Results 1 to 10 of about 2,421 (145)

Cancer-associated fibroblast-derived COL17A1 promotes gemcitabine resistance and tumorigenesis in pancreatic cancer cells by interacting with ACTN4 [PDF]

open access: yesDiscover Oncology
Background Cancer-associated fibroblasts (CAFs) are key components of tumor microenvironment and have been identified to be involved in modulating drug resistance in cancers by secreting molecules.
Rongyu Shi   +6 more
exaly   +4 more sources

Identifying six single nucleotide variants in the COL17A1 gene that alter RNA splicing: database analysis and minigene assays [PDF]

open access: yesScientific Reports
Collagen type XVII alpha 1 chain (COL17A1) is a protein in the collagen family crucial for maintaining the integrity of skin and epithelial tissues. It is also vital for enamel formation and plays a significant role in the differentiation of ameloblasts.
Yingfei Shao, Ran Zhang
exaly   +4 more sources

Mechanical Stretch‐Induced Interlayer Coordination between MMP2 and COL17A1 Exacerbates Regenerative Exhaustion in Skin [PDF]

open access: yesAdvanced Science
The layered structure of skin necessitates highly sophisticated tissue coordination during regeneration. The unmet clinical need of long‐term skin expansion therapy stems from limited regenerative capacity, yet the underlying mechanism remains enigmatic ...
Yidan Sun   +13 more
doaj   +3 more sources

Association of immune checkpoint inhibitor-induced bullous pemphigoid with underlying cancer type: A lack of association with cancer tissue COL17A1 mutations and dysregulation [PDF]

open access: yesJID Innovations
Bullous pemphigoid (BP) is an autoimmune blistering disease caused by autoantibodies to collagen type 17 (COL17A1) and is a recognized immune-related adverse event in patients receiving immune checkpoint inhibitors (ICIs).
Rachel C. Chang   +10 more
doaj   +3 more sources

The Deubiquitinase USP22-Stabilized COL17A1 Promotes Lung Adenocarcinoma Progression

open access: yesClinical Respiratory Journal
Background Lung adenocarcinoma (LUAD) is a highly aggressive and rapidly fatal malignancy worldwide. Collagen XVII (COL17A1) has been implicated in various protumorigenic processes.
Huifeng Li
exaly   +3 more sources

COL17A1 editing via homology-directed repair in junctional epidermolysis bullosa

open access: yesFrontiers in Medicine, 2022
BackgroundEpidermolysis bullosa (EB), a severe genetic disorder characterized by blister formation in skin, is caused by mutations in genes encoding dermal-epidermal junction proteins that function to hold the skin layers together.
Julia Reichelt   +2 more
exaly   +4 more sources

NEIL1 drives the initiation of colorectal cancer through transcriptional regulation of COL17A1

open access: yesCell Reports
Summary: Deficiency of DNA repair pathways drives the development of colorectal cancer. However, the role of the base excision repair (BER) pathway in colorectal cancer initiation remains unclear.
Jin-Long Lin
exaly   +4 more sources

Morphological abnormalities in the ureter of type XVII collagen–deficient mice [PDF]

open access: yesScientific Reports
Non-fibrillar type XVII collagen (COL17A1) is a hemidesmosomal component of the epidermis and a key skin-disease molecule. We previously reported that COL17A1 is expressed in the urothelium of multiple species at low constitutive or in inducible levels ...
Amy Suzui   +8 more
doaj   +2 more sources

Mesenchymal stem cell-derived exosomes promote scalp rejuvenation through type XVII collagen regulation via the miR-21-5p/DKK2/Wnt pathway [PDF]

open access: yesFrontiers in Cell and Developmental Biology
BackgroundHair follicle aging is driven by COL17A1 proteolysis in hair follicle stem cells (HFSCs). Mesenchymal stem cell (MSC)-derived exosomes show promise in tissue regeneration, but their effects on COL17A1 and hair follicle aging remain unexplored ...
Shiyue Cui   +4 more
doaj   +2 more sources

First case report of complete paternal isodisomy of chromosome 10 harbouring a novel variant in COL17A1 that causes junctional epidermolysis bullosa intermediate

open access: yesBMC Medical Genomics, 2022
Background Uniparental disomy (UPD) is a condition in which both chromosomes are inherited from the same parent, except for imprinting disorders. Uniparental isodisomy (UPiD) may result in a homozygous variant contributing to an autosomal recessive ...
Yao Wang   +11 more
doaj   +3 more sources

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