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

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

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

IL16 gene variations may affect the risk of alopecia areata in Koreans.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

MC4R gene variants not linked to female hair loss.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Certain gene variations increase the risk of alopecia areata in Koreans.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

New models predict male pattern baldness better than old ones but still need improvement.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Male pattern baldness does not cause an increased risk of prostate cancer.