Martine Vaxillaire

Martine Vaxillaire

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Martine Vaxillaire

Martine Vaxillaire

Publications by authors named "Martine Vaxillaire"

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67Publications

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How Recent Advances in Genomics Improve Precision Diagnosis and Personalized Care of Maturity-Onset Diabetes of the Young.

Curr Diab Rep 2019 Aug 5;19(9):79. Epub 2019 Aug 5.

Univ. Lille, CNRS, CHU Lille, Institut Pasteur de Lille, UMR 8199 - European Genomic Institute for Diabetes (EGID), University Lille, F-59000, Lille, France.

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http://dx.doi.org/10.1007/s11892-019-1202-xDOI Listing
August 2019

The unique clinical spectrum of maturity onset diabetes of the young type 3.

Diabetes Res Clin Pract 2018 Jan 28;135:18-22. Epub 2017 Oct 28.

The Jesse Z. and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva 49202, Israel; Felsenstein Medical Research Center, Petah Tikva 49100, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

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http://dx.doi.org/10.1016/j.diabres.2017.10.024DOI Listing
January 2018

Monogenic diabetes: Implementation of translational genomic research towards precision medicine.

J Diabetes 2016 Nov 7;8(6):782-795. Epub 2016 Sep 7.

CNRS-UMR 8199, Integrative Genomics and Modelling of Metabolic Diseases, Pasteur Institute of Lille, Lille, France.

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http://dx.doi.org/10.1111/1753-0407.12446DOI Listing
November 2016

Impact of statistical models on the prediction of type 2 diabetes using non-targeted metabolomics profiling.

Mol Metab 2016 Oct 23;5(10):918-925. Epub 2016 Aug 23.

CNRS UMR8199, Pasteur Institute of Lille, Lille, France; European Genomic Institute for Diabetes (EGID), FR-3508, Lille, France; Lille University, France; Department of Genomics of Common Disease, School of Public Health, Imperial College London, Hammersmith Hospital, London, UK. Electronic address:

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034686PMC
http://dx.doi.org/10.1016/j.molmet.2016.08.011DOI Listing
October 2016

Comment on Beltrand et al. Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations. Diabetes Care 2015;38:2033-2041.

Diabetes Care 2016 09;39(9):e153-4

UMR 8199-European Genomic Institute for Diabetes, University of Lille, Lille, France CNRS UMR 8199, Lille, France Institut Pasteur de Lille, Lille, France Department of Endocrinology, Diabetology and Metabolism, Centre Hospitalier Régional Universitaire de Lille, Lille, France Department of Genomics of Common Disease, School of Public Health and Hammersmith Hospital, Imperial College London, London, U.K.

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http://dx.doi.org/10.2337/dc15-2703DOI Listing
September 2016

The lessons of early-onset monogenic diabetes for the understanding of diabetes pathogenesis.

Best Pract Res Clin Endocrinol Metab 2012 Apr;26(2):171-87

Centre National de la Recherche Scientifique UMR, Genomics and Metabolic Diseases, Lille Pasteur Institute, Lille Nord de France University, France.

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http://dx.doi.org/10.1016/j.beem.2011.12.001DOI Listing
April 2012

Human mutation within Per-Arnt-Sim (PAS) domain-containing protein kinase (PASK) causes basal insulin hypersecretion.

J Biol Chem 2011 Dec 7;286(51):44005-14. Epub 2011 Nov 7.

Department of Medicine, Section of Cell Biology, Division of Diabetes Endocrinology and Metabolism, School of Public Health, Imperial College London, London, UK.

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http://dx.doi.org/10.1074/jbc.M111.254995DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243507PMC
December 2011

Mechanism of KATP hyperactivity and sulfonylurea tolerance due to a diabetogenic mutation in L0 helix of sulfonylurea receptor 1 (ABCC8).

FEBS Lett 2011 Nov 19;585(22):3555-9. Epub 2011 Oct 19.

Pacific Northwest Research Institute, University of Washington Diabetes Endocrinology Research Center, Seattle, WA 98122, United States.

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http://dx.doi.org/10.1016/j.febslet.2011.10.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215797PMC
November 2011

Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations.

Pediatr Diabetes 2011 May 9;12(3 Pt 2):266-9. Epub 2011 Jan 9.

Department of Pediatrics, Second Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.

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http://dx.doi.org/10.1111/j.1399-5448.2010.00719.xDOI Listing
May 2011

The emerging genetics of type 2 diabetes.

Trends Mol Med 2010 Sep 20;16(9):407-16. Epub 2010 Aug 20.

Univ Lille Nord de France, F-59000 Lille, France.

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http://linkinghub.elsevier.com/retrieve/pii/S147149141000097
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http://dx.doi.org/10.1016/j.molmed.2010.06.004DOI Listing
September 2010

Study of TNFalpha -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population.

Clin Biochem 2010 Apr 2;43(6):549-52. Epub 2010 Feb 2.

Laboratory of Genetics, Immunology and Human Pathologies, Faculty of Sciences of Tunis, 2092 Tunis, Tunisia.

