Reiner A Veitia

Reiner A Veitia

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Reiner A Veitia

Reiner A Veitia

Publications by authors named "Reiner A Veitia"

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Insights into the loss of the Y chromosome with age in control individuals and in patients with age-related macular degeneration using genotyping microarray data.

Hum Genet 2020 Mar 27;139(3):401-407. Epub 2019 May 27.

Institut Jacques Monod, Université Paris Diderot, 15 rue Hélène Brion, 75013, Paris, France.

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http://dx.doi.org/10.1007/s00439-019-02029-1DOI Listing
March 2020

Special issue on "Molecular genetics of aging and longevity": a critical time in the field of geroscience.

Hum Genet 2020 Mar;139(3):275-276

Institut Jacques Monod, CNRS UMR7592, Université de Paris, Paris, France.

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http://dx.doi.org/10.1007/s00439-020-02125-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041886PMC
March 2020

Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysis.

FASEB J 2020 Jan 25;34(1):571-587. Epub 2019 Nov 25.

Institut Jacques Monod, CNRS UMR7592, Université de Paris, Paris, France.

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http://dx.doi.org/10.1096/fj.201901573RDOI Listing
January 2020

The Gene Balance Hypothesis: Epigenetics and Dosage Effects in Plants.

Methods Mol Biol 2020 ;2093:161-171

Division of Biological Sciences, University of Missouri, Columbia, MO, USA.

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http://dx.doi.org/10.1007/978-1-0716-0179-2_12DOI Listing
January 2020

MIRAGE Syndrome: Phenotypic Rescue by Somatic Mutation and Selection.

Authors:
Reiner A Veitia

Trends Mol Med 2019 Nov 14;25(11):937-940. Epub 2019 Oct 14.

Institut Jacques Monod, Université Paris Diderot, Paris, France; Université Paris-Diderot, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.molmed.2019.08.008DOI Listing
November 2019

Causes and effects of haploinsufficiency.

Biol Rev Camb Philos Soc 2019 10 31;94(5):1774-1785. Epub 2019 May 31.

Institut Jacques Monod, Université de Paris, Paris, 75205, France.

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http://dx.doi.org/10.1111/brv.12527DOI Listing
October 2019

AFF3: a new player in maintaining XIST monoallelic expression.

Authors:
Reiner A Veitia

J Mol Cell Biol 2019 Sep;11(9):723-724

Institut Jacques Monod, Université Paris Diderot, Paris, France.

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http://dx.doi.org/10.1093/jmcb/mjy082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821381PMC
September 2019

Darwinian selection within an individual or somatic selection: facts and models.

Authors:
Reiner A Veitia

J Mol Cell Biol 2019 Aug;11(8):719-722

Institut Jacques Monod, Université Paris Diderot, 75013 Paris, France.

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http://dx.doi.org/10.1093/jmcb/mjz014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788724PMC
August 2019

DNA Content, Cell Size, and Cell Senescence.

Authors:
Reiner A Veitia

Trends Biochem Sci 2019 Aug 31;44(8):645-647. Epub 2019 May 31.

Institut Jacques Monod, Université Paris Diderot, Paris, France; Université Paris-Diderot, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.tibs.2019.04.013DOI Listing
August 2019

Further quantitative insights into the decrease of heteroplasmy of m.3243A>G with age in leukocytes.

Authors:
Reiner A Veitia

Clin Genet 2019 04 28;95(4):542-543. Epub 2019 Jan 28.

Institut Jacques Monod, Université Paris Diderot, Paris, France.

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http://doi.wiley.com/10.1111/cge.13496
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http://dx.doi.org/10.1111/cge.13496DOI Listing
April 2019

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

EBioMedicine 2019 Apr 15;42:524-531. Epub 2019 Apr 15.

Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France; Université Paris Diderot-Paris 7, 75205 Paris Cedex 13, France. Electronic address:

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http://dx.doi.org/10.1016/j.ebiom.2019.03.075DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491878PMC
April 2019

Genomic Balance and Speciation.

Epigenet Insights 2019 31;12:2516865719840291. Epub 2019 Mar 31.

Institut Jacques Monod, Universite Paris Diderot, Paris, France.

