-
2
-
-
0036387220
-
Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: Correlation with phenotype and genotype
-
E. Orvisky, J. K. Park, M. E. LaMarca, E. I. Ginns, B. M. Martin, N. Tayebi, E. Sidransky, Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: Correlation with phenotype and genotype. Mol. Genet. Metab. 76, 262-270 (2002).
-
(2002)
Mol. Genet. Metab.
, vol.76
, pp. 262-270
-
-
Orvisky, E.1
Park, J.K.2
LaMarca, M.E.3
Ginns, E.I.4
Martin, B.M.5
Tayebi, N.6
Sidransky, E.7
-
3
-
-
0014348167
-
The fine structure of the cerebroside occurring in Gaucher's disease
-
R. E. Lee, The fine structure of the cerebroside occurring in Gaucher's disease. Proc. Natl. Acad. Sci. U.S.A. 61, 484-489 (1968).
-
(1968)
Proc. Natl. Acad. Sci. U.S.A.
, vol.61
, pp. 484-489
-
-
Lee, R.E.1
-
4
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
E. Sidransky, M. A. Nalls, J. O. Aasly, J. Aharon-Peretz, G. Annesi, E. R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, A. Brice, C. M. Chen, L. N. Clark, C. Condroyer, E. V. De Marco, A. Dürr, M. J. Eblan, S. Fahn, M. J. Farrer, H. C. Fung, Z. Gan-Or, T. Gasser, R. Gershoni-Baruch, N. Giladi, A. Griffith, T. Gurevich, C. Januario, P. Kropp, A. E. Lang, G. J. Lee-Chen, S. Lesage, K. Marder, I. F. Mata, A. Mirelman, J. Mitsui, I. Mizuta, G. Nicoletti, C. Oliveira, R. Ottman, A. Orr-Urtreger, L. V. Pereira, A. Quattrone, E. Rogaeva, A. Rolfs, H. Rosenbaum, R. Rozenberg, A. Samii, T. Samaddar, C. Schulte,M. Sharma,A. Singleton, M. Spitz, E. K. Tan, N. Tayebi, T. Toda, A. R. Troiano, S. Tsuji, M. Wittstock, T. G. Wolfsberg, Y. R. Wu, C. P. Zabetian, Y. Zhao, S. G. Ziegler, Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N. Engl. J. Med. 361, 1651-1661 (2009).
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1651-1661
-
-
Sidransky, E.1
Nalls, M.A.2
Aasly, J.O.3
Aharon-Peretz, J.4
Annesi, G.5
Barbosa, E.R.6
Bar-Shira, A.7
Berg, D.8
Bras, J.9
Brice, A.10
Chen, C.M.11
Clark, L.N.12
Condroyer, C.13
De Marco, E.V.14
Dürr, A.15
Eblan, M.J.16
Fahn, S.17
Farrer, M.J.18
Fung, H.C.19
Gan-Or, Z.20
Gasser, T.21
Gershoni-Baruch, R.22
Giladi, N.23
Griffith, A.24
Gurevich, T.25
Januario, C.26
Kropp, P.27
Lang, A.E.28
Lee-Chen, G.J.29
Lesage, S.30
Marder, K.31
Mata, I.F.32
Mirelman, A.33
Mitsui, J.34
Mizuta, I.35
Nicoletti, G.36
Oliveira, C.37
Ottman, R.38
Orr-Urtreger, A.39
Pereira, L.V.40
Quattrone, A.41
Rogaeva, E.42
Rolfs, A.43
Rosenbaum, H.44
Rozenberg, R.45
Samii, A.46
Samaddar, T.47
Schulte, C.48
Sharma, M.49
Singleton, A.50
Spitz, M.51
Tan, E.K.52
Tayebi, N.53
Toda, T.54
Troiano, A.R.55
Tsuji, S.56
Wittstock, M.57
Wolfsberg, T.G.58
Wu, Y.R.59
Zabetian, C.P.60
Zhao, Y.61
Ziegler, S.G.62
more..
