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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Polyamines are important for hair growth, but more research is needed to understand their functions and treatment potential.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Aging alone barely affects the number of hair follicles, meaning hair loss is minimal without other conditions like androgenetic alopecia.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Hair follicles and deer antlers regenerate similarly through stem cells and are influenced by hormones and growth factors.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Advanced nanocarrier and microneedle drug delivery methods are more effective, safer, and less invasive for treating skin diseases.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A new method using gentian violet and a protective spray can improve symmetry and reduce surgery time in hair restoration, but it's only effective for total hair loss, not diffuse hair loss or follow-up treatments.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Epidermal stem cells are diverse and vary in activity, playing key roles in skin maintenance and repair.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

We need more research to better understand human hair follicle stem cells for improved treatments for hair loss and skin cancer.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Certain immune cells worsen post-surgery gut paralysis by activating a specific immune response.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

The Hairless gene is crucial for healthy skin and hair growth.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.