PITX2 gain-of-function induced defects in mouse forelimb development.
Holmberg, Johan; Ingner, Gorel; Johansson, Curt; Leander, Peter; Hjalt, Tord A.
BMC Dev Biol
; 8: 25, 2008 Feb 29.
Artigo em Inglês | MEDLINE | ID: mdl-18312615
Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex.
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
PRMT5 is essential for the maintenance of chondrogenic progenitor cells in the limb bud.
Fibulin-4 E57K Knock-in Mice Recapitulate Cutaneous, Vascular and Skeletal Defects of Recessive Cutis Laxa 1B with both Elastic Fiber and Collagen Fibril Abnormalities.
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?
Murine model indicates 22q11.2 signaling adaptor <i>CRKL</i> is a dosage-sensitive regulator of genitourinary development.
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies.