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Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

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

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The SOSTDC1 gene is crucial for determining sheep wool type.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Retinoic acid helps activate hair growth in people with common hair loss by working on a specific cell growth pathway.

STK11 gene polymorphism does not predict metformin response in PCOS.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Blocking DPP4 can potentially speed up hair growth and regeneration, especially after injury or in cases of hair loss.

VEGFR-2 activation is likely involved in hair follicle growth, survival, and development.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The gene Prss53 affects hair shape and bone development in rabbits.

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.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.