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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Increasing Smurf2 hinders hair follicle stem cell differentiation and wound healing.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

KRT72 gene helps form hair.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

SQSTM1 is linked to increased risk of alopecia areata.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Slug (Snai2) helps regulate hair growth timing in mice.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Researchers found a non-functional sheep keratin gene due to mutations.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The HCR gene contributes to psoriasis risk.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

The E2 protein affects gene activity in hair follicles of mice.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.