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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.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

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

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

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.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

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

Adult stem cells are effective and ethically acceptable for treating various diseases.

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.

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

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

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

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

A rare skin condition causes red and dark patches on the face and limbs.

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.

High DHEA and short cervical length in women with PCOS and recurrent miscarriages may harm pregnancy outcomes.

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.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

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