-
1
-
-
0021320516
-
Rimmed vacuole myopathy sparing the quadriceps. A unique disorder in Iranian Jews
-
Argov Z, Yarom R (1984) "Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews. J Neurol Sci 64 (1): 33-43.
-
(1984)
J Neurol Sci
, vol.64
, Issue.1
, pp. 33-43
-
-
Argov, Z.1
Yarom, R.2
-
2
-
-
0027407477
-
Vacuolar myopathy sparing the quadriceps
-
Sadeh M, Gadoth N, Hadar H, Ben-David E (1993) Vacuolar myopathy sparing the quadriceps. Brain 116 (Pt 1): 217-232.
-
(1993)
Brain
, vol.116
, Issue.Pt 1
, pp. 217-232
-
-
Sadeh, M.1
Gadoth, N.2
Hadar, H.3
Ben-David, E.4
-
3
-
-
36349012566
-
Muscle sonography in six patients with hereditary inclusion body myopathy
-
Adler RS, Garolfalo G, Paget S, Kagen L (2008) Muscle sonography in six patients with hereditary inclusion body myopathy. Skeletal Radiol 37 (1): 43-48.
-
(2008)
Skeletal Radiol
, vol.37
, Issue.1
, pp. 43-48
-
-
Adler, R.S.1
Garolfalo, G.2
Paget, S.3
Kagen, L.4
-
4
-
-
0019481203
-
Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation
-
Nonaka I, Sunohara N, Ishiura S, Satoyoshi E (1981) Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation. J Neurol Sci 51 (1): 141-155.
-
(1981)
J Neurol Sci
, vol.51
, Issue.1
, pp. 141-155
-
-
Nonaka, I.1
Sunohara, N.2
Ishiura, S.3
Satoyoshi, E.4
-
5
-
-
0031926006
-
Distal myopathy with rimmed vacuoles
-
Nonaka I, Murakami N, Suzuki Y, Kawai M (1998) Distal myopathy with rimmed vacuoles. Neuromuscul Disord 8 (5): 333-337.
-
(1998)
Neuromuscul Disord
, vol.8
, Issue.5
, pp. 333-337
-
-
Nonaka, I.1
Murakami, N.2
Suzuki, Y.3
Kawai, M.4
-
6
-
-
0033377221
-
Distal myopathies
-
Nonaka I (1999) Distal myopathies. Curr Opin Neurol 12 (5): 493-499.
-
(1999)
Curr Opin Neurol
, vol.12
, Issue.5
, pp. 493-499
-
-
Nonaka, I.1
-
7
-
-
0031799116
-
Immunohistochemical study of clathrin in distal myopathy with rimmed vacuoles
-
Kumamoto T, Abe T, Nagao S, Ueyama H, Tsuda T (1998) Immunohistochemical study of clathrin in distal myopathy with rimmed vacuoles. Acta Neuropathol 95 (6): 571-575.
-
(1998)
Acta Neuropathol
, vol.95
, Issue.6
, pp. 571-575
-
-
Kumamoto, T.1
Abe, T.2
Nagao, S.3
Ueyama, H.4
Tsuda, T.5
-
8
-
-
17944366749
-
The UDPN- acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
-
Eisenberg I, Avidan N, Potikha T, Hochner H, Chen M, et al. (2001) The UDPN- acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nat Genet 29 (1): 83-87.
-
(2001)
Nat Genet
, vol.29
, Issue.1
, pp. 83-87
-
-
Eisenberg, I.1
Avidan, N.2
Potikha, T.3
Hochner, H.4
Chen, M.5
-
9
-
-
0030063986
-
Hereditary inclusion body myopathy maps to chromosome 9p1-q1
-
Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, Seidman CE, Seidman JG (1996) Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Hum Mol Genet 5 (1): 159-163.
