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Ronald Cohn

Research Profile

Disorders

Living Beings

Anatomy

Muscle, Skeletal

Chemicals & Drugs

Physiology

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Publications

TOP 3
Eva Andres-Mateos; Heinrich Brinkmeier; Tyesha N Burks; Diego Alvarez de la Rosa; Daniel C Files; Erika Finanger Hedderick; Michael Föller; Ivan Hernandez-Diaz; Christophe Hourdé; Dietmar Kuhl; Florian Lang; Leslie A Leinwand; Benjamin Lin; Brian M Lin; Tom G Marr; RUTH MARX-RATTNER; Rebeca Mejias; Jessica L Simmers; Arshia Soleimani; Martin Steinberger; Dana K Vaughan; Silke Vogelsang; Ronald D Cohn
Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy.
Ronald D Cohn
Stem cells in severe infantile spinal muscular atrophy (SMA1).
Elizabeth M MacDonald; Ronald D Cohn
TGFβ signaling: its role in fibrosis formation and myopathies.

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All Publications

2013: Eva Andres-Mateos; Heinrich Brinkmeier; Tyesha N Burks; Diego Alvarez de la Rosa; Daniel C Files; Erika Finanger Hedderick; Michael Föller; Ivan Hernandez-Diaz; Christophe Hourdé; Dietmar Kuhl; Florian Lang; Leslie A Leinwand; Benjamin Lin; Brian M Lin; Tom G Marr; RUTH MARX-RATTNER; Rebeca Mejias; Jessica L Simmers; Arshia Soleimani; Martin Steinberger; Dana K Vaughan; Silke Vogelsang; Ronald D Cohn
Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy.
EMBO molecular medicine 2013;5(1):80-91.
2012: Ronald D Cohn
Stem cells in severe infantile spinal muscular atrophy (SMA1).
Neuromuscular disorders : NMD 2012;22(12):1106-7.
2012: Elizabeth M MacDonald; Ronald D Cohn
TGFβ signaling: its role in fibrosis formation and myopathies.
Current opinion in rheumatology 2012;24(6):628-34.
2012: K M Williams; T Chung; Ronald D Cohn; Andrea M Corse; David M Loeb; Alex Mammen; L W Ostrow; Allen R Chen
Immunohistochemistry of affected tissue may guide cGVHD treatment decisions.
Bone marrow transplantation 2012;47(5):731-3.
2012: D Clark Files; J David Furlow; Brian T Garibaldi; Laura F Johnston; Priya Kesari; Landon S King; Chun Liu; Maria L Messi; Jason R Mock; Jared Murdoch; Cam Patterson; Jessica L Simmers; Clarke G Tankersley; Monte S Willis; Neil R Aggarwal; Sue Bodine; Ronald D Cohn; Franco RAFAEL D'Alessio; Antonio DeGorordo; Osvaldo Delbono; Michael T Crow
A critical role for muscle ring finger-1 in acute lung injury-associated skeletal muscle wasting.
American journal of respiratory and critical care medicine 2012;185(8):825-34.
2012: Eva Andres-Mateos; Tyesha N Burks; David L Huso; Leslie A Leinwand; Benjamin Lin; Brian M Lin; Tom G Marr; RUTH MARX-RATTNER; Rebeca Mejias; Dana K Merriman; Arshia Soleimani; RICHARD ZELLARS; Yonggang Zhang; Ronald D Cohn
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrels.
PloS one 2012;7(11):e48884.
2012: Abha Gupta; Courtney L Robertson; Lewis H Romer; Melania Bembea; Anna Brown; Ronald D Cohn
Respiratory failure secondary to human metapneumovirus requiring extracorporeal membrane oxygenation in a 32-month-old child.
Case reports in pediatrics 2012;2012():268074.
2011: Tyesha N Burks; Ronald D Cohn
One size may not fit all: anti-aging therapies and sarcopenia.
