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

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Targeting the TNFRSF1B gene may help treat hair loss.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Researchers found a genetic region that influences the number of coat layers in dogs.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Certain gene variations increase the risk of alopecia areata in Koreans.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

The FA2H gene improves cashmere fineness by enhancing hair growth in goats.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

A specific gene mutation causes a severe skin disorder in a family.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

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.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Spt4 and Spt6 are essential for fat cell development.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A new treatment using a DNA aptamer can promote hair growth by targeting a specific receptor.