-
5
-
-
26844468253
-
Cell-surface calreticulin initiates clearance of viable or apoptotic cells through trans-activation of LRP on the phagocyte
-
S. J. Gardai, K. A. McPhillips, S. C. Frasch, W. J. Janssen, A. Starefeldt, J. E. Murphy-Ullrich, D. L. Bratton, P. A. Oldenborg, M. Michalak, P. M. Henson, Cell-surface calreticulin initiates clearance of viable or apoptotic cells through trans-activation of LRP on the phagocyte. Cell 123, 321-334 (2005).
-
(2005)
Cell
, vol.123
, pp. 321-334
-
-
Gardai, S.J.1
McPhillips, K.A.2
Frasch, S.C.3
Janssen, W.J.4
Starefeldt, A.5
Murphy-Ullrich, J.E.6
Bratton, D.L.7
Oldenborg, P.A.8
Michalak, M.9
Henson, P.M.10
-
8
-
-
84876793140
-
Chaperone therapy update: Fabry disease, GM1-gangliosidosis and Gaucher disease
-
Y. Suzuki, Chaperone therapy update: Fabry disease, GM1-gangliosidosis and Gaucher disease. Brain Dev. 35, 515-523 (2013).
-
(2013)
Brain Dev.
, vol.35
, pp. 515-523
-
-
Suzuki, Y.1
-
9
-
-
84894528843
-
Reduced glucocerebrosidase is associated with increased a-synuclein in sporadic Parkinson's disease
-
K. E.Murphy, A. M.Gysbers, S. K. Abbott, N. Tayebi,W. S. Kim, E. Sidransky, A. Cooper, B. Garner, G. M. Halliday, Reduced glucocerebrosidase is associated with increased a-synuclein in sporadic Parkinson's disease. Brain 137, 834-848 (2014).
-
(2014)
Brain
, vol.137
, pp. 834-848
-
-
Murphy, K.E.1
Gysbers, A.M.2
Abbott, S.K.3
Tayebi, N.4
Kim, W.S.5
Sidransky, E.6
Cooper, A.7
Garner, B.8
Halliday, G.M.9
-
10
-
-
84867036900
-
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains
-
M. E. Gegg, D. Burke, S. J. Heales, J. M. Cooper, J. Hardy, N. W. Wood, A. H. Schapira, Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains. Ann. Neurol. 72, 455-463 (2012).
-
(2012)
Ann. Neurol.
, vol.72
, pp. 455-463
-
-
Gegg, M.E.1
Burke, D.2
Heales, S.J.3
Cooper, J.M.4
Hardy, J.5
Wood, N.W.6
Schapira, A.H.7
-
11
-
-
84855845987
-
High throughput screening for small molecule therapy for Gaucher disease using patient tissue as the source of mutant glucocerebrosidase
-
E. Goldin, W. Zheng, O. Motabar, N. Southall, J. H. Choi, J. Marugan, C. P. Austin, E. Sidransky, High throughput screening for small molecule therapy for Gaucher disease using patient tissue as the source of mutant glucocerebrosidase. PLOS One 7, e29861 (2012).
-
(2012)
PLOS One
, vol.7
-
-
Goldin, E.1
Zheng, W.2
Motabar, O.3
Southall, N.4
Choi, J.H.5
Marugan, J.6
Austin, C.P.7
Sidransky, E.8
-
12
-
-
84863083762
-
Discovery, structure-activity relationship, and biological evaluation of noninhibitory small molecule chaperones of glucocerebrosidase
-
S. Patnaik, W. Zheng, J. H. Choi, O. Motabar, N. Southall, W. Westbroek, W. A. Lea, A. Velayati, E. Goldin, E. Sidransky, W. Leister, J. J. Marugan, Discovery, structure-activity relationship, and biological evaluation of noninhibitory small molecule chaperones of glucocerebrosidase. J. Med. Chem. 55, 5734-5748 (2012).
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5734-5748
-
-
Patnaik, S.1
Zheng, W.2
Choi, J.H.3
Motabar, O.4
Southall, N.5
Westbroek, W.6
Lea, W.A.7
Velayati, A.8
Goldin, E.9
Sidransky, E.10
Leister, W.11
Marugan, J.J.12
-
13
-
-
84868089871
-
Induced pluripotent stem cell model recapitulates pathologic hallmarks of Gaucher disease
-
L.M. Panicker, D. Miller, T. S. Park, B. Patel, J. L. Azevedo, O. Awad,M. A.Masood, T. D. Veenstra, E. Goldin, B. K. Stubblefield, N. Tayebi, S. K. Polumuri, S. N. Vogel, E. Sidransky, E. T. Zambidis, R. A. Feldman, Induced pluripotent stem cell model recapitulates pathologic hallmarks of Gaucher disease. Proc. Natl. Acad. Sci. U.S.A. 109, 18054-18059 (2012).
