Now showing items 21-30 of 121
Chromosomal localization of the zinc finger protein 15, Zfp15 , on Mouse Chromosome 4
(Springer-Verlag, 1995-04)
mnd2: A New Mouse Model of Inherited Motor Neuron Disease
(Elsevier, 1993-06)
The autosomal recessive mutation mnd2 results in early onset motor neuron disease with rapidly progressive paralysis, severe muscle wasting, regression of thymus and spleen, and death before 40 days of age. mnd2 has been ...
Gene expression of the insulin-like growth factors and their receptors in human neuroblastoma cell lines
(Elsevier, 1992-10)
Insulin-like growth factors (IGF) I and II are polypeptides with both growth-promoting and insulin-like metabolic effects. The developmentally specific expression of IGF I and II in the nervous system implies a role for ...
Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backross
(Elsevier, 1991-07)
Ames dwarf (df) is an autosomal recessive mutation characterized by severe dwarfism and infertility. This mutation provides a mouse model for panhypopituitarism. The dwarf phenotype results from failure in the differentiation ...
Corticotropin-releasing hormone ( Crh ) maps to mouse Chromosome 3
(Springer-Verlag; Springer-Verlag New York, Inc., 1993-10)
Heterogeneity of the blood pressure distribution among Solomon Islands societies with increasing acculturation
(Wiley Subscription Services, Inc., A Wiley Company, 1990-04)
This study illustrates the very complex nature of gene by environmental interactions influencing the blood pressure (BP) distribution in a series of genetically distinctive populations undergoing rapid acculturation. We ...
Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth
(John Wiley & Sons, Inc., 1998-01-06)
We report on a family with early-onset sensorineural hearing loss, abnormal retinal pigment epithelium granularity, accumulation of creamy-white lesions at the level of the retinal pigment epithelium particularly superior ...
Steroid hormone responsiveness of a family of closely related mouse proviral elements
(Springer-Verlag; Springer-Verlag New York Inc., 1997-11)
Regulation of the mouse sex-limited protein ( Slp ) gene is unusual in that hormone response is conferred by the 5′ LTR of an upstream inserted provirus, dubbed the imposon ( imp1 ). In a search for additional genes whose ...
Mutation watch:PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness
(Springer-Verlag; Springer-Verlag New York Inc., 1997-08)
An assessment of teratology training provided by masters level genetic counseling programs
(Kluwer Academic Publishers-Human Sciences Press; National Society of Genetic Counselors, Inc. ; Springer Science+Business Media, 1995-12)
The increasing demand in the clinical genetics setting for information about teratogen exposures has created a need for genetic counselors to have the capabilities to appropriately address patient concerns. In order to ...