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TP0427736 may help treat hair loss by blocking a specific protein and promoting hair growth.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

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

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

PCOS is a common condition in women that causes various symptoms and health issues, treatable with lifestyle changes and medication.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Eating a high-glycemic diet may worsen acne by increasing certain protein levels and expressions in the skin.

A substance from hair follicle stem cells helps heal skin wounds in diabetic mice by promoting cell growth and preventing cell death.

Keratin 33A is a key protein in goat winter coats, especially in high-producing breeds.

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

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The document concludes that a deeper understanding of skin aging and photodamage is needed to create better skin treatments.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Psoriasis is linked to other autoimmune diseases and involves a specific inflammatory process.

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.

Certain essential oils can activate a human skin receptor, potentially helping with skin disorders.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Non-immune factors play a significant role in alopecia areata.

A woman with anorexia and Cushing's syndrome improved after tumor removal, highlighting the need to consider hormonal issues in psychiatric conditions.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

Versican, a protein, is less present in thinning hair follicles and this decrease might contribute to common hair loss in men.

The S100A4 protein is more common in psoriatic skin and could be a target for treating psoriasis.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Antiandrogens like flutamide are effective in treating conditions like prostate cancer and hair loss, but there's a need for more potent versions. Understanding their structure can help develop better treatments.