Search

everythinglearnresearchcommunity

for

Search:↓

A genetic marker linked to a type of hair loss was found in most patients studied.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Finasteride helps female-pattern hair loss.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Blocking a specific enzyme can reduce the negative impact of stress hormones on hair growth cells.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

High CCL11 levels may indicate poor response to baricitinib in severe alopecia areata.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

A new gene mutation causes a rare type of hair loss.

A new gene mutation is linked to monilethrix in the studied family.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

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

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A specific gene mutation causes severe skin and nail issues and hair loss.

A specific gene mutation causes congenital hair loss.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.