Search

everythinglearnresearchcommunity

for

Search:↓

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

pCLCA2 protein may help maintain skin structure and function.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Tenascin-C and tenascin-W help control stem cell movement and growth in whisker follicles.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Corin helps control salt and sweat release in sweat glands.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Celtis choseniana may help treat hair loss by reducing androgen effects and boosting hair growth signals.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

A CCS patient with severe complications was successfully treated using combined therapies.

Trichothiodystrophy causes unusual hair and developmental issues.

A new gene, JMJD1C, may affect testosterone levels in men.

Wnt-10b helps skin cells develop into hair-related structures.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Circ 0020938 slows down hair growth in cashmere goats.

Cystatin M/E helps in the final stages of hair and nail formation by controlling certain enzymes.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

TCDD changes skin cell growth and keratin production in mice.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Claudin 6 is crucial for normal skin and hair development.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A specific gene mutation causes a severe skin disorder in a family.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

New mouse models help study melanocytic cells for melanoma research.

CTP-543 is generally safe for treating alopecia areata.