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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Dock5 is important for skin healing and could help treat diabetic wounds.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Certain gene variations are linked to the thickness of cashmere goat hair.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Activating mitophagy may help manage a key immune response involved in the hair loss condition alopecia areata.

Researchers found four genes that could help diagnose severe alopecia areata early.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

ILC1 cells contribute to hair loss in alopecia areata.

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

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Cyclosporin A promotes hair cell growth and affects protein kinase C levels.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Blocking CCR5 can prevent and improve hair loss in alopecia areata.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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

Keratin 10 end domains may increase skin cancer risk by reducing cell death.