Cerebellar defects in Pdss2 conditional knockout mice during embryonic development and in adulthood

The mouse <i>Fgf8</i> gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo

Philip H. Crossley, Gail R. Martin · Development · 1995 · 1.2K citations

Life Sciences, Developmental Biology, Genetics +17

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S

Michael J. McLeod · Teratology · 1980 · 623 citations

Life Sciences, Anatomy, Developmental Biology +11

Widespread recombinase expression using FLPeR (Flipper) mice

Francis W. Farley, Philippe Soriano, Leta S. Steffen et al. · genesis · 2000 · 608 citations

Life Sciences, Genetics, Molecular Biology +11

Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations

Luís C. López, Markus Schuelke, Catarina M. Quinzii et al. · The American Journal of Human Genetics · 2006 · 394 citations · Full text

Medicine, Genetics, Molecular Genetics +10

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

Jack Favor, Rodica Sandulache, A. Neuhäuser-Klaus et al. · Proceedings of the National Academy of Sciences · 1996 · 391 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17