Ralf Spörle - Publications, H-index & Citations

Ralf Spörle

机构信息待补充

14H指数

25论文数

1.4K被引数

收录论文 6

发表时间

Multiple roles for neurofibromin in skeletal development and growth

HUMAN MOLECULAR GENETICS

IF3.2

2007-02-22

121

OAAI

Kolanczyk, Mateusz; Kossler, Nadine; Kuehnisch, Jirko; Lavitas, Liron; Stricker, Sigmar; Wilkening, Ulrich; Manjubala, Inderchand; Fratzl, Peter; Sporle, Ralf; Herrmann, Bernhard G.; Parada, Luis F.; Kornak, Uwe; Mundlos, Stefan

Computer-based three-dimensional visualization of developmental gene expression

NATURE GENETICS

IF31.8

2000-06-01

PREAI

Streicher, J; Donat, MA; Strauss, B; Spörle, R; Schughart, K; Müller, GB

Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndrome

HUMAN MOLECULAR GENETICS

IF3.2

1999-04-01

PREAI

Grimm, C; Spörle, R; Schmid, TE; Adler, ID; Adamski, J; Schughart, K; Graw, J

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome

GENOMICS

IF3

1999-04-01

OAAI

Wang, YK; Spörle, R; Paperna, T; Schughart, K; Francke, U

Neural tube morphogenesis

CURRENT OPINION IN GENETICS & DEVELOPMENT

IF3.6

1997-08-01

PREAI

Sporle, R; Schughart, K

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

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

IF9.1

1996-11-26

351

OAAI

Favor, J; Sandulache, R; NeuhauserKlaus, A; Pretsch, W; Chatterjee, B; Senft, E; Wurst, W; Blanquet, V; Grimes, P; Sporle, R; Schughart, K

研究方向