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 18054-18059
-
-
Panicker, L.M.1
Miller, D.2
Park, T.S.3
Patel, B.4
Azevedo, J.L.5
Awad, O.6
Masood, M.A.7
Veenstra, T.D.8
Goldin, E.9
Stubblefield, B.K.10
Tayebi, N.11
Polumuri, S.K.12
Vogel, S.N.13
Sidransky, E.14
Zambidis, E.T.15
Feldman, R.A.16
-
14
-
-
49349094179
-
Homogeneous monocytes and macrophages from human embryonic stem cells following coculture-free differentiation in M-CSF and IL-3
-
K. R. Karlsson, S. Cowley, F. O. Martinez, M. Shaw, S. L. Minger, W. James, Homogeneous monocytes and macrophages from human embryonic stem cells following coculture-free differentiation in M-CSF and IL-3. Exp. Hematol. 36, 1167-1175 (2008).
-
(2008)
Exp. Hematol.
, vol.36
, pp. 1167-1175
-
-
Karlsson, K.R.1
Cowley, S.2
Martinez, F.O.3
Shaw, M.4
Minger, S.L.5
James, W.6
-
15
-
-
77953782625
-
NADPH oxidase activity controls phagosomal proteolysis in macrophages through modulation of the lumenal redox environment of phagosomes
-
J. M. Rybicka, D. R. Balce, M. F. Khan, R. M. Krohn, R. M. Yates, NADPH oxidase activity controls phagosomal proteolysis in macrophages through modulation of the lumenal redox environment of phagosomes. Proc. Natl. Acad. Sci. U.S.A. 107, 10496-10501 (2010).
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 10496-10501
-
-
Rybicka, J.M.1
Balce, D.R.2
Khan, M.F.3
Krohn, R.M.4
Yates, R.M.5
-
16
-
-
0742269462
-
Plasma level of the macrophagederived soluble CD163 is increased and positively correlates with severity in Gaucher's disease
-
H. J. Møller, M. de Fost, H. Aerts, C. Hollak, S. K. Moestrup, Plasma level of the macrophagederived soluble CD163 is increased and positively correlates with severity in Gaucher's disease. Eur. J. Haematol. 72, 135 -139 (2004).
-
(2004)
Eur. J. Haematol.
, vol.72
, pp. 135-139
-
-
Møller, H.J.1
De Fost, M.2
Aerts, H.3
Hollak, C.4
Moestrup, S.K.5
-
18
-
-
78650614891
-
Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage
-
P. K. Mistry, J. Liu, M. Yang, T. Nottoli, J. McGrath, D. Jain, K. Zhang, J. Keutzer, W. L. Chuang, W. Z. Mehal, H. Zhao, A. Lin, S. Mane, X. Liu, Y. Z. Peng, J. H. Li, M. Agrawal, L. L. Zhu, H. C. Blair, L. J. Robinson, J. Iqbal, L. Sun, M. Zaidi, Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage. Proc. Natl. Acad. Sci. U.S.A. 107, 19473-19478 (2010).
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 19473-19478
-
-
Mistry, P.K.1
Liu, J.2
Yang, M.3
Nottoli, T.4
McGrath, J.5
Jain, D.6
Zhang, K.7
Keutzer, J.8
Chuang, W.L.9
Mehal, W.Z.10
Zhao, H.11
Lin, A.12
Mane, S.13
Liu, X.14
Peng, Y.Z.15
Li, J.H.16
Agrawal, M.17
Zhu, L.L.18
Blair, H.C.19
Robinson, L.J.20
Iqbal, J.21
Sun, L.22
Zaidi, M.23
more..
