J Hered. 1978 Jul-Aug;69(4):251-4.

Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model for congenital lipoid adrenal hyperplasia.

Abstract

One-hundred-twenty-nine cases of adrenal hyperplasia in the rabbit were shown to be associated with a fully penetrant autosomal recessive gene, symbolized ah. The mutant is viable prenatally, may be recognized by gross examination of the adrenal at least as early as 19 days of gestation, but dies soon after birth. There is an external feminizing effect of the gene and the model is similar to the feminizing congenital lipoid adrenal hyperplasia reported in man. This mutant is being maintained in strain IIIVO/ahJ.

PMID:: 731013; [PubMed - indexed for MEDLINE]

MeSH Terms

LinkOut - more resources

Full Text Sources

HighWire Press - PDF

Other Literature Sources

Labome Researcher Resource - ExactAntigen/Labome

Medical

Supplemental Content

Save items

Related citations in PubMed

Hereditary chondrodystrophy in the rabbit. Genetics and pathology of a new mutant, a model for metatropic dwarfism. [J Hered. 1975]
Hereditary chondrodystrophy in the rabbit. Genetics and pathology of a new mutant, a model for metatropic dwarfism.
Fox RR, Crary DD. J Hered. 1975 Sep-Oct; 66(5):271-6.
Targeted disruption of the mouse gene encoding steroidogenic acute regulatory protein provides insights into congenital lipoid adrenal hyperplasia. [Proc Natl Acad Sci U S A. 1997]
Targeted disruption of the mouse gene encoding steroidogenic acute regulatory protein provides insights into congenital lipoid adrenal hyperplasia.
Caron KM, Soo SC, Wetsel WC, Stocco DM, Clark BJ, Parker KL. Proc Natl Acad Sci U S A. 1997 Oct 14; 94(21):11540-5.
Evidence of a steroidogenic enzyme gene dose effect on adrenal gene expression in hereditary rabbit congenital adrenal hyperplasia. [Pediatr Res. 1994]
Evidence of a steroidogenic enzyme gene dose effect on adrenal gene expression in hereditary rabbit congenital adrenal hyperplasia.
Iwamoto K, Yang X, Rogerson FM, Mason JI, Artwohl J, Bolin K, Klimah P, Swart P, Pang S. Pediatr Res. 1994 Nov; 36(5):660-6.
Review Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome. [Am J Med Genet. 1988]
Review Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome.
Burke BA, Wick MR, King R, Thompson T, Hansen J, Darrae BT, Francke U, Seltzer WK, McCabe ER, Scheithauer BW. Am J Med Genet. 1988 Sep; 31(1):75-97.
Review NIH conference. Future directions in the study and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Ann Intern Med. 2002]
Review NIH conference. Future directions in the study and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Merke DP, Bornstein SR, Avila NA, Chrousos GP. Ann Intern Med. 2002 Feb 19; 136(4):320-34.

See reviews... See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIA
Online Mendelian Inheritance in Animals (OMIA) records that cite the current articles.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.

Recent activity

Clear Turn Off Turn On

Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model ...
Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model for congenital lipoid adrenal hyperplasia.
J Hered. 1978 Jul-Aug ;69(4):251-4.

PubMed
Identification of a new physically induced urticaria: cold-induced cholinergic u...
Identification of a new physically induced urticaria: cold-induced cholinergic urticaria.
J Allergy Clin Immunol. 1981 Dec ;68(6):438-41.

PubMed
Measuring the quality of life of cancer patients: a concise QL-index for use by ...
Measuring the quality of life of cancer patients: a concise QL-index for use by physicians.
J Chronic Dis. 1981 ;34(12):585-97.

PubMed
Geriatric patients who improve in token economy and general milieu treatment pro...
Geriatric patients who improve in token economy and general milieu treatment programs: a multivariate analysis.
J Consult Clin Psychol. 1978 Dec ;46(6):1340-8.

PubMed
[2,3-diphosphoglycerate level in the red blood cells, inorganic phosphorus in th...
[2,3-diphosphoglycerate level in the red blood cells, inorganic phosphorus in the blood serum and the acid-base equilibrium indicators in different periods of normal pregnancy].
Ginekol Pol. 1981 Aug ;52(8):687-92.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

Genetics and pathology of hereditary adrenal hyperplasia in the rabbit: a model for congenital lipoid adrenal hyperplasia.

Abstract

MeSH Terms

MeSH Terms

LinkOut - more resources

Full Text Sources

Other Literature Sources

Medical

Supplemental Content

Save items

Related citations in PubMed

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information