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Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

GDNF signaling helps in hair growth and skin healing after a wound.

NAG-1 may help prevent some metabolic issues related to PCOS.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Blocking EGFR in mice causes hair loss and skin changes.

TGFβ1 expression in skin causes hair loss and skin thickening, but these effects are reversible.

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

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Twist1 is crucial for UVB-induced skin cancer development.

Miz1 is essential for proper hair structure and growth.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The Celsr1 gene is crucial for normal hair patterning in mice.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

Deleting MED1 in skin cells causes hair loss and skin changes.

NG2 is crucial for normal skin and hair development in mice.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.