-
19
-
-
80054841258
-
Elevated plasma glucosylsphingosine in Gaucher disease: Relation to phenotype, storage cell markers, and therapeutic response
-
N. Dekker, L. van Dussen, C. E. Hollak, H. Overkleeft, S. Scheij, K. Ghauharali, M. J. van Breemen, M. J. Ferraz, J. E. Groener, M. Maas, F. A. Wijburg, D. Speijer, A. Tylki-Szymanska, P. K. Mistry, R. G. Boot, J. M. Aerts, Elevated plasma glucosylsphingosine in Gaucher disease: Relation to phenotype, storage cell markers, and therapeutic response. Blood 118, e118-e127 (2011).
-
(2011)
Blood
, vol.118
-
-
Dekker, N.1
Van Dussen, L.2
Hollak, C.E.3
Overkleeft, H.4
Scheij, S.5
Ghauharali, K.6
Van Breemen, M.J.7
Ferraz, M.J.8
Groener, J.E.9
Maas, M.10
Wijburg, F.A.11
Speijer, D.12
Tylki-Szymanska, A.13
Mistry, P.K.14
Boot, R.G.15
Aerts, J.M.16
-
21
-
-
0037159549
-
Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: A report from the Gaucher Registry
-
N. J. Weinreb, J. Charrow, H. C. Andersson, P. Kaplan, E. H. Kolodny, P. Mistry, G. Pastores, B. E. Rosenbloom, C. R. Scott, R. S. Wappner, A. Zimran, Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: A report from the Gaucher Registry. Am. J. Med. 113, 112-119 (2002).
-
(2002)
Am. J. Med.
, vol.113
, pp. 112-119
-
-
Weinreb, N.J.1
Charrow, J.2
Andersson, H.C.3
Kaplan, P.4
Kolodny, E.H.5
Mistry, P.6
Pastores, G.7
Rosenbloom, B.E.8
Scott, C.R.9
Wappner, R.S.10
Zimran, A.11
-
22
-
-
0035049241
-
The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease
-
G. Altarescu, S. Hill, E. Wiggs, N. Jeffries, C. Kreps, C. C. Parker, R. O. Brady, N. W. Barton, R. Schiffmann, The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease. J. Pediatr. 138, 539-547 (2001).
-
(2001)
J. Pediatr.
, vol.138
, pp. 539-547
-
-
Altarescu, G.1
Hill, S.2
Wiggs, E.3
Jeffries, N.4
Kreps, C.5
Parker, C.C.6
Brady, R.O.7
Barton, N.W.8
Schiffmann, R.9
-
23
-
-
34447309572
-
Effect of mannose chain length on targeting of glucocerebrosidase for enzyme replacement therapy of Gaucher disease
-
S. M. Van Patten, H. Hughes, M. R. Huff, P. A. Piepenhagen, J. Waire, H. Qiu, C. Ganesa, D. Reczek, P. V. Ward, J. P. Kutzko, T. Edmunds, Effect of mannose chain length on targeting of glucocerebrosidase for enzyme replacement therapy of Gaucher disease. Glycobiology 17, 467-478 (2007).
-
(2007)
Glycobiology
, vol.17
, pp. 467-478
-
-
Van Patten, S.M.1
Hughes, H.2
Huff, M.R.3
Piepenhagen, P.A.4
Waire, J.5
Qiu, H.6
Ganesa, C.7
Reczek, D.8
Ward, P.V.9
Kutzko, J.P.10
Edmunds, T.11
-
24
-
-
77949643182
-
The pharmacological chaperone isofagomine increases the activity of the Gaucher disease L444P mutant form of b-glucosidase
-
R. Khanna, E. R. Benjamin, L. Pellegrino, A. Schilling, B. A. Rigat, R. Soska, H. Nafar, B. E. Ranes, J. Feng, Y. Lun, A. C. Powe, D. J. Palling, B. A. Wustman, R. Schiffmann, D. J. Mahuran, D. J. Lockhart, K. J. Valenzano, The pharmacological chaperone isofagomine increases the activity of the Gaucher disease L444P mutant form of b-glucosidase. FEBS J. 277, 1618-1638 (2010).
-
(2010)
FEBS J.
