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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.

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

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

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

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

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

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

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

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

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

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

Some vaccines, like the hepatitis B vaccine, might be linked to the hair loss condition Alopecia Areata, but more research is needed.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

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.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.