Klein A - Search Results

1

Mass spectrometric approach for screening modifications of total serum N-glycome in human diseases: application to cirrhosis.

Morelle W, Flahaut C, Michalski JC, Louvet A, Mathurin P, Klein A. Morelle W, et al. Among authors: klein a. Glycobiology. 2006 Apr;16(4):281-93. doi: 10.1093/glycob/cwj067. Epub 2005 Dec 8. Glycobiology. 2006. PMID: 16339757

2

Modifications of human total serum N-glycome during liver fibrosis-cirrhosis, is it all about immunoglobulins?

Klein A, Michalski JC, Morelle W. Klein A, et al. Proteomics Clin Appl. 2010 Apr;4(4):372-8. doi: 10.1002/prca.200900151. Epub 2010 Mar 5. Proteomics Clin Appl. 2010. PMID: 21137057 Review.

3

Immunoglobulins are the major glycoproteins involved in the modifications of total serum N-glycome in cirrhotic patients.

Klein A, Carre Y, Louvet A, Michalski JC, Morelle W. Klein A, et al. Proteomics Clin Appl. 2010 Apr;4(4):379-93. doi: 10.1002/prca.200900133. Epub 2010 Feb 3. Proteomics Clin Appl. 2010. PMID: 21137058

4

Human total serum N-glycome.

Klein A. Klein A. Adv Clin Chem. 2008;46:51-85. Adv Clin Chem. 2008. PMID: 19004187 Review.

5

Manganese-induced turnover of TMEM165.

Potelle S, Dulary E, Climer L, Duvet S, Morelle W, Vicogne D, Lebredonchel E, Houdou M, Spriet C, Krzewinski-Recchi MA, Peanne R, Klein A, de Bettignies G, Morsomme P, Matthijs G, Marquardt T, Lupashin V, Foulquier F. Potelle S, et al. Among authors: klein a. Biochem J. 2017 Apr 19;474(9):1481-1493. doi: 10.1042/BCJ20160910. Biochem J. 2017. PMID: 28270545 Free PMC article.

6

Cohen syndrome is associated with major glycosylation defects.

Duplomb L, Duvet S, Picot D, Jego G, El Chehadeh-Djebbar S, Marle N, Gigot N, Aral B, Carmignac V, Thevenon J, Lopez E, Rivière JB, Klein A, Philippe C, Droin N, Blair E, Girodon F, Donadieu J, Bellanné-Chantelot C, Delva L, Michalski JC, Solary E, Faivre L, Foulquier F, Thauvin-Robinet C. Duplomb L, et al. Among authors: klein a. Hum Mol Genet. 2014 May 1;23(9):2391-9. doi: 10.1093/hmg/ddt630. Epub 2013 Dec 13. Hum Mol Genet. 2014. PMID: 24334764

7

Golgi post-translational modifications and associated diseases.

Potelle S, Klein A, Foulquier F. Potelle S, et al. Among authors: klein a. J Inherit Metab Dis. 2015 Jul;38(4):741-51. doi: 10.1007/s10545-015-9851-7. Epub 2015 May 13. J Inherit Metab Dis. 2015. PMID: 25967285 Review.

8

Variation of the serum N-glycosylation during the pregnancy of a MPI-CDG patient.

Lebredonchel E, Duvet S, Douillard C, Foulquier F, Klein A. Lebredonchel E, et al. Among authors: klein a. JIMD Rep. 2021 Sep 17;62(1):22-29. doi: 10.1002/jmd2.12247. eCollection 2021 Nov. JIMD Rep. 2021. PMID: 34765394 Free PMC article.

9

Endoplasmic reticulum-associated degradation of glycoproteins bearing Man5GlcNAc2 and Man9GlcNAc2 species in the MI8-5 CHO cell line.

Foulquier F, Duvet S, Klein A, Mir AM, Chirat F, Cacan R. Foulquier F, et al. Among authors: klein a. Eur J Biochem. 2004 Jan;271(2):398-404. doi: 10.1046/j.1432-1033.2003.03938.x. Eur J Biochem. 2004. PMID: 14717707 Free article.

10

Congenital disorder of glycosylation Ib (CDG-Ib) without gastrointestinal symptoms.

Penel-Capelle D, Dobbelaere D, Jaeken J, Klein A, Cartigny M, Weill J. Penel-Capelle D, et al. Among authors: klein a. J Inherit Metab Dis. 2003;26(1):83-5. doi: 10.1023/a:1024044017385. J Inherit Metab Dis. 2003. PMID: 12872847

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