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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1973 2
1974 1
1978 1
1980 1
1981 4
1982 1
1983 4
1984 8
1985 11
1986 12
1987 5
1988 9
1989 8
1990 21
1991 11
1992 24
1993 19
1994 21
1995 45
1996 36
1997 46
1998 39
1999 57
2000 49
2001 74
2002 70
2003 74
2004 83
2005 98
2006 109
2007 121
2008 132
2009 122
2010 126
2011 140
2012 142
2013 179
2014 198
2015 209
2016 205
2017 207
2018 230
2019 236
2020 245
2021 272
2022 221
2023 215
2024 108

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3,772 results

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Quoted phrase not found in phrase index: "COG6-ongenital disorder of glycosylation"
Page 1
Roles of CA19-9 in pancreatic cancer: Biomarker, predictor and promoter.
Luo G, Jin K, Deng S, Cheng H, Fan Z, Gong Y, Qian Y, Huang Q, Ni Q, Liu C, Yu X. Luo G, et al. Biochim Biophys Acta Rev Cancer. 2021 Apr;1875(2):188409. doi: 10.1016/j.bbcan.2020.188409. Epub 2020 Aug 19. Biochim Biophys Acta Rev Cancer. 2021. PMID: 32827580 Review.
Carbohydrate antigen 19-9 (CA19-9) is the best validated biomarker and an indicator of aberrant glycosylation in pancreatic cancer. CA19-9 functions as a biomarker, predictor, and promoter in pancreatic cancer. ...As a promoter, CA19-9 could be used to evaluate the biology …
Carbohydrate antigen 19-9 (CA19-9) is the best validated biomarker and an indicator of aberrant glycosylation in pancreatic cancer. C …
Protein glycosylation in cancer.
Stowell SR, Ju T, Cummings RD. Stowell SR, et al. Annu Rev Pathol. 2015;10:473-510. doi: 10.1146/annurev-pathol-012414-040438. Annu Rev Pathol. 2015. PMID: 25621663 Free PMC article. Review.
Although genetic alterations underpin the development of neoplastic disease, epigenetic changes can exert an equally significant effect on neoplastic transformation. Among neoplasia-associated epigenetic alterations, changes in cellular glycosylation have recently r …
Although genetic alterations underpin the development of neoplastic disease, epigenetic changes can exert an equally significant effe …
MUC1: An emerging target in cancer treatment and diagnosis.
Qing L, Li Q, Dong Z. Qing L, et al. Bull Cancer. 2022 Nov;109(11):1202-1216. doi: 10.1016/j.bulcan.2022.08.001. Epub 2022 Sep 30. Bull Cancer. 2022. PMID: 36184332 Review.
MUC1 is a highly glycosylated transmembrane mucin on the luminal surface of epithelial cells, protecting them from extreme factors. ...MUC1 glycosylation insufficiency leads to exposure of novel antigenic epitopes that can be used as specific targets for therapy and …
MUC1 is a highly glycosylated transmembrane mucin on the luminal surface of epithelial cells, protecting them from extreme factors. . …
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up.
Altassan R, Péanne R, Jaeken J, Barone R, Bidet M, Borgel D, Brasil S, Cassiman D, Cechova A, Coman D, Corral J, Correia J, de la Morena-Barrio ME, de Lonlay P, Dos Reis V, Ferreira CR, Fiumara A, Francisco R, Freeze H, Funke S, Gardeitchik T, Gert M, Girad M, Giros M, Grünewald S, Hernández-Caselles T, Honzik T, Hutter M, Krasnewich D, Lam C, Lee J, Lefeber D, Marques-de-Silva D, Martinez AF, Moravej H, Õunap K, Pascoal C, Pascreau T, Patterson M, Quelhas D, Raymond K, Sarkhail P, Schiff M, Seroczyńska M, Serrano M, Seta N, Sykut-Cegielska J, Thiel C, Tort F, Vals MA, Videira P, Witters P, Zeevaert R, Morava E. Altassan R, et al. J Inherit Metab Dis. 2019 Jan;42(1):5-28. doi: 10.1002/jimd.12024. J Inherit Metab Dis. 2019. PMID: 30740725
Phosphomannomutase 2 (PMM2-CDG) is the most common congenital disorder of N-glycosylation and is caused by a deficient PMM2 activity. ...