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http://dx.doi.org/10.1177/2516865719840291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444768PMC
March 2019

On the loss of human sex chromosomes in lymphocytes with age: a quantitative treatment.

Authors:
Reiner A Veitia

Eur J Hum Genet 2018 12 10;26(12):1875-1878. Epub 2018 Aug 10.

Institut Jacques Monod, Université Paris Diderot, Paris, France.

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http://dx.doi.org/10.1038/s41431-018-0225-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244361PMC
December 2018

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.

Trends Endocrinol Metab 2018 06 26;29(6):400-419. Epub 2018 Apr 26.

Medical Faculty, Univ. Paris Sud and Paris Saclay, Bicetre Hospital 94275, Le Kremlin Bicêtre, France. Electronic address:

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http://dx.doi.org/10.1016/j.tem.2018.03.010DOI Listing
June 2018

Dosage effects in morphogenetic gradients of transcription factors: insights from a simple mathematical model.

Authors:
Reiner A Veitia

J Genet 2018 Jun;97(2):365-370

Institut Jacques Monod, Université Paris-Diderot, 75013 Paris, France.

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June 2018

Gene Expression Dominance in Allopolyploids: Hypotheses and Models.

Trends Plant Sci 2018 05 9;23(5):393-402. Epub 2018 Feb 9.

Université Paris Diderot-Paris VII, 75205 Paris Cedex 13, France; Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France. Electronic address:

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http://dx.doi.org/10.1016/j.tplants.2018.01.002DOI Listing
May 2018

How the most common mitochondrial DNA mutation (m.3243A>G) vanishes from leukocytes: a mathematical model.

Authors:
Reiner A Veitia

Hum Mol Genet 2018 05;27(9):1565-1571

Institut Jacques Monod, Université Paris Diderot, Paris, France.

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http://dx.doi.org/10.1093/hmg/ddy063DOI Listing
May 2018

Natural and molecular history of prolactinoma: insights from a mouse model.

Oncotarget 2018 Jan 27;9(5):6144-6155. Epub 2017 Dec 27.

Unité INSERM 1185, Faculté de Médecine Paris Sud, Université Paris-Saclay, le Kremlin-Bicêtre, France.

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http://www.oncotarget.com/fulltext/23713
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http://dx.doi.org/10.18632/oncotarget.23713DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814201PMC
January 2018

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.

Clin Endocrinol (Oxf) 2017 Nov 13;87(5):539-544. Epub 2017 Aug 13.

Université Paris Diderot, Sorbonne Paris Cité, Paris, France.

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http://dx.doi.org/10.1111/cen.13420DOI Listing
November 2017

Gene Duplicates: Agents of Fragility? - A Reply to Landry and Diss.

Authors:
Reiner A Veitia

Trends Genet 2017 10 17;33(10):658-660. Epub 2017 Aug 17.

Institut Jacques Monod, Université Paris Diderot, Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche 7592, Paris 75013, France; Université Paris Diderot-Paris VII, 75205 Paris CEDEX 13, France. Electronic address:

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http://dx.doi.org/10.1016/j.tig.2017.07.013DOI Listing
October 2017

A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.

Hum Mol Genet 2017 08;26(16):3161-3166

Center For Research in Genetics and Genomics-CIGGUR, GENIUROS Research Group, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.

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http://dx.doi.org/10.1093/hmg/ddx199DOI Listing
August 2017

Gene Duplicates: Agents of Robustness or Fragility?

Authors:
Reiner A Veitia

Trends Genet 2017 06 20;33(6):377-379. Epub 2017 Apr 20.

Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France; Université Paris Diderot-Paris VII, 75205 Paris Cedex 13, France. Electronic address:

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http://dx.doi.org/10.1016/j.tig.2017.03.006DOI Listing
June 2017

Hill function-based models of transcriptional switches: impact of specific, nonspecific, functional and nonfunctional binding.

Biol Rev Camb Philos Soc 2017 May 8;92(2):953-963. Epub 2016 Apr 8.

Université Paris Diderot, Sorbonne Paris Cité, 75013 Paris, France.

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http://dx.doi.org/10.1111/brv.12262DOI Listing
May 2017

A homozygous mutation of in a familial case diagnosed with polycystic ovary syndrome.

