Search

everythinglearnresearchcommunity

for

Search:↓

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Fzd2 is important for skin and hair development through various signaling ways.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Dacomitinib can cause nail and skin issues, but these can be managed without stopping the drug.

Immune cells and plasma proteins are linked to hair loss, suggesting new treatment options.

A substance called miR-1246 may help treat severe hair loss by reducing certain immune cell activities.

Two siblings had a rare hair condition with banded hair, which doesn't need treatment.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Alopecia areata is influenced by genetics and immune system factors, and better understanding could improve treatments.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

Topical rapamycin may effectively treat fibrous papules on the face.

Targeting SIRT1 with antisense oligonucleotides could be a promising treatment for hair loss.

A gene mutation in Lama3 is linked to a common type of hair loss.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Tick-bite alopecia can be identified by a bite-centered mark and treated with topical steroids, while SENLAT needs doxycycline.

Ritlecitinib provides new treatment options for diverse alopecia areata patients.

Increasing SSAT makes skin more prone to cancer.