Search

everythinglearnresearchcommunity

for

Search:↓

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Removing SIX1 in fat cells reduces skin fibrosis.

Laminin 332 is essential for normal skin cell behavior and structure.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Researchers created a long-lasting mouse skin cell strain that may help with hair growth research and treatments.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

PAD type III enzyme is specific to rat skin and hair follicles.

Rac1 is essential for proper hair structure and color.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

miR-195-5p reduces hair growth ability in cells by blocking a specific growth signal.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

EGFR helps hair follicles transition properly by controlling Stathmin levels.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

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

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

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

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.