Search

everythinglearnresearchcommunity

for

Search:↓

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A new method can detect mutations in mice by observing changes in hair follicle cells.

The HCR gene contributes to psoriasis risk.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Two mouse mutations cause similar hair loss despite different skin changes.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Two siblings have a rare hair condition caused by a new genetic variant.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Rac1 is essential for proper hair structure and color.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A specific gene change in APCDD1 increases the risk of hair loss.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.