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New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

The Foxn1 gene is essential for normal nail and hair development.

A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.

Nitrogen mustard causes DNA damage and structural changes in mouse skin hair follicles, but some recovery occurs after 5 days.

The hr gene is linked to hair loss in Valle del Belice sheep.

Artemis dysfunction might cause hair loss through telomere shortening.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

Hand-foot-mouth disease may cause nail loss in children.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Imatinib can cause hair loss due to lichen planopilaris.

Laminin 332 is essential for normal skin cell behavior and structure.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Specific RNA patterns are linked to alopecia areata.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.