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A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

DHT in the human prostate is produced through multiple pathways, not just from testosterone.

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

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Non-coding RNAs could help detect and treat radiation damage.

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Intermediate filaments are crucial for cell differentiation and stem cell function.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A woman had a rare liver tumor causing male-like physical changes, highlighting the need for thorough checks when such symptoms appear.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

Tradescantia plants can effectively test for the toxicity of harmful algae.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Sulforaphane from broccoli may help treat certain cancers, hormone issues, and hair loss.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Telomerase-positive cells are mainly in the bulb matrix and outer root sheath of hair follicles.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Intralesional triamcinolone acetonide can effectively limit the progression of GLPLS.

The document's conclusion cannot be provided because the document is not accessible or understandable.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Activating the Sonic hedgehog gene in mice can start the hair growth phase.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.