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MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

A male with aromatase deficiency improved bone health with estradiol treatment.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Whale genes show changes that help them live in water, like less hair and better flippers.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

New drugs for Alzheimer's and rheumatoid arthritis advanced, a Zika vaccine is in development, and there were business deals in anesthesia and oncology.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

The European Society of Endocrinology advises individualized long-term management for PCOS, focusing on lifestyle changes, accurate diagnosis, and treatments for associated health risks and symptoms.

Wnt signaling is crucial for pigmented hair regeneration by controlling stem cell activation and differentiation.

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

Skin cells produce and activate vitamin D, which regulates skin functions and supports hair growth.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Four-amino acid part makes enzyme sensitive to finasteride.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

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