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Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

PNU157706 reduced rat sperm movement and fertility without affecting offspring health.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

ESR2 gene variations may be linked to female pattern hair loss.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

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

AR gene not major factor in female hair loss; different from male hair loss.

No link found between new male baldness genes and female hair loss.

Whale genes show changes that help them live in water, like less hair and better flippers.

Less AgNOR protein production is linked to hair loss.

Researchers found a new mutation causing total hair loss from birth.

Metabolic syndrome in kids and teens is linked to obesity and increases diabetes and heart disease risk; early lifestyle changes are crucial for management.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The 25Up study collected extensive data on mental disorders and related factors in Australian twins and siblings to investigate the genetics of psychiatric illnesses.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

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.

Some skin diseases and their treatments can negatively affect male fertility.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

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.

Various treatments exist for hair loss, but more research is needed for better options.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

The document concludes that early diagnosis is key for treating common baldness in women, but reassurance is often the best approach as hair thinning can be a normal part of aging.