Now showing items 21-30 of 35
Linkage mapping of murine homolog of the yeast SPT6 gene to MMU11B1
(Springer-Verlag; Springer-Verlag New York Inc., 1996-06)
WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth
(Wiley-Liss, Inc., 2008-06)
WNT5A deficiency causes pituitary dysmorphology and ectopic melanotrope differentiation. Immunohistochemistry for prohormone convertase 2 (PC2) marks melanotrope cells, which are normally confined to the intermediate lobe ...
Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system
(Blackwell Publishing Ltd, 2007-02)
A dominant mutation of the gene encoding the POU4F3 transcription factor underlies human non-syndromic progressive hearing loss DFNA15. Using oligonucleotide microarrays to generate expression profiles of inner ears of ...
The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation
(Elsevier, 1990-11)
Two nonallelic mouse mutations with severe dwarf phenotypes are characterized by a lack of growth hormone, prolactin, and thyroid stimulating hormone. The cells that normally synthesize these pituitary hormones express a ...
Localization of the peptidylglycine α-amidating monooxygenase gene ( Pam ) introduces a region of homology between human Chromosome 5q and mouse Chromosome 1
(Springer-Verlag; Springer-Verlag New York Inc, 1994-11)
Cre-mediated recombination in the pituitary gland
(John Wiley & Sons, Inc., 2000-11)
Summary: Organ-specific expression of a cre recombinase transgene allows for the analysis of gene function in a particular tissue or cell type. Using a 4.6 kb promoter from the mouse glycoprotein hormone Α-subunit (Α GSU ...
Exclusion of PITX2 mutations as a major cause of CHARGE association
(Wiley Subscription Services, Inc., A Wiley Company, 2002-07-22)
CHARGE is a nonrandom association of ocular coloboma, congenital heart defects, atresia of the choanae, retarded growth and development, genital hypoplasia, and ear anomalies including deafness. The cause of CHARGE remains ...
Chromosomal localization of the transcription factor YY1 in the mouse and human
(Springer-Verlag, 1994-04)
Meeting report: 10th International Mouse Genome Conference
(Springer-Verlag; Springer-Verlag New York Inc., 1997-07)