Search

everythinglearnresearchcommunity

for

Search:↓

Melatonin affects when and how goat hair follicle genes turn on and off during growth cycles.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

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

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

The study found key genes and pathways involved in cashmere goat hair growth stages.

GLP-1 receptor agonists, like Dulaglutide, Liraglutide, and Semaglutide, have potential benefits beyond the pancreas, including neuroprotection, pain suppression, cardiovascular protection, obesity management, and cancer treatment, but there are concerns about pancreatitis and pancreatic cancer risks.

RXRα is crucial for proper immune response and links diet to immune function.

Miz1 is essential for proper hair structure and growth.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

A mouse gene mutation increases the risk of skin cancer.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

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

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Mild oxidative stress can prevent hair loss from chemotherapy.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.