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3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

The Itpr3 gene causes a specific hair pattern in mice.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

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.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Melanocyte stem cells in hair follicles are key for hair color and could help treat greying and pigment disorders.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

The method can effectively extract biomedical information without needing expert annotation, performing better than previous models.

The Rotterdam Study aims to understand various diseases in older adults.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Alopecia areata involves immune activation in the scalp, suggesting treatments targeting TH1, TH2, and IL-23 pathways.

CDP is crucial for lung and hair follicle cell development.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.