Human Molecular Genetics

Journal Abbreviation: HUM MOL GENET
ISSN: 0964-6906
eISSN: 1460-2083
Publisher: Oxford University Press (OUP): Policy B - Oxford Open Option B

Publications (51)

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Abstract

Human-induced pluripotent stem cells pave the road for a better understanding of motor neuron disease (2014) Winner B, Marchetto MC, Winkler J, Gage FH Journal article Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons (2014) Havlicek S, Kohl Z, Mishra HK, Prots I, Eberhardt E, Denguir N, Wend H, et al. Journal article, Original article A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium (2014) Milne RL, Herranz J, Michailidou K, Dennis J, Tyrer JP, Zamora MP, Arias-Perez JI, et al. Journal article SUCLG2 identified as both a determinator of CSF A?1-42 levels and an attenuator of cognitive decline in Alzheimer's disease (2014) Ramirez A, Van Der Flier WM, Herold C, Ramonet D, Heilmann S, Lewczuk P, Popp J, et al. Journal article Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia (2014) Meissner B, Bartram T, Eckert C, Trka J, Panzer-Grümayer R, Hermanova I, Ellinghaus E, et al. Journal article Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice (2014) Casadei N, Pöhler AM, Tomas-Zapico C, Torres-Peraza J, Schwedhelm I, Witz A, Zamolo I, et al. Journal article The small GTPase Rab11 co-localizes with ?-synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity (2014) Chutna O, Goncalves S, Villar-Pique A, Guerreiro P, Marijanovic Z, Mendes T, Ramalho J, et al. Journal article DNA mismatch repair gene MSH6 implicated in determining age at natural menopause (2014) Perry JRB, Hsu YH, Chasman DI, Johnson AD, Elks C, Albrecht E, Andrulis IL, et al. Journal article Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium (2014) Milne RL, Burwinkel B, Michailidou K, Arias-Perez JI, Pilar Zamora M, Menendez-Rodriguez P, Hardisson D, et al. Journal article Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia (2014) Perez-Branguli F, Mishra HK, Prots I, Havlicek S, Kohl Z, Saul D, Rummel C, et al. Journal article
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