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TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

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

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

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

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

FOXN1 gene variants cause low T cells and immune issues from birth.

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

Krox20 overexpression in fibroblasts may play a role in abnormal scar formation and could be a target for new treatments.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A new gene mutation causes a rare type of hair loss.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

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

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

A KRT32 gene variant causes loose anagen hair syndrome.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

A new therapy for a skin blistering condition has not been developed yet.