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Select item 107674151.

“Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene”

Mohammed Ahmed Mohammed Oshi, Jaber Alfaifi, Youssef Ali M. Alqahtani, Mohammed Fahad Aljabri, Naglaa M. Kamal, Jwaher Althopaity, Khalid A. Althobaiti, Abdullah M. Almalki, Salma A. S. Abosabie, Sara A. Abosabie, Hanan Sakr Sherbiny, Saif K. Almanjoomi, Enas A. A. Abdallah

Mol Genet Genomic Med. 2024 Jan; 12(1): e2282. Published online 2023 Oct 6. doi: 10.1002/mgg3.2282

PMCID:: PMC10767415

Abstract Article PDF–708K

Select item 68221892.

Association between oral cleft and transcobalamin 2 polymorphism in a sample study from Nassiriya, Iraq

Francesco Carinci, Annalisa Palmieri, Luca Scapoli, Francesca Cura, Fabio Abenavoli, Aldo Bruno Giannì, Antonio Russillo, Raffaella Docimo, Marcella Martinelli

Int J Immunopathol Pharmacol. 2019 Jan-Dec; 33: 2058738419855571. Published online 2019 Oct 30. doi: 10.1177/2058738419855571

PMCID:: PMC6822189

Abstract Article PDF–434K

Select item 56719993.

Proteome Analysis of Hypoxic Glioblastoma Cells Reveals Sequential Metabolic Adaptation of One-Carbon Metabolic Pathways

Kangling Zhang, Pei Xu, James L. Sowers, Daniel F. Machuca, Barsam Mirfattah, Jason Herring, Hui Tang, Yan Chen, Bing Tian, Allan R. Brasier, Lawrence C. Sowers

Mol Cell Proteomics. 2017 Nov; 16(11): 1906–1921. Published online 2017 Aug 18. doi: 10.1074/mcp.RA117.000154

PMCID:: PMC5671999

Abstract Article PDF–3.1M

Select item 56117834.

Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studies

Abderrahim Oussalah, Julien Levy, Pierre Filhine-Trésarrieu, Fares Namour, Jean-Louis Guéant

Am J Clin Nutr. 2017 Oct; 106(4): 1142–1156. Published online 2017 Aug 16. doi: 10.3945/ajcn.117.156349

PMCID:: PMC5611783

Abstract Article PDF–1.9M

Select item 51187345.

Transcobalamin 776C→G polymorphism is associated with peripheral neuropathy in elderly individuals with high folate intake

Hathairat Sawaengsri, Peter R Bergethon, Wei Qiao Qiu, Tammy M Scott, Paul F Jacques, Jacob Selhub, Ligi Paul

Am J Clin Nutr. 2016 Dec; 104(6): 1665–1670. Published online 2016 Oct 12. doi: 10.3945/ajcn.116.139030

PMCID:: PMC5118734

Abstract Article PDF–488K

Select item 48053276.

Transcobalamin II Deficiency in Four Cases with Novel Mutations

Şule Ünal, Tony Rupar, Sevgi Yetgin, Neşe Yaralı, Ali Dursun, Türkiz Gürsel, Mualla Çetin

Turk J Haematol. 2015 Dec; 32(4): 317–322. Published online 2015 Dec 3. doi: 10.4274/tjh.2014.0154

PMCID:: PMC4805327

Abstract Article PDF–179K

Select item 35049457.

Association of transcobalamin c. 776C>G with overall survival in patients with primary central nervous system lymphoma

M Linnebank, S Moskau, A Kowoll, A Semmler, C Bangard, M Vogt-Schaden, G Egerer, G Schackert, H Reichmann, I G H Schmidt-Wolf, H Pels, U Schlegel

Br J Cancer. 2012 Nov 20; 107(11): 1840–1843. Published online 2012 Oct 25. doi: 10.1038/bjc.2012.476

PMCID:: PMC3504945

Abstract Article PDF–442K

Select item 31989748.

Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk

F.-C. Hsu, E.G. Sides, J.C. Mychaleckyj, B.B. Worrall, G.A. Elias, Y. Liu, W.-M. Chen, B.M. Coull, J.F. Toole, S.S. Rich, K.L. Furie, M.M. Sale

Neurology. 2011 Oct 18; 77(16): 1543–1550. doi: 10.1212/WNL.0b013e318233b1f9

Correction in:: Neurology. 2012 Jul 24; 79(4): 393.

