Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

AR gene not major factor in female hair loss; different from male hair loss.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Mutations in the hairless protein gene cause hair loss.

CD8+ T cells drive alopecia areata, while regulatory T cells are protective.

Certain VDR gene changes can affect melanoma risk.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A mutation in the Sgkl gene causes defective hair growth in mice.

Certain genes help dermal papillae cells in hair follicles grow and group together.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

DNMT3A is crucial for healthy skin and hair growth.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The humanized AA mouse model is better for testing new alopecia areata treatments.

Alopecia areata is an autoimmune hair loss condition linked to genetic factors.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A mutation in mice causes hair loss and immune problems.

Different autoantibody groups in pediatric SLE are linked to specific symptoms and disease outcomes.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

DLQI is a reasonable quality-of-life measure for alopecia patients, but more research is needed.

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

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

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

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