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A very low-calorie ketogenic diet led to weight loss and improved metabolic and hormonal health in obese men, with better sperm motility.

Lower LDL-c levels predict higher COVID-19 mortality.

Human hair keratins can be turned into useful 3D biomedical scaffolds through a freeze-thaw process.

COVID-19 pneumonia may cause lasting lung damage like fibrosis.

Reducing iron levels didn't improve heart health or metabolism in women with certain ovarian issues.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

Modified laparoscopic sleeve gastrectomy effectively controls diabetes and treats obesity with minimal complications.

A vitamin D receptor mutation causes rickets and affects immune responses.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Hair properties vary by ethnicity and environment, affecting surface charge and particle deposition.

Calorie restriction changes the elemental and isotopic makeup of mouse hair and bone.

Keratin from human hair shows promise for medical uses like wound healing and tissue engineering.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

Dentin sialoprotein and phosphophoryn are present in rodent hair follicles and may help hair growth and development.

Tirzepatide might help manage PCOS in obese patients but needs more research to confirm safety and effectiveness.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

PPX causes much less hair loss than traditional taxanes.

Serine is vital for hair follicle stem cells to balance hair growth and skin repair.

Poor blood supply in hair follicles is linked to nutrient deficiency in patients with female pattern hair loss, and adding more nutrients could potentially fix this.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Hair cuticles remain stable and resilient under stress due to strong protein content and crosslinking.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

TGase 3 helps build hair structure by forming strong bonds between proteins.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Bioengineered microneedles and nanomedicine offer promising, precise treatments for tissue regeneration.

IVIg treatment improved symptoms but caused permanent dark hair loss.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.