-
1
-
-
0015129206
-
Inclusion body myositis
-
Yunis EJ, Samaha FJ. Inclusion body myositis. Lab. Invest. 25(3), 240-248 (1971).
-
(1971)
Lab. Invest.
, vol.25
, Issue.3
, pp. 240-248
-
-
Yunis, E.J.1
Samaha, F.J.2
-
2
-
-
0028787389
-
Inclusion body myositis and myopathies
-
Griggs RC, Askanas V, DiMauro S et al. Inclusion body myositis and myopathies. Ann. Neurol. 38(5), 705-713 (1995).
-
(1995)
Ann. Neurol.
, vol.38
, Issue.5
, pp. 705-713
-
-
Griggs, R.C.1
Askanas, V.2
Dimauro, S.3
-
3
-
-
0028832396
-
New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies
-
Askanas V, Engel WK. New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies. Curr. Opin. Rheumatol. 7(6), 486-496 (1995).
-
(1995)
Curr. Opin. Rheumatol.
, vol.7
, Issue.6
, pp. 486-496
-
-
Askanas, V.1
Engel, W.K.2
-
4
-
-
0021320516
-
"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews
-
Argov Z, Yarom R. "Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews. J. Neurol. Sci. 64(1), 33-43 (1984).
-
(1984)
J. Neurol. Sci.
, vol.64
, Issue.1
, pp. 33-43
-
-
Argov, Z.1
Yarom, R.2
-
5
-
-
53049089196
-
The hereditary inclusion body myopathy enigma and its future therapy
-
Argov Z, Mitrani-Rosenbaum S. The hereditary inclusion body myopathy enigma and its future therapy. Neurotherapeutics 5(4), 633-637 (2008).
-
(2008)
Neurotherapeutics
, vol.5
, Issue.4
, pp. 633-637
-
-
Argov, Z.1
Mitrani-Rosenbaum, S.2
-
6
-
-
70249085865
-
Hereditary inclusion body myopathy: A decade of progress
-
Huizing M, Krasnewich DM. Hereditary inclusion body myopathy: a decade of progress. Biochim. Biophys. Acta 1792(9), 881-887 (2009).
-
(2009)
Biochim. Biophys. Acta
, vol.1792
, Issue.9
, pp. 881-887
-
-
Huizing, M.1
Krasnewich, D.M.2
-
7
-
-
84906264260
-
-
Scriver's Online Metabolic and Molecular Bases of Inherited Disease
-
Scriver's Online Metabolic and Molecular Bases of Inherited Disease. http://ommbid.mh me dical.com/book.aspx+bookID +474
-
-
-
-
8
-
-
17944366749
-
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
-
Eisenberg I, Avidan N, Potikha T et al. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nat. Genet. 29(1), 83-87 (2001).
-
(2001)
Nat. Genet.
, vol.29
, Issue.1
, pp. 83-87
-
-
Eisenberg, I.1
Avidan, N.2
Potikha, T.3
-
9
-
-
0030827128
-
A bifunctional enzyme catalyzes the frst two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purifcation and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase
-
Hinderlich S, Stasche R, Zeitler R, Reutter W. A bifunctional enzyme catalyzes the frst two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purifcation and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase. J. Biol. Chem. 272(39), 24313-24318 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, Issue.39
, pp. 24313-24318
-
-
Hinderlich, S.1
Stasche, R.2
Zeitler, R.3
Reutter, W.4
-
10
-
-
77957183382
-
Diversity in the sialic acids
-
Varki A. Diversity in the sialic acids. Glycobiology 2(1), 25-40 (1992).
-
(1992)
Glycobiology
, vol.2
, Issue.1
, pp. 25-40
-
-
Varki, A.1
-
11
-
-
0033591388
-
UDP-GlcNAc 2-epimerase: A regulator of cell surface sialylation
-
Keppler OT, Hinderlich S, Langner J, Schwartz-Albiez R, Reutter W, Pawlita M. UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation. Science 284(5418), 1372-1376 (1999).
