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Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Prolactin affects when mice shed and grow hair.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Men with male pattern baldness have a higher risk of dying from prostate cancer.

Statins may be linked to reproductive organ conditions, and their risks should be monitored.

Intense pulsed light treatment mainly damages pigmented hair parts but spares stem cells, allowing hair to regrow.

Precision medicine is crucial for early diagnosis and personalized treatment in prediabetes.

Taking vitamin C and vitamin E twice a day can help prevent sunburn and DNA damage from UVB exposure.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Melatonin helps Cashmere goats grow more hair by affecting certain genes and cell pathways.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

Older ovarian cancer patients live longer and tolerate weekly chemotherapy better than three-weekly treatments.

Researchers found 44 proteins that change during different hair growth stages and may be important for hair follicle function.

Temozolomide improves survival in grade III glioma patients without harming quality of life.

Virus infection risk is linked to heat tolerance and size, but decreases with high humidity and mutation rate.

Higher fasting insulin levels increase the risk of androgenetic alopecia.

Found new possible treatments for hair loss.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

A specific gene mutation causes congenital hair loss.

Mutations in the SNRPE gene cause hereditary hair loss.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new method can detect mutations in mice by observing changes in hair follicle cells.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Mutations in the LIPH gene cause woolly hair in a child.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.