-
(1996)
Hum Mol Genet
, vol.5
, Issue.1
, pp. 159-163
-
-
Mitrani-Rosenbaum, S.1
Argov, Z.2
Blumenfeld, A.3
Seidman, C.E.4
Seidman, J.G.5
-
10
-
-
0030827128
-
A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/Nacetylmannosamine kinase
-
Hinderlich S, Stasche R, Zeitler R, Reutter W (1997) A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/Nacetylmannosamine kinase. J Biol Chem 272 (39): 24313-24318.
-
(1997)
J Biol Chem
, vol.272
, Issue.39
, pp. 24313-24318
-
-
Hinderlich, S.1
Stasche, R.2
Zeitler, R.3
Reutter, W.4
-
11
-
-
0027318961
-
Biological roles of oligosaccharides: All of the theories are correct
-
Varki A (1993) Biological roles of oligosaccharides: all of the theories are correct. Glycobiology 3 (2): 97-130.
-
(1993)
Glycobiology
, vol.3
, Issue.2
, pp. 97-130
-
-
Varki, A.1
-
12
-
-
0030993576
-
Sialic acids as ligands in recognition phenomena
-
Varki A (1997) Sialic acids as ligands in recognition phenomena. Faseb J 11 (4): 248-255.
-
(1997)
Faseb J
, vol.11
, Issue.4
, pp. 248-255
-
-
Varki, A.1
-
13
-
-
29444437433
-
Siglecs-the major subfamily of I-type lectins
-
Varki A, Angata T (2006) Siglecs-the major subfamily of I-type lectins. Glycobiology 16 (1): 1R-27R.
-
(2006)
Glycobiology
, vol.16
, Issue.1
-
-
Varki, A.1
Angata, T.2
-
14
-
-
0037117532
-
Sialylation is essential for early development in mice
-
Schwarzkopf M, Knobeloch KP, Rohde E, Hinderlich S, Wiechens N, et al. (2002) Sialylation is essential for early development in mice. Proc Natl Acad Sci U S A 99 (8): 5267-5270.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, Issue.8
, pp. 5267-5270
-
-
Schwarzkopf, M.1
Knobeloch, K.P.2
Rohde, E.3
Hinderlich, S.4
Wiechens, N.5
-
15
-
-
2442555152
-
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/Nacetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy
-
Hinderlich S, Salama I, Eisenberg I, Potikha T, Mantey LR, et al. (2004) The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/Nacetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy. FEBS Lett 566 (1-3): 105-109.
-
(2004)
FEBS Lett
, vol.566
, Issue.1-3
, pp. 105-109
-
-
Hinderlich, S.1
Salama, I.2
Eisenberg, I.3
Potikha, T.4
Mantey, L.R.5
-
16
-
-
12144287262
-
Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distalmyopathy with rimmed vacuoles
-
Noguchi S, Keira Y, Murayama K, Ogawa M, Fujita M, et al. (2004) Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distalmyopathy with rimmed vacuoles. J Biol Chem 279 (12): 11402-11407.
-
(2004)
J Biol Chem
, vol.279
, Issue.12
, pp. 11402-11407
-
-
Noguchi, S.1
Keira, Y.2
Murayama, K.3
Ogawa, M.4
Fujita, M.5
-
17
-
-
27944459314
-
Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and Nacetylmannosamine kinase activities in human hereditary inclusion body myopathy
-
Sparks SE, Ciccone C, Lalor M, Orvisky E, Klootwijk R, et al. (2005) Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and Nacetylmannosamine kinase activities in human hereditary inclusion body myopathy. Glycobiology 15 (11): 1102-1110.
-
(2005)
Glycobiology
, vol.15
, Issue.11
, pp. 1102-1110
-
-
Sparks, S.E.1
Ciccone, C.2
Lalor, M.3
Orvisky, E.4
Klootwijk, R.5
-
18
-
-
33644689755
-
Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy
-
Penner J, Mantey LR, Elgavish S, Ghaderi D, Cirak S, et al. (2006) Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy. Biochemistry 45 (9): 2968-2977.
