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CGRP MAbs treatment for migraines may also improve rosacea symptoms, but more research is needed to confirm its effectiveness and safety.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

OsPRX83 helps rice survive stress by improving stress response and antioxidant activity.

Early diagnosis of pseudopelade of Brocq in men is crucial to prevent permanent hair loss.

Disruptions in sleep-wake cycles can cause health problems like mental, metabolic, and heart diseases, and cancer.

Blocking CRF-R1 can reduce alcohol intake in stressed mice.

MCSP may help identify and regulate skin stem cells, affecting hair growth and regeneration.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

New biological pathways and potential treatment targets for male pattern baldness were identified.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Wnt/β-catenin signaling is crucial for cell fusion in placental development.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

AP collagen peptides help hair grow and improve hair health.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Higher TGF-β signaling may increase skin cancer risk in organ transplant recipients.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

Obese children respond worse to CARP treatment than non-obese children.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.