Ronald D Cohn

Ronald D Cohn

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Ronald D Cohn

Publications by authors named "Ronald D Cohn"

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Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing.

Cell Rep 2019 Nov;29(7):1739-1746.e5

Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1M1, Canada; Department of Biochemistry, University of Toronto, Toronto, ON M5G 1M1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2019.10.017DOI Listing
November 2019

A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene.

Nature 2019 Aug 24;572(7767):125-130. Epub 2019 Jul 24.

Program in Genetics and Genome Biology, the Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/s41586-019-1430-xDOI Listing
August 2019

Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy.

Curr Gene Ther 2017 ;17(4):301-308

Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

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http://www.eurekaselect.com/157532/article
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http://dx.doi.org/10.2174/1566523217666171121165046DOI Listing
April 2019

MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature review.

Seizure 2019 Apr 22;67:86-90. Epub 2019 Mar 22.

Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

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http://dx.doi.org/10.1016/j.seizure.2019.03.015DOI Listing
April 2019

Letter to the Editor.

Authors:
Ronald D Cohn

Forensic Sci Int 2019 Mar 11;296:144. Epub 2019 Jan 11.

Department of Paediatrics University of Toronto, Canada; The Hospital for Sick Children R.S. McLaughlin Foundation Chair in Paediatrics, Canada; Department of Molecular Genetics, University of Toronto, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03790738193000
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http://dx.doi.org/10.1016/j.forsciint.2019.01.002DOI Listing
March 2019

Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.

Am J Hum Genet 2019 Mar 28;104(3):466-483. Epub 2019 Feb 28.

Division of Neurology, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1X8, Canada; Program in Genetics and Genome Biology, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 0A4, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029297193001
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http://dx.doi.org/10.1016/j.ajhg.2019.01.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407525PMC
March 2019

Genetic landscape of pediatric movement disorders and management implications.

Neurol Genet 2018 Oct 26;4(5):e265. Epub 2018 Sep 26.

Division of Clinical and Metabolic Genetics (D.C., G.B., R.D.C., S.M.-A.), Department of Pediatrics, Toronto, Ontario, Canada; Department of Medical Genetics (K.S.), University of Alberta, Edmonton, Canada; Department of Pediatrics (A.E., J.K., R.D.C., S.M.-A.), University of Toronto; the Emergency Medicine Division (A.E.), Department of Paediatrics, The Hospital for Sick Children; Division of Neurology (J.K.), Department of Paediatrics, The Hospital for Sick Children,; Genetics and Genome Biology Program (R.D.C., S.M.-A.), Research Institute, The Hospital for Sick Children; and Institute of Medical Sciences (S.M.-A.), University of Toronto, Toronto, Ontario, Canada.

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http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
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http://dx.doi.org/10.1212/NXG.0000000000000265DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167181PMC
October 2018

Outcome of Patients With Inherited Neurotransmitter Disorders.

Can J Neurol Sci 2018 09 15;45(5):571-576. Epub 2018 Aug 15.

1Department of Pediatrics,Division of Clinical and Metabolic Genetics,University of Toronto,Toronto,Ontario,Canada.

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https://www.cambridge.org/core/product/identifier/S031716711
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http://dx.doi.org/10.1017/cjn.2018.266DOI Listing
September 2018

ERCC6L2-associated inherited bone marrow failure syndrome.

Mol Genet Genomic Med 2018 05 6;6(3):463-468. Epub 2018 Apr 6.

Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada.

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http://dx.doi.org/10.1002/mgg3.388DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014454PMC
May 2018

Treating pediatric neuromuscular disorders: The future is now.

Am J Med Genet A 2018 Apr 10;176(4):804-841. Epub 2017 Sep 10.

Department of Pediatrics, Clinical Neurological Sciences, Epidemiology, Western University, London, Ontario, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.38418
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http://dx.doi.org/10.1002/ajmg.a.38418DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900978PMC
April 2018

Professional opportunity for pharmacists to integrate pharmacogenomics in medication therapy.

Can Pharm J (Ott) 2018 May-Jun;151(3):167-169. Epub 2018 Apr 2.

Hospital for Sick Children (I. Cohn, R. D. Cohn, Ito), University of Toronto, Toronto.

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http://dx.doi.org/10.1177/1715163518766376DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5958433PMC
April 2018

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.