-
(2006)
Biochemistry
, vol.45
, Issue.9
, pp. 2968-2977
-
-
Penner, J.1
Mantey, L.R.2
Elgavish, S.3
Ghaderi, D.4
Cirak, S.5
-
19
-
-
1242292943
-
Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations
-
Huizing M, Rakocevic G, Sparks SE, Mamali I, Shatunov A, et al. (2004) Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations. Mol Genet Metab 81 (3): 196-202.
-
(2004)
Mol Genet Metab
, vol.81
, Issue.3
, pp. 196-202
-
-
Huizing, M.1
Rakocevic, G.2
Sparks, S.E.3
Mamali, I.4
Shatunov, A.5
-
20
-
-
13444262055
-
Alpha- Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy
-
Broccolini A, Gliubizzi C, Pavoni E, Gidaro T, Morosetti R, et al. (2005) alpha- Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy. Neuromuscul Disord 15 (2): 177-184.
-
(2005)
Neuromuscul Dis
, vol.15
, Issue.2
, pp. 177-184
-
-
Broccolini, A.1
Gliubizzi, C.2
Pavoni, E.3
Gidaro, T.4
Morosetti, R.5
-
21
-
-
33645870439
-
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations
-
Ricci E, Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, et al. (2006) NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations. Neurology 66 (5): 755-758.
-
(2006)
Neurology
, vol.66
, Issue.5
, pp. 755-758
-
-
Ricci, E.1
Broccolini, A.2
Gidaro, T.3
Morosetti, R.4
Gliubizzi, C.5
-
22
-
-
42449147150
-
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle
-
Broccolini A, Gidaro T, De Cristofaro R, Morosetti R, Gliubizzi C, et al. (2008) Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle. J Neurochem 105 (3): 971-981.
-
(2008)
J Neurochem
, vol.105
, Issue.3
, pp. 971-981
-
-
Broccolini, A.1
Gidaro, T.2
de Cristofaro, R.3
Morosetti, R.4
Gliubizzi, C.5
-
23
-
-
0033753384
-
Increased lysosome-related proteins in the skeletal muscles of distal myopathy with rimmed vacuoles
-
Kumamoto T, Ito T, Horinouchi H, Ueyama H, Toyoshima I, et al. (2000) Increased lysosome-related proteins in the skeletal muscles of distal myopathy with rimmed vacuoles. Muscle Nerve 23 (11): 1686-1693.
-
(2000)
Muscle Nerve
, vol.23
, Issue.11
, pp. 1686-1693
-
-
Kumamoto, T.1
Ito, T.2
Horinouchi, H.3
Ueyama, H.4
Toyoshima, I.5
-
24
-
-
0034919522
-
Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles
-
Tsuruta Y, Furuta A, Furuta K, Yamada T, Kira J, et al. (2001) Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles. Acta Neuropathol 101 (6): 579-584.
-
(2001)
Acta Neuropathol
, vol.101
, Issue.6
, pp. 579-584
-
-
Tsuruta, Y.1
Furuta, A.2
Furuta, K.3
Yamada, T.4
Kira, J.5
-
25
-
-
19944433043
-
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation
-
Salama I, Hinderlich S, Shlomai Z, Eisenberg I, Krause S, et al. (2005) No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation. Biochem Biophys Res Commun 328 (1): 221-226.
-
(2005)
Biochem Biophys Res Commun
, vol.328
, Issue.1
, pp. 221-226
-
-
Salama, I.1
Hinderlich, S.2
Shlomai, Z.3
Eisenberg, I.4
Krause, S.5
-
26
-
-
33847650003
-
Reduced sialylation status in UDP-N-acetylglucosamine-2-epimerase/Nacetylmannosamine kinase (GNE)-deficient mice
-
Gagiannis D, Orthmann A, Danssmann I, Schwarzkopf M, Weidemann W, et al. (2007) Reduced sialylation status in UDP-N-acetylglucosamine-2-epimerase/Nacetylmannosamine kinase (GNE)-deficient mice. Glycoconj J 24 (2-3): 125-130.