Eur J Endocrinol 2017 May;176(5):K9-K14

Institut Jacques MonodUniversité Paris Diderot, Paris, France.

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http://dx.doi.org/10.1530/EJE-16-0968DOI Listing
May 2017

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.

Genet Med 2017 04 4;19(4):367-376. Epub 2016 Aug 4.

Department of Pediatrics, Division of Pediatric Endocrinology, Ghent University Hospital and Ghent University, Ghent, Belgium.

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http://dx.doi.org/10.1038/gim.2016.118DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392598PMC
April 2017

Aging: Somatic Mutations, Epigenetic Drift and Gene Dosage Imbalance.

Trends Cell Biol 2017 04 9;27(4):299-310. Epub 2016 Dec 9.

Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.

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http://dx.doi.org/10.1016/j.tcb.2016.11.006DOI Listing
April 2017

A Fresh Look at 'Aging' Proteins.

Authors:
Reiner A Veitia

Trends Biochem Sci 2017 02 14;42(2):86-89. Epub 2016 Nov 14.

Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France; Université Paris Diderot-Paris VII, 75205 Paris Cedex 13, France. Electronic address:

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http://dx.doi.org/10.1016/j.tibs.2016.11.001DOI Listing
February 2017

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.

J Clin Endocrinol Metab 2016 12 7;101(12):4541-4550. Epub 2016 Sep 7.

Inserm 1185 (J.B., I.B., S.B., J.F., J.Y., N.B.), Le Kremlin-Bicêtre, Université Paris-Saclay, Faculté de Médecine Paris Sud, 94270 Le Kremlin-Bicêtre, France; Service de Biochimie et Génétique Moléculaire (K.A., C.B., C.D.), Hôpital Cochin, AP-HP, Université Paris-Descartes, 75004 Paris, France; Service d'Endocrinologie-Diabète-Nutrition (A.F., B.D.), CHU de Reims-Hôpital Robert-Debré, 51100 Reims, France; Institut Jacques Monod (A.L.T., R.A.V.), Université Paris Diderot-PARIS 7/CNRS UMR7592, 75013 Paris, France; and Service d'Endocrinologie et des Maladies de la Reproduction (J.Y.), APHP, Hôpital de Bicêtre, 94270 Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1210/jc.2016-2152DOI Listing
December 2016

The transcription factor FOXL2 in ovarian function and dysfunction.

Folia Histochem Cytobiol 2009 ;47(5):S43-9

Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.2478/v10042-009-0062-7DOI Listing
April 2016

Kinetics genetics: Incorporating the concept of genomic balance into an understanding of quantitative traits.

Plant Sci 2016 Apr 6;245:128-34. Epub 2016 Feb 6.

Institut Jacques Monod, 15 rue Helene Brion, 75013 Paris, France; Universite Paris Diderot, Paris, France.

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http://dx.doi.org/10.1016/j.plantsci.2016.02.002DOI Listing
April 2016

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Hum Mol Genet 2015 Dec 11;24(23):6687-98. Epub 2015 Sep 11.

Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France, Faculty of Biological Sciences, Université Paris Diderot-Paris VII, 75205 Paris, France,

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http://dx.doi.org/10.1093/hmg/ddv373DOI Listing
December 2015

Models of buffering of dosage imbalances in protein complexes.

Biol Direct 2015 Aug 15;10:42. Epub 2015 Aug 15.

University of Missouri, Division of Biological Sciences, Columbia, MO, 65211, USA.

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http://dx.doi.org/10.1186/s13062-015-0063-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537584PMC
August 2015

Gene dosage imbalances: action, reaction, and models.

Trends Biochem Sci 2015 Jun 27;40(6):309-17. Epub 2015 Apr 27.

Sorbonne Universités, Université Pierre et Marie Curie (UPMC), Université Paris 06, Institut National de la Santé et de la Recherche Médicale (INSERM) and Centre National de la Recherche Scientifique (CNRS) Unités de Recherche U75, U1127, U7225, and Institut du Cerveau et de la Moelle Épinière (ICM), 75013 Paris, France.

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http://dx.doi.org/10.1016/j.tibs.2015.03.011DOI Listing
June 2015

A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors.

EBioMedicine 2015 May 6;2(5):421-31. Epub 2015 Mar 6.