CMAJ 2018 02;190(5):E126-E136

The Centre for Applied Genomics (Reuter, Walker, Thiruvahindrapuram, Whitney, Yuen, Trost, Paton, Pereira, Herbrick, Wintle, Merico, Howe, MacDonald, Lu, Nalpathamkalam, Sung, Wang, Patel, Pellecchia, J. Wei, Strug, Bell, Kellam, Mahtani, Hosseini, Fiume, Marshall, Buchanan, Scherer); Divisions of Clinical Pharmacology and Toxicology (I. Cohn), or Clinical, and Metabolic Genetics (Sondheimer, Weksberg, Shuman, Bowdin, Meyn, Monfared), The Hospital for Sick Children; Departments of Paediatrics (Sondheimer, R. Cohn) and Molecular Genetics (Yuen, Weksberg, Shuman, R. Cohn, Ellis, Meyn), University of Toronto; Deep Genomics Inc. (Merico); Department of Psychiatry (Bassett), University Health Network and Centre for Addiction and Mental Health, University of Toronto; Li Ka Shing Knowledge Institute (Bombard), St. Michael's Hospital; Institute of Health Policy, Management and Evaluation (Bombard), University of Toronto; Centre for Genetic Medicine (Stavropoulos, Bowdin, Ray, Monfared); Molecular Genetics Laboratory (Stavropoulos, Ray, Marshall), Division of Genome Diagnostics, Paediatric Laboratory Medicine; Developmental and Stem Cell Biology (Hildebrandt, W. Wei, Romm, Pasceri, Ellis); Ted Rogers Cardiac Genome Clinic (Hosseini); Cytogenetics Laboratory (Joseph-George), Division of Genome Diagnostics, Paediatric Laboratory Medicine, The Hospital for Sick Children; Departments of Biochemistry and Laboratory Medicine, and Pathobiology (Keeley), University of Toronto; DNAstack (Cook, Fiume); McLaughlin Centre (Lee, Scherer), University of Toronto; Medcan Health Management Inc. (Davies, Hazell); Dalla Lana School of Public Health (Szego), Department of Family and Community Medicine, and The Joint Centre for Bioethics, University of Toronto; Centre for Clinical Ethics (Szego), St. Joseph's Health Centre, Toronto, Ont.

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http://dx.doi.org/10.1503/cmaj.171151DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798982PMC
February 2018

Genetic Testing among Children in a Complex Care Program.

Children (Basel) 2017 May 22;4(5). Epub 2017 May 22.

Division of Paediatric Medicine, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.

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http://dx.doi.org/10.3390/children4050042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448000PMC
May 2017

Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study.

NPJ Genom Med 2017 26;2:19. Epub 2017 May 26.

Division of Clinical Pharmacology and Toxicology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON Canada M5G 1X8.

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http://dx.doi.org/10.1038/s41525-017-0021-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677914PMC
May 2017

Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.

Mol Genet Metab 2017 03 3;120(3):235-242. Epub 2017 Jan 3.

Division of Clinical and Metabolic Genetics, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2016.12.014DOI Listing
March 2017

Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L.

J Pediatr 2016 Apr 26;171:313-6.e1-2. Epub 2016 Jan 26.

Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.jpeds.2015.12.060DOI Listing
April 2016

Exon Snipping in Duchenne Muscular Dystrophy.

Trends Mol Med 2016 Mar 5;22(3):187-189. Epub 2016 Feb 5.

Genetics and Genome Biology Program, the Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; Department of Pediatrics, University of Toronto, Toronto, ON, Canada; Division of Clinical and Metabolic Genetics, the Hospital for Sick Children, Toronto, ON, Canada; Centre for Genetic Medicine, the Hospital for Sick Children, Toronto, ON, Canada. Electronic address:

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http://www.cell.com/trends/molecular-medicine/pdf/S1471-4914
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http://dx.doi.org/10.1016/j.molmed.2016.01.007DOI Listing
March 2016

Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.

Am J Hum Genet 2016 Jan 10;98(1):90-101. Epub 2015 Dec 10.