, vol.277
, pp. 1618-1638
-
-
Khanna, R.1
Benjamin, E.R.2
Pellegrino, L.3
Schilling, A.4
Rigat, B.A.5
Soska, R.6
Nafar, H.7
Ranes, B.E.8
Feng, J.9
Lun, Y.10
Powe, A.C.11
Palling, D.J.12
Wustman, B.A.13
Schiffmann, R.14
Mahuran, D.J.15
Lockhart, D.J.16
Valenzano, K.J.17
-
26
-
-
33845240108
-
Chemical chaperones and permissive temperatures alter localization of Gaucher disease associated glucocerebrosidase variants
-
A. R. Sawkar, M. Schmitz, K. P. Zimmer, D. Reczek, T. Edmunds, W. E. Balch, J. W. Kelly, Chemical chaperones and permissive temperatures alter localization of Gaucher disease associated glucocerebrosidase variants. ACS Chem. Biol. 1, 235-251 (2006).
-
(2006)
ACS Chem. Biol.
, vol.1
, pp. 235-251
-
-
Sawkar, A.R.1
Schmitz, M.2
Zimmer, K.P.3
Reczek, D.4
Edmunds, T.5
Balch, W.E.6
Kelly, J.W.7
-
27
-
-
34548650256
-
Three classes of glucocerebrosidase inhibitors identified by quantitative high-throughput screening are chaperone leads for Gaucher disease
-
W. Zheng, J. Padia, D. J. Urban, A. Jadhav, O. Goker-Alpan, A. Simeonov, E. Goldin, D. Auld, M. E. LaMarca, J. Inglese, C. P. Austin, E. Sidransky, Three classes of glucocerebrosidase inhibitors identified by quantitative high-throughput screening are chaperone leads for Gaucher disease. Proc. Natl. Acad. Sci. U.S.A. 104, 13192-13197 (2007).
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 13192-13197
-
-
Zheng, W.1
Padia, J.2
Urban, D.J.3
Jadhav, A.4
Goker-Alpan, O.5
Simeonov, A.6
Goldin, E.7
Auld, D.8
LaMarca, M.E.9
Inglese, J.10
Austin, C.P.11
Sidransky, E.12
-
28
-
-
84862907612
-
Non-iminosugar glucocerebrosidase small molecule chaperones
-
J. J. Marugan, W. Huang, O. Motabar, W. Zheng, J. Xiao, S. Patnaik, N. Southall, W. Westbroek, W. A. Lea, A. Simeonov, E. Goldin, M. A. Debernardi, E. Sidransky, Non-iminosugar glucocerebrosidase small molecule chaperones. Medchemcomm 3, 56-60 (2012).
-
(2012)
Medchemcomm
, vol.3
, pp. 56-60
-
-
Marugan, J.J.1
Huang, W.2
Motabar, O.3
Zheng, W.4
Xiao, J.5
Patnaik, S.6
Southall, N.7
Westbroek, W.8
Lea, W.A.9
Simeonov, A.10
Goldin, E.11
Debernardi, M.A.12
Sidransky, E.13
-
29
-
-
0035965237
-
phox component of NADPH oxidase is not the voltage-gated proton channel in phagocytes, but it helps
-
phox component of NADPH oxidase is not the voltage-gated proton channel in phagocytes, but it helps. J. Biol. Chem. 276, 36063-36066 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 36063-36066
-
-
DeCoursey, T.E.1
Cherny, V.V.2
Morgan, D.3
Katz, B.Z.4
Dinauer, M.C.5
-
30
-
-
15944372262
-
Activation and assembly of the NADPH oxidase: A structural perspective
-
Y. Groemping, K. Rittinger, Activation and assembly of the NADPH oxidase: A structural perspective. Biochem. J. 386, 401-416 (2005).
-
(2005)
Biochem. J.
, vol.386
, pp. 401-416
-
-
Groemping, Y.1
Rittinger, K.2
-
31
-
-
0037039667
-
phox PX domains of NADPH oxidase target cell membranes via direct and indirect recruitment by phosphoinositides
-
phox PX domains of NADPH oxidase target cell membranes via direct and indirect recruitment by phosphoinositides. J. Biol. Chem. 277, 4512-4518 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 4512-4518
-
-
Zhan, Y.1
Virbasius, J.V.2
Song, X.3
Pomerleau, D.P.4
Zhou, G.W.5
-
32
-
-
79960009804
-
Gaucher disease glucocerebrosidase and a-synuclein form a bidirectional pathogenic loop in synucleinopathies
-
J. R. Mazzulli, Y. H. Xu, Y. Sun, A. L. Knight, P. J. McLean, G. A. Caldwell, E. Sidransky, G. A. Grabowski, D. Krainc, Gaucher disease glucocerebrosidase and a-synuclein form a bidirectional pathogenic loop in synucleinopathies. Cell 146, 37-52 (2011).
