PubMed (GeneRIF) for id: 9719

Year	Number of Results
2008	1
2011	1
2013	1
2016	1
2017	2
2018	1
2019	2
2020	1
2021	5
2022	3
2023	2
2024	0

1

Secreted ADAMTS-like 2 promotes myoblast differentiation by potentiating WNT signaling.

Taye N, Singh M, Baldock C, Hubmacher D. Taye N, et al. Matrix Biol. 2023 Jun;120:24-42. doi: 10.1016/j.matbio.2023.05.003. Epub 2023 May 14. Matrix Biol. 2023. PMID: 37187448

2

Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders.

Batkovskyte D, McKenzie F, Taylan F, Simsek-Kiper PO, Nikkel SM, Ohashi H, Stevenson RE, Ha T, Cavalcanti DP, Miyahara H, Skinner SA, Aguirre MA, Akçören Z, Utine GE, Chiu T, Shimizu K, Hammarsjö A, Boduroglu K, Moore HW, Louie RJ, Arts P, Merrihew AN, Babic M, Jackson MR, Papadogiannakis N, Lindstrand A, Nordgren A, Barnett CP, Scott HS, Chagin AS, Nishimura G, Grigelioniene G. Batkovskyte D, et al. J Bone Miner Res. 2023 May;38(5):692-706. doi: 10.1002/jbmr.4799. Epub 2023 Mar 27. J Bone Miner Res. 2023. PMID: 36896612 Free article.

3

Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis.

Liu B, Zhao S, Liu L, Du H, Zhao H, Wang S, Niu Y, Li X, Qiu G; Deciphering disorders Involving Scoliosis COmorbidities (DISCO) study group; Wu Z, Zhang TJ, Wu N. Liu B, et al. Gene. 2022 Mar 10;814:146126. doi: 10.1016/j.gene.2021.146126. Epub 2021 Dec 24. Gene. 2022. PMID: 34958866 Free article.

4

The relationship of ADAMTSL2 and LRPAP1 gene methylation level with rheumatoid arthritis activity.

Podgórska D, Cieśla M, Majdan M, Podgórski R, Kolarz B. Podgórska D, et al. Clin Exp Rheumatol. 2022 Nov;40(11):2052-2059. doi: 10.55563/clinexprheumatol/ogk9sd. Epub 2021 Dec 22. Clin Exp Rheumatol. 2022. PMID: 34936547

5

The extracellular matrix glycoprotein ADAMTSL2 is increased in heart failure and inhibits TGFβ signalling in cardiac fibroblasts.

Rypdal KB, Erusappan PM, Melleby AO, Seifert DE, Palmero S, Strand ME, Tønnessen T, Dahl CP, Almaas V, Hubmacher D, Apte SS, Christensen G, Lunde IG. Rypdal KB, et al. Sci Rep. 2021 Oct 5;11(1):19757. doi: 10.1038/s41598-021-99032-2. Sci Rep. 2021. PMID: 34611183 Free PMC article.

6

ADAMTSL2 protein and a soluble biomarker signature identify at-risk non-alcoholic steatohepatitis and fibrosis in adults with NAFLD.

Corey KE, Pitts R, Lai M, Loureiro J, Masia R, Osganian SA, Gustafson JL, Hutter MM, Gee DW, Meireles OR, Witkowski ER, Richards SM, Jacob J, Finkel N, Ngo D, Wang TJ, Gerszten RE, Ukomadu C, Jennings LL. Corey KE, et al. J Hepatol. 2022 Jan;76(1):25-33. doi: 10.1016/j.jhep.2021.09.026. Epub 2021 Oct 1. J Hepatol. 2022. PMID: 34600973 Free PMC article.

7

ADAMTSL2 gene variant in patients with features of autosomal dominant connective tissue disorders.

Steinle J, Hossain WA, Lovell S, Veatch OJ, Butler MG. Steinle J, et al. Am J Med Genet A. 2021 Mar;185(3):743-752. doi: 10.1002/ajmg.a.62030. Epub 2020 Dec 27. Am J Med Genet A. 2021. PMID: 33369194 Free PMC article.

8

Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia.

Hubmacher D, Taye N, Balic Z, Thacker S, Adams SM, Birk DE, Schweitzer R, Apte SS. Hubmacher D, et al. Matrix Biol. 2019 Sep;82:38-53. doi: 10.1016/j.matbio.2019.02.001. Epub 2019 Feb 7. Matrix Biol. 2019. PMID: 30738849 Free PMC article.

9

Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix families.

Aviram R, Zaffryar-Eilot S, Hubmacher D, Grunwald H, Mäki JM, Myllyharju J, Apte SS, Hasson P. Aviram R, et al. Matrix Biol. 2019 Jan;75-76:114-125. doi: 10.1016/j.matbio.2018.05.003. Epub 2018 May 17. Matrix Biol. 2019. PMID: 29758265 Free PMC article.

10

A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2.

Li D, Dong H, Zheng H, Song J, Li X, Jin Y, Liu Y, Yang Y. Li D, et al. Eur J Med Genet. 2017 Dec;60(12):685-689. doi: 10.1016/j.ejmg.2017.09.003. Epub 2017 Sep 14. Eur J Med Genet. 2017. PMID: 28917829

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