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The DNA hydrogel helps heal diabetic wounds by absorbing fluids, warming, sticking to tissue, killing bacteria, and aiding tissue and hair regrowth.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The HR protein's role as a repressor is essential for controlling hair growth.

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

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

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

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

Sox2-positive dermal papilla cells have unique characteristics and contribute more to skin and hair follicle formation than Sox2-negative cells.

Msx2 and Foxn1 are both crucial for hair growth and health.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Karl E. Weick suggested focusing on everyday events and smaller groups to improve organizational theory and urged the inclusion of nonobvious aspects for better explanations.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Mutations in keratin genes cause cell fragility and various skin disorders.

About 13% of women had idiopathic hirsutism and 8.5% had polycystic ovary syndrome in a group of Iranian women.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The dietary supplement helped increase hair growth in women with hair loss.