Search

everythinglearnresearchcommunity

for

Search:↓

Neurosteroids change how GABA_A receptors work in the brain, which could be important for treating temporal lobe epilepsy.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

The dietary supplement significantly improved skin, nails, and hair in older adults.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Advanced human skin models improve drug development and could replace animal testing.

The article concludes that developing in vitro models for human hair structures is important for research and reducing animal testing, but there are challenges like obtaining suitable samples and the models' limitations.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

The sebaceous gland has more roles than just producing sebum and contributing to acne, and new research could lead to better skin disease treatments.

Topical drugs and near-infrared light therapy show potential for treating alopecia.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

A specific gene mutation causes long hair in Angora rabbits.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

New methods to test hair growth treatments have been developed.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

The document concludes that veterinary dermatologists need more experience and a better approach to treating skin diseases in nonhuman primates.

SGK3 is essential for proper hair growth and health.

Mice can regenerate ear tissue without the p53 protein.

Myrtle has various health benefits and potential for medicine development.

Wnt activation shows promise for regenerative medicine but requires selective targeting to minimize risks like cancer.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Taurine might help prevent hair loss caused by stress.