78 citations
,
November 2005 in “Endocrinology” Hairless protein can block vitamin D activation in skin cells.
137 citations
,
September 2005 in “Proceedings of the National Academy of Sciences of the United States of America” The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.
250 citations
,
November 2003 in “The Journal of Cell Biology” BMP receptor IA is essential for proper hair cell differentiation in mice.
215 citations
,
September 2003 in “Journal of Biological Chemistry” Vitamin D receptor and hairless protein are essential for hair growth.
132 citations
,
February 2002 in “Journal of Biological Chemistry” HOXC13 is crucial for regulating hair keratin genes in hair follicles.
178 citations
,
October 2001 in “Genes & Development” The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.
114 citations
,
May 2001 in “Development” Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.
36 citations
,
October 2000 in “British Journal of Dermatology” A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.
22 citations
,
September 2000 in “Journal of Investigative Dermatology” μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.
37 citations
,
June 2000 in “Experimental dermatology” The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.
75 citations
,
April 2000 in “Developmental Dynamics” Whn is essential for hair growth, and its malfunction causes hair loss.
79 citations
,
December 1999 in “Mechanisms of Development” Whn is crucial for hair growth in certain areas by controlling a specific gene.
126 citations
,
October 1998 in “Experimental Dermatology” The hr gene is crucial for skin and hair health, with mutations causing hair disorders.
86 citations
,
June 1998 in “Journal of Investigative Dermatology” The hairless gene mutation causes baldness by disrupting hair follicle structure.
245 citations
,
January 1998 in “Genes & Development” The study on Hoxc13 mutant mice revealed that mutations in the Hoxc13 gene led to significant defects in hair, nail, and filiform papilla development, resulting in hairlessness due to brittle hair fracturing at the skin surface. Homozygous mutant mice exhibited malformed nails and broken filiform papillae, and most did not survive past two weeks. The research indicated that Hoxc13 was crucial for the development of hair follicles, nails, and filiform papillae, suggesting a novel function for this gene in structural protein synthesis. Additionally, Hoxc13 mutants showed skeletal changes, highlighting the gene's role in a developmental program affecting various structures. This study was the first to demonstrate significant effects of an Antennapedia-class homeobox gene on hair development, implying broader developmental roles for Hox genes.