PubMed for id: 148789

Year	Number of Results
2002	1
2003	1
2004	3
2006	1
2011	1
2012	2
2013	4
2014	2
2015	2
2017	4
2018	1
2019	1
2020	3
2021	1
2022	6
2023	1
2024	0

1

[Genetic analysis of a Chinese family affected with α-dystroglycanopathy due to variant of B3GALNT2 gene].

Zeng L, Lin L, Zhang Y, Lin K, Xu Q, Lin C. Zeng L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Jul 10;40(7):802-806. doi: 10.3760/cma.j.cn511374-20220624-00426. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37368380 Chinese.

2

Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene.

Wang P, Jin P, Zhu L, Chen M, Qian Y, Zeng W, Wang M, Xu Y, Xu Y, Dong M. Wang P, et al. J Gene Med. 2022 May;24(5):e3417. doi: 10.1002/jgm.3417. Epub 2022 Apr 6. J Gene Med. 2022. PMID: 35338537 Free PMC article.

3

Novel mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients.

Chen XY, Song DY, Fan YB, Tan DD, Chang XZ, Xiao JX, Toda T, Xiong H. Chen XY, et al. Chin Med J (Engl). 2020 Dec 7;134(12):1483-1485. doi: 10.1097/CM9.0000000000001283. Chin Med J (Engl). 2020. PMID: 33290285 Free PMC article. No abstract available.

4

Identification of mammalian glycoproteins with type-I LacdiNAc structures synthesized by the glycosyltransferase B3GALNT2.

Nakane T, Angata K, Sato T, Kaji H, Narimatsu H. Nakane T, et al. J Biol Chem. 2019 May 3;294(18):7433-7444. doi: 10.1074/jbc.RA118.006892. Epub 2019 Mar 21. J Biol Chem. 2019. PMID: 30898876 Free PMC article.

5

Increased B3GALNT2 in hepatocellular carcinoma promotes macrophage recruitment via reducing acetoacetate secretion and elevating MIF activity.

Yang T, Wang Y, Dai W, Zheng X, Wang J, Song S, Fang L, Zhou J, Wu W, Gu J. Yang T, et al. J Hematol Oncol. 2018 Apr 4;11(1):50. doi: 10.1186/s13045-018-0595-3. J Hematol Oncol. 2018. PMID: 29618368 Free PMC article.

6

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.

Maroofian R, Riemersma M, Jae LT, Zhianabed N, Willemsen MH, Wissink-Lindhout WM, Willemsen MA, de Brouwer APM, Mehrjardi MYV, Ashrafi MR, Kusters B, Kleefstra T, Jamshidi Y, Nasseri M, Pfundt R, Brummelkamp TR, Abbaszadegan MR, Lefeber DJ, van Bokhoven H. Maroofian R, et al. Genome Med. 2017 Dec 22;9(1):118. doi: 10.1186/s13073-017-0505-2. Genome Med. 2017. PMID: 29273094 Free PMC article.

7

Involvement of B3GALNT2 overexpression in the cell growth of breast cancer.

Matsuo T, Komatsu M, Yoshimaru T, Kiyotani K, Miyoshi Y, Sasa M, Katagiri T. Matsuo T, et al. Int J Oncol. 2014 Feb;44(2):427-34. doi: 10.3892/ijo.2013.2187. Epub 2013 Nov 27. Int J Oncol. 2014. PMID: 24285400

8

B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations.

Hedberg C, Oldfors A, Darin N. Hedberg C, et al. Eur J Hum Genet. 2014 May;22(5):707-10. doi: 10.1038/ejhg.2013.223. Epub 2013 Oct 2. Eur J Hum Genet. 2014. PMID: 24084573 Free PMC article.

9

A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAc.

Hiruma T, Togayachi A, Okamura K, Sato T, Kikuchi N, Kwon YD, Nakamura A, Fujimura K, Gotoh M, Tachibana K, Ishizuka Y, Noce T, Nakanishi H, Narimatsu H. Hiruma T, et al. J Biol Chem. 2004 Apr 2;279(14):14087-95. doi: 10.1074/jbc.M310614200. Epub 2004 Jan 14. J Biol Chem. 2004. PMID: 14724282 Free article.

10

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.

Stevens E, Carss KJ, Cirak S, Foley AR, Torelli S, Willer T, Tambunan DE, Yau S, Brodd L, Sewry CA, Feng L, Haliloglu G, Orhan D, Dobyns WB, Enns GM, Manning M, Krause A, Salih MA, Walsh CA, Hurles M, Campbell KP, Manzini MC; UK10K Consortium; Stemple D, Lin YY, Muntoni F. Stevens E, et al. Am J Hum Genet. 2013 Mar 7;92(3):354-65. doi: 10.1016/j.ajhg.2013.01.016. Epub 2013 Feb 28. Am J Hum Genet. 2013. PMID: 23453667 Free PMC article.

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