Aging 2011;3(12):1142-53.
2011: Peter M Abadir; Tyesha N Burks; Robert M Carey; Ronald D Cohn; CA Cooke; Michael T Crow; Neal S Fedarko; Darren Foster; Alka Jain; Brian O'Rourke; Jasma J Rucker; Barbara J Smith; Jeremy Walston
Identification and characterization of a functional mitochondrial angiotensin system.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(36):14849-54.
2011: Emily C Lisi; Ronald D Cohn
Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature.
Developmental medicine and child neurology 2011;53(7):586-99.
2011: Tyesha N Burks; Eva Andres-Mateos; RUTH MARX-RATTNER; Rebeca Mejias; Christel Van Erp; Jessica L Simmers; Jeremy Walston; Christopher Ward; Ronald D Cohn
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia.
Science translational medicine 2011;3(82):82ra37.
2011: Tammy M Holm; JENNIFER HABASHI; Jefferson J Doyle; Djahida Bedja; YiChun Chen; Christel van Erp; Mark E Lindsay; David Kim; Florian Schoenhoff; Ronald D Cohn; Bart Loeys; Craig J Thomas; Samarjit Patnaik; Juan J Marugan; Daniel P Judge; Harry C Dietz
Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
Science (New York, N.Y.) 2011;332(6027):358-61.
2011: Ronald D Cohn
Muscle cramps and coffee.
Neuromuscular disorders : NMD 2011;21(4):311.
2011: E L Finanger Hedderick; J L Simmers; A Soleimani; E Andres-Mateos; RUTH MARX-RATTNER; D C Files; Landon S King; Thomas O Crawford; Andrea M Corse; Ronald D Cohn
Loss of sarcolemmal nNOS is common in acquired and inherited neuromuscular disorders.
Neurology 2011;76(11):960-7.
2011: Tyesha N Burks; Ronald D Cohn
Role of TGF-β signaling in inherited and acquired myopathies.
Skeletal muscle 2011;1(1):19.
2010: Ching H Wang; Carsten G Bonnemann; Anne Rutkowski; Thomas Sejersen; Jonathan Bellini; Vanessa Battista; Julaine M Florence; Ulrike Schara; Pamela M Schuler; Karim Wahbi; Annie Aloysius; Robert O Bash; Christophe Béroud; Enrico Bertini; Kate Bushby; Ronald D Cohn; Anne M Connolly; Nicolas Deconinck; Isabelle Desguerre; Michelle Eagle; Brigitte Estournet-Mathiaud; Ana Ferreiro; Albert Fujak; Nathalie Goemans; Susan T Iannaccone; Patricia Jouinot; Marion Main; Paola Melacini; Wolfgang Mueller-Felber; Francesco Muntoni; Leslie L Nelson; Jes Rahbek; Susana Quijano-Roy; Caroline Sewry; Kari Storhaug; Anita Simonds; Brian Tseng; Jiri Vajsar; Andrea Vianello; Reinhard Zeller
Consensus statement on standard of care for congenital muscular dystrophies.
Journal of child neurology 2010;25(12):1559-81.
2010: Se-Jin Lee; Yun-Sil Lee; Teresa Zimmers; Arshia Soleimani; Martin M Matzuk; Kunihiro Tsuchida; Ronald D Cohn; Elisabeth R Barton
Regulation of muscle mass by follistatin and activins.
Molecular endocrinology (Baltimore, Md.) 2010;24(10):1998-2008.
2010: Ronald D Cohn
Best practice in Duchenne dystrophy.
Neuromuscular disorders : NMD 2010;20(4):292.
2009: Moon-Jung Goo; Mi-Ran Ki; Hye-Rim Lee; Hai-Jie Yang; Dong-Wei Yuan; Il-Hwa Hong; Jin-Kyu Park; Kyung-Sook Hong; Jung-Youn Han; Ok-Kyung Hwang; Dong-Hwan Kim; Sun-Hee Do; Ronald D Cohn; Kyu-Shik Jeong
Helicobacter pylori promotes hepatic fibrosis in the animal model.
Laboratory investigation; a journal of technical methods and pathology 2009;89(11):1291-303.