Institut Jacques Monod, Université Paris Diderot, CNRS UMR7592, Paris 75013, France ; Université Paris Diderot-Paris VII, 75205 Paris Cedex 13, France.

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http://dx.doi.org/10.1016/j.ebiom.2015.03.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485906PMC
May 2015

Synthetic lethals in HIV: ways to avoid drug resistance : Running title: Preventing HIV resistance.

Biol Direct 2015 Apr 17;10:17. Epub 2015 Apr 17.

Univ Paris Diderot, Sorbonne Paris Cité, F-75013, Paris, France.

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http://dx.doi.org/10.1186/s13062-015-0044-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399722PMC
April 2015

X chromosome inactivation and active X upregulation in therian mammals: facts, questions, and hypotheses.

J Mol Cell Biol 2015 Feb 6;7(1):2-11. Epub 2015 Jan 6.

Division of Biological Sciences, University of Missouri, Columbia, MO, USA.

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http://dx.doi.org/10.1093/jmcb/mjv001DOI Listing
February 2015

FOXL2, GATA4, and SMAD3 co-operatively modulate gene expression, cell viability and apoptosis in ovarian granulosa cell tumor cells.

PLoS One 2014 9;9(1):e85545. Epub 2014 Jan 9.

Children's Hospital, Pediatric Research Center, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland ; Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085545PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887065PMC
September 2014

The Gene Balance Hypothesis: dosage effects in plants.

Methods Mol Biol 2014 ;1112:25-32

Division of Biological Sciences, University of Missouri, Columbia, MO, USA.

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http://dx.doi.org/10.1007/978-1-62703-773-0_2DOI Listing
September 2014

STAG3 is a strong candidate gene for male infertility.

Hum Mol Genet 2014 Jul 7;23(13):3421-31. Epub 2014 Mar 7.

Instituto de Biología Molecular y Celular del Cáncer (CSIC-USAL), 37007 Salamanca, Spain

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http://dx.doi.org/10.1093/hmg/ddu051DOI Listing
July 2014

Transcription factors: specific DNA binding and specific gene regulation.

Trends Genet 2014 Jun 26;30(6):211-9. Epub 2014 Apr 26.

Institut Jacques Monod, Paris, France; Université Paris Diderot, Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.tig.2014.04.002DOI Listing
June 2014

Of adrenaline and SRY in males (comment on DOI 10.1002/bies.201100159).

Authors:
Reiner A Veitia

Bioessays 2014 May 7;36(5):438. Epub 2014 Mar 7.

CNRS UMR7592, Institut Jacques Monod, Paris, France; Université Paris Diderot, Paris VII, Paris, France.

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http://dx.doi.org/10.1002/bies.201400026DOI Listing
May 2014

NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis.

J Mol Cell Biol 2014 Apr 11;6(2):175-7. Epub 2014 Mar 11.

Inserm U693, Le Kremlin-Bicêtre, F-94276, France.

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http://dx.doi.org/10.1093/jmcb/mju006DOI Listing
April 2014

Mutant cohesin in premature ovarian failure.

N Engl J Med 2014 Mar;370(10):943-949

Institut Jacques Monod, Université Paris Diderot (S.C., M.F., R.A.V.), and Institut Cochin, Université Paris Descartes, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, INSERM (D.V., M.F.) - both in Paris; the Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles (V.A.A., E.V.); Departamento de Fisiología y Farmacología, Universidad de Salamanca (E.L.), and Instituto de Biología Molecular y Celular del Cáncer (E.L., I.G.-T., A.M.P.) - both in Salaman ca, Spain; the Department of Molecular Cellular Biology, Baylor College of Medicine, Houston (P.A.O., K.O., W.H.); Centro de In vestigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid (J.L.B.); and the Department of Genetics, Hadassah University Hospital, Jerusalem (Z.B.-N.).

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http://dx.doi.org/10.1056/NEJMoa1309635DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4068824PMC
March 2014

FOXL2: a central transcription factor of the ovary.

J Mol Endocrinol 2014 Feb 19;52(1):R17-33. Epub 2013 Dec 19.

CNRS UMR 7592, Institut Jacques Monod, 15 Rue Hélène Brion, 75013 Paris, France Université Paris Diderot, Paris VII, Paris, France.

