Work

Urogenital and caudal dysgenesis in adrenocortical dysplasia ( acd ) mice is caused by a splicing mutation in a novel telomeric regulator

Year: 2004

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/ddi011

Authors: Catherine E. Keegan, Janna E. Hutz, Tobias Else, Maja Adamska, Sonalee P. Shah, Amy E. Kent, John M. Howes, Wesley G. Beamer, Gary D. Hammer

Institutions: University of Michigan, Jackson Laboratory

Language: English

Topic: Developmental Biology and Gene Regulation

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G2055771504, Gene Interaction in Development and Disease, G3711721818, The acd mouse: a model for congenital adrenal hypoplasia, University of Michigan Rogel Cancer Center Support Grant 2023-2028, Advancing Child Health Through Cellular and Molecular Biology, Mechanisms of Adrenal Differentiation

OpenAlex ID: W2114719839

FWCI: 0.947

Cites: 51

Cited by: 68

Related to: 10