Work

PKHDL1, a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression

Year: 2003

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/12.6.685

Authors: M. C. Hogan, M. D. Griffin, S. Rossetti, V. E. Torres, C. J. Ward, P. C. Harris

Institution: Mayo Clinic

Language: English

Topic: Genetic and Kidney Cyst Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: PKD Foundation, Mayo Foundation for Medical Education and Research, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G249753797, G6984968209, Role of Vitamin D in Dendritic Cell Immune Functions, ADPKD: Disease Spectrum & Genotype-Phenotype Correlations, Investigation of common disease mechanisms in nonsyndromic and syndromic PKD, G945531938

OpenAlex ID: W2140344774

FWCI: 2.466

Cites: 39

Cited by: 69

Related to: 10