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http://dx.doi.org/10.1530/JME-13-0159DOI Listing
February 2014

Dominance and interloci interactions in transcriptional activation cascades: models explaining compensatory mutations and inheritance patterns.

Bioessays 2014 Jan 18;36(1):84-92. Epub 2013 Nov 18.

Université Paris-Sud, IGM, UMR8621, Orsay, France; CNRS, Orsay, France.

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http://dx.doi.org/10.1002/bies.201300109DOI Listing
January 2014

Why preeclampsia still exists?

Med Hypotheses 2013 Aug 10;81(2):259-63. Epub 2013 May 10.

INSERM u1016, Institut Cochin, Paris, France; CNRS, UMR8104, Paris, France.

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http://dx.doi.org/10.1016/j.mehy.2013.04.034DOI Listing
August 2013

The transience of transient overexpression.

Nat Methods 2013 Aug;10(8):715-21

Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.

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http://dx.doi.org/10.1038/nmeth.2534DOI Listing
August 2013

Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation.

Trends Genet 2013 Jul 17;29(7):385-93. Epub 2013 May 17.

Centre national de la recherche Scientifique, UMR7592, Institut Jacques Monod, Paris, France.

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http://dx.doi.org/10.1016/j.tig.2013.04.004DOI Listing
July 2013

The transcription factor encyclopedia.

Authors:
Dimas Yusuf Stefanie L Butland Magdalena I Swanson Eugene Bolotin Amy Ticoll Warren A Cheung Xiao Yu Cindy Zhang Christopher T D Dickman Debra L Fulton Jonathan S Lim Jake M Schnabl Oscar H P Ramos Mireille Vasseur-Cognet Charles N de Leeuw Elizabeth M Simpson Gerhart U Ryffel Eric W-F Lam Ralf Kist Miranda S C Wilson Raquel Marco-Ferreres Jan J Brosens Leonardo L Beccari Paola Bovolenta Bérénice A Benayoun Lara J Monteiro Helma D C Schwenen Lars Grontved Elizabeth Wederell Susanne Mandrup Reiner A Veitia Harini Chakravarthy Pamela A Hoodless M Michela Mancarelli Bruce E Torbett Alison H Banham Sekhar P Reddy Rebecca L Cullum Michaela Liedtke Mario P Tschan Michelle Vaz Angie Rizzino Mariastella Zannini Seth Frietze Peggy J Farnham Astrid Eijkelenboom Philip J Brown David Laperrière Dominique Leprince Tiziana de Cristofaro Kelly L Prince Marrit Putker Luis del Peso Gieri Camenisch Roland H Wenger Michal Mikula Marieke Rozendaal Sylvie Mader Jerzy Ostrowski Simon J Rhodes Capucine Van Rechem Gaylor Boulay Sam W Z Olechnowicz Mary B Breslin Michael S Lan Kyster K Nanan Michael Wegner Juan Hou Rachel D Mullen Stephanie C Colvin Peter John Noy Carol F Webb Matthew E Witek Scott Ferrell Juliet M Daniel Jason Park Scott A Waldman Daniel J Peet Michael Taggart Padma-Sheela Jayaraman Julien J Karrich Bianca Blom Farhad Vesuna Henriette O'Geen Yunfu Sun Richard M Gronostajski Mark W Woodcroft Margaret R Hough Edwin Chen G Nicholas Europe-Finner Magdalena Karolczak-Bayatti Jarrod Bailey Oliver Hankinson Venu Raman David P LeBrun Shyam Biswal Christopher J Harvey Jason P DeBruyne John B Hogenesch Robert F Hevner Christophe Héligon Xin M Luo Marissa Cathleen Blank Kathleen Joyce Millen David S Sharlin Douglas Forrest Karin Dahlman-Wright Chunyan Zhao Yuriko Mishima Satrajit Sinha Rumela Chakrabarti Elodie Portales-Casamar Frances M Sladek Philip H Bradley Wyeth W Wasserman

Genome Biol 2012 ;13(3):R24

Department of Medical Genetics, Faculty of Medicine, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, Canada.

