-
1
-
-
0037366067
-
Neuroblastoma: Biological insights into a clinical enigma
-
Brodeur GM: Neuroblastoma: biological insights into a clinical enigma. Nat Rev Cancer 3: 203-216, 2003.
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 203-216
-
-
Brodeur, G.M.1
-
2
-
-
0017698493
-
Chromosomal aberrations in human neuroblastomas
-
Brodeur GM, Sekhon G and Goldstein MN: Chromosomal aberrations in human neuroblastomas. Cancer 40: 2256-2263, 1977.
-
(1977)
Cancer
, vol.40
, pp. 2256-2263
-
-
Brodeur, G.M.1
Sekhon, G.2
Goldstein, M.N.3
-
3
-
-
33745193454
-
Loss in chromosome 11q identifies tumors with increased risk for metastatic relapses in localized and 4S neuroblastoma
-
Spitz R, Hero B, Simon T and Berthold F: Loss in chromosome 11q identifies tumors with increased risk for metastatic relapses in localized and 4S neuroblastoma. Clin Cancer Res 12: 3368-3373, 2006.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 3368-3373
-
-
Spitz, R.1
Hero, B.2
Simon, T.3
Berthold, F.4
-
4
-
-
0033517349
-
Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas
-
Guo C, White PS, Weiss MJ, et al: Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas. Oncogene 18: 4948-4957, 1999.
-
(1999)
Oncogene
, vol.18
, pp. 4948-4957
-
-
Guo, C.1
White, P.S.2
Weiss, M.J.3
-
5
-
-
0035166044
-
Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma
-
Maris JM, Guo C, White PS, et al: Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma. Med Pediatr Oncol 36: 24-27, 2001.
-
(2001)
Med Pediatr Oncol
, vol.36
, pp. 24-27
-
-
Maris, J.M.1
Guo, C.2
White, P.S.3
-
6
-
-
0347503601
-
Identification and high-resolution mapping of a constitutional 11q deletion in an infant with multifocal neuroblastoma
-
Mosse Y, Greshock J, King A, Khazi D, Weber BL and Maris JM: Identification and high-resolution mapping of a constitutional 11q deletion in an infant with multifocal neuroblastoma. Lancet Oncol 4: 769-771, 2003.
-
(2003)
Lancet Oncol
, vol.4
, pp. 769-771
-
-
Mosse, Y.1
Greshock, J.2
King, A.3
Khazi, D.4
Weber, B.L.5
Maris, J.M.6
-
7
-
-
40249110396
-
Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis
-
Krona C, Caren H, Sjoberg RM, et al: Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis. Int J Oncol 32: 575-583, 2008.
-
(2008)
Int J Oncol
, vol.32
, pp. 575-583
-
-
Krona, C.1
Caren, H.2
Sjoberg, R.M.3
-
8
-
-
4544265599
-
Germline PHOX2B mutation in hereditary neuroblastoma
-
Mosse YP, Laudenslager M, Khazi D, et al: Germline PHOX2B mutation in hereditary neuroblastoma. Am J Hum Genet 75: 727-730, 2004.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 727-730
-
-
Mosse, Y.P.1
Laudenslager, M.2
Khazi, D.3
-
9
-
-
12144291333
-
Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma
-
Trochet D, Bourdeaut F, Janoueix-Lerosey I, et al: Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma. Am J Hum Genet 74: 761-764, 2004.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 761-764
-
-
Trochet, D.1
Bourdeaut, F.2
Janoueix-Lerosey, I.3
-
10
-
-
19944426569
-
The Phox2B homeobox gene is mutated in sporadic neuroblastomas
-
van Limpt V, Schramm A, van Lakeman A, et al: The Phox2B homeobox gene is mutated in sporadic neuroblastomas. Oncogene 23: 9280-9288, 2004.
-
(2004)
Oncogene
, vol.23
, pp. 9280-9288
-
-
van Limpt, V.1
Schramm, A.2
van Lakeman, A.3
-
11
-
-
14544286852
-
The role of Phox2B in chromaffin cell development
-
Huber K, Karch N, Ernsberger U, Goridis C and Unsicker K: The role of Phox2B in chromaffin cell development. Dev Biol 279: 501-508, 2005.
-
(2005)
Dev Biol
, vol.279
, pp. 501-508
-
-
Huber, K.1
Karch, N.2
Ernsberger, U.3
Goridis, C.4
Unsicker, K.5
-
12
-
-
0034034865
-
Specification of the central noradrenergic phenotype by the homeobox gene Phox2b
-
Pattyn A, Goridis C and Brunet JF: Specification of the central noradrenergic phenotype by the homeobox gene Phox2b. Mol Cell Neurosci 15: 235-243, 2000.