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http://dx.doi.org/10.1016/j.clinbiochem.2010.01.008DOI Listing
April 2010

Monogenic forms of diabetes mellitus: an update.

Endocrinol Nutr 2009 Dec;56S4:26-29

Genomics and Molecular Physiology of Metabolic Diseases. CNRS UMR8090. Lille Institute of Biology. Lille. France.

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http://dx.doi.org/10.1016/S1575-0922(09)73513-2DOI Listing
December 2009

Monogenic forms of diabetes mellitus: an update.

Endocrinol Nutr 2009 Dec;56 Suppl 4:26-9

Genomics and Molecular Physiology of Metabolic Diseases, CNRS UMR8090, Lille Institute of Biology, Lille, France.

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December 2009

Breakthroughs in monogenic diabetes genetics: from pediatric forms to young adulthood diabetes.

Pediatr Endocrinol Rev 2009 Mar;6(3):405-17

CNRS UMR 8090, Institute of Biology & Pasteur Institute, Lille, France.

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March 2009

Neonatal diabetes mellitus because of pancreatic agenesis with dysmorphic features and recurrent bacterial infections.

Pediatr Diabetes 2008 Jun;9(3 Pt 1):240-4

Division of Pediatric Endocrinology, Department of Pediatrics, King Faisal Specialist Hospital and Research Centre - Jeddah, Jeddah, Saudi Arabia.

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http://doi.wiley.com/10.1111/j.1399-5448.2007.00365.x
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http://dx.doi.org/10.1111/j.1399-5448.2007.00365.xDOI Listing
June 2008

Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes.

Endocr Rev 2008 May 24;29(3):254-64. Epub 2008 Apr 24.

Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8090, Institute of Biology and Pasteur Institute, Lille, France.

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https://academic.oup.com/edrv/article-lookup/doi/10.1210/er.
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http://dx.doi.org/10.1210/er.2007-0024DOI Listing
May 2008

Neonatal hyperglycaemia and abnormal development of the pancreas.

Best Pract Res Clin Endocrinol Metab 2008 Feb;22(1):17-40

Clinique des Maladies du Développement, Unité d'Endocrinologie, Diabétologie et Gynécologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, France.

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http://dx.doi.org/10.1016/j.beem.2007.08.003DOI Listing
February 2008

Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study.

Diabetes 2008 Jan 31;57(1):244-54. Epub 2007 Oct 31.

UMR8090 and Institute of Biology, Lille 2 University, CNRS and Pasteur Institute, Lille, France.

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http://dx.doi.org/10.2337/db07-0615DOI Listing
January 2008

Diabetes in very young children and mutations in the insulin-secreting cell potassium channel genes: therapeutic consequences.

Endocr Dev 2007 ;12:86-98

Clinique des Maladies du Développement, Unité d'Endocrinologie, Diabétologie et Gynécologie Pédiatrique, Hôpital Necker-Enfants Malades, France.

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https://www.karger.com/Article/FullText/109636
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http://dx.doi.org/10.1159/000109636DOI Listing
December 2007

New ABCC8 mutations in relapsing neonatal diabetes and clinical features.

Diabetes 2007 Jun 27;56(6):1737-41. Epub 2007 Mar 27.

Centre National de la Recherche Scientifique, UMR8090, Institute of Biology, Pasteur Institute, Lille, France.

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http://dx.doi.org/10.2337/db06-1540DOI Listing
June 2007

MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients.

Diabetes Res Clin Pract 2007 Jan 7;75(1):99-106. Epub 2006 Jul 7.

Research Unit of Haematological and Autoimmune Diseases, Faculty of Pharmacy, Monastir, Center University, Tunisia.

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http://dx.doi.org/10.1016/j.diabres.2006.05.018DOI Listing
January 2007

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.

N Engl J Med 2006 Aug;355(5):456-66

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, USA.

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http://dx.doi.org/10.1056/NEJMoa055068DOI Listing
August 2006

Genetic basis of maturity-onset diabetes of the young.

Endocrinol Metab Clin North Am 2006 Jun;35(2):371-84, x

CNRS UMR8090 Unit, Institute of Biology and Pasteur Institute of Lille, 1 rue du Professeur Calmette BP 245 59019, Lille, France.

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http://dx.doi.org/10.1016/j.ecl.2006.02.009DOI Listing
June 2006

Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.

Hum Genet 2005 Dec 28;118(3-4):348-55. Epub 2005 Sep 28.

Department of Medicine, The University of Chicago, 5841 S. Maryland Avenue, MC3090, Chicago, IL, 60637, USA.

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http://dx.doi.org/10.1007/s00439-005-0036-6DOI Listing
December 2005

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

Diabetes 2004 Oct;53(10):2719-22

Centre National de la Recherche Scientifique UMR 8090, Institut of Biology and Pasteur Institute, Lille, France.

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http://dx.doi.org/10.2337/diabetes.53.10.2719DOI Listing
October 2004