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Activins and follistatins, part of the TGFβ family, are crucial for hair follicle development and skin health, affecting growth, repair, and the hair cycle.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Hair analysis shows infants and mothers in north-western Spain are exposed to environmental pollutants, with factors like diet and residence affecting pollutant levels.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Constant light exposure during pregnancy changes newborn rabbits' skin, affecting hair follicles, skin thickness, and pigment cells.

Girls conceived via assisted reproductive technologies show early puberty signs and larger ovaries.

YH0618 helps reduce chemotherapy-induced hair loss by targeting specific proteins and pathways.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

Diagnosing and treating PCOS in teenagers is difficult, and the focus is on lifestyle changes and medication to improve health and prevent future issues.

Women with type 1 diabetes often have polycystic ovary syndrome and excess male hormones, which are frequently undiagnosed.

Pregnancy with Cushing's syndrome is rare and risky for both mother and baby, needing early diagnosis and treatment.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Testosterone may have a dual role in COVID-19, potentially worsening outcomes in men, and testosterone therapy could help some patients, but more research is needed.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Manage women's cholesterol with diet, exercise, and careful treatment choices, especially during pregnancy, PCOS, and menopause.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Treatment of acromegaly can improve women's reproductive health issues caused by hormonal imbalances or tumors.

Women with acromegaly often have irregular periods due to hormone imbalances and growth hormone effects.

AMH helps estimate ovarian reserve but doesn't predict pregnancy chances; age is more important.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

A new gene mutation causes insulin resistance in a girl and her mother.

Hyperthyroidism can hide signs of high androgen levels in females.

The guideline suggests using specific criteria to diagnose PCOS, recommends various treatments for its symptoms, and advises screening for related health issues.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.