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ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

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

The WIF1 gene is crucial for hair growth in Angora rabbits.

Two gene areas linked to male pattern baldness found, more research needed.

Vitamin D receptor is crucial for bone health and mineral metabolism.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

Finasteride improves heart function and repairs damage after heart attack in mice.

Finasteride improves heart function and repairs damage after heart attack in mice.

Common gene patterns may cause skin autoimmune diseases.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

Disabling the FGF5 gene in sheep leads to longer wool.

Deleting the CRIF1 gene in mice disrupts skin and hair formation, certain proteins affect hair growth, a new compound may improve skin and hair health, blood cell-derived stem cells can create skin-like structures, and hair follicle stem cells come from embryonic cells needing specific signals for development.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

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.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Oestrogens help maintain healthy skin, heal wounds, and may protect against skin aging and cancer.

Scientists developed a method to regenerate salivary glands using stem cells.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.