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The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Different hair follicles in the skin are innervated by unique combinations of mechanosensory neurons, crucial for touch sensation.

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

TCDD speeds up skin barrier formation by increasing certain gene expressions.

A specific gene mutation causes congenital hair loss.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Stopping S100A3 activity slows down hair growth in mice.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

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

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.