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Year Number of Results
2001 1
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23 results

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Page 1
Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate.
Mohamad Shah NS, Sulong S, Wan Sulaiman WA, Halim AS. Mohamad Shah NS, et al. Mol Genet Genomic Med. 2019 May;7(5):e635. doi: 10.1002/mgg3.635. Epub 2019 Mar 28. Mol Genet Genomic Med. 2019. PMID: 30924295 Free PMC article.

RESULTS: Genome-wide linkage analysis had discovered several genes including TOX3 and COL21A1 in four different loci 4p15.2-p16.1, 6p11.2-p12.3, 14q13-q21, and 16q12.1. There was significant decreased, p < 0.05 of SATB2, COL21A1, and TOX3 copy number in extended

…
RESULTS: Genome-wide linkage analysis had discovered several genes including TOX3 and COL21A1 in four different loci 4p15.2-p16.1, 6p …
A new FACIT of the collagen family: COL21A1.
Fitzgerald J, Bateman JF. Fitzgerald J, et al. FEBS Lett. 2001 Sep 14;505(2):275-80. doi: 10.1016/s0014-5793(01)02754-5. FEBS Lett. 2001. PMID: 11566190 Free article.
The organization of these motifs predict that collagen XXI is a new member of the FACIT collagen sub-family. Expression analysis indicated that COL21A1 mRNA is present in many tissues including heart, stomach, kidney, skeletal muscle and placenta, and radiation hybrid mapp …
The organization of these motifs predict that collagen XXI is a new member of the FACIT collagen sub-family. Expression analysis indicated t …
Genomic organization and characterization of the human type XXI collagen (COL21A1) gene.
Chou MY, Li HC. Chou MY, et al. Genomics. 2002 Mar;79(3):395-401. doi: 10.1006/geno.2002.6712. Genomics. 2002. PMID: 11863369
Assembly of the genomic data reveals a complete sequence of the human gene COL21A1. COL21A1 is localized to chromosome 6p11.2-12.3, spanning 337 kb in size. ...The expression of COL21A1 in human tissues is developmentally regulated, with a higher level at fet …
Assembly of the genomic data reveals a complete sequence of the human gene COL21A1. COL21A1 is localized to chromosome 6p11.2- …
Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionary breakpoints in the rodent lineage.
Fitzgerald J, Bateman JF. Fitzgerald J, et al. Trends Genet. 2004 Sep;20(9):408-12. doi: 10.1016/j.tig.2004.07.002. Trends Genet. 2004. PMID: 15313548
One possible consequence of these rearrangements is the deletion of genes that are located within evolutionary breakpoint regions. In this article, we present evidence of four human genes (COL21A1, STK17A, GPR145 and ARHI) that are located in regions corresponding to evolu …
One possible consequence of these rearrangements is the deletion of genes that are located within evolutionary breakpoint regions. In this a …
Identification of hub genes and pathways in the development of gastric cancer by gene co‑expression network analysis.
Qin LH, Zhu XJ, Zhang LY, Chen JQ, Jin GY, Xiang LJ. Qin LH, et al. J Biol Regul Homeost Agents. 2021 Jan-Feb;35(1):35-44. doi: 10.23812/20-478-A. J Biol Regul Homeost Agents. 2021. PMID: 33601878
In each module, genes with the most connectivity were selected as hub genes, including G antigen 12J (GAGE12J) in blue, proline, histidine and glycine rich 1 (PHGR1) in dark orange, DNA polymerase gamma 2, accessory subunit (POLG2) in dark red and collagen type XXI alpha 1 chain …
In each module, genes with the most connectivity were selected as hub genes, including G antigen 12J (GAGE12J) in blue, proline, histidine a …
Extracellular Matrix and Integrin Expression Profiles in Fuchs Endothelial Corneal Dystrophy Cells and Tissue Model.
