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Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Chemotherapy causes complex changes in hair follicle cells that can lead to hair loss.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Men, especially older ones with health issues like prostate cancer, may have worse COVID-19 outcomes and could benefit from therapies targeting male hormones.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Dental pulp stem cells might not reliably become neurons.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

Immune cells are essential for early hair and skin development and healing.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Genetic mutations can affect female sexual development, requiring personalized medical care.

WWP2 is crucial for tooth development in mice.

Neuregulin3 affects cell development in the skin and mammary glands.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Different immune cells like platelets, mast cells, neutrophils, macrophages, T cells, B cells, and innate lymphoid cells all play roles in skin wound healing, but more research is needed due to inconsistent results and the complex nature of the immune response.

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

VDR regulation varies by tissue and is crucial for its biological functions.

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.

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

The conclusion is that understanding how hair follicle stem cells live or die is important for maintaining healthy tissue and repairing injuries, and could help treat hair loss, but there are still challenges to overcome.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.