Jane Gitschier - Publications, H-index & Citations

Jane Gitschier

机构信息待补充

43H指数

102论文数

1.4W被引数

收录论文 11

发表时间

Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome)

AMERICAN JOURNAL OF OPHTHALMOLOGY

IF4.2

2005-08-01

OAAI

Egan, RA; Weleber, RG; Hogarth, P; Gregory, A; Coryell, J; Westaway, SK; Gitschier, J; Das, S; Hayflick, SJ

Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia

HUMAN MOLECULAR GENETICS

IF3.2

2004-11-03

114

OAAI

Kuo, YM; Duncan, JL; Westaway, SK; Yang, H; Nune, G; Xu, EYJ; Hayflick, SJ; Gitschier, J

The adaptive response to dietary zinc in mice involves the differential cellular localization and zinc regulation of the zinc transporters ZIP4 and ZIP5

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2004-11-01

221

OAAI

Dufner-Beattie, J; Kuo, YM; Gitschier, J; Andrews, GK

The acrodermatitis enteropathica gene ZIP4 encodes a tissue-specific, zinc-regulated zinc transporter in mice

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2003-08-01

274

OAAI

Dufner-Beattie, J; Wang, FD; Kuo, YM; Gitschier, J; Eide, D; Andrews, GK

A novel member of a zinc transporter family is defective in acrodermatitis enteropathica

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2002-07-01

418

OAAI

Wang, K; Zhou, B; Kuo, YM; Zemansky, J; Gitschier, J

Genetics of disease - Surprises still in store - Editorial overview

CURRENT OPINION IN GENETICS & DEVELOPMENT

IF3.6

2002-06-01

PREAI

Gitschier, J; Zoghbi, HY

The copper transporter CTR1 provides an essential function in mammalian embryonic development

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2001-06-05

363

OAAI

Kuo, YM; Zhou, B; Cosco, D; Gitschier, J

Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2001-04-01

OAAI

Wang, K; Pugh, EW; Griffen, S; Doheny, KF; Mostafa, WZ; al-Aboosi, MM; el-Shanti, H; Gitschier, J

The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

NATURE GENETICS

IF31.8

1999-11-01

165

PREAI

Huang, LP; Kuo, YM; Gitschier, J

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

NATURE GENETICS

IF31.8

1999-02-01

1.0K

PREAI

Vulpe, CD; Kuo, YM; Murphy, TL; Cowley, L; Askwith, C; Libina, N; Gitschier, J; Anderson, GJ

Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease

PEDIATRIC RESEARCH

IF3.1

1997-10-01

OAAI

Murata, Y; Kodama, H; Abe, T; Ishida, N; Nishimura, M; Levinson, B; Gitschier, J; Packman, S

研究方向