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A new method accurately measures nine specific hormones in human blood.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

Keratin-associated proteins are part of the developing hair fiber cuticle.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Testosterone increases acidification in the vas deferens by up-regulating V-ATPase.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

New treatments targeting androgen receptors show promise for drug-resistant prostate cancer.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

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

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Mutations in certain receptors can cause diseases and offer new treatment options.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

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

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.