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Topical 17 alpha-propylmesterolone increases hair cell growth in androgenetic alopecia.

Certain gene variations may increase the risk and severity of alopecia areata.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

CAG repeat polymorphism and prostate zone volume are not reliable markers of long-term androgen sensitivity.

Cyclosporin A promotes hair growth in mice and increases a protein linked to hair growth, but it may not work the same way in humans.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Clofazimine may be effective for treating ashy dermatosis.

Machine learning identified three unique subtypes of androgen excess in women with PCOS, each with different metabolic risks.

Scalp hair 17-OHP and androstenedione levels can help monitor treatment in CAH patients.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Lack of a key enzyme causes severe skin issues and death in mice.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

PPAR alpha may help in hair growth and could be a target for treatment.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.