Program in Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada; Department of Paediatrics, University of Toronto, Toronto, ON M5G 1X8, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Centre for Genetic Medicine, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. Electronic address:

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http://www.cell.com/cms/attachment/2040911867/2054828527/mmc
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http://linkinghub.elsevier.com/retrieve/pii/S000292971500457
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http://dx.doi.org/10.1016/j.ajhg.2015.11.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716669PMC
January 2016

Duchenne muscular dystrophy: Ringo to the rescue?

Neuromuscul Disord 2016 Jan;26(1):5-6

Dubowitz Neuromuscular Centre, UCL Institute of Child Health, London, UK.. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2015.12.001DOI Listing
January 2016

Dystrophin and Duchenne dystrophy.

Neuromuscul Disord 2015 May;25(5):361-2

Department of Pediatrics and Division of Clinical & Metabolic Genetics, Hospital for Sick Children, Toronto, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2015.03.013DOI Listing
May 2015

Stem cells on alert: priming quiescent stem cells after remote injury.

Cell Stem Cell 2014 Jul;15(1):7-8

Program in Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Department of Paediatrics and Molecular Genetics, University of Toronto, Toronto, ON M5R 0A3, Canada; Centre for Genetic Medicine, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.stem.2014.06.012DOI Listing
July 2014

The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical care.

Hum Mutat 2014 May 7;35(5):513-9. Epub 2014 Apr 7.

Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada; The Centre for Genetic Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1002/humu.22536DOI Listing
May 2014

Maintaining skeletal muscle mass: lessons learned from hibernation.

Exp Physiol 2014 Apr 17;99(4):632-7. Epub 2014 Jan 17.

* The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8.

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http://dx.doi.org/10.1113/expphysiol.2013.074344DOI Listing
April 2014

Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition.

Dis Model Mech 2014 Apr 6;7(4):471-81. Epub 2014 Feb 6.

McKusick-Nathans Institute of Genetic Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1242/dmm.014126DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974457PMC
April 2014

Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilization.

Exp Neurol 2013 Sep 16;247:392-401. Epub 2013 Jan 16.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S00144886130001
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http://dx.doi.org/10.1016/j.expneurol.2013.01.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706566PMC
September 2013

Stem cells in severe infantile spinal muscular atrophy (SMA1).

Authors:
Ronald D Cohn

Neuromuscul Disord 2012 Dec;22(12):1106-7

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http://dx.doi.org/10.1016/j.nmd.2012.10.023DOI Listing
December 2012

TGFβ signaling: its role in fibrosis formation and myopathies.

Curr Opin Rheumatol 2012 Nov;24(6):628-34

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

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http://dx.doi.org/10.1097/BOR.0b013e328358df34DOI Listing
November 2012

One size may not fit all: anti-aging therapies and sarcopenia.

Aging (Albany NY) 2011 Dec;3(12):1142-53

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273894PMC
http://dx.doi.org/10.18632/aging.100409DOI Listing
December 2011

Identification and characterization of a functional mitochondrial angiotensin system.

Proc Natl Acad Sci U S A 2011 Sep 18;108(36):14849-54. Epub 2011 Aug 18.

Division of Geriatric Medicine and Gerontology, Biology of Healthy Aging Program, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1073/pnas.1101507108DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169127PMC
September 2011

Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature.

Dev Med Child Neurol 2011 Jul 21;53(7):586-99. Epub 2011 Mar 21.

Johns Hopkins Center for Hypotonia, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://doi.wiley.com/10.1111/j.1469-8749.2011.03918.x
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http://dx.doi.org/10.1111/j.1469-8749.2011.03918.xDOI Listing
July 2011

Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia.

Sci Transl Med 2011 May;3(82):82ra37

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1126/scitranslmed.3002227DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140459PMC
May 2011

Role of TGF-β signaling in inherited and acquired myopathies.

Skelet Muscle 2011 May 4;1(1):19. Epub 2011 May 4.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://skeletalmusclejournal.biomedcentral.com/articles/10.1
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http://dx.doi.org/10.1186/2044-5040-1-19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156642PMC
May 2011

Muscle cramps and coffee.

Authors:
Ronald D Cohn

Neuromuscul Disord 2011 Apr 5;21(4):311. Epub 2011 Mar 5.

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http://dx.doi.org/10.1016/j.nmd.2011.02.011DOI Listing
April 2011

Regulation of muscle mass by follistatin and activins.