-
(2007)
Glycoconj J
, vol.24
, Issue.2-3
, pp. 125-130
-
-
Gagiannis, D.1
Orthmann, A.2
Danssmann, I.3
Schwarzkopf, M.4
Weidemann, W.5
-
27
-
-
0037567649
-
Evidence for a sialic acid salvaging pathway in epidopteran insect cells
-
Hollister J, Conradt H, Jarvis DL (2003) Evidence for a sialic acid salvaging pathway in epidopteran insect cells. Glycobiology 13 (6): 487-495.
-
(2003)
Glycobiology
, vol.13
, Issue.6
, pp. 487-495
-
-
Hollister, J.1
Conradt, H.2
Jarvis, D.L.3
-
28
-
-
0034825538
-
Evidence for efficient uptake and incorporation of sialic acid by eukaryotic cells
-
Oetke C, Hinderlich S, Brossmer R, Reutter W, Pawlita M, et al. (2001) Evidence for efficient uptake and incorporation of sialic acid by eukaryotic cells. Eur J Biochem 268 (16): 4553-4561.
-
(2001)
Eur J Biochem
, vol.268
, Issue.16
, pp. 4553-4561
-
-
Oetke, C.1
Hinderlich, S.2
Brossmer, R.3
Reutter, W.4
Pawlita, M.5
-
29
-
-
34250826506
-
Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
-
Malicdan MC, Noguchi S, Nishino I (2007) Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy. Autophagy 3 (4): 396-398.
-
(2007)
Autophagy
, vol.3
, Issue.4
, pp. 396-398
-
-
Malicdan, M.C.1
Noguchi, S.2
Nishino, I.3
-
30
-
-
34547895110
-
GNE protein expression and subcellular distribution are unaltered in HIBM
-
Krause S, Aleo A, Hinderlich S, Merlini L, Tournev I, et al. (2007) GNE protein expression and subcellular distribution are unaltered in HIBM. Neurology 69 (7): 655-659.
-
(2007)
Neurology
, vol.69
, Issue.7
, pp. 655-659
-
-
Krause, S.1
Aleo, A.2
Hinderlich, S.3
Merlini, L.4
Tournev, I.5
-
31
-
-
35548931584
-
Characterization of hereditary inclusion body myopathy myoblasts: Possible primary impairment of apoptotic events
-
Amsili S, Shlomai Z, Levitzki R, Krause S, Lochmuller H, et al. (2007) Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events. Cell Death Differ.
-
(2007)
Cell Death Differ
-
-
Amsili, S.1
Shlomai, Z.2
Levitzki, R.3
Krause, S.4
Lochmuller, H.5
-
32
-
-
14644446021
-
Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells
-
Krause S, Hinderlich S, Amsili S, Horstkorte R, Wiendl H, et al. (2005) Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells. Exp Cell Res 304 (2): 365-379.
-
(2005)
Exp Cell Res
, vol.304
, Issue.2
, pp. 365-379
-
-
Krause, S.1
Hinderlich, S.2
Amsili, S.3
Horstkorte, R.4
Wiendl, H.5
-
33
-
-
33751540141
-
The collapsin response mediator protein 1 (CRMP-1) and the promyelocytic leukemia zinc finger protein (PLZF) bind to UDP-N-acetylglucosamine 2- epimerase/N-acetylmannosamine kinase (GNE), the key enzyme of sialic acid biosynthesis
-
Weidemann W, Stelzl U, Lisewski U, Bork K, Wanker EE, et al. (2006) The collapsin response mediator protein 1 (CRMP-1) and the promyelocytic leukemia zinc finger protein (PLZF) bind to UDP-N-acetylglucosamine 2- epimerase/N-acetylmannosamine kinase (GNE), the key enzyme of sialic acid biosynthesis. FEBS Lett 580 (28-29): 6649-6654.
-
(2006)
FEBS Lett
, vol.580
, Issue.28-29
, pp. 6649-6654
-
-
Weidemann, W.1
Stelzl, U.2
Lisewski, U.3
Bork, K.4
Wanker, E.E.5
-
34
-
-
0034123470
-
Plzf regulates limb and axial skeletal patterning
-
Barna M, Hawe N, Niswander L, Pandolfi PP (2000) Plzf regulates limb and axial skeletal patterning. Nat Genet 25 (2): 166-172.
