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Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

The new microneedle method delivers hair loss treatment more effectively by enhancing growth pathways.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

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

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

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

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Chemokine signaling is important for hair development.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

EdnrB signaling helps melanocyte stem cells regenerate and could be targeted to treat pigmentation issues.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

The circadian clock influences the behavior and regeneration of stem cells in the body.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.