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TIP39 and PTH2R help control calcium levels and skin cell development.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

KRTAP6 genes affect wool quality in sheep.

c-Kit is important for heart regeneration and cancer development.

A KRT32 gene variant causes loose anagen hair syndrome.

Activating PKCα in skin causes cell death and inflammation through different pathways.

Phosphatide distribution in mouse skin remains consistent in both normal and cancerous growths.

TRPV1 affects sebaceous gland function and could help treat acne.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

A specific mutation in PA-PLA1α causes abnormal hair growth.

The Apc gene is crucial for normal skin and thymus development.

Human-induced stem cell-created skin models can help understand skin diseases by studying the skin's layers.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

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

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A peptide in shampoo can promote hair growth and improve hair condition.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.