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People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Hairless gene not strongly linked to baldness.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Bioluminescence imaging can track hair follicle cells and help study hair regrowth.

Progesterone and its byproducts control a specific receptor in the brain independently of progesterone receptors, affecting conditions related to the menstrual cycle.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Haplogroup X found in Altaian population supports Amerindian origin.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

A 1-day or 3-day itraconazole treatment is effective for acute vulvovaginal candidosis, but recurrent cases may need longer treatment.

Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Overexpressing SIMK in alfalfa boosts root hair growth, nodule clustering, and shoot biomass.

Spironolactone may make some cancer treatments more effective by blocking a protein that helps cancer cells survive.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.