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Human Molecular Genetics|January 18, 2011
Germline competency of parthenogenetic embryonic stem cells from immature oocytes of adult mouse ovaryZhong Liu, Zhe Hu, Xinghua Pan, et al.
Human Molecular Genetics|February 16, 2011
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entityManuela Pigors, Dimitra Kiritsi, Sebastian Krümpelmann, et al.
Human Molecular Genetics|February 16, 2011
Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1Atsushi Shiga, Hiroaki Nozaki, Akio Yokoseki, et al.
Human Molecular Genetics|January 20, 2011
Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx miceMichelle H Kim, Danielle I Kay, Renuka T Rudra, et al.
Human Molecular Genetics|December 15, 2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsKonrad Oexle, Janina S Ried, Andrew A Hicks, et al.
Human Molecular Genetics|December 15, 2010
Genome-wide association study identifies HLA-A*3101 allele as a genetic risk factor for carbamazepine-induced cutaneous adverse drug reactions in Japanese populationTakeshi Ozeki, Taisei Mushiroda, Amara Yowang, et al.
Human Molecular Genetics|September 10, 2010
Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosisA Sharifi, M Kousi, C Sagné, et al.
Human Molecular Genetics|September 14, 2010
Genome-wide association study identifies genetic determinants of warfarin responsiveness for JapanesePei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, et al.
Human Molecular Genetics|September 7, 2010
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisLena F Burbulla, Carina Schelling, Hiroki Kato, et al.
Human Molecular Genetics|September 7, 2010
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndromeAmanda J Walne, Tom Vulliamy, Richard Beswick, et al.
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