Search

everythinglearnresearchcommunity

for

Search:↓

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

The ASIP gene is crucial for determining cattle coat color.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

CCCA is a common, scarring hair loss in Black women that needs early detection.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

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

Researchers found a genetic region that influences the number of coat layers in dogs.

A new keratin gene was found in mice, explaining hair growth.

New genetic variants linked to albinism were found in Pakistani families.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

HPV8 E6 gene causes growth of certain skin stem cells.

FLCN helps control iron levels in cells.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

KRT72 gene helps form hair.

A specific mutation in PA-PLA1α causes abnormal hair growth.