PubMed for id: 226531226

Year	Number of Results
2003	1
2008	1
2010	1
2011	2
2017	1
2018	1
2019	1
2020	1
2021	1
2022	1
2024	0

1

Disruption of Trip11 in cranial neural crest cells is associated with increased ER and Golgi stress contributing to skull defects in mice.

Yamaguchi H, Meyer MD, He L, Komatsu Y. Yamaguchi H, et al. Dev Dyn. 2022 Jul;251(7):1209-1222. doi: 10.1002/dvdy.461. Epub 2022 Feb 18. Dev Dyn. 2022. PMID: 35147267 Free PMC article.

2

The molecular complex of ciliary and golgin protein is crucial for skull development.

Yamaguchi H, Meyer MD, He L, Senavirathna L, Pan S, Komatsu Y. Yamaguchi H, et al. Development. 2021 Jul 1;148(13):dev199559. doi: 10.1242/dev.199559. Epub 2021 Jul 1. Development. 2021. PMID: 34128978 Free PMC article.

3

Abnormal fertility, acrosome formation, IFT20 expression and localization in conditional Gmap210 knockout mice.

Wang Z, Shi Y, Ma S, Huang Q, Yap YT, Shi L, Zhang S, Zhou T, Li W, Hu B, Zhang L, Krawetz SA, Pazour GJ, Hess RA, Zhang Z. Wang Z, et al. Am J Physiol Cell Physiol. 2020 Jan 1;318(1):C174-C190. doi: 10.1152/ajpcell.00517.2018. Epub 2019 Oct 2. Am J Physiol Cell Physiol. 2020. PMID: 31577511 Free PMC article.

4

The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects.

Bird IM, Kim SH, Schweppe DK, Caetano-Lopes J, Robling AG, Charles JF, Gygi SP, Warman ML, Smits PJ. Bird IM, et al. Development. 2018 Jan 8;145(1):dev156588. doi: 10.1242/dev.156588. Development. 2018. PMID: 29180569 Free PMC article.

5

BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia.

Monis WJ, Faundez V, Pazour GJ. Monis WJ, et al. J Cell Biol. 2017 Jul 3;216(7):2131-2150. doi: 10.1083/jcb.201611138. Epub 2017 Jun 2. J Cell Biol. 2017. PMID: 28576874 Free PMC article.

6

IFT20 is required for opsin trafficking and photoreceptor outer segment development.

Keady BT, Le YZ, Pazour GJ. Keady BT, et al. Mol Biol Cell. 2011 Apr;22(7):921-30. doi: 10.1091/mbc.E10-09-0792. Epub 2011 Feb 9. Mol Biol Cell. 2011. PMID: 21307337 Free PMC article.

7

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype.

Dwyer ND, Manning DK, Moran JL, Mudbhary R, Fleming MS, Favero CB, Vock VM, O'Leary DD, Walsh CA, Beier DR. Dwyer ND, et al. Neural Dev. 2011 Jan 7;6:3. doi: 10.1186/1749-8104-6-3. Neural Dev. 2011. PMID: 21214893 Free PMC article.

8

Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210.

Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, Krakow D, Cohn DH, Kirchhausen T, Warman ML, Beier DR. Smits P, et al. N Engl J Med. 2010 Jan 21;362(3):206-16. doi: 10.1056/NEJMoa0900158. N Engl J Med. 2010. PMID: 20089971 Free PMC article.

9

The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex.

Follit JA, San Agustin JT, Xu F, Jonassen JA, Samtani R, Lo CW, Pazour GJ. Follit JA, et al. PLoS Genet. 2008 Dec;4(12):e1000315. doi: 10.1371/journal.pgen.1000315. Epub 2008 Dec 26. PLoS Genet. 2008. PMID: 19112494 Free PMC article.

10

BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.

Stryke D, Kawamoto M, Huang CC, Johns SJ, King LA, Harper CA, Meng EC, Lee RE, Yee A, L'Italien L, Chuang PT, Young SG, Skarnes WC, Babbitt PC, Ferrin TE. Stryke D, et al. Nucleic Acids Res. 2003 Jan 1;31(1):278-81. doi: 10.1093/nar/gkg064. Nucleic Acids Res. 2003. PMID: 12520002 Free PMC article.

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