Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

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

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

CD34+ and CD34- melanocyte stem cells have different regenerative abilities.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Inhibiting certain proteins harms hair follicle immunity and increases IL-33, affecting hair health.

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

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Whn is crucial for hair growth in certain areas by controlling a specific gene.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.