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

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

New genetic mutations causing hair loss were found in a Chinese family.

A new mouse mutation causes skin and hair defects due to a gene change.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Certain gene variations might be linked to severe acne in women but not in men.

Vitamin D receptor is crucial for bone health and mineral metabolism.