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Acne is caused by hormones, genetics, skin cell buildup, oil production, bacteria, and inflammation.

A specific gene mutation causes long hair in Angora rabbits.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Alopecia areata significantly impacts patients' mental health and quality of life.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Keratins are crucial for cell structure, growth, and disease risk.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Losing weight, fixing varicoceles, and using advanced sperm selection methods improve male infertility treatment outcomes.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

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

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Hypothyroidism may cause certain types of hair loss.

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

New treatments and diagnostic methods for various animal skin conditions showed promising results.

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

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.