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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A mutation in the KRT74 gene causes tightly curled hair.

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

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

CLE14 peptide promotes root hair growth in Arabidopsis.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

MCHR2 gene duplications may be linked to alopecia areata.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

New mutations in the hairless gene may cause hair loss and affect bone development.

A specific gene mutation causes congenital hair loss.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

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

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.