-
(2000)
Nat Genet
, vol.25
, Issue.2
, pp. 166-172
-
-
Barna, M.1
Hawe, N.2
Niswander, L.3
Pandolfi, P.P.4
-
35
-
-
49349097189
-
UDPN- acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: Novel pathways in skeletal muscle?
-
Amsili S, Zer H, Hinderlich S, Krause S, Becker-Cohen M, et al. (2008) UDPN- acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle? PLoS ONE 3 (6): e2477.
-
(2008)
PLoS ONE
, vol.3
, Issue.6
-
-
Amsili, S.1
Zer, H.2
Hinderlich, S.3
Krause, S.4
Becker-Cohen, M.5
-
36
-
-
33748755610
-
Roles for UDP-GlcNAc 2- epimerase/ManNAc 6-kinase outside of sialic acid biosynthesis: Modulation of sialyltransferase and BiP expression, GM3 and GD3 biosynthesis, proliferation, and apoptosis, and ERK1/2 phosphorylation
-
Wang Z, Sun Z, Li AV, Yarema KJ (2006) Roles for UDP-GlcNAc 2- epimerase/ManNAc 6-kinase outside of sialic acid biosynthesis: modulation of sialyltransferase and BiP expression, GM3 and GD3 biosynthesis, proliferation, and apoptosis, and ERK1/2 phosphorylation. J Biol Chem 281 (37): 27016-27028.
-
(2006)
J Biol Chem
, vol.281
, Issue.37
, pp. 27016-27028
-
-
Wang, Z.1
Sun, Z.2
Li, A.V.3
Yarema, K.J.4
-
37
-
-
0031047961
-
Glycosphingolipid expression in human skeletal and heart muscle assessed by immunostaining thin-layer chromatography
-
Muthing J, Cacic M (1997) Glycosphingolipid expression in human skeletal and heart muscle assessed by immunostaining thin-layer chromatography. Glycoconj J 14 (1): 19-28.
-
(1997)
Glycoconj J
, vol.14
, Issue.1
, pp. 19-28
-
-
Muthing, J.1
Cacic, M.2
-
38
-
-
0028848435
-
Immunohistological analyses of neutral glycosphingolipids and gangliosides in normal mouse skeletal muscle and in mice with neuromuscular diseases
-
Cacic M, Sostaric K, Weber-Schurholz S, Muthing J (1995) Immunohistological analyses of neutral glycosphingolipids and gangliosides in normal mouse skeletal muscle and in mice with neuromuscular diseases. Glycoconj J 12 (5): 721-728.
-
(1995)
Glycoconj J
, vol.12
, Issue.5
, pp. 721-728
-
-
Cacic, M.1
Sostaric, K.2
Weber-Schurholz, S.3
Muthing, J.4
-
39
-
-
0028114635
-
Expression of neutral glycosphingolipids and gangliosides in human skeletal and heart muscle determined by indirect immunofluorescence staining
-
Cacic M, Muthing J, Kracun I, Neumann U, Weber-Schurholz S (1994) Expression of neutral glycosphingolipids and gangliosides in human skeletal and heart muscle determined by indirect immunofluorescence staining. Glycoconj J 11 (5): 477-485.
-
(1994)
Glycoconj J
, vol.11
, Issue.5
, pp. 477-485
-
-
Cacic, M.1
Muthing, J.2
Kracun, I.3
Neumann, U.4
Weber-Schurholz, S.5
-
40
-
-
0028052885
-
Different distributions of glycosphingolipids inmouse and rabbit skeletalmuscle demonstrated by biochemical and immunohistological analyses
-
Muthing J, Maurer U, Sostaric K, Neumann U, Brandt H, et al. (1994) Different distributions of glycosphingolipids inmouse and rabbit skeletalmuscle demonstrated by biochemical and immunohistological analyses. J Biochem 115 (2): 248-256.
