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A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A new gene, JMJD1C, may affect testosterone levels in men.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

A specific gene mutation causes long hair in Angora rabbits.

Timely zinc treatment is crucial for preventing severe complications in Acrodermatitis enteropathica.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

All-trans retinoic acid slows cell growth and increases cell death in goat hair follicles through a specific pathway.

The Itpr3 gene causes a specific hair pattern in mice.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Mutations in certain receptors can cause diseases and offer new treatment options.

Targeting androgen receptor signaling may improve acute myeloid leukemia treatment.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.