Search

everythinglearnresearchcommunity

for

Search:↓

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

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

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Researchers found a new mutation causing total hair loss from birth.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Deleting part of a gene in mice causes wavy hair and high pup loss.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

RNase L suppresses regeneration in mammals.

Hedgehog signaling can create new hair follicles but may also cause tumors.

ILC1-like cells can cause alopecia areata by themselves.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Human cathepsin V can replace mouse cathepsin L to maintain normal skin and hair in mice.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.