-
(1999)
Science
, vol.284
, Issue.5418
, pp. 1372-1376
-
-
Keppler, O.T.1
Hinderlich, S.2
Langner, J.3
Schwartz-Albiez, R.4
Reutter, W.5
Pawlita, M.6
-
12
-
-
48149090000
-
Sialic acids in human health and disease
-
Varki A. Sialic acids in human health and disease. Trends Mol. Med. 14(8), 351-360 (2008).
-
(2008)
Trends Mol. Med.
, vol.14
, Issue.8
, pp. 351-360
-
-
Varki, A.1
-
13
-
-
12144287262
-
Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles
-
Noguchi S, Keira Y, Murayama K et al. Reduction of UDP-N- acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles. J. Biol. Chem. 279(12), 11402-11407 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, Issue.12
, pp. 11402-11407
-
-
Noguchi, S.1
Keira, Y.2
Murayama, K.3
-
14
-
-
27944459314
-
Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy
-
Sparks SE, Ciccone C, Lalor M et al. Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. Glycobiology 15(11), 1102-1110 (2005).
-
(2005)
Glycobiology
, vol.15
, Issue.11
, pp. 1102-1110
-
-
Sparks, S.E.1
Ciccone, C.2
Lalor, M.3
-
16
-
-
20244374708
-
Distal myopathy with rimmed vacuoles: Impaired O-glycan formation in muscular glycoproteins
-
Tajima Y, Uyama E, Go S et al. Distal myopathy with rimmed vacuoles: impaired O-glycan formation in muscular glycoproteins. Am. J. Pathol. 166(4), 1121-1130 (2005).
-
(2005)
Am. J. Pathol.
, vol.166
, Issue.4
, pp. 1121-1130
-
-
Tajima, Y.1
Uyama, E.2
Go, S.3
-
17
-
-
1242292943
-
Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations
-
Huizing M, Rakocevic G, Sparks SE et al. Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations. Mol. Genet. Metab. 81(3), 196-202 (2004).
-
(2004)
Mol. Genet. Metab.
, vol.81
, Issue.3
, pp. 196-202
-
-
Huizing, M.1
Rakocevic, G.2
Sparks, S.E.3
-
18
-
-
42449147150
-
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle
-
Broccolini A, Gidaro T, De Cristofaro R et al. Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle. J. Neurochem. 105(3), 971-981 (2008).
-
(2008)
J. Neurochem.
, vol.105
, Issue.3
, pp. 971-981
-
-
Broccolini, A.1
Gidaro, T.2
De Cristofaro, R.3
-
19
-
-
33645870439
-
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations
-
Ricci E, Broccolini A, Gidaro T et al. NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations. Neurology 66(5), 755-758 (2006).
-
(2006)
Neurology
, vol.66
, Issue.5
, pp. 755-758
-
-
Ricci, E.1
Broccolini, A.2
Gidaro, T.3
-
20
-
-
77956322898
-
Ganglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease
-
Paccalet T, Coulombe Z, Tremblay JP. Ganglioside GM3 levels are altered in a mouse model of HIBM: GM3 as a cellular marker of the disease. PLoS ONE 5(4), e10055 (2010).
-
(2010)
PLoS ONE
, vol.5
, Issue.4
-
-
Paccalet, T.1
Coulombe, Z.2
Tremblay, J.P.3
-
21
-
-
34249874096
-
Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine
-
Galeano B, Klootwijk R, Manoli I et al. Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine. J. Clin. Invest. 117(6), 1585-1594 (2007).
-
(2007)
J. Clin. Invest.
, vol.117
, Issue.6
, pp. 1585-1594
-
-
Galeano, B.1
Klootwijk, R.2
Manoli, I.3
-
22
-
-
67349234199
-
Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model
-
Malicdan MC, Noguchi S, Hayashi YK, Nonaka I, Nishino I. Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model. Nat. Med. 15(6), 690-695 (2009).
-
(2009)
Nat. Med.
, vol.15
, Issue.6
, pp. 690-695
-
-
Malicdan, M.C.1
Noguchi, S.2
Hayashi, Y.K.3
Nonaka, I.4
Nishino, I.5
-
23
-
-
33846946820
-
Intravenous immune globulin in hereditary inclusion body myopathy: A pilot study
-
Sparks S, Rakocevic G, Joe G et al. Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study. BMC Neurol. 7, 3 (2007).