2009: Stefani Fontana; Ronald D Cohn
SP-litting the satellite niche to repopulate muscle.
Cell stem cell 2009;4(3):194-5.
2008: Tina Cheng; Ronald D Cohn; George J Dover
The genetics revolution and primary care pediatrics.
JAMA : the journal of the American Medical Association 2008;299(4):451-3.
2007: Ronald D Cohn; Hsin-Yueh Liang; Reena Shetty; Theodore P Abraham; Kathryn R Wagner
Myostatin does not regulate cardiac hypertrophy or fibrosis.
Neuromuscular disorders : NMD 2007;17(4):290-6.
2007: Ronald D Cohn; Christel van Erp; JENNIFER HABASHI; Arshia A Soleimani; Erin C Klein; Matthew T Lisi; Matthew Gamradt; Colette ApRhys; Tammy M Holm; Bart Loeys; Francesco Ramirez; Daniel P Judge; Christopher Ward; Harry C Dietz
Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states.
Nature medicine 2007;13(2):204-10.
2007: Matthew T Lisi; Ronald D Cohn
Congenital muscular dystrophies: new aspects of an expanding group of disorders.
Biochimica et biophysica acta 2007;1772(2):159-72.
2006: Ronald D Cohn; Erik Eklund; Amanda L Bergner; James F Casella; S Lee Woods; Janyne E Althaus; Karin J Blakemore; Harold E Fox; Julie E Hoover-Fong; Ada Hamosh; Nancy Braverman; Hudson H Freeze; Simeon Boyd
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.
Pediatrics 2006;118(2):e514-21.
2006: Stacie B Peddy; Luca A Vricella; Jane Crosson; Gretchen L Oswald; Ronald D Cohn; Duke E Cameron; David Valle; Bart Loeys
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene.
Pediatrics 2006;117(5):1830-3.
2006: JENNIFER HABASHI; Daniel P Judge; Tammy M Holm; Ronald D Cohn; Bart Loeys; Timothy K Cooper; Loretha Myers; Erin C Klein; Guosheng Liu; Carla Calvi; Megan Podowski; Enid R Neptune; Marc K Halushka; Djahida Bedja; Kathleen L Gabrielson; Daniel B Rifkin; Luca Carta; Francesco Ramirez; David L Huso; Harry C Dietz
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.
Science (New York, N.Y.) 2006;312(5770):117-21.
2005: Ronald D Cohn
Dystroglycan: important player in skeletal muscle and beyond.
Neuromuscular disorders : NMD 2005;15(3):207-17.
2004: Rita Barresi; Daniel Michele; Motoi Kanagawa; Hollie A Harper; Sherri A Dovico; Jakob S Satz; Steven A Moore; Wenli Zhang; Harry Schachter; Jan P Dumanski; Ronald D Cohn; Ichizo Nishino; Kevin P Campbell
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
Nature medicine 2004;10(7):696-703.
2003: Fumiaki Saito; Steven A Moore; Rita Barresi; Michael Henry; Albee Messing; Susan E Ross-Barta; Ronald D Cohn; Roger A Williamson; Kathleen A Sluka; Diane L Sherman; Peter J Brophy; James D Schmelzer; Phillip A Low; Lawrence Wrabetz; M Laura Feltri; Kevin P Campbell
Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization.
Neuron 2003;38(5):747-58.
2002: Ronald D Cohn; Michael Henry; Daniel Michele; Rita Barresi; Fumiaki Saito; Steven A Moore; Jason D Flanagan; Mark Skwarchuk; Michael E Robbins; Jerry R Mendell; Roger A Williamson; Kevin P Campbell
Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
Cell 2002;110(5):639-48.
2002: Steven A Moore; Fumiaki Saito; Jianguo Chen; Daniel Michele; Michael Henry; Albee Messing; Ronald D Cohn; Susan E Ross-Barta; Steve Westra; Roger A Williamson; Toshinori Hoshi; Kevin P Campbell
