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Hair count is important to distinguish between genetic hair thinning (Androgenetic Alopecia) and hair thinning caused by disrupted hair growth (Chronic Telogen Effluvium).

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Trichotillomania can occur in unusual patterns and sites, highlighting the need for awareness and treatment options.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

Curly hair is influenced by specific genetic variations.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

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

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Title change to "Central Centrifugal Cicatricial Alopecia (CCCA)"; common in African American women; hair-grooming methods may contribute; no effective therapy found; trials needed.

A genetic variant in the KRT25 gene causes tightly curled hair.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

The improved genome of the African spiny mouse helps study its tissue regeneration.

Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

Chemotherapy caused hair loss with specific patterns, but most patients had hair regrowth after treatment, while some had lasting hair loss.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

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

Mutations in the hHb6 gene cause the hair disorder monilethrix.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.