PubMed (GeneRIF) for id: 80781

Year	Number of Results
2001	3
2002	10
2003	8
2004	12
2005	10
2006	7
2007	10
2008	11
2009	20
2010	13
2011	8
2012	8
2013	9
2014	6
2015	9
2016	4
2017	6
2018	8
2019	1
2020	7
2021	4
2023	1
2024	0

1

Temporally and spatially regulated collagen XVIII isoforms are involved in ureteric tree development via the TSP1-like domain.

Rinta-Jaskari MM, Naillat F, Ruotsalainen HJ, Koivunen JT, Sasaki T, Pietilä I, Elamaa HP, Kaur I, Manninen A, Vainio SJ, Pihlajaniemi TA. Rinta-Jaskari MM, et al. Matrix Biol. 2023 Jan;115:139-159. doi: 10.1016/j.matbio.2023.01.001. Epub 2023 Jan 6. Matrix Biol. 2023. PMID: 36623578 Free article.

2

Knobloch Syndrome Associated with Novel COL18A1 Variants in Chinese Population.

Li S, Wang Y, Sun L, Yan W, Huang L, Zhang Z, Zhang T, Ding X. Li S, et al. Genes (Basel). 2021 Sep 26;12(10):1512. doi: 10.3390/genes12101512. Genes (Basel). 2021. PMID: 34680907 Free PMC article.

3

Elevated Endostatin Expression Is Regulated by the pIgA Immune Complex and Associated with Disease Severity of IgA Nephropathy.

Zhai Y, Long X, Gao J, Yao X, Wang X, Zhao Z. Zhai Y, et al. Kidney Blood Press Res. 2021;46(1):31-40. doi: 10.1159/000508079. Epub 2020 Dec 18. Kidney Blood Press Res. 2021. PMID: 33341801 Free article.

4

Collagen type XVIII alpha 1 chain (COL18A1) variants affect the risk of anti-tuberculosis drug-induced hepatotoxicity: A prospective study.

Cheng Y, Jiao L, Li W, Wang J, Lin Z, Lai H, Ying B. Cheng Y, et al. J Clin Lab Anal. 2021 Feb;35(2):e23630. doi: 10.1002/jcla.23630. Epub 2020 Dec 9. J Clin Lab Anal. 2021. PMID: 33296124 Free PMC article.

5

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children.

Levinger N, Hendler K, Banin E, Hanany M, Kimchi A, Mechoulam H, Meiner V, Parag Y, Sharon D, Macarov M, Yahalom C. Levinger N, et al. Eur J Ophthalmol. 2021 Nov;31(6):3349-3354. doi: 10.1177/1120672120977343. Epub 2020 Nov 25. Eur J Ophthalmol. 2021. PMID: 33238767

6

Knobloch syndrome in a patient from Chile.

Nakousi-Capurro N, Huserman J, Castillo S, Herrera L, Romero P, Pizarro F, Quezada C, Cea F. Nakousi-Capurro N, et al. Am J Med Genet A. 2020 Oct;182(10):2239-2242. doi: 10.1002/ajmg.a.61760. Epub 2020 Jul 22. Am J Med Genet A. 2020. PMID: 32700429

7

Three cases of molecularly confirmed Knobloch syndrome.

Balikova I, Sanak NS, Fanny D, Smits G, Soblet J, de Baere E, Cordonnier M. Balikova I, et al. Ophthalmic Genet. 2020 Feb;41(1):83-87. doi: 10.1080/13816810.2020.1737948. Epub 2020 Mar 17. Ophthalmic Genet. 2020. PMID: 32178553

8

Serum Endostatin Is a Novel Marker for COPD Associated with Lower Lung Function, Exacerbation and Systemic Inflammation.

Wu Y, Qin J, He J, Shen Y, Wang H, Li Y, Zeng Q, Dong J, An Y, Xiong S, Feng M, Wen F. Wu Y, et al. Int J Chron Obstruct Pulmon Dis. 2020 Feb 25;15:397-407. doi: 10.2147/COPD.S234760. eCollection 2020. Int J Chron Obstruct Pulmon Dis. 2020. PMID: 32158205 Free PMC article.

9

Functional Impact of Human Genetic Variants of COL18A1/Endostatin on Pulmonary Endothelium.

Goyanes AM, Moldobaeva A, Marimoutou M, Varela LC, Wang L, Johnston LF, Aladdin MM, Peloquin GL, Kim BS, Damarla M, Suresh K, Sato T, Kolb TM, Hassoun PM, Damico RL. Goyanes AM, et al. Am J Respir Cell Mol Biol. 2020 Apr;62(4):524-534. doi: 10.1165/rcmb.2019-0056OC. Am J Respir Cell Mol Biol. 2020. PMID: 31922883 Free PMC article.

10

Type XVIII Collagen Modulates Keratohyalin Granule Formation and Keratinization in Oral Mucosa.

Nguyen HTT, Ono M, Hara ES, Komori T, Edamatsu M, Yonezawa T, Kimura-Ono A, Maekawa K, Kuboki T, Oohashi T. Nguyen HTT, et al. Int J Mol Sci. 2019 Sep 24;20(19):4739. doi: 10.3390/ijms20194739. Int J Mol Sci. 2019. PMID: 31554264 Free PMC article.

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