Search

everythinglearnresearchcommunity

for

Search:↓

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

AKR1C3 could be a treatment target for metabolic issues in PCOS.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

The ABHRS held a test in Capri, Italy.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Hair follicles can be used to study gene mutations in Stargardt disease.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Higher androgen levels and site-specific AR expression cause sex-related skeletal differences, and certain steroids can boost AR expression and androgen effects in bone cells.

RCS-01 cell therapy is safe and improves skin gene expression.

Male pattern baldness is linked to higher levels of a certain receptor in the scalp, which leads to the shrinking of blood vessels and hair loss. Early treatment targeting this receptor could be more effective.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

These gene variations are not linked to alopecia areata in Egyptians.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Vitamin C derivative may promote hair growth by activating specific genes.

A KRT32 gene variant causes loose anagen hair syndrome.

DNA analysis can help tailor alopecia treatment.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Therapies targeting the androgen receptor are being developed to treat prostate cancer and improve bone and muscle health.