Search

everythinglearnresearchcommunity

for

Search:↓

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new mutation in the HR gene causes hair loss in a specific family.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

EZH2 is essential for hair growth and skin cell development.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

All-trans retinoic acid helps amelanotic melanocytes in hair follicles develop and produce pigment while reducing their growth.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

HoxC genes are crucial for normal hair and nail development.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Hair samples can't reliably detect hypercortisolism in anorexia nervosa patients.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

HMG-CoA reductase is crucial for skin wound healing by regulating keratinocyte growth and blood vessel formation.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

A20 protein is crucial for normal skin and hair development.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Different keratin types have unique amino acid patterns that are evolutionarily conserved.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

Hormone therapy for excessive hair growth is as good with GnRHa as with high-dose CPA, but GnRHa has longer-lasting results.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The HCR gene contributes to psoriasis risk.