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A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Adding a topical agent to IPL improves hair reduction and satisfaction without extra side effects.

Lichen planopilaris can occur with multiple autoimmune diseases.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Aromatase gene variation may increase female hair loss risk.

No link found between aromatase gene and female hair loss.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

High levels of testosterone and anti-Müllerian hormone before pregnancy are linked to a higher risk of newborns needing intensive care.

Notch1 helps skin heal by attracting specific immune cells.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Pseudomonas sp. T5-6-I bacteria increase selenium uptake in Brassica oleracea plants by 130%.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

Genetic markers can help predict ear shapes for forensic use.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

c-Kit is important for heart regeneration and cancer development.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

There's no significant genetic link between male pattern baldness and COVID-19.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

People with rheumatoid arthritis have a higher risk of developing alopecia areata.

Taking Saw palmetto and Pygeum africana can change the levels of certain steroids in urine, which could cause confusion in doping tests.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Ulcerative colitis involves immune activation, chronic inflammation, and metabolic issues, some of which persist even during remission.

Hair cell loss usually happens after hearing loss starts.

Genetics can help tailor treatments for male pattern hair loss, improving outcomes like stabilization or modest regrowth.