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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Overexpression of ALK2 in hair follicles disrupts skin development and slows wound healing.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

p2y5, now called LPA6, is a receptor important for human hair growth.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

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

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

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

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

MEF2C is crucial for normal hair cycle progression.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The HCR gene contributes to psoriasis risk.

Keratin mutations cause skin diseases and could lead to new treatments.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Suppressing ODC activity reduces tumor growth in hair follicles.

TEDAR is crucial for skin cell differentiation and barrier formation.