Search

everythinglearnresearchcommunity

for

Search:↓

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

Hair cells grown in a lab showed specific hair proteins.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

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

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Removing SIX1 in fat cells reduces skin fibrosis.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

The gene HDC is important for the development of hair follicles in newborn mice.

Specific keratin gene mutations can cause monilethrix.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Keratin from human hair shows promise for medical uses like wound healing and tissue engineering.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Most mouse hair keratin genes are on chromosomes 11 and 15.

Nonimmunogenic forms of keratins K71 and K31 can delay and prevent alopecia areata.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A20 protein is crucial for normal skin and hair development.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.