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Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

The E2 protein affects gene activity in hair follicles of mice.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Lhx2 helps retinal cells respond to signals for eye development.

Different parts of the nail express different keratins, showing unique patterns of differentiation.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Type XIX Collagen is present in specific skin and hair cells during development.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Hsc70 protein may influence hair growth by responding to androgens.

CK 19 expression is higher in more severe skin cancers.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Most mouse hair keratin genes are on chromosomes 11 and 15.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

WWP2 is crucial for tooth development in mice.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Keratin 79 cells help form and regenerate hair canals.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.