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Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The research identifies genes linked to wool quality in sheep and provides insights to improve wool production.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Autophagy prevents early aging and maintains lipid and pheromone balance in mouse glands.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

Female pattern hair loss has multiple causes and treatments, with new therapies showing promise.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

The document concludes that significant investment in agricultural innovation is necessary to achieve global food security and nutrition.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Methotrexate treats various disorders by inhibiting DNA synthesis, but careful monitoring is needed to avoid toxicity and manage side effects.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

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

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

The monkey's hair loss was due to an autoimmune disease, not genetics.

Mutation in hairless gene may increase hair loss risk.

The AC 2 peptide from Trapa japonica fruit helps protect hair cells and may treat hair loss.

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.

Mutation in hairless gene may increase hair loss risk.

Nerve growth factor helps cashmere goat hair cells grow and is more active during the hair growth phase.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.