-
(1994)
J Biochem
, vol.115
, Issue.2
, pp. 248-256
-
-
Muthing, J.1
Maurer, U.2
Sostaric, K.3
Neumann, U.4
Brandt, H.5
-
41
-
-
33845645834
-
Ganglioside GM3 is involved in neuronal cell death
-
Sohn H, Kim YS, Kim HT, Kim CH, Cho EW, et al. (2006) Ganglioside GM3 is involved in neuronal cell death. Faseb J 20 (8): 1248-1250.
-
(2006)
Faseb J
, vol.20
, Issue.8
, pp. 1248-1250
-
-
Sohn, H.1
Kim, Y.S.2
Kim, H.T.3
Kim, C.H.4
Cho, E.W.5
-
42
-
-
23444435304
-
The ganglioside GD3 as the Greek goddess Hecate: Several faces turned towards as many directions
-
Malisan F, Testi R (2005) The ganglioside GD3 as the Greek goddess Hecate: several faces turned towards as many directions. IUBMB Life 57 (7): 477-482.
-
(2005)
IUBMB Life
, vol.57
, Issue.7
, pp. 477-482
-
-
Malisan, F.1
Testi, R.2
-
43
-
-
28544442735
-
Cancer stem cells in the mammalian central nervous system
-
Pilkington GJ (2005) Cancer stem cells in the mammalian central nervous system. Cell Prolif 38 (6): 423-433.
-
(2005)
Cell Prolif
, vol.38
, Issue.6
, pp. 423-433
-
-
Pilkington, G.J.1
-
44
-
-
0028327467
-
Glycosphingolipids during skeletal muscle cell differentiation: Comparison of normal and fusion-defective myoblasts
-
Cambron LD, Leskawa KC (1994) Glycosphingolipids during skeletal muscle cell differentiation: comparison of normal and fusion-defective myoblasts. Mol Cell Biochem 130 (2): 173-185.
-
(1994)
Mol Cell Biochem
, vol.130
, Issue.2
, pp. 173-185
-
-
Cambron, L.D.1
Leskawa, K.C.2
-
45
-
-
0023767395
-
Glycosphingolipid biosynthesis during myogenesis of rat L6 cells in vitro
-
Leskawa KC, Erwin RE, Buse PE, Hogan EL (1988) Glycosphingolipid biosynthesis during myogenesis of rat L6 cells in vitro. Mol Cell Biochem 83 (1): 47-54.
-
(1988)
Mol Cell Biochem
, vol.83
, Issue.1
, pp. 47-54
-
-
Leskawa, K.C.1
Erwin, R.E.2
Buse, P.E.3
Hogan, E.L.4
-
46
-
-
0025353024
-
Regulation of glycolipid synthesis during differentiation of clonal murine muscle cells
-
Leskawa KC, Hogan EL (1990) Regulation of glycolipid synthesis during differentiation of clonal murine muscle cells. Mol Cell Biochem 96 (2): 163-173.
-
(1990)
Mol Cell Biochem
, vol.96
, Issue.2
, pp. 163-173
-
-
Leskawa, K.C.1
Hogan, E.L.2
-
47
-
-
34249874096
-
Mutation in he key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria nd is rescued by N-acetylmannosamine
-
Galeano B, Klootwijk R, Manoli I, Sun M, Ciccone C, et al. (2007) Mutation in he key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria nd is rescued by N-acetylmannosamine. J Clin Invest 117 (6): 1585-1594.