-
(2007)
BMC Neurol.
, vol.7
, pp. 3
-
-
Sparks, S.1
Rakocevic, G.2
Joe, G.3
-
24
-
-
77952558706
-
Hereditary inclusion body myopathy: Single patient response to GNE gene Lipoplex therapy
-
Nemunaitis G, Maples PB, Jay C et al. Hereditary inclusion body myopathy: single patient response to GNE gene Lipoplex therapy. J. Gene Med. 12(5), 403-412 (2010).
-
(2010)
J. Gene Med.
, vol.12
, Issue.5
, pp. 403-412
-
-
Nemunaitis, G.1
Maples, P.B.2
Jay, C.3
-
25
-
-
81855184520
-
Hereditary inclusion body myopathy: Single patient response to intravenous dosing of GNE gene lipoplex
-
Nemunaitis G, Jay CM, Maples PB et al. Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplex. Hum. Gene Ther. 22(11), 1331-1341 (2011).
-
(2011)
Hum. Gene Ther.
, vol.22
, Issue.11
, pp. 1331-1341
-
-
Nemunaitis, G.1
Jay, C.M.2
Maples, P.B.3
-
26
-
-
77954974790
-
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy
-
Broccolini A, Gidaro T, Tasca G et al. Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy. Neurology 75(3), 265-272 (2010).
-
(2010)
Neurology
, vol.75
, Issue.3
, pp. 265-272
-
-
Broccolini, A.1
Gidaro, T.2
Tasca, G.3
-
27
-
-
33645100936
-
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fbres of inclusion body myositis
-
Broccolini A, Gidaro T, Morosetti R et al. Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fbres of inclusion body myositis. J. Neurochem. 96(3), 777-789 (2006).
-
(2006)
J. Neurochem.
, vol.96
, Issue.3
, pp. 777-789
-
-
Broccolini, A.1
Gidaro, T.2
Morosetti, R.3
-
28
-
-
84861512568
-
Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy
-
Valles-Ayoub Y, Esfandiarifard S, Sinai P et al. Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy. Genet. Test. Mol. Biomarkers 16(5), 313-317 (2012).
-
(2012)
Genet. Test. Mol. Biomarkers
, vol.16
, Issue.5
, pp. 313-317
-
-
Valles-Ayoub, Y.1
Esfandiarifard, S.2
Sinai, P.3
-
29
-
-
33746305634
-
Normal sialylation of serum N-linked and O-GalNAc-linked glycans in hereditary inclusion-body myopathy
-
Savelkoul PJ, Manoli I, Sparks SE et al. Normal sialylation of serum N-linked and O-GalNAc-linked glycans in hereditary inclusion-body myopathy. Mol. Genet. Metab. 88(4), 389-390 (2006).
-
(2006)
Mol. Genet. Metab.
, vol.88
, Issue.4
, pp. 389-390
-
-
Savelkoul, P.J.1
Manoli, I.2
Sparks, S.E.3
-
30
-
-
33847354287
-
Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N-and O-glycan biosynthesis defects
-
Wopereis S, Grunewald S, Huijben KM et al. Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N-and O-glycan biosynthesis defects. Clin. Chem. 53(2), 180-187 (2007).
-
(2007)
Clin. Chem.
, vol.53
, Issue.2
, pp. 180-187
-
-
Wopereis, S.1
Grunewald, S.2
Huijben, K.M.3
-
31
-
-
84864353995
-
N-and O-linked glycosylation of total plasma glycoproteins in galactosemia
-
Liu Y, Xia B, Gleason TJ et al. N-and O-linked glycosylation of total plasma glycoproteins in galactosemia. Mol. Genet. Metab. 106(4), 442-454 (2012).
-
(2012)
Mol. Genet. Metab.
, vol.106
, Issue.4
, pp. 442-454
-
-
Liu, Y.1
Xia, B.2
Gleason, T.J.3
-
32
-
-
0014408452
-
Structures and immunochemical properties of oligosaccharides isolated from pig submaxillary mucins
-
Carlson DM. Structures and immunochemical properties of oligosaccharides isolated from pig submaxillary mucins. J. Biol. Chem. 243(3), 616-626 (1968).
