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The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Researchers found genes in sheep that may affect hair growth and wool quality.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

A mutation in the KRT25 gene causes woolly hair and hair loss.

No link found between specific genes and female pattern hair loss.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

A gene mutation in mice causes permanent hair loss and skin issues.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Vitamin D receptor helps control hair growth genes in skin cells.

The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

A mutation in the IL2RA gene increases the risk of alopecia areata.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Sea cucumbers have unique genes that help them regenerate their intestines.

A mutation in the KRTHB5 gene causes hair and nail issues.

VEGFR-2 activation is likely involved in hair follicle growth, survival, and development.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

SOX9 is crucial for cell development and repair but can cause fibrosis and cancer if misregulated.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

RNase L suppresses regeneration in mammals.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Transfected cells with VEGF and FGF2 genes improve skin wound healing by enhancing blood flow and regeneration.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.