Search

everythinglearnresearchcommunity

for

Search:↓

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

AMPK activation may reduce melanoma risk in red-haired individuals.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Rac1 is essential for proper hair structure and color.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Grasp protein helps maintain skin health after UVB exposure.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

β-catenin affects hair growth and can lead to tumors, needing more research for better understanding.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.