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Artemis protein may help control hair growth and health by influencing cell processes.

Deleting MED1 in skin cells causes hair loss and skin changes.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Gene differences found in hair follicles linked to male baldness.

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

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

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.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Researchers found a gene mutation responsible for a rare hair loss condition.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Short-term finasteride treatment may lower some cell death factors in prostate cancer cells.

Collagen and TGF-β2 help maintain hair cell shape and youthfulness.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

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

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.