-
(1968)
J. Biol. Chem.
, vol.243
, Issue.3
, pp. 616-626
-
-
Carlson, D.M.1
-
33
-
-
34250330012
-
A rapid mass spectrometric strategy for the characterization of Nand O-glycan chains in the diagnosis of defects in glycan biosynthesis
-
Faid V, Chirat F, Seta N, Foulquier F, Morelle W. A rapid mass spectrometric strategy for the characterization of Nand O-glycan chains in the diagnosis of defects in glycan biosynthesis. Proteomics 7(11), 1800-1813 (2007).
-
(2007)
Proteomics
, vol.7
, Issue.11
, pp. 1800-1813
-
-
Faid, V.1
Chirat, F.2
Seta, N.3
Foulquier, F.4
Morelle, W.5
-
34
-
-
84884498276
-
Serum N-glycan and O-glycan analysis by mass spectrometry for diagnosis of congenital disorders of glycosylation
-
Xia B, Zhang W, Li X et al. Serum N-glycan and O-glycan analysis by mass spectrometry for diagnosis of congenital disorders of glycosylation. Anal. Biochem. 442(2), 178-185 (2013).
-
(2013)
Anal. Biochem.
, vol.442
, Issue.2
, pp. 178-185
-
-
Xia, B.1
Zhang, W.2
Li, X.3
-
35
-
-
79954626850
-
Plasma N-glycan profling by mass spectrometry for congenital disorders of glycosylation type II
-
Guillard M, Morava E, Van Delft FL et al. Plasma N-glycan profling by mass spectrometry for congenital disorders of glycosylation type II. Clin. Chem. 57(4), 593-602 (2011).
-
(2011)
Clin. Chem.
, vol.57
, Issue.4
, pp. 593-602
-
-
Guillard, M.1
Morava, E.2
Van Delft, F.L.3
-
36
-
-
27344457893
-
Application of tandem mass spectrometry in the structure determination of permethylated sialic acid-containing oligosaccharides
-
Yoo E, Yoon I. Application of tandem mass spectrometry in the structure determination of permethylated sialic acid-containing oligosaccharides. Bull. Korean Chem. Soc. 26(9), 1347-1353 (2005).
-
(2005)
Bull. Korean Chem. Soc.
, vol.26
, Issue.9
, pp. 1347-1353
-
-
Yoo, E.1
Yoon, I.2
-
37
-
-
0023186308
-
Brackenbury. Neural cell adhesion molecule: Structure, immunoglobulin-like domains, cell surface modulation, and alternative RNA splicing
-
Cunningham BA, Hemperly JJ, Murray BA, Prediger EA, Brackenbury. Neural cell adhesion molecule: structure, immunoglobulin-like domains, cell surface modulation, and alternative RNA splicing. Science 236(4803), 799-806 (1987).
-
(1987)
Science
, vol.236
, Issue.4803
, pp. 799-806
-
-
Cunningham, B.A.1
Hemperly, J.J.2
Murray, B.A.3
Prediger, E.A.4
-
38
-
-
0023600981
-
Identifcation of a cDNA clone that contains the complete coding sequence for a 140-kD rat NCAM polypeptide
-
Small SJ, Shull GE, Santoni MJ, Akeson R. Identifcation of a cDNA clone that contains the complete coding sequence for a 140-kD rat NCAM polypeptide. J. Cell. Biol. 105(5), 2335-2345 (1987).
-
(1987)
J. Cell. Biol.
, vol.105
, Issue.5
, pp. 2335-2345
-
-
Small, S.J.1
Shull, G.E.2
Santoni, M.J.3
Akeson, R.4
-
39
-
-
34047255890
-
Lectins: Carbohydrate-specifc reagents and biological recognition molecules
-
Sharon N. Lectins: carbohydrate-specifc reagents and biological recognition molecules. J. Biol. Chem. 282(5), 2753-2764 (2007).
