Now showing items 1-10 of 15
STATISTICAL TESTS FOR TAXONOMIC DISTINCTIVENESS FROM OBSERVATIONS OF MONOPHYLY
(Blackwell Publishing Inc, 2007-02)
Hair cells in the inner ear of the pirouette and shaker 2 mutant mice
(Kluwer Academic Publishers; Springer Science+Business Media, 2000-04)
The shaker 2 ( sh2 ) and pirouette ( pi ) mouse mutants display severe inner ear dysfunction that involves both auditory and vestibular manifestation. Pathology of the stereocilia of hair cells has been found in both ...
Evolution of N-terminal sequences of the vertebrate HOXA13 protein
(Springer-Verlag; Springer-Verlag New York Inc., 2000-02)
While the the role of the homeodomain in HOX function has been evaluated extensively, little attention has been given to the non-homeodomain portions of the HOX proteins. To investigate the evolution of the HOXA13 protein ...
Genetic and phenotypic analysis of the mouse mutant mh 2J , an Ap3d allele caused by IAP element insertion
(Springer-Verlag; Springer-Verlag New York Inc., 2003-03)
Abstract
Absence or Reduction of Carbonic Anhydrase II in the Red Cells of the Beluga Whale and Llama: Implications for Adaptation to Hypoxia
(Kluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Media, 2000-08)
Carbonic anhydrase (CA) expression was examined in the red cells of two mammals that have adapted to low oxygen stress: the llama, which has adapted to high altitudes, and the beluga (or white) whale, which routinely dives ...
Expanded HOXA13 polyalanine tracts in a monotreme
(Blackwell Publishing Inc, 2008-07)
The N-terminal region of human HOXA13 has seven discrete polyalanine tracts. Our previous analysis of these tracts in multiple major vertebrate clades suggested that three are mammal-specific. We now report the N-terminal ...
Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Na v 1.6) and a genetically linkedretinal mutation, rd13
(Springer-Verlag, 2004-05)
The goal of The Jackson Laboratory Neuroscience Mutagenesis Facility is to generate mouse models of human neurological disease. We describe three new models obtained from a three-generation screen for recessive mutations. ...
BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital bud
(Blackwell Publishing Inc, 2008-07)
We previously demonstrated that a ∼1 Mb domain of genes upstream of and including Hoxa13 is co-expressed in the developing mouse limbs and genitalia. A highly conserved non-coding sequence, mmA13CNS, was shown to be ...
Identification of members of the Wnt signaling pathway in the embryonic pituitary gland
(Springer-Verlag; Springer-Verlag New York Inc., 2001-11)
Prop1 is one of several transcription factors important for the development of the pituitary gland. Downstream targets of PROP1 and other critical pituitary transcription factors remain largely unknown. We have generated ...
Strain-specific modification of lethality in fucose-deficient mice
(Springer-Verlag; Springer-Verlag New York Inc., 2003-02)
Abstract