Search

everythinglearnresearchcommunity

for

Search:↓

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Vitamin D receptor interacts with certain dietary components to help prevent diseases and regulate hair growth.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

Male pattern hair loss could hint at androgens affecting COVID-19 severity.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

EDA2R gene linked to hair loss.

Muscles and nerves that cause goosebumps also help control hair growth.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

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

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

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.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Patient-derived melanocytes can potentially treat vitiligo by restoring skin pigmentation.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

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.