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The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

The document concludes that PCOS in teenagers is hard to diagnose, influenced by various factors, and should be managed with lifestyle changes and medication.

The scraggly mutation causes hair loss and skin defects in mice.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

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

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Losing weight, fixing varicoceles, and using advanced sperm selection methods improve male infertility treatment outcomes.

Understanding skin structure and development helps diagnose and treat skin disorders.

Light diffraction helps in eye surgery, brain treatments, and detecting hair loss and genetic diseases.

Biotechnology could lead to new hair growth products.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Childhood hair and scalp disorders can be managed with treatments like cortisone and corticosteroids.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Pig hair cortisol levels are inheritable and linked to stress responses, which could help select for more resilient pigs.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

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

Glycerol may improve wound healing and prevent keloids, a device can measure itch intensity, male pattern baldness is highly heritable, and fumaric acid esters may work for psoriasis by causing cell death in T cells.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Men can have genetic risks for PCOS-related traits like obesity and diabetes.