-
(2007)
J Clin Invest
, vol.117
, Issue.6
, pp. 1585-1594
-
-
Galeano, B.1
Klootwijk, R.2
Manoli, I.3
Sun, M.4
Ciccone, C.5
-
48
-
-
35549010650
-
A Gne nockout mouse expressing human GNE D176V mutation develops features imilar to distal myopathy with rimmed vacuoles or hereditary inclusion body yopathy
-
Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I (2007) A Gne nockout mouse expressing human GNE D176V mutation develops features imilar to distal myopathy with rimmed vacuoles or hereditary inclusion body yopathy. Hum Mol Genet 16 (22): 2669-2682.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.22
, pp. 2669-2682
-
-
Malicdan, M.C.1
Noguchi, S.2
Nonaka, I.3
Hayashi, Y.K.4
Nishino, I.5
-
49
-
-
3242730231
-
Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides ollowing ceramide glycanase digestion and anthranilic acid labeling
-
Neville DC, Coquard V, Priestman DA, te Vruchte DJ, Sillence DJ, et al. (2004) Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides ollowing ceramide glycanase digestion and anthranilic acid labeling. Anal iochem 331 (2): 275-282.
-
(2004)
Anal Iochem
, vol.331
, Issue.2
, pp. 275-282
-
-
Neville, D.C.1
Coquard, V.2
Priestman, D.A.3
Te Vruchte, D.J.4
Sillence, D.J.5
-
50
-
-
0025877969
-
Structure and function of renal glycosphingolipids
-
Shayman JA, Radin NS (1991) Structure and function of renal glycosphingolipids. m J Physiol 260 (3 Pt 2): F291-F302.
-
(1991)
M J Physiol
, vol.260
, Issue.3 pt 2
-
-
Shayman, J.A.1
Radin, N.S.2
-
51
-
-
0014692743
-
Glomerular sialoprotein
-
Mohos SC, Skoza L (1969) Glomerular sialoprotein. Science 164 (887): 519-521.
-
(1969)
Science
, vol.164
, Issue.887
, pp. 519-521
-
-
Mohos, S.C.1
Skoza, L.2
-
52
-
-
0029765799
-
Decrease of lomerular disialogangliosides in puromycin nephrosis of the rat
-
Holthofer H, Reivinen J, Solin ML, Haltia A, Miettinen A (1996) Decrease of lomerular disialogangliosides in puromycin nephrosis of the rat. Am J Pathol 49 (3): 1009-1015.
-
(1996)
Am J Pathol
, vol.49
, Issue.3
, pp. 1009-1015
-
-
Holthofer, H.1
Reivinen, J.2
Solin, M.L.3
Haltia, A.4
Miettinen, A.5
-
53
-
-
0037436732
-
Decreases of anglioside GM3 in streptozotocin-induced diabetic glomeruli of rats
-
Kwak DH, Rho YI, Kwon OD, Ahan SH, Song JH, et al. (2003) Decreases of anglioside GM3 in streptozotocin-induced diabetic glomeruli of rats. Life Sci 72 17): 1997-2006.
-
(2003)
Life Sci
, vol.72
, Issue.17
, pp. 1997-2006
-
-
Kwak, D.H.1
Rho, Y.I.2
Kwon, O.D.3
Ahan, S.H.4
Song, J.H.5
-
54
-
-
35548931584
-
Characterization of hereditary inclusion body myopathy myoblasts: Possible rimary impairment of apoptotic events
-
Amsili S, Shlomai Z, Levitzki R, Krause S, Lochmuller H, et al. (2007) Characterization of hereditary inclusion body myopathy myoblasts: possible rimary impairment of apoptotic events. Cell Death Differ 14 (11): 1916-1924.
-
(2007)
Cell Death Differ
, vol.14
, Issue.11
, pp. 1916-1924
-
-
Amsili, S.1
Shlomai, Z.2
Levitzki, R.3
Krause, S.4
Lochmuller, H.5
-
55
-
-
61349094775
-
NEU3 ialidase strictly modulates GM3 levels in skeletal myoblasts C2C12 thus avoring their differentiation and protecting them from apoptosis
-
Anastasia L, Papini N, Colazzo F, Palazzolo G, Tringali C, et al. (2008) NEU3 ialidase strictly modulates GM3 levels in skeletal myoblasts C2C12 thus avoring their differentiation and protecting them from apoptosis. J Biol Chem 83 (52): 36265-36271.
