Search

everythinglearnresearchcommunity

for

Search:↓

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Activin A and Follistatin affect how mouse hair follicles grow.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

PCS rats show significant inner ear damage and zinc deficiency, similar to liver cirrhosis patients.

The hair defect is due to abnormal inner root sheath keratinization.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

Deleting part of a gene in mice causes wavy hair and high pup loss.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The laser system helps study brain cell functions by precisely removing specific cells and observing changes.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Mutations in the HOXC13 gene cause hair and nail development issues.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

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

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

MicroRNA-21 could help diagnose and treat skin fibrosis.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Key genes can rewire networks, changing skin appendage types.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.