-
(2000)
Mol Cell Neurosci
, vol.15
, pp. 235-243
-
-
Pattyn, A.1
Goridis, C.2
Brunet, J.F.3
-
13
-
-
0035885066
-
Sp proteins and Phox2b regulate the expression of the human Phox2a gene
-
Flora A, Lucchetti H, Benfante R, Goridis C, Clementi F and Fornasari D: Sp proteins and Phox2b regulate the expression of the human Phox2a gene. J Neurosci 21: 7037-7045, 2001.
-
(2001)
J Neurosci
, vol.21
, pp. 7037-7045
-
-
Flora, A.1
Lucchetti, H.2
Benfante, R.3
Goridis, C.4
Clementi, F.5
Fornasari, D.6
-
14
-
-
0031908025
-
MASH1 activates expression of the paired homeodomain transcription factor Phox2a, and couples pan-neuronal and subtype-specific components of autonomic neuronal identity
-
Lo L, Tiveron MC and Anderson DJ: MASH1 activates expression of the paired homeodomain transcription factor Phox2a, and couples pan-neuronal and subtype-specific components of autonomic neuronal identity. Development 125: 609-620, 1998.
-
(1998)
Development
, vol.125
, pp. 609-620
-
-
Lo, L.1
Tiveron, M.C.2
Anderson, D.J.3
-
15
-
-
0036668282
-
Phox2 genes - from patterning to connectivity
-
Brunet JF and Pattyn A: Phox2 genes - from patterning to connectivity. Curr Opin Genet Dev 12: 435-440, 2002.
-
(2002)
Curr Opin Genet Dev
, vol.12
, pp. 435-440
-
-
Brunet, J.F.1
Pattyn, A.2
-
16
-
-
27644592012
-
Phox2 and dHAND transcription factors select shared and unique target genes in the noradrenergic cell type
-
Rychlik JL, Hsieh M, Eiden LE and Lewis EJ: Phox2 and dHAND transcription factors select shared and unique target genes in the noradrenergic cell type. J Mol Neurosci 27: 281-292, 2005.
-
(2005)
J Mol Neurosci
, vol.27
, pp. 281-292
-
-
Rychlik, J.L.1
Hsieh, M.2
Eiden, L.E.3
Lewis, E.J.4
-
17
-
-
0027239723
-
Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment
-
Brodeur GM, Pritchard J, Berthold F, et al: Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 11: 1466-1477, 1993.
-
(1993)
J Clin Oncol
, vol.11
, pp. 1466-1477
-
-
Brodeur, G.M.1
Pritchard, J.2
Berthold, F.3
-
18
-
-
0345596397
-
Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours
-
Martinsson T, Sjoberg RM, Hallstensson K, Nordling M, Hedborg F and Kogner P: Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours. Eur J Cancer 33: 1997-2001, 1997.
-
(1997)
Eur J Cancer
, vol.33
, pp. 1997-2001
-
-
Martinsson, T.1
Sjoberg, R.M.2
Hallstensson, K.3
Nordling, M.4
Hedborg, F.5
Kogner, P.6
-
19
-
-
0028853718
-
Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms
-
Martinsson T, Sjoberg RM, Hedborg F and Kogner P: Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms. Cancer Res 55: 5681-5686, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 5681-5686
-
-
Martinsson, T.1
Sjoberg, R.M.2
Hedborg, F.3
Kogner, P.4
-
20
-
-
50849086751
-
High-resolution array copy number analyses and MLPA for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors; Four cases of homozygous deletions of the CDKN2A gene
-
Carén H, Erichsen J, Olsson L, et al: High-resolution array copy number analyses and MLPA for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors; Four cases of homozygous deletions of the CDKN2A gene. BMC Genomics 9: 353, 2008.
-
(2008)
BMC Genomics
, vol.9
, pp. 353
-
-
Carén, H.1
Erichsen, J.2
Olsson, L.3
-
21
-
-
0035179560
-
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2
-
Nakano M, Yamada K, Fain J, et al: Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2. Nat Genet 29: 315-320, 2001.
-
(2001)
Nat Genet
, vol.29
, pp. 315-320
-
-
Nakano, M.1
Yamada, K.2
Fain, J.3
-
22
-
-
0037129827
-
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
-
Research0034
-
Vandesompele J, De Preter K, Pattyn F, et al: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3: Research0034, 2002.
-
(2002)
Genome Biol
, vol.3
-
-
Vandesompele, J.1
De Preter, K.2
Pattyn, F.3
-
23
-
-
0027517354
-
Dynamic expression of the murine Achaete-Scute homologue Mash-1 in the developing nervous system
-
Guillemot F and Joyner AL: Dynamic expression of the murine Achaete-Scute homologue Mash-1 in the developing nervous system. Mech Dev 42: 171-185, 1993.
