Search

everythinglearnresearchcommunity

for

Search:↓

MCHR2 gene duplications may be linked to alopecia areata.

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

Trichohyalin is a versatile protein involved in hair and skin structure.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

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

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Removing Mediator 1 causes teeth cells to turn into hair cells.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Adults with classic congenital adrenal hyperplasia value medication that prevents weight gain from glucocorticoids the most.

Specific keratin gene mutations can cause monilethrix.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

TCDD reduces EGF receptor activity and causes various developmental changes in animals.

Mice without certain skin proteins had abnormal skin and hair development.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

Unique genes in hair follicle cells help tissue regeneration.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Toluene diisocyanate exposure can cause immune sensitization by interacting with proteins in hair follicles and sebaceous glands.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

AHCC reduces hair loss and liver injury caused by chemotherapy in rodents.