Human Molecular Genetics,volume 9,issue 1  (01-2013)

Period of time： 2013年1期

Publisher： Oxford University Press

Founded in： 1992

Total resources： 344

ISSN： 1460-2083

Subject： Q3 Genetics

Favorite

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Human Molecular Genetics,volume 9,issue 1

Menu

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2 1Neu +/– mutant mice

By Porteous Sarah,Torban Elena in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 1-11

Oxford University Press

Abstract Access to resources Recommend Favorite

Expanded polyglutamine peptides alone are intrinsically cytotoxic and cause neurodegeneration in Drosophila

By Marsh J. Lawrence,Walker Heli,Theisen Heidi,Zhu Ya-Zhen,Fielder Tom,Purcell Judy,Thompson Leslie M. in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 13-25

Oxford University Press

Abstract Access to resources Recommend Favorite

A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

By Maw Marion A.,Corbeil Denis in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 27-34

Oxford University Press

Abstract Access to resources Recommend Favorite

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences

By Dorschner Michael O.,Sybert Virginia P.,Weaver Molly,Pletcher Beth A.,Stephens Karen in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 35-46

Oxford University Press

Abstract Access to resources Recommend Favorite

Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord

By Pagliardini Silvia,Giavazzi Alessio,Setola Veronica,Lizier Carlotta,Di Luca Monica in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 47-56

Oxford University Press

Abstract Access to resources Recommend Favorite

Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations—the ECTIM Study

By Lambert Jean-Charles in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 57-61

Oxford University Press

Abstract Access to resources Recommend Favorite

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

By Liu Xue-Zhong in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 63-67

Oxford University Press

Abstract Access to resources Recommend Favorite

Cell cycle arrest enhances the in vitro cellular toxicity of the truncated Machado–Joseph disease gene product with an expanded polyglutamine stretch

By Yoshizawa Toshihiro,Yamagishi Yasuaki,Koseki Naoteru,Goto Jun in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 69-78

Oxford University Press

Abstract Access to resources Recommend Favorite

The sex-linked fidget mutation abolishes Brn4 / Pou3f4 gene expression in the embryonic inner ear

By Phippard Deborah,Boyd Yvonne in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 79-85

Oxford University Press

Abstract Access to resources Recommend Favorite

Significant evidence for linkage of febrile seizures to chromosome 5q14–q15

By Nakayama Junko in (2000)

Human Molecular Genetics,volume 9,issue 1 , Vol. 9, Iss. 1, 2000-01 , pp. 87-91

Oxford University Press

Abstract Access to resources Recommend Favorite

Previous 1 2 Next Display item(s) per page Total 16 item(s)