Search

everythinglearnresearchcommunity

for

Search:↓

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.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

Changing YBX1 protein activity affects skin stem cell function and aging.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A specific gene mutation causes long hair in Angora rabbits.

The hr gene is linked to hair loss in Valle del Belice sheep.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Mutations in the HOXC13 gene cause hair and nail development issues.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Genetic factors play a major role in acne.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Dermal EZH2 controls skin cell development and hair growth in mice.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.