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
Nature 2002;418(6896):422-5.
2002: Daniel Michele; Rita Barresi; Motoi Kanagawa; Fumiaki Saito; Ronald D Cohn; Jakob S Satz; James Dollar; Ichizo Nishino; Richard I Kelley; Hannu Somer; Volker Straub; Katherine D Mathews; Steven A Moore; Kevin P Campbell
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.
Nature 2002;418(6896):417-22.
2001: Thomas Voit; P Kutz; B Leube; E Neuen-Jacob; JM Schröder; D Cavallotti; M L Vaccario; Jörg Schaper; P Broich; Ronald D Cohn; M Baethmann; G Göhlich-Ratmann; Ciriaco Scoppetta; R Herrmann
Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus.
Neuromuscular disorders : NMD 2001;11(1):11-9.
2001: Ronald D Cohn; Madeleine Durbeej; Steven A Moore; R Coral-Vazquez; S Prouty; Kevin P Campbell
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.
The Journal of clinical investigation 2001;107(2):R1-7.
2000: Ronald D Cohn; Kevin P Campbell
Molecular basis of muscular dystrophies.
Muscle & nerve 2000;23(10):1456-71.
2000: Wolfgang M Franz; M Müller; O J Müller; R Herrmann; T Rothmann; M Cremer; Ronald D Cohn; T Voit; Hugo A Katus
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.
Lancet 2000;355(9217):1781-5.
2000: Kevin M Flanigan; L Kerr; Mark B Bromberg; C Leonard; Jay S Tsuruda; P Zhang; I Gonzalez-Gomez; Ronald D Cohn; K P Campbell; Mark Leppert
Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
Annals of neurology 2000;47(2):152-61.
2000: Madeleine Durbeej; Ronald D Cohn; Ronald Hrstka; Steven A Moore; Valérie Allamand; Beverly L Davidson; Roger A Williamson; Kevin P Campbell
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.
Molecular cell 2000;5(1):141-51.
1999: R Coral-Vazquez; Ronald D Cohn; Steven A Moore; James A Hill; Robert M Weiss; Robin L Davisson; Volker Straub; Rita Barresi; D Bansal; Ronald Hrstka; Roger Williamson; Kevin P Campbell
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.
Cell 1999;98(4):465-74.
1999: Ronald D Cohn; Ulrike Mayer; Gesine Saher; R Herrmann; Arjan van der Flier; A Sonnenberg; L Sorokin; Thomas Voit
Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle.
Journal of the neurological sciences 1999;163(2):140-52.
1999: Thomas Voit; Ronald D Cohn; J Sperner; B Leube; L Sorokin; T Toda; R Herrmann
Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation.
Neuromuscular disorders : NMD 1999;9(2):95-101.
1998: Arpad von Moers; Frank K H van Landeghem; Ronald D Cohn; E Baumgarten; Joachim Bürger; Gisela Stoltenburg-Didinger
Dystrophinopathy in a boy with Chediak-Higashi syndrome.
Neuromuscular disorders : NMD 1998;8(7):489-94.
1998: Ronald D Cohn; R Herrmann; L Sorokin; U M Wewer; Thomas Voit
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases.
Neurology 1998;51(1):94-100.
1997: Ronald D Cohn; R Herrmann; U M Wewer; Thomas Voit
Changes of laminin beta 2 chain expression in congenital muscular dystrophy.
Neuromuscular disorders : NMD 1997;7(6-7):373-8.
1996: Ronald D Cohn; Gabriele Gillessen-Kaesbach; W B Dobyns; Thomas Kahn; H G Lenard; Thomas Voit
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.
American journal of medical genetics 1996;63(1):314-7.