PMCID:: PMC3198974

Abstract Article PDF–392K

Select item 16855739.

Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma.

S P Daiger, M L Labowe, M Parsons, L Wang, L L Cavalli-Sforza

Am J Hum Genet. 1978 Mar; 30(2): 202–214.

PMCID:: PMC1685573

Summary Page Browse PDF–1.6M

Select item 113712110.

Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patients.

N Li, S Seetharam, D S Rosenblatt, B Seetharam

Biochem J. 1994 Jul 15; 301(Pt 2): 585–590. doi: 10.1042/bj3010585

PMCID:: PMC1137121

Summary Page Browse PDF–1.5M

Select item 664225011.

Genetic polymorphisms of the cobalamin transport system are associated with idiopathic recurrent implantation failure

Han Sung Park, Jung Oh Kim, Hui Jeong An, Chang Soo Ryu, Eun Ju Ko, Young Ran Kim, Eun Hee Ahn, Woo Sik Lee, Ji Hyang Kim, Nam Keun Kim

J Assist Reprod Genet. 2019 Jul; 36(7): 1513–1522. Published online 2019 May 23. doi: 10.1007/s10815-019-01455-4

PMCID:: PMC6642250

Abstract Article PDF–285K

Select item 404243012.

Immunohistochemical Quantification of the Vitamin B12 Transport Protein (TCII), Cell Surface Receptor (TCII-R) and Ki-67 in Human Tumor Xenografts

Annette M. Sysel, Victor E. Valli, Ray B. Nagle, Joseph A. Bauer

Anticancer Res. Author manuscript; available in PMC 2014 Oct 1.

Published in final edited form as: Anticancer Res. 2013 Oct; 33(10): 4203–4212.

PMCID:: PMC4042430

Abstract Article PDF–917K

Select item 286478713.

Transcobalamin C776G Genotype Modifies the Association between Vitamin B12 and Homocysteine in Older Hispanics

Marjorie G. Garrod, Lindsay H. Allen, Mary N. Haan, Ralph Green, Joshua W. Miller

Eur J Clin Nutr. Author manuscript; available in PMC 2010 Nov 1.

Published in final edited form as: Eur J Clin Nutr. 2010 May; 64(5): 503–509. Published online 2010 Mar 10. doi: 10.1038/ejcn.2010.20

PMCID:: PMC2864787

Abstract Article PDF–790K

Select item 274087914.

Environmental influence on the worldwide prevalence of a 776C→G variant in the transcobalamin gene (TCN2)

Jean‐Louis Guéant, Nicodème W Chabi, Rosa‐Maria Guéant‐Rodriguez, Osvaldo M Mutchinick, Renée Debard, Corinne Payet, Xiaohong Lu, Christian Villaume, Jean‐Pierre Bronowicki, Edward V Quadros, Ambaliou Sanni, Emile Amouzou, Bing Xia, Min Chen, Guido Anello, Paolo Bosco, Corrado Romano, Heidy R Arrieta, Beatríz E Sánchez, Antonino Romano, Bernard Herbeth, Wafaa Anwar, Fares Namour

J Med Genet. 2007 Jun; 44(6): 363–367. Published online 2007 Jan 12. doi: 10.1136/jmg.2006.048041

PMCID:: PMC2740879

Abstract Article PDF–224K

Select item 271895515.

Association of genetic variants of methionine metabolism with methotrexate-induced CNS white matter changes in patients with primary CNS lymphoma

Michael Linnebank, Susanna Moskau, Annika Jürgens, Matthias Simon, Alexander Semmler, Katjana Orlopp, Axel Glasmacher, Christopher Bangard, Marlies Vogt-Schaden, Horst Urbach, Ingo G.H. Schmidt-Wolf, Hendrik Pels, Uwe Schlegel

Neuro Oncol. 2009 Feb; 11(1): 2–8. doi: 10.1215/15228517-2008-082

PMCID:: PMC2718955

Abstract Article PDF–258K

Select item 692335216.

Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressure

Shan Liu, Mengwei Liu, Qian Li, Xiuping Liu, Yue Wang, Michael Mambiya, Kaili Zhang, Luping Yang, Qian Zhang, Mengke Shang, Fanxin Zeng, Fangfang Nie, Wanyang Liu

Biosci Rep. 2019 Dec 20; 39(12): BSR20191454. Published online 2019 Dec 17. doi: 10.1042/BSR20191454