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A specific gene mutation causes varying hair loss severity in a Pakistani family.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

MCHR2 gene duplications may be linked to alopecia areata.

Sex steroids affect the MafB gene differently in male and female hamsters.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

AMPK activation may reduce melanoma risk in red-haired individuals.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

BMP receptor IA is essential for proper hair cell differentiation in mice.

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

Acne patients have higher mTOR gene expression.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

FGF5s can block the effects of FGF5, which may help control hair growth in cashmere goats.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

The testes significantly contribute to vitamin D metabolism and may affect male reproductive health and conditions like hair loss.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

H3K4me3 helps control RSPO3 to influence hair growth and development.

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

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.