Search

everythinglearnresearchcommunity

for

Search:↓

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Combining genetic models helps improve heat tolerance in beef cattle.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Cactus extract from Notocactus ottonis may help promote hair growth.

Lysophospholipids can act as anti-inflammatory agents through specific receptors, but more research is needed.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

WNT10B is important for body functions and linked to diseases like osteoporosis, obesity, and cancer.

Microvascular damage and platelet issues persist in ulcerative colitis remission, helping assess disease states.

PP2Acα is essential for proper hair and skin development.

Osteoma cutis is a rare, benign skin condition where bone forms in the skin.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Thymosin beta-4 promotes hair growth in mice.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

Certain genetic variants increase the risk of aggressive prostate cancer.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Two new gene mutations cause a rare hair disorder.

Specific keratin gene mutations can cause monilethrix.