Goyer B, Thériault M, Gendron SP, Brunette I, Rochette PJ, Proulx S. Goyer B, et al. Tissue Eng Part A. 2018 Apr;24(7-8):607-615. doi: 10.1089/ten.TEA.2017.0128. Epub 2017 Sep 28. Tissue Eng Part A. 2018. PMID: 28726551 Free PMC article.
Microarray analysis showed nonstatistical twofold downregulation of collagen-coding genes (COL4A4, COL8A2, and COL21A1) and a twofold upregulation of the COL6A1, laminin alpha3 gene LAMA3, and integrin subunit alpha10 gene ITGA10 in FECD cells. ...
Microarray analysis showed nonstatistical twofold downregulation of collagen-coding genes (COL4A4, COL8A2, and COL21A1) and a twofold …
The cross talk between type II diabetic microenvironment and the regenerative capacities of human adipose tissue-derived pericytes: a promising cell therapy.
Ahmed TA, Ahmed SM, Elkhenany H, El-Desouky MA, Magdeldin S, Osama A, Anwar AM, Mohamed IK, Abdelgawad ME, Hanna DH, El-Badri N. Ahmed TA, et al. Stem Cell Res Ther. 2024 Feb 8;15(1):36. doi: 10.1186/s13287-024-03643-1. Stem Cell Res Ther. 2024. PMID: 38331889 Free PMC article.
DS caused impaired angiogenic differentiation of PCs as confirmed by tube formation, decreased VEGF-A and IGF-1 gene expression, upregulated TSP1, PF4, actin-related protein 2/3 complex, and downregulated COL21A1 protein expression. These cells suffered more pronounced apo …
DS caused impaired angiogenic differentiation of PCs as confirmed by tube formation, decreased VEGF-A and IGF-1 gene expression, upregulated …
A potential prognostic prediction model for metastatic osteosarcoma based on bioinformatics analysis.
Wang Y, Ming G, Gao B. Wang Y, et al. Acta Orthop Belg. 2023 Sep;89(3):373-380. doi: 10.52628/89.2.10491. Acta Orthop Belg. 2023. PMID: 37935218
Furthermore, four optimized prognostic gene signatures (ALOX5AP, COL21A1, HLA-DQB1, and LDHB) were further screened, and the prognostic prediction model for metastatic OS was constructed. ...
Furthermore, four optimized prognostic gene signatures (ALOX5AP, COL21A1, HLA-DQB1, and LDHB) were further screened, and the prognost …
Genome-wide association study of atypical psychosis.
Kanazawa T, Ikeda M, Glatt SJ, Tsutsumi A, Kikuyama H, Kawamura Y, Nishida N, Miyagawa T, Hashimoto R, Takeda M, Sasaki T, Tokunaga K, Koh J, Iwata N, Yoneda H. Kanazawa T, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Oct;162B(7):679-86. doi: 10.1002/ajmg.b.32164. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 24132900
The most significant SNPs were detected around the CHN2/CPVL genes (rs245914, P = 1.6 10(-7)) , COL21A1 gene (rs12196860, P = 2.45 10(-7) ), and PYGL/TRIM9 genes (rs1959536, P = 7.73 10(-7) ), although none of the single-nucleotide polymorphisms exhibited genome-wide signi …
The most significant SNPs were detected around the CHN2/CPVL genes (rs245914, P = 1.6 10(-7)) , COL21A1 gene (rs12196860, P = 2.45 10 …
Association Analyses of Predicted Loss-of-Function Variants Prioritized 15 Genes as Blood Pressure Regulators.
Lecluze E, Lettre G. Lecluze E, et al. Can J Cardiol. 2023 Dec;39(12):1888-1897. doi: 10.1016/j.cjca.2023.07.011. Epub 2023 Jul 13. Can J Cardiol. 2023. PMID: 37451613 Free article.
We also found a burden of rare pLoF variants in 5 additional genes associated with BP (TTN, NOS3, FES, SMAD6, COL21A1). Except for PNCK, which is located on the X-chromosome, these genes map near variants previously associated with BP by GWAS, validating the study of pLoF …
We also found a burden of rare pLoF variants in 5 additional genes associated with BP (TTN, NOS3, FES, SMAD6, COL21A1). Except for PN …
23 results