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http://digital.csic.es/bitstream/10261/53044/2/gb-2012-13-3-
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http://genomebiology.com/2012/13/3/R24
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http://dx.doi.org/10.1186/gb-2012-13-3-r24DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439975PMC
September 2012

Gene balance hypothesis: connecting issues of dosage sensitivity across biological disciplines.

Proc Natl Acad Sci U S A 2012 Sep 20;109(37):14746-53. Epub 2012 Aug 20.

Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.

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http://dx.doi.org/10.1073/pnas.1207726109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443177PMC
September 2012

Protein-Protein and Protein-DNA Dosage Balance and Differential Paralog Transcription Factor Retention in Polyploids.

Front Plant Sci 2011 11;2:64. Epub 2011 Oct 11.

Division of Biological Sciences, University of Missouri Columbia, MO, USA.

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http://dx.doi.org/10.3389/fpls.2011.00064DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355771PMC
August 2012

Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles.

Hum Mol Genet 2012 Jul 27;21(14):3264-74. Epub 2012 Apr 27.

Institut Jacques Monod, UMR 7592 CNRS-Université Paris Diderot, Paris 75205, France.

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http://dx.doi.org/10.1093/hmg/dds170DOI Listing
July 2012

The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology.

Mol Cell Endocrinol 2012 Jun 8;356(1-2):55-64. Epub 2011 Jul 8.

CNRS UMR 7592, Institut Jacques Monod, Equipe Génétique et Génomique du Développement Gonadique, 75205 Paris Cedex 13, France.

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http://dx.doi.org/10.1016/j.mce.2011.06.019DOI Listing
June 2012

Dynamics of the subcellular localization of RalBP1/RLIP through the cell cycle: the role of targeting signals and of protein-protein interactions.

FASEB J 2012 May 8;26(5):2164-74. Epub 2012 Feb 8.

Mécanismes Moléculaires du Développement, Institut Jacques Monod, CNRS, UMR 7592, Université Paris Diderot, Sorbonne Paris Cité. 15, rue Hélène Brion. 75205 Paris, France.

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http://dx.doi.org/10.1096/fj.11-196451DOI Listing
May 2012

A regulatory domain is required for Foxn4 activity during retinogenesis.

J Mol Neurosci 2012 Feb 24;46(2):315-23. Epub 2011 Jun 24.

Centre de Recherche des Cordeliers, INSERM UMR S872, 15, Rue de L'Ecole de Médecine, 75006, Paris, France.

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http://link.springer.com/10.1007/s12031-011-9585-4
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http://dx.doi.org/10.1007/s12031-011-9585-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518883PMC
February 2012

Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.

Hum Mol Genet 2011 Jul 19;20(13):2642-50. Epub 2011 Apr 19.

Evolution des Régulations Endocriniennes, CNRS UMR 7221, Muséum National d'Histoire Naturelle, Paris, France.

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http://dx.doi.org/10.1093/hmg/ddr166DOI Listing
July 2011

Forkhead transcription factors: key players in health and disease.

Trends Genet 2011 Jun 18;27(6):224-32. Epub 2011 Apr 18.

CNRS UMR 7592, Institut Jacques Monod, Equipe Génétique et Génomique du Développement Gonadique, 75205 Paris Cedex 13, France.

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http://dx.doi.org/10.1016/j.tig.2011.03.003DOI Listing
June 2011

Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.

Hum Mol Genet 2011 May 2;20(9):1673-86. Epub 2011 Feb 2.

CNRS UMR 7592, Institut Jacques Monod, Equipe Génétique et Génomique du Développement Gonadique 75205 Paris Cedex 13, France.

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http://dx.doi.org/10.1093/hmg/ddr042DOI Listing
May 2011

Exploring the mechanistic bases of heterosis from the perspective of macromolecular complexes.

FASEB J 2011 Feb 9;25(2):476-82. Epub 2010 Nov 9.

Institut Jacques Monod, CNRS-UMR 7592, Bâtiment Buffon, 15 Rue Hélène Brion, Paris Cedex 13, France.

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http://dx.doi.org/10.1096/fj.10-170639DOI Listing
February 2011

Heterosis.

Plant Cell 2010 Jul 9;22(7):2105-12. Epub 2010 Jul 9.

Division of Biological Sciences, University of Missouri, Columbia, Missouri 65211, USA.