-
(2008)
J Biol Chem
, vol.83
, Issue.52
, pp. 36265-36271
-
-
Anastasia, L.1
Papini, N.2
Colazzo, F.3
Palazzolo, G.4
Tringali, C.5
-
57
-
-
84860493578
-
Lipid ediators of insulin resistance
-
Holland WL, Knotts TA, Chavez JA, Wang LP, Hoehn KL, et al. (2007) Lipid ediators of insulin resistance. Nutr Rev 65 (6 Pt 2): S39-S46.
-
(2007)
Nutr Rev
, vol.65
, Issue.6 pt 2
-
-
Holland, W.L.1
Knotts, T.A.2
Chavez, J.A.3
Wang, L.P.4
Hoehn, K.L.5
-
58
-
-
40849113048
-
Type I Gaucher disease, a glycosphingolipid storage disorder, is ssociated with insulin resistance
-
Langeveld M, Ghauharali KJ, Sauerwein HP, Ackermans MT, Groener JE, t al. (2008) Type I Gaucher disease, a glycosphingolipid storage disorder, is ssociated with insulin resistance. J Clin Endocrinol Metab 93 (3): 845-851.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.3
, pp. 845-851
-
-
Langeveld, M.1
Ghauharali, K.J.2
Sauerwein, H.P.3
Ackermans, M.T.4
Groener, J.E.5
-
59
-
-
0037452930
-
Enhanced insulin sensitivity in mice lacking ganglioside GM3
-
Yamashita T, Hashiramoto A, Haluzik M, Mizukami H, Beck S, et al. (2003) Enhanced insulin sensitivity in mice lacking ganglioside GM3. Proc Natl Acad ci U S A 100 (6): 3445-3449.
-
(2003)
Proc Natl Acad Ci U S A
, vol.100
, Issue.6
, pp. 3445-3449
-
-
Yamashita, T.1
Hashiramoto, A.2
Haluzik, M.3
Mizukami, H.4
Beck, S.5
-
60
-
-
56149107232
-
Muscle weakness orrelates with muscle atrophy and precedes the development of inclusion body r rimmed vacuoles in the mouse model of DMRV/hIBM
-
Malicdan MC, Noguchi S, Hayashi YK, Nishino I (2008) Muscle weakness orrelates with muscle atrophy and precedes the development of inclusion body r rimmed vacuoles in the mouse model of DMRV/hIBM. Physiol Genomics 35 (1): 106-115.
-
(2008)
Physiol Genomics
, vol.35
, Issue.1
, pp. 106-115
-
-
Malicdan, M.C.1
Noguchi, S.2
Hayashi, Y.K.3
Nishino, I.4
-
61
-
-
13444291036
-
Improved real-time RT-PCR method for high-throughput measurements using second derivative calculation and double correction
-
Luu-The V, Paquet N, Calvo E, Cumps J (2005) Improved real-time RT-PCR method for high-throughput measurements using second derivative calculation and double correction. Biotechniques 38 (2): 287-293.
-
(2005)
Biotechniques
, vol.38
, Issue.2
, pp. 287-293
-
-
Luu-The, V.1
Paquet, N.2
Calvo, E.3
Cumps, J.4
-
62
-
-
0018890975
-
A procedure for the quantitative isolation of brain gangliosides
-
Svennerholm L, Fredman P (1980) A procedure for the quantitative isolation of brain gangliosides. Biochim Biophys Acta 617 (1): 97-109.
-
(1980)
Biochim Biophys Acta
, vol.617
, Issue.1
, pp. 97-109
-
-
Svennerholm, L.1
Fredman, P.2
-
63
-
-
0021954882
-
A solvent partition method for microscale ganglioside purification
-
Ladisch S, Gillard B (1985) A solvent partition method for microscale ganglioside purification. Anal Biochem 146 (1): 220-231.
-
(1985)
Anal Biochem
, vol.146
, Issue.1
, pp. 220-231
-
-
Ladisch, S.1
Gillard, B.2
|