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

Syphilis patients showed abnormal hair root changes, with no difference between primary and secondary stages.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

A gene mutation in mice causes permanent hair loss and skin issues.

New genetic mutations causing hair loss were found in a Chinese family.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

A unique gene mutation was found in a family with monilethrix.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.