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http://www.plantcell.org/cgi/doi/10.1105/tpc.110.076133
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929104PMC
July 2010

FOXL2: at the crossroads of female sex determination and ovarian function.

Adv Exp Med Biol 2009 ;665:207-26

Institut Jacques Monod, Bâtiment Buffon, 15 rue Hélèna Brion, 75205 Paris Cx 13, France.

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http://dx.doi.org/10.1007/978-1-4419-1599-3_16DOI Listing
May 2010

FOXL2 versus SOX9: a lifelong "battle of the sexes".

Authors:
Reiner A Veitia

Bioessays 2010 May;32(5):375-80

Institut Jacques Monod, CNRS-UMR 7592, Bâtiment Buffon, Paris Cedex, France.

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http://dx.doi.org/10.1002/bies.200900193DOI Listing
May 2010

The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution.

New Phytol 2010 Apr 19;186(1):54-62. Epub 2009 Nov 19.

Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.

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http://dx.doi.org/10.1111/j.1469-8137.2009.03087.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858765PMC
April 2010

A generalized model of gene dosage and dominant negative effects in macromolecular complexes.

Authors:
Reiner A Veitia

FASEB J 2010 Apr 9;24(4):994-1002. Epub 2009 Dec 9.

Institut Jacques Monod, Unité Mixte de Recherche 7592, Centre National de la Recherche Scientifique, and Université Paris-Diderot/Paris 7, Paris, France.

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http://dx.doi.org/10.1096/fj.09-146969DOI Listing
April 2010

BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

Clin Endocrinol (Oxf) 2010 Mar 8;72(3):425-6. Epub 2009 Jun 8.

Department of Cytogenetics and Reproductive Biology, Farhat Hached University Teaching Hospital, Sousse, Tunisia.

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http://dx.doi.org/10.1111/j.1365-2265.2009.03651.xDOI Listing
March 2010

Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?

FASEB J 2010 Feb 17;24(2):346-56. Epub 2009 Sep 17.

Unité Mixte de Recherche 7592-Centre National de la Recherche Scientifique, Institut Jacques Monod, Paris, France.

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http://dx.doi.org/10.1096/fj.09-142117DOI Listing
February 2010

The forkhead factor FOXL2: a novel tumor suppressor?

Biochim Biophys Acta 2010 Jan 10;1805(1):1-5. Epub 2009 Sep 10.

Institut Jacques Monod, UMR 7592-CNRS, 15 rue Hélène Brion, Paris, France.

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http://dx.doi.org/10.1016/j.bbcan.2009.09.002DOI Listing
January 2010

Dominance and gene dosage balance in health and disease: why levels matter!

J Pathol 2010 Jan;220(2):174-85

Institut Jacques Monod, CNRS-UMR 7592, Bâtiment Buffon, Paris Cedex 13, France.

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http://dx.doi.org/10.1002/path.2623DOI Listing
January 2010

Whole genome duplications and a 'function' for junk DNA? Facts and hypotheses.

PLoS One 2009 Dec 14;4(12):e8201. Epub 2009 Dec 14.

CNRS-UMR 7592, Institut Jacques Monod, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0008201PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788606PMC
December 2009

Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.

Hum Mol Genet 2009 Sep 10;18(17):3324-33. Epub 2009 Jun 10.

UMR7592-CNRS, Institut Jacques Monod, 75013 Paris, France.

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http://dx.doi.org/10.1093/hmg/ddp273DOI Listing
September 2009

Dominant negative factors in health and disease.

Authors:
Reiner A Veitia

J Pathol 2009 Aug;218(4):409-18

Institut Jacques Monod, CNRS-UMR 7592, Bâtiment Buffon, 15 Rue Hélène Brion, Paris Cedex 13, France.

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http://dx.doi.org/10.1002/path.2583DOI Listing
August 2009

The new molecular biology of granulosa cell tumors of the ovary.

Genome Med 2009 Aug 25;1(8):81. Epub 2009 Aug 25.

Service d'Hormonologie, Hôpital Lapeyronie, CHU Montpellier et UM1, Montpellier, France.

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http://dx.doi.org/10.1186/gm81DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768967PMC
August 2009

A post-translational modification code for transcription factors: sorting through a sea of signals.

