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Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Organoids can help study COVID-19 and develop treatments, but face challenges like instability and limited renewal.

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.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Changing light periods synchronized wool growth cycles in sheep.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A specific gene mutation causes Olmsted syndrome.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A gene called BMAL1 plays a role in controlling hair growth.

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

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Melandrium firmum extract helps mice grow hair by blocking a hair loss enzyme and changing hair growth genes.

TrichoTech™ may help hair growth and skin repair by increasing fibroblast growth and activity.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new gene variant causes glucocorticoid resistance in a mother and son.

Finasteride may help reduce COVID-19 infection by altering a key gene.