Search

everythinglearnresearchcommunity

for

Search:↓

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

AR gene not major factor in female hair loss; different from male hair loss.

Inhibiting connective tissue sheath contraction may improve hair growth in male pattern baldness.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

AGA linked to inflammation, stress, fibrosis, and disturbed hair follicle stem cells.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

Gene differences found in hair follicles linked to male baldness.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

The KRTAP36-2 gene in sheep affects wool yield.

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

ATP-sensitive potassium channels play a role in chloroquine-induced itch in mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

AH-001 could be a safer and more effective treatment for hair loss.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

Wnt/β-catenin and TGF-β pathways affect hair loss, and activating Wnt/β-catenin could be a potential treatment.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

TGase 3 helps build hair structure by forming strong bonds between proteins.

TG5 helps maintain hair follicle health, while TG3 aids in hair shaft development.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

TBX3 gene affects horse coat color, with higher expression in darker areas.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Different genes are linked to various types of hair loss.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

The scalp fat tissue of men with hair loss shows changes in gene activity that may contribute to their condition.