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A pet ferret had a serious infection from Mycobacterium xenopi, which can spread to humans.

Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

Alopecia areata involves specific T-cells, unlike androgenetic alopecia.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

BAF200 is essential for proper heart and coronary artery formation.

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

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The Endocrine Society advised against routine testosterone therapy for women, citing a need for more research on long-term safety and a clear definition of androgen deficiency.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Correct skin biopsy techniques are crucial to avoid misdiagnosis of skin diseases.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Keratins are important for skin cell health and their problems can cause diseases.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

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.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Apple extract called procyanidin B-2 was found to greatly increase hair growth.

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.

New drugs for heart disease may be developed from molecules secreted by stem cells.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Fisetin, a type of polyphenol, may help hair grow by increasing certain protein activities in cells.

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

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.