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The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Thyrotropin-Releasing Hormone helps heal wounds in frog and human skin.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

Spt4 and Spt6 are essential for fat cell development.

A genetic variant linked to hair thinning in Japanese women was found.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

TRH in hair follicles can influence hair color by increasing melanin.

Keratin 6A increases skin inflammation, suggesting it could be a target for treating certain skin diseases.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Whn is essential for hair growth, and its malfunction causes hair loss.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.