Search

everythinglearnresearchcommunity

for

Search:↓

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Hormone imbalances from the pituitary, thyroid, and adrenal glands can cause infertility, but treating these disorders can improve fertility.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Certain molecules in hair change with age and could be used for cosmetic treatments.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Hidradenitis suppurativa is a skin disease caused by the breakdown of the skin's natural immune barriers, especially around hair follicles.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

New treatments targeting specific genes show promise for treating keratin disorders.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.

JAK inhibitors show promise in effectively treating hair loss from alopecia areata.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Fat-derived stem cell therapies can potentially increase hair growth and thickness in people with hair loss.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Oxidative stress is important in causing alopecia areata.

Chemotherapy drugs can cause abnormal growth and changes in healthy skin and gland cells.

Researchers found potential new targets for treating melanoma and nonmelanoma skin cancers, and identified a possible cause and treatment for male pattern baldness and eczema.

SDF-1/CXCL12 and its receptor CXCR4 are crucial for melanocyte movement in mouse hair follicles.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

Correcting trace element imbalances may help reduce alopecia areata symptoms.