Phosphomannomutase 2 (PMM2-CDG) is the most common congenital disorder of N-glycosylation and is caused by a deficient PMM2 ac …
What is new in CDG?
Jaeken J, Péanne R. Jaeken J, et al. J Inherit Metab Dis. 2017 Jul;40(4):569-586. doi: 10.1007/s10545-017-0050-6. Epub 2017 May 8. J Inherit Metab Dis. 2017. PMID: 28484880 Review.
Congenital disorders of glycosylation (CDG) are one group among the disorders of glycosylation. ...Genetic diseases with hypoglycosylation can be divided in primary congenital disorders of glycosylation (CDG) and in genetic diseases causi …
Congenital disorders of glycosylation (CDG) are one group among the disorders of glycosylation. ...Genetic disea …
2022 Overview of Metabolic Epilepsies.
Tumiene B, Ferreira CR, van Karnebeek CDM. Tumiene B, et al. Genes (Basel). 2022 Mar 12;13(3):508. doi: 10.3390/genes13030508. Genes (Basel). 2022. PMID: 35328062 Free PMC article. Review.
Six hundred metabolic epilepsies have been identified, accounting for as much as 37% of all currently described inherited metabolic diseases (IMD). Epilepsy is a particularly common symptom in disorders of energy metabolism, congenital disorders of glycosylation …
Six hundred metabolic epilepsies have been identified, accounting for as much as 37% of all currently described inherited metabolic diseases …
Altered glycosylation in pancreatic cancer and beyond.
Lumibao JC, Tremblay JR, Hsu J, Engle DD. Lumibao JC, et al. J Exp Med. 2022 Jun 6;219(6):e20211505. doi: 10.1084/jem.20211505. Epub 2022 May 6. J Exp Med. 2022. PMID: 35522218 Free PMC article. Review.
Aberrant glycosylation is a feature of cancer progression and influences a broad range of signaling pathways to promote disease onset and progression. ...A deeper understanding of the functional consequences of altered glycosylation will facilitate future hyp …
Aberrant glycosylation is a feature of cancer progression and influences a broad range of signaling pathways to promote disease …
The challenge of CDG diagnosis.
Francisco R, Marques-da-Silva D, Brasil S, Pascoal C, Dos Reis Ferreira V, Morava E, Jaeken J. Francisco R, et al. Mol Genet Metab. 2019 Jan;126(1):1-5. doi: 10.1016/j.ymgme.2018.11.003. Epub 2018 Nov 9. Mol Genet Metab. 2019. PMID: 30454869 Review.
Congenital disorders of glycosylation (CDG) are a rapidly growing family of genetic diseases that currently includes some 130 different types. ...In addition, the classical screening test, serum transferrin isoelectrofocusing, is only positive in about 60% of CDG, a …
Congenital disorders of glycosylation (CDG) are a rapidly growing family of genetic diseases that currently includes some 130 …
Congenital disorders of glycosylation: narration of a story through its patents.
Monticelli M, D'Onofrio T, Jaeken J, Morava E, Andreotti G, Cubellis MV. Monticelli M, et al. Orphanet J Rare Dis. 2023 Aug 29;18(1):247. doi: 10.1186/s13023-023-02852-w. Orphanet J Rare Dis. 2023. PMID: 37644541 Free PMC article. Review.
Congenital disorders of glycosylation are a group of more than 160 rare genetic defects in protein and lipid glycosylation. ...
Congenital disorders of glycosylation are a group of more than 160 rare genetic defects in protein and lipid glycosylation …
Artificial intelligence in the analysis of glycosylation data.
Li H, Chiang AWT, Lewis NE. Li H, et al. Biotechnol Adv. 2022 Nov;60:108008. doi: 10.1016/j.biotechadv.2022.108008. Epub 2022 Jun 20. Biotechnol Adv. 2022. PMID: 35738510 Free PMC article. Review.
They are involved in diverse essential organismal functions. Aberrant glycosylation may lead to disease development, such as cancer, autoimmune diseases, and inflammatory diseases. ...Finally, we propose how to leverage the gained knowledge for developing predictive …
They are involved in diverse essential organismal functions. Aberrant glycosylation may lead to disease development, such as c …
3,772 results