Search

everythinglearnresearchcommunity

for

Search:↓

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Pioglitazone improved insulin sensitivity and altered cortisol metabolism in PCOS patients.

Finasteride treatment changes urine metabolomics and steroid signatures, potentially monitoring effectiveness but may cause sexual side effects.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Using a special laser and skin medication together successfully cleared a skin condition in a pregnant woman.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The conclusion is that a safe donor area for hair transplants varies and should be chosen based on individual factors like race, future hair loss, family history, and specific thinning patterns.

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

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

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

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Selective Androgen Receptor Modulators (SARMs) are drugs that can control the effects of androgens in different tissues, potentially having fewer side effects and promising for treating various conditions.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

The conference highlighted new dermatological treatments and emphasized early intervention and addressing conditions lacking evidence-based treatments.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The study concluded that the new wound model can be used to evaluate skin regeneration and nerve growth.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The study found that expanded skin regenerates similarly to normal skin, with 77 genes playing a role in the process.

Genomic approach finds new possible treatments for hair loss.