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Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

FOXN1 gene variants cause low T cells and immune issues from birth.

New hybrid compound found to effectively prevent hair loss.

Most children with CNS tumors on targeted therapy had skin reactions, which were generally treatable without stopping the therapy.

Diabetex improves diabetic wound healing better than metformin.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Panitumumab can cause excessive ear hair growth.

The Hairless gene is crucial for healthy skin and hair growth.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Facial rejuvenation surgery has evolved to yield natural results with low complication rates, and more men and older patients are choosing this surgery.

Finasteride helps hair regrowth in frontal fibrosing alopecia.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Voriconazole can cause serious side effects, especially in long-term use.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Hair follicles can be used to quickly assess drug effects in cancer treatment.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

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.

S100A3 protein is crucial for hair shaft formation in mice.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.