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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

A missing mK6irs1 gene causes hair loss in mice.

Mutations in the Whn gene affect hair keratin gene expression differently.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Immune activities and specific genes are important in male pattern baldness.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

AKR1C enzymes in scalp glands decrease with age, possibly affecting hair loss.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Hair root sheaths can be used to accurately analyze genetic markers.

TEDAR is crucial for skin cell differentiation and barrier formation.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

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

Lack of a key enzyme causes severe skin issues and death in mice.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A genetic variant in the KRT25 gene causes tightly curled hair.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.