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Human Molecular Genetics|August 2, 2013
Reducing CTGF/CCN2 slows down mdx muscle dystrophy and improves cell therapyMaria Gabriela Morales, Jaime Gutierrez, Claudio Cabello-Verrugio, et al.Human Molecular Genetics|August 3, 2013
Quantification of shape and cell polarity reveals a novel mechanism underlying malformations resulting from related FGF mutations during facial morphogenesisXin Li, Nathan M Young, Stephen Tropp, et al.Human Molecular Genetics|June 21, 2013
Skeletal and cardiac α-actin isoforms differently modulate myosin cross-bridge formation and myofibre force productionJulien Ochala, Hiroyuki Iwamoto, Gianina Ravenscroft, et al.Human Molecular Genetics|June 22, 2013
MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein functionChristine Grill, Kristín Bergsteinsdóttir, Margrét H Ogmundsdóttir, et al.Human Molecular Genetics|July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationMorad Ansari, Paul M McKeigue, Christine Skerka, et al.Human Molecular Genetics|July 23, 2013
MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposisKyungsoo Ha, Jillian G Buchan, David M Alvarado, et al.Human Molecular Genetics|June 19, 2013
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM studyPeter Bauer, David J Balding, Hans H Klünemann, et al.Human Molecular Genetics|June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophyNatacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.Human Molecular Genetics|June 7, 2013
Bioenergetic flux, mitochondrial mass and mitochondrial morphology dynamics in AD and MCI cybrid cell linesDiana F Silva, J Eva Selfridge, Jianghua Lu, et al.Pageof 1,196