Search

everythinglearnresearchcommunity

for

Search:↓

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Hair growth and development are controlled by specific signaling pathways.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Genetic factors and diet significantly increase the risk of male pattern baldness.

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

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

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

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Dutasteride is effective for treating prostate enlargement and reducing related surgery risk, but is not approved for preventing prostate cancer.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

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

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Birth control pills increase the risk of blood clots, especially within the first year and with certain types.

The E2 protein affects gene activity in hair follicles of mice.

Hair grays due to oxidative stress and fewer functioning melanocytes.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.