Search

everythinglearnresearchcommunity

for

Search:↓

MicroRNA miR-22 causes hair loss by making hair follicles regress early.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Hoxc13 is essential for hair growth and follicle development.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Genetic analysis of Cashmere goats identified key genes for wool, reproduction, and high-altitude adaptation.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

UTX is important for skin health and its loss can lead to skin issues, especially in females.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

RXRα is crucial for proper immune response and links diet to immune function.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.