Search

everythinglearnresearchcommunity

for

Search:↓

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

Two gene areas linked to male pattern baldness found, more research needed.

Methamphetamine affects gene expression in rat whisker follicles, with key genes linked to addiction.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Akt2 protein is essential for normal cell division in early mouse embryos.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Alopecia areata involves specific immune cells, offering potential treatment targets.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

IgG4-related disease can cause scalp hair loss that looks like acne keloidalis nuchae.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Impaired ABCA5 activity disrupts cholesterol balance in hair follicle cells, affecting hair growth.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The scraggly mutation causes hair loss and skin defects in mice.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Spt4 and Spt6 are essential for fat cell development.