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S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

A new gene mutation is linked to monilethrix in the studied family.

Lhx2 helps retinal cells respond to signals for eye development.

The model can effectively test gene functions and drug responses in human skin.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

p120-catenin helps control skin inflammation by regulating cadherin levels.

RXRα is crucial for proper immune response and links diet to immune function.

EGFR helps control how hair grows and forms without needing p53 protein.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Early over-expression of FoxN1 harms immune and skin development.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

Eyelid cells share signaling components but differ in pathway activity.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

Researchers found a non-functional sheep keratin gene due to mutations.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Mutations in specific genes cause different types of ectodermal dysplasias.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Blimp1 is crucial for hair follicle growth and skin health.