Mol Endocrinol 2010 Oct 1;24(10):1998-2008. Epub 2010 Sep 1.

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

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https://academic.oup.com/mend/article-lookup/doi/10.1210/me.
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http://dx.doi.org/10.1210/me.2010-0127DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954636PMC
October 2010

Best practice in Duchenne dystrophy.

Authors:
Ronald D Cohn

Neuromuscul Disord 2010 Apr;20(4):292

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http://dx.doi.org/10.1016/j.nmd.2010.03.012DOI Listing
April 2010

Helicobacter pylori promotes hepatic fibrosis in the animal model.

Lab Invest 2009 Nov 7;89(11):1291-303. Epub 2009 Sep 7.

Department of Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu, Buk-ku 702-701, Republic of Korea.

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http://dx.doi.org/10.1038/labinvest.2009.90DOI Listing
November 2009

SP-litting the satellite niche to repopulate muscle.

Cell Stem Cell 2009 Mar;4(3):194-5

Department of Pediatrics and Neurology, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, 733 North Broadway, BRB 529 Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1016/j.stem.2009.02.002DOI Listing
March 2009

The genetics revolution and primary care pediatrics.

JAMA 2008 Jan;299(4):451-3

Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland 21287, USA.

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http://dx.doi.org/10.1001/jama.299.4.451DOI Listing
January 2008

Myostatin does not regulate cardiac hypertrophy or fibrosis.

Neuromuscul Disord 2007 Apr 2;17(4):290-6. Epub 2007 Mar 2.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

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http://dx.doi.org/10.1016/j.nmd.2007.01.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2562651PMC
April 2007

Congenital muscular dystrophies: new aspects of an expanding group of disorders.

Biochim Biophys Acta 2007 Feb 20;1772(2):159-72. Epub 2006 Sep 20.

McKusick-Nathans Institute of Genetic Medicine, Department of Pediatrics and Neurology, Johns Hopkins University School of Medicine, 600 N Wolfe Street, Blalock 1008 Baltimore, MD 21287, USA.

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http://dx.doi.org/10.1016/j.bbadis.2006.09.006DOI Listing
February 2007

Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.

Pediatrics 2006 Aug 30;118(2):e514-21. Epub 2006 Jun 30.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins Hospital, Children's Center, Johns Hopkins University School of Medicine, 600 N Wolfe St, Blalock 1008, Baltimore, Maryland 21205, USA.

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http://dx.doi.org/10.1542/peds.2005-1307DOI Listing
August 2006

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene.

Pediatrics 2006 May;117(5):1830-3

Department of Pediatric Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

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http://dx.doi.org/10.1542/peds.2005-2301DOI Listing
May 2006

Dystroglycan: important player in skeletal muscle and beyond.

Authors:
Ronald D Cohn

Neuromuscul Disord 2005 Mar 28;15(3):207-17. Epub 2005 Jan 28.

Johns Hopkins Hospital, Children's Center, McKusick-Nathans Institute of Genetic Medicine, 600 N Wolfe Street, Blalock 1008, Baltimore, MD 21287, USA.

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http://dx.doi.org/10.1016/j.nmd.2004.11.005DOI Listing
March 2005

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

Nat Med 2004 Jul 6;10(7):696-703. Epub 2004 Jun 6.

Howard Hughes Medical Institute, Department of Physiology and Biophysics, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.

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http://www.nature.com/doifinder/10.1038/nm1059
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http://dx.doi.org/10.1038/nm1059DOI Listing
July 2004

Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization.

Neuron 2003 Jun;38(5):747-58

Howard Hughes Medical Institute, Department of Physiology and Biophysics, University of Iowa Roy J. and Lucille A. Carver College of Medicine, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.1016/s0896-6273(03)00301-5DOI Listing
June 2003

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

Cell 2002 Sep;110(5):639-48

Howard Hughes Medical Institute, Department of Physiology and Biophysics, Department of Neurology, Iowa City, IA 52242, USA.

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http://dx.doi.org/10.1016/s0092-8674(02)00907-8DOI Listing
September 2002

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Nature 2002 Jul;418(6896):417-22

Howard Hughes Medical Institute, Department of Physiology and Biophysics, University of Iowa, Iowa City, Iowa 52242-1101, USA.

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http://dx.doi.org/10.1038/nature00837DOI Listing
July 2002