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Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

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.

Male pattern baldness is an unintended side effect of the body's use of androgens for muscle growth, especially in those genetically prone to it.

Using hemocoagulase with platelet-rich plasma in hip replacement can lessen blood loss and improve healing and blood clotting.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

About half the patients treated with capecitabine and docetaxel developed severe hand-foot syndrome.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Sonic hedgehog signaling is crucial for hair growth and maintaining hair follicle identity.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

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

Hedgehog signaling is crucial for mammary gland development over hair follicles.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.