Search

everythinglearnresearchcommunity

for

Search:↓

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

Too much or too little selenium in the diet can cause hair loss and graying in mice.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Nestin-expressing progenitor cells become outer root sheath keratinocytes.

The molecule Wise is involved in the development of various structures in chick embryos.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

Hair shaft miniaturization leads to hair follicle stem cell loss, suggesting Piezo1 as a potential treatment target.

Noncoding RNAs help determine cashmere quality in goats.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

Ceramide Synthase 4 is essential for normal hair growth and preventing hair loss.

SCD1 inhibitors can cause skin issues in rodents.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

HAPLN1 can promote hair growth and may help treat hair loss.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

ILC1-like cells can cause alopecia areata by themselves.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Mouse and human skin development share similar fibroblast timelines.

Sox2-positive cells determine specific hair follicle types in mammals.

Sper-12 nanoparticles may help treat hair loss by delivering siRNA to target androgen receptors.