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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

CDP is crucial for lung and hair follicle cell development.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

A new gene variant causes curly coats in some dog breeds.

New genetic locations explain much of hair color variation in Europeans.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

The FGF5 gene determines hair length in dogs.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

Some people with congenital triangular alopecia have a central tuft of hair in the bald patch, but the cause is unknown.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Genetic factors and diet significantly increase the risk of male pattern baldness.

hHbl gene is active in hair shaft cells and some pilomatricomas.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.