Trends Cell Biol 2009 May 26;19(5):189-97. Epub 2009 Mar 26.

Institut Jacques Monod, Bâtiment Buffon, 15 Rue Hélène Brion, Paris Cedex 13, France.

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http://dx.doi.org/10.1016/j.tcb.2009.02.003DOI Listing
May 2009

Gene expression regulation in the context of mouse interspecific mosaic genomes.

Genome Biol 2008 27;9(8):R133. Epub 2008 Aug 27.

U567 Department of Genetics and Development, Institut Cochin, INSERM, 24 rue du Faubourg St Jacques, Paris, 75014, France.

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http://dx.doi.org/10.1186/gb-2008-9-8-r133DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575523PMC
December 2008

One thousand and one ways of making functionally similar transcriptional enhancers.

Authors:
Reiner A Veitia

Bioessays 2008 Nov;30(11-12):1052-7

Institut Cochin, Département de Génétique et Développement, Inserm, Université Paris, France.

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http://dx.doi.org/10.1002/bies.20849DOI Listing
November 2008

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.

Hum Mol Genet 2008 Oct 16;17(20):3118-27. Epub 2008 Jul 16.

INSERM U567, Team 21, Département de Génétique et Développement, Institut Cochin 75014, Paris, France.

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http://dx.doi.org/10.1093/hmg/ddn209DOI Listing
October 2008

Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.

Hum Mutat 2008 Aug;29(8):E123-31

Department of Genetics, Dr. G.Venkataswamy Eye Research Institute, Aravind Medical Research Foundation, Aravind Eye Hospital, Madurai 625020, India.

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http://dx.doi.org/10.1002/humu.20809DOI Listing
August 2008

Cellular reactions to gene dosage imbalance: genomic, transcriptomic and proteomic effects.

Trends Genet 2008 Aug 26;24(8):390-7. Epub 2008 Jun 26.

INSERM U567, Team21 Genomics and Epigenetics of Placental Diseases, Genetics and Development Department, Institut Cochin, 75014 Paris, France.

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http://dx.doi.org/10.1016/j.tig.2008.05.005DOI Listing
August 2008

The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways.

Proteomics 2008 Aug;8(15):3118-23

INSERM U567, Team21, Genetics and Development Department, Institut Cochin, Paris, France.

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http://dx.doi.org/10.1002/pmic.200800084DOI Listing
August 2008

Preservation of genes involved in sterol metabolism in cholesterol auxotrophs: facts and hypotheses.

PLoS One 2008 Aug 6;3(8):e2883. Epub 2008 Aug 6.

Département de Génétique et Développement Inserm, Faculté de Médecine Paris Descartes, Institut Cochin, U567, CNRS, UMR 8104, Université Paris 5, UM 3, Paris, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0002883PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2478713PMC
August 2008

Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.

Arch Ophthalmol 2008 May;126(5):700-8

Department of Genetics, Dr. G. Venkataswamy Eye Research Institute, Aravind Medical Research Foundation, Madurai, India.

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http://dx.doi.org/10.1001/archopht.126.5.700DOI Listing
May 2008

Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development.

Hum Mol Genet 2008 Apr 24;17(7):1010-9. Epub 2007 Dec 24.

Department of Genetics and Development, INSERM U567, Team21 Genomics and Epigenetics of Placental Diseases, Paris, France.

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http://dx.doi.org/10.1093/hmg/ddm373DOI Listing
April 2008

Recent advances in the study of genes involved in non-syndromic premature ovarian failure.

Mol Cell Endocrinol 2008 Jan 19;282(1-2):101-11. Epub 2007 Nov 19.

Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France; Inserm, U567 Paris, France.

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http://dx.doi.org/10.1016/j.mce.2007.11.005DOI Listing
January 2008

Exploring the molecular etiology of dominant-negative mutations.

Authors:
Reiner A Veitia

Plant Cell 2007 Dec 14;19(12):3843-51. Epub 2007 Dec 14.

Université Denis Diderot/Paris VII (Unité de Formation et de Recherche/Department of Biology), 75005 Paris, France.

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http://dx.doi.org/10.1105/tpc.107.055053DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217636PMC
December 2007