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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Enzymes involved in Vitamin A metabolism affect hair growth and type in mice.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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

The model and estimator can predict drug exposure in kidney transplant patients well.

The document concludes that diagnosing and treating Human African Trypanosomiasis is challenging, but new treatments like fexinidazole are promising.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Skin can heal wounds without hair follicle stem cells, but it takes a bit longer.

A group has developed therapies that show promise for treating cancer and various other conditions.

A specific genetic deletion in goats affects cashmere yield and thickness.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

MOF controls skin development by regulating genes for mitochondria and cilia.

Lower SMAD2/3 activation predicts more severe skin cancer.

Autophagy helps control skin inflammation and cancer responses and regulates hair growth by affecting stem cell activity.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

RANKL causes lymph nodes to grow by making certain cells multiply.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.