PubMed for id: 2572895192

Year	Number of Results
1989	2
1993	2
1995	1
1996	2
1999	1
2000	1
2022	1
2023	4
2024	0

1

Autosomal recessive otospondylo-mega-epiphyseal dysplasia: comprehensive clinical review of a pediatric cohort.

Mutlu H, Elçioğlu N, Kiliç E. Mutlu H, et al. Clin Dysmorphol. 2023 Oct 1;32(4):151-155. doi: 10.1097/MCD.0000000000000467. Epub 2023 Jul 4. Clin Dysmorphol. 2023. PMID: 37646720

2

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis.

Rebello D, Wohler E, Erfani V, Li G, Aguilera AN, Santiago-Cornier A, Zhao S, Hwang SW, Steiner RD, Zhang TJ, Gurnett CA, Raggio C, Wu N, Sobreira N, Giampietro PF, Ciruna B. Rebello D, et al. Hum Mol Genet. 2023 Sep 16;32(19):2913-2928. doi: 10.1093/hmg/ddad117. Hum Mol Genet. 2023. PMID: 37462524

3

The Association of Variants within Types V and XI Collagen Genes with Knee Joint Laxity Measurements.

Beckley S, Dey R, Stinton S, van der Merwe W, Branch T, September AV, Posthumus M, Collins M. Beckley S, et al. Genes (Basel). 2022 Dec 14;13(12):2359. doi: 10.3390/genes13122359. Genes (Basel). 2022. PMID: 36553626 Free PMC article.

4

Genetic Hearing Loss Overview.

Shearer AE, Hildebrand MS, Schaefer AM, Smith RJH. Shearer AE, et al. 1999 Feb 14 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1999 Feb 14 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301607 Free Books & Documents. Review.

5

Stickler Syndrome.

Mortier G. Mortier G. 2000 Jun 9 [updated 2023 Sep 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2000 Jun 9 [updated 2023 Sep 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301479 Free Books & Documents. Review.

6

The human alpha 2(XI) collagen gene (COL11A2): completion of coding information, identification of the promoter sequence, and precise localization within the major histocompatibility complex reveal overlap with the KE5 gene.

Lui VC, Ng LJ, Sat EW, Cheah KS. Lui VC, et al. Genomics. 1996 Mar 15;32(3):401-12. doi: 10.1006/geno.1996.0135. Genomics. 1996. PMID: 8838804

7

Extensive alternative splicing within the amino-propeptide coding domain of alpha2(XI) procollagen mRNAs. Expression of transcripts encoding truncated pro-alpha chains.

Lui VC, Ng LJ, Sat EW, Nicholls J, Cheah KS. Lui VC, et al. J Biol Chem. 1996 Jul 12;271(28):16945-51. doi: 10.1074/jbc.271.28.16945. J Biol Chem. 1996. PMID: 8663204 Free article.

8

The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens.

Vuristo MM, Pihlajamaa T, Vandenberg P, Prockop DJ, Ala-Kokko L. Vuristo MM, et al. J Biol Chem. 1995 Sep 29;270(39):22873-81. doi: 10.1074/jbc.270.39.22873. J Biol Chem. 1995. PMID: 7559422 Free article.

9

The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization.

Kimura T, Cheah KS, Chan SD, Lui VC, Mattei MG, van der Rest M, Ono K, Solomon E, Ninomiya Y, Olsen BR. Kimura T, et al. J Biol Chem. 1989 Aug 15;264(23):13910-6. J Biol Chem. 1989. PMID: 2760050 Free article.

10

The human alpha 2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6.

Hanson IM, Gorman P, Lui VC, Cheah KS, Solomon E, Trowsdale J. Hanson IM, et al. Genomics. 1989 Nov;5(4):925-31. doi: 10.1016/0888-7543(89)90135-3. Genomics. 1989. PMID: 2591970

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