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About 12% of children in Kota, Rajasthan, experience hair loss, mainly due to fungal infections, with early treatment advised to prevent worsening.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Mice without Vitamin D receptors have hair growth problems because of issues in the hedgehog signaling pathway.

The HR protein's role as a repressor is essential for controlling hair growth.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Hair follicle regeneration possible, more research needed.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Vitamin D receptor helps control hair growth genes in skin cells.

Wnt signaling is crucial for skin and hair development and its disruption can cause skin tumors.

Using neurohormones to control keratin can lead to new skin disease treatments.

Keratin mutations cause skin diseases and could lead to new treatments.

CD2 might be a new treatment target for patchy alopecia areata.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

Hair loss in children is often caused by scalp infections, immune disorders, hair pulling, stress, and requires careful treatment due to emotional effects.