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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.

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

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Porphyra-334 may help reduce wrinkles and promote hair growth.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

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.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

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

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A rare ear-area hair cyst was successfully removed from a 10-year-old boy.

FGF5 gene mutations cause long hair in domestic cats.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.