-
(2007)
J. Biol. Chem.
, vol.282
, Issue.5
, pp. 2753-2764
-
-
Sharon, N.1
-
40
-
-
59749086716
-
Specifcity analysis of lectins and antibodies using remodeled glycoproteins
-
Iskratsch T, Braun A, Paschinger K, Wilson IB. Specifcity analysis of lectins and antibodies using remodeled glycoproteins. Anal. Biochem. 386(2), 133-146 (2009).
-
(2009)
Anal. Biochem.
, vol.386
, Issue.2
, pp. 133-146
-
-
Iskratsch, T.1
Braun, A.2
Paschinger, K.3
Wilson, I.B.4
-
41
-
-
0020488865
-
Specifcity of isolectins of wheat germ agglutinin for sialyloligosaccharides: A 360-MHz proton nuclear magnetic resonance binding study
-
Kronis KA, Carver JP. Specifcity of isolectins of wheat germ agglutinin for sialyloligosaccharides: a 360-MHz proton nuclear magnetic resonance binding study. Biochemistry 21(13), 3050-3057 (1982).
-
(1982)
Biochemistry
, vol.21
, Issue.13
, pp. 3050-3057
-
-
Kronis, K.A.1
Carver, J.P.2
-
42
-
-
0023644482
-
The elderberry (Sambucus nigra L.) bark lectin recognizes the Neu5Ac(alpha 2-6)Gal/GalNAc sequence
-
Shibuya N, Goldstein IJ, Broekaert WF, Nsimba-Lubaki M, Peeters B, Peumans WJ. The elderberry (Sambucus nigra L.) bark lectin recognizes the Neu5Ac(alpha 2-6)Gal/GalNAc sequence. J. Biol. Chem. 262(4), 1596-1601 (1987).
-
(1987)
J. Biol. Chem.
, vol.262
, Issue.4
, pp. 1596-1601
-
-
Shibuya, N.1
Goldstein, I.J.2
Broekaert, W.F.3
Nsimba-Lubaki, M.4
Peeters, B.5
Peumans, W.J.6
-
43
-
-
0026481151
-
Carbohydrate binding specifcity of the Tn-antigen binding lectin from Vicia villosa seeds (VVLB4)
-
Puri KD, Gopalakrishnan B, Surolia A. Carbohydrate binding specifcity of the Tn-antigen binding lectin from Vicia villosa seeds (VVLB4). FEBS Lett 312(2-3), 208-212 (1992).
-
(1992)
FEBS Lett
, vol.312
, Issue.2-3
, pp. 208-212
-
-
Puri, K.D.1
Gopalakrishnan, B.2
Surolia, A.3
-
44
-
-
84869883180
-
Oral monosaccharide therapies to reverse renal and muscle hyposialylation in a mouse model of GNE myopathy
-
Niethamer TK, Yardeni T, Leoyklang P et al. Oral monosaccharide therapies to reverse renal and muscle hyposialylation in a mouse model of GNE myopathy. Mol. Genet. Metab. 107(4), 748-755 (2012).
-
(2012)
Mol. Genet. Metab.
, vol.107
, Issue.4
, pp. 748-755
-
-
Niethamer, T.K.1
Yardeni, T.2
Leoyklang, P.3
-
45
-
-
0034850831
-
The human sialyltransferase family
-
Harduin-Lepers A, Vallejo-Ruiz V, Krzewinski-Recchi MA, Samyn-Petit B, Julien S, Delannoy P. The human sialyltransferase family. Biochimie 83(8), 727-737 (2001).
-
(2001)
Biochimie
, vol.83
, Issue.8
, pp. 727-737
-
-
Harduin-Lepers, A.1
Vallejo-Ruiz, V.2
Krzewinski-Recchi, M.A.3
Samyn-Petit, B.4
Julien, S.5
Delannoy, P.6
-
46
-
-
84865583094
-
New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa
-
Giacopuzzi E, Bresciani R, Schauer R, Monti E, Borsani G. New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa. PLoS ONE 7(8), e44193 (2012).
-
(2012)
PLoS ONE
, vol.7
, Issue.8
-
-
Giacopuzzi, E.1
Bresciani, R.2
Schauer, R.3
Monti, E.4
Borsani, G.5
-
47
-
-
84880279999
-
Desialylation of surface receptors as a new dimension in cell signaling
-
Pshezhetsky AV, Ashmarina LI. Desialylation of surface receptors as a new dimension in cell signaling. Biochemistry (Mosc.) 78(7), 736-745 (2013).
