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Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

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

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

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

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Haircuts and medical growth factors do not cause cancer.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

CDP is crucial for lung and hair follicle cell development.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Personalized medicine is important for treating skin disorders, with new treatments and connections to hormones and genetics being explored.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

Low androgen levels might delay prostate cancer but could lead to more aggressive, therapy-resistant cancers.