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A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

Toxic Shock Syndrome cases increased due to new factors, but decreased with public health measures and changes in tampon use.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Genetics may play a significant role in gender dysphoria.

Researchers created human cells that can turn into sebocytes, which may help study and treat skin conditions like acne.

Temporary scalp trichopigmentation creates a shaved hair look on the scalp using pigments that fade over time.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Using both TGA and DTDG in hair straightening reduces hair damage compared to using TGA alone.

Women with PCOS who have low SHBG are more likely to have low good cholesterol and metabolic syndrome.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Thymic stromal lymphopoietin (TSLP) promotes hair growth by stimulating specific skin cells.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The procedure involving seminal vesiculoscopy, TURED, and balloon dilation effectively treated a man's hematospermia and improved his dysorgasmia.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.