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Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

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

Early-onset baldness is linked to a higher risk of aggressive prostate cancer in African-American men, especially before age 60.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Skin problems are common in thyroid disorders, with dry skin in hypothyroidism and warm, soft skin in hyperthyroidism.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

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

Alisertib was found to be an effective and tolerable treatment for children with recurrent brain tumors.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

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

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Female hair loss is often hereditary and can be treated with medication, hair transplants, and lasers.

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.

Skin issues can indicate immune system problems.

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

Targeted cancer therapies often cause skin problems that need careful management to improve patient quality of life and treatment success.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.

New genetic locations explain much of hair color variation in Europeans.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.