Search

everythinglearnresearchcommunity

for

Search:↓

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Donor lymphocyte infusions effectively treated leukemia relapse but caused vitiligo and alopecia areata.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A truncated protein linked to breast cancer may change cell adhesion.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Crash dieting can cause hair loss due to severe calorie restriction.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Somatic BHD mutations are rare in Japanese renal tumors.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A vitamin D receptor mutation causes rickets and affects immune responses.

A specific gene mutation causes different hair defects in Indian monilethrix families.

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

Autoimmune reactions may cause both alopecia areata and HAM.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

The hr gene is linked to hair loss in Valle del Belice sheep.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.