-
(2011)
Cell
, vol.146
, pp. 37-52
-
-
Mazzulli, J.R.1
Xu, Y.H.2
Sun, Y.3
Knight, A.L.4
McLean, P.J.5
Caldwell, G.A.6
Sidransky, E.7
Grabowski, G.A.8
Krainc, D.9
-
33
-
-
0033951675
-
Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease
-
D. L. Stone, N. Tayebi, E. Orvisky, B. Stubblefield, V. Madike, E. Sidransky, Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease. Hum. Mutat. 15, 181-188 (2000).
-
(2000)
Hum. Mutat.
, vol.15
, pp. 181-188
-
-
Stone, D.L.1
Tayebi, N.2
Orvisky, E.3
Stubblefield, B.4
Madike, V.5
Sidransky, E.6
-
34
-
-
0019164190
-
The uptake of iron by reticulocytes. The influence of purification of the ghosts on iron-containing components in the ghost suspension
-
C. von der Heul, M. J. Kroos, C. M. de Jeu-Jaspars, H. G. von Eijk, The uptake of iron by reticulocytes. The influence of purification of the ghosts on iron-containing components in the ghost suspension. Biochim. Biophys. Acta 601, 572-583 (1980).
-
(1980)
Biochim. Biophys. Acta
, vol.601
, pp. 572-583
-
-
Von Der Heul, C.1
Kroos, M.J.2
De Jeu-Jaspars, C.M.3
Von Eijk, H.G.4
-
35
-
-
84873040393
-
Neuronopathic Gaucher's disease: Induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds
-
G. Tiscornia, E. Lorenzo Vivas, L. Matalonga, I. Berniakovich, M. Barragán Monasterio, C. Eguizábal, L. Gort, F. González, C. Ortiz Mellet, J. M. García Fernández, A. Ribes, A. Veiga, J. C. Izpisua Belmonte, Neuronopathic Gaucher's disease: Induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds. Hum. Mol. Genet. 22, 633-645 (2013).
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 633-645
-
-
Tiscornia, G.1
Lorenzo Vivas, E.2
Matalonga, L.3
Berniakovich, I.4
Barragán Monasterio, M.5
Eguizábal, C.6
Gort, L.7
González, F.8
Ortiz Mellet, C.9
García Fernández, J.M.10
Ribes, A.11
Veiga, A.12
Izpisua Belmonte, J.C.13
-
36
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
E. Schröck, S. du Manoir, T. Veldman, B. Schoell, J. Wienberg, M. A. Ferguson-Smith, Y. Ning, D. H. Ledbetter, I. Bar-Am, D. Soenksen, Y. Garini, T. Ried, Multicolor spectral karyotyping of human chromosomes. Science 273, 494-497 (1996).
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
38
-
-
82255175222
-
Impaired Rho GTPase activation abrogates cell polarization and migration in macrophages with defective lipolysis
-
E. Aflaki, N. A. Balenga, P. Luschnig-Schratl, H. Wolinski, S. Povoden, P. G. Chandak, J. G. Bogner-Strauss, S. Eder, V. Konya, S. D. Kohlwein, A. Heinemann, D. Kratky, Impaired Rho GTPase activation abrogates cell polarization and migration in macrophages with defective lipolysis. Cell. Mol. Life Sci. 68, 3933-3947 (2011).
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 3933-3947
-
-
Aflaki, E.1
Balenga, N.A.2
Luschnig-Schratl, P.3
Wolinski, H.4
Povoden, S.5
Chandak, P.G.6
Bogner-Strauss, J.G.7
Eder, S.8
Konya, V.9
Kohlwein, S.D.10
Heinemann, A.11
Kratky, D.12
|