-
(2013)
Biochemistry (Mosc.)
, vol.78
, Issue.7
, pp. 736-745
-
-
Pshezhetsky, A.V.1
Ashmarina, L.I.2
-
48
-
-
0030848719
-
Immunoreactive T and Tn epitopes in cancer diagnosis, prognosis, and immunotherapy
-
Springer GF. Immunoreactive T and Tn epitopes in cancer diagnosis, prognosis, and immunotherapy. J. Mol. Med. (Berl.) 75(8), 594-602 (1997).
-
(1997)
J. Mol. Med. (Berl.)
, vol.75
, Issue.8
, pp. 594-602
-
-
Springer, G.F.1
-
49
-
-
0028818113
-
Expression of Thomsen-Friedenreich-related antigens in primary and metastatic colorectal carcinomas. A re-evaluation
-
Cao Y, Karsten UR, Liebrich W, Haensch W, Springer GF, Schlag PM. Expression of Thomsen-Friedenreich-related antigens in primary and metastatic colorectal carcinomas. A re-evaluation. Cancer 76(10), 1700-1708 (1995).
-
(1995)
Cancer
, vol.76
, Issue.10
, pp. 1700-1708
-
-
Cao, Y.1
Karsten, U.R.2
Liebrich, W.3
Haensch, W.4
Springer, G.F.5
Schlag, P.M.6
-
50
-
-
1642562900
-
Thomsen-Friedenreich antigen: The "hidden" tumor antigen
-
Goletz S, Cao Y, Danielczyk A, Ravn P, Schoeber U, Karsten U. Thomsen-Friedenreich antigen: the "hidden" tumor antigen. Adv. Exp. Med. Biol. 535, 147-162 (2003).
-
(2003)
Adv. Exp. Med. Biol.
, vol.535
, pp. 147-162
-
-
Goletz, S.1
Cao, Y.2
Danielczyk, A.3
Ravn, P.4
Schoeber, U.5
Karsten, U.6
-
51
-
-
0035003195
-
Immunohistochemical expression of T Tn and sialyl-Tn antigens and clinical outcome in human breast carcinoma
-
Imai J, Ghazizadeh M, Naito Z, Asano G. Immunohistochemical expression of T, Tn and sialyl-Tn antigens and clinical outcome in human breast carcinoma. Anticancer Res. 21(2B), 1327-1334 (2001).
-
(2001)
Anticancer Res.
, vol.21
, Issue.2 B
, pp. 1327-1334
-
-
Imai, J.1
Ghazizadeh, M.2
Naito, Z.3
Asano, G.4
-
52
-
-
84856005825
-
Distal myopathies-new genetic entities expand diagnostic challenge
-
Udd B. Distal myopathies-new genetic entities expand diagnostic challenge. Neuromusc. Disord. 22(1), 5-12 (2012).
-
(2012)
Neuromusc. Disord.
, vol.22
, Issue.1
, pp. 5-12
-
-
Udd, B.1
-
53
-
-
80052472115
-
Muscular dystrophies due to glycosylation defects: Diagnosis and therapeutic strategies
-
Muntoni F, Torelli S, Wells DJ, Brown SC. Muscular dystrophies due to glycosylation defects: diagnosis and therapeutic strategies. Curr. Opin. Neurol. 24(5), 437-442 (2011).
-
(2011)
Curr. Opin. Neurol.
, vol.24
, Issue.5
, pp. 437-442
-
-
Muntoni, F.1
Torelli, S.2
Wells, D.J.3
Brown, S.C.4
-
54
-
-
77951886324
-
Impact of glycosylation on effector functions of therapeutic IgG
-
Abes R, Teillaud J-L. Impact of glycosylation on effector functions of therapeutic IgG. Pharmaceuticals 3, 146-157 (2010).
-
(2010)
Pharmaceuticals
, vol.3
, pp. 146-157
-
-
Abes, R.1
Teillaud, J.-L.2
|