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Neoadjuvant chemotherapy followed by surgery leads to fewer severe complications and better quality of life than immediate surgery in advanced ovarian cancer patients with high tumor load.

Hair follicle stem cells might help treat traumatic brain injury.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A new skin treatment using a patient's own cells healed chronic wounds effectively and was preferred over traditional grafts.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

The Spanish HSS-29 scale effectively measures changes in life quality due to female-pattern hair loss.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Gingerol may help treat chronic graft-versus-host disease by improving immune cell balance.

Hair follicle stem cells may help treat strokes.

A mix of specific inhibitors and a growth factor helps keep hair growth cells from losing their properties in the lab.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Cutaneous keratocyst and steatocystoma should be called "sebaceous duct cyst" due to their similarities.

Selenium therapy improved health in cystic fibrosis patients with fewer side effects at a lower dose.

Effective management of side effects is crucial for safe use of sacituzumab govitecan in advanced breast cancer treatment.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

More research is needed to understand chemotherapy-induced hair loss and its phases.

CE-PTG detects early hair follicle issues in balding areas, helping measure male hair loss.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Human skin cells with stem-like features can help create new hair follicles and sebaceous glands when combined with other cells.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.