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Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

The study found nine new hair protein genes in human hair follicles.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

A new gene mutation linked to a skin condition was found in a Spanish family.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

HLD10 can include increased body hair and Mongolian spots.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Two new gene mutations cause a rare hair disorder.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Lipase H is important for hair follicle function and shaping hair fibers.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A protein called HIF-1a helps control hair growth genes and could be targeted to treat hair loss.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.