Search

everythinglearnresearchcommunity

for

Search:↓

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

Resveratrol-loaded nanoparticles show promise for lung cancer treatment.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

A new gene mutation is linked to monilethrix in the studied family.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

PTCH gene mutations contribute to basal cell carcinoma development.

WNT10B affects hair growth by altering gene activity in hair cells.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

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

miR-148a and miR-10a affect hair growth in Hu sheep.

MicroRNAs play a key role in wool growth in Tibetan sheep.

Certain genes may influence hair loss differently in men and women.

ILC1-like cells can cause alopecia areata by attacking hair follicles.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Certain genetic variations are linked to hair loss in Mexican men.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

High DKK1 levels predict worse survival in head and neck cancer.

New LSS gene variants help understand congenital hypotrichosis 14 better.

FoxN1 overexpression in young mice harms immune cell and skin development.

Basal cell carcinomas may use IDO to protect themselves from the immune system.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Mutations in the hairless protein gene cause hair loss.