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A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Hair loss gene linked to prostate issues.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

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

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

Stopping the pill and giving birth both caused hair loss.

Less AgNOR protein production is linked to hair loss.

Anticonvulsant drugs may cause temporary chromosomal abnormalities.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

The document suggests that hair loss after stopping birth control may be similar to post-pregnancy hair loss and could recur with future pregnancies.

Busulfan/cyclophosphamide and total bone irradiation are equally effective for AML transplants.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.