Results 31 to 40 of about 21,356 (260)

A Functional Single-Nucleotide Polymorphism Upstream of the Collagen Type III Gene Is Associated with Catastrophic Fracture Risk in Thoroughbred Horses

open access: yesAnimals, 2023
Fractures caused by bone overloading are a leading cause of euthanasia in Thoroughbred racehorses. The risk of fatal fracture has been shown to be influenced by both environmental and genetic factors but, to date, no specific genetic mechanisms ...
Esther Palomino Lago   +6 more
doaj   +1 more source

Relative mRNA expression of HSP47, ATF6, ATG5 and ATG7 in thoracic aorta of Col3a1+/G182R and Col3a1+/+ mice determined by q-PCR.

open access: yes, 2022
The expression of HSP47, ATF6, ATG5 and ATG7 is significantly different in the thoracic aorta of Col3a1+/G182R mice compared to Col3a1+/+ controls (Student t-test, p (TIFF)
Irmine Loisel-Ferreira (12197672)   +11 more
core   +1 more source

Genetic testing for vascular Ehlers-Danlos syndrome and other variants with fragility of the middle arteries

open access: yesThe EuroBiotech Journal, 2018
Ehlers-Danlos syndrome (EDS) is an umbrella term for various inherited connective tissue disorders associated with mutations in genes involved in extracellular matrix formation.
Rakhmanov Yeltay   +6 more
doaj   +1 more source

RNAi‐mediated inhibition of COL1A1 and COL3A1 in human skin fibroblasts [PDF]

open access: yesExperimental Dermatology, 2007
Abstract:  Types I and III collagens are the major collagens comprising skin connective tissue. Defects in these collagens lead to diseases of dermal connective tissue and fibre hyperplasia. RNA interference (RNAi) provides a powerful tool to inhibit specific gene expression.
Qiong, Wang   +5 more
openaire   +2 more sources

COL3A1 rs1800255 polymorphism is associated with pelvic organ prolapse susceptibility in Caucasian individuals: Evidence from a meta-analysis.

open access: yesPLoS ONE, 2021
BackgroundThe collagen 3 alpha 1 (COL3A1) rs1800255 polymorphism has been reported to be associated with women pelvic organ prolapse (POP) susceptibility, but the results of these previous studies have been contradictory.
Ke Niu, Xu Chen, Yongxian Lu
doaj   +1 more source

Comprehensive analysis of endoplasmic reticulum-related and secretome gene expression profiles in the progression of non-alcoholic fatty liver disease

open access: yesFrontiers in Endocrinology, 2022
Endoplasmic reticulum (ER) is the principal organelle for protein synthesis, such as hepatokines and transmembrane proteins, and is critical for maintaining physiological function. Dysfunction of ER is associated with metabolic disorders.
Rong Gao   +17 more
doaj   +1 more source

COL3A1 and Its Related Molecules as Potential Biomarkers in the Development of Human Ewing’s Sarcoma [PDF]

open access: yesBioMed Research International, 2021
Background. Ewing’s sarcoma (ES) is the most common malignant primary bone tumor in children and adolescents. This study is aimed at developing new prognostic markers and building a microRNA‐mRNA network in the development of ES. Method. GSE80201 and GSE39262 were downloaded from the Gene Expression Omnibus (GEO) database.
Min Tang   +7 more
openaire   +2 more sources

COL3A1对胃癌细胞增殖及侵袭影响的实验研究

open access: yesZhongguo shiyan zhenduanxue, 2022
目的 研究COL3A1在胃癌细胞增殖、迁移及侵袭过程中的作用。方法 以靶向COL3A1的干扰慢病毒(3个靶点)及阴性对照慢病毒转染胃癌细胞株MGC803,嘌呤霉素筛选稳转细胞株。qRT-PCR验证转染后MGC803细胞中COL3A1的mRNA表达,筛选出2个转染效率最高的细胞株,再以Western blot法进一步检测转染后胃癌细胞中COL3A1的蛋白表达量。采用MTT、Transwell法检测COL3A1干扰组、对照组胃癌细胞增殖、侵袭、迁移表型,观察COL3A1敲减前后胃癌细胞生物学特性的变化。结果
姜洪伟   +6 more
doaj  

Soft Tissues: Lipoblastoma with t(2;8)(q31;q12.1) COL3A1/PLAG1 [PDF]

open access: yes, 2015
Review on lipoblastoma with t(2;8)(q31;q12.1) COL3A1/PLAG1, with data on clinics, and the genes ...
Miyachi, Mitsuru   +2 more
core   +1 more source

Immunofluorescence of descending TA sections in Col3a1+/G182R mice.

open access: yes, 2022
A. Immunofluorescent staining of descending TA sections of Col3a1+/+ (n = 10) and Col3a1+/G182R (n = 10) mice to show the distribution of collagens I and III.
Irmine Loisel-Ferreira (12197672)   +11 more
core   +1 more source

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