Search

everythinglearnresearchcommunity

for

Search:↓

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

Stress hormone CRF causes hair loss and stops hair cell growth.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

CTCF protein is essential for skin and hair follicle development in mice.

Inhibiting SFRP1 may help treat hair loss.

Mrp3 helps in wound healing and hair growth.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Trps1 plays a key role in hair follicle development and cycling.

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

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Blocking mTORC1 reduces skin tumor growth in mice.

The Celsr1 gene is crucial for normal hair patterning in mice.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

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

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.