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Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Loss of keratin K2 causes skin problems and inflammation.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

Stem cells and their surrounding environment in hair follicles work closely together, affecting hair growth and having implications for cancer and tissue regeneration.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Oral zinc sulphate reduces dark hair color in mice.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Meis1 is crucial for skin health and tumor development.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

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

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

Genetic marker rs12558842 strongly linked to male hair loss.

Activin activation in skin cells speeds up wound healing without affecting scar quality.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A gene deletion causes the "hairless" trait in Iffa Credo rats.