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The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

Mice with CBS deficiency are healthier on a low-methionine diet.

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

Caffeine intake during pregnancy and lactation can cause skin lesions in mother rats and their babies, not linked to cortisol levels.

Standardized procedures are crucial for collecting and preparing biological samples to ensure accurate clinical metabolomics results.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Delayed ejaculation is a complex issue caused by psychological, biological, and lifestyle factors, requiring a holistic treatment approach.

Isotretinoin can cause serious birth defects and needs careful use, especially in pregnant women.

Ultrasound shows 80% of Hidradenitis Suppurativa patients have abnormal hair tracts that may worsen the condition.

Chemotherapy caused hair loss with specific patterns, but most patients had hair regrowth after treatment, while some had lasting hair loss.

Melatonin may protect inner ear cells from damage by reducing cell death and oxidative stress, potentially treating sudden hearing loss.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

Ectopic adrenal rests can cause androgen excess after adrenalectomy and may need targeted surgery.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

Early over-expression of FoxN1 harms immune and skin development.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

A woman had severe reactions to methotrexate, including skin issues and organ problems, but improved after 38 days in the hospital.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The modified wash test is better than TrichoScan® for diagnosing hair loss.