Search

everythinglearnresearchcommunity

for

Search:↓

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

RNase L hinders hair growth by altering immune signals.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Local injections of nanosized rhEPO can speed up skin healing and improve quality after deep second-degree burns.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

MCSP may help identify and regulate skin stem cells, affecting hair growth and regeneration.

Lgr5+ stem cells do not cause skin tumors.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Calretinin can help identify certain skin structures and tumors.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Estrogen receptor α controls hair growth cycles and skin thickness in male mice.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

A new gene variant causes glucocorticoid resistance in a mother and son.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Nestin-expressing progenitor cells become outer root sheath keratinocytes.

Krox20 is crucial for hair growth and maintaining skin stem cells.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.