-
(1993)
Mech Dev
, vol.42
, pp. 171-185
-
-
Guillemot, F.1
Joyner, A.L.2
-
24
-
-
0031910150
-
Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system
-
Hirsch MR, Tiveron MC, Guillemot F, Brunet JF and Goridis C: Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system. Development 125: 599-608, 1998.
-
(1998)
Development
, vol.125
, pp. 599-608
-
-
Hirsch, M.R.1
Tiveron, M.C.2
Guillemot, F.3
Brunet, J.F.4
Goridis, C.5
-
25
-
-
28844459839
-
The cAMP pathway regulates both transcription and activity of the paired homeobox transcription factor Phox2a required for development of neural crest-derived and central nervous system-derived catecholaminergic neurons
-
Chen S, Ji M, Paris M, Hullinger RL and Andrisani OM: The cAMP pathway regulates both transcription and activity of the paired homeobox transcription factor Phox2a required for development of neural crest-derived and central nervous system-derived catecholaminergic neurons. J Biol Chem 280: 41025-41036, 2005.
-
(2005)
J Biol Chem
, vol.280
, pp. 41025-41036
-
-
Chen, S.1
Ji, M.2
Paris, M.3
Hullinger, R.L.4
Andrisani, O.M.5
-
26
-
-
0025838235
-
Antibody markers identify a common progenitor to sympathetic neurons and chromaffin cells in vivo and reveal the timing of commitment to neuronal differentiation in the sympathoadrenal lineage
-
Anderson DJ, Carnahan JF, Michelsohn A and Patterson PH: Antibody markers identify a common progenitor to sympathetic neurons and chromaffin cells in vivo and reveal the timing of commitment to neuronal differentiation in the sympathoadrenal lineage. J Neurosci 11: 3507-3519, 1991.
-
(1991)
J Neurosci
, vol.11
, pp. 3507-3519
-
-
Anderson, D.J.1
Carnahan, J.F.2
Michelsohn, A.3
Patterson, P.H.4
-
27
-
-
34047144947
-
Classification of neuroblastoma patients by published gene-expression markers reveals a low sensitivity for unfavorable courses of MYCN non-amplified disease
-
Oberthuer A, Warnat P, Kahlert Y, et al: Classification of neuroblastoma patients by published gene-expression markers reveals a low sensitivity for unfavorable courses of MYCN non-amplified disease. Cancer Lett 250: 250-267, 2007.
-
(2007)
Cancer Lett
, vol.250
, pp. 250-267
-
-
Oberthuer, A.1
Warnat, P.2
Kahlert, Y.3
-
28
-
-
20244385561
-
Expression profiling using a tumor-specific cDNA microarray predicts the prognosis of intermediate risk neuroblastomas
-
Ohira M, Oba S, Nakamura Y, et al: Expression profiling using a tumor-specific cDNA microarray predicts the prognosis of intermediate risk neuroblastomas. Cancer Cell 7: 337-350, 2005.
-
(2005)
Cancer Cell
, vol.7
, pp. 337-350
-
-
Ohira, M.1
Oba, S.2
Nakamura, Y.3
-
29
-
-
33745700217
-
Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number
-
Wang Q, Diskin S, Rappaport E, et al: Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number. Cancer Res 66: 6050-6062, 2006.
-
(2006)
Cancer Res
, vol.66
, pp. 6050-6062
-
-
Wang, Q.1
Diskin, S.2
Rappaport, E.3
-
30
-
-
0030936255
-
Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a
-
Morin X, Cremer H, Hirsch MR, Kapur RP, Goridis C and Brunet JF: Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a. Neuron 18: 411-423, 1997.
-
(1997)
Neuron
, vol.18
, pp. 411-423
-
-
Morin, X.1
Cremer, H.2
Hirsch, M.R.3
Kapur, R.P.4
Goridis, C.5
Brunet, J.F.6
-
31
-
-
0032841987
-
The Phox2 homeodomain proteins are sufficient to promote the development of sympathetic neurons
-
Stanke M, Junghans D, Geissen M, Goridis C, Ernsberger U and Rohrer H: The Phox2 homeodomain proteins are sufficient to promote the development of sympathetic neurons. Development 126: 4087-4094, 1999.
-
(1999)
Development
, vol.126
, pp. 4087-4094
-
-
Stanke, M.1
Junghans, D.2
Geissen, M.3
Goridis, C.4
Ernsberger, U.5
Rohrer, H.6
-
32
-
-
0033609337
-
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
-
Pattyn A, Morin X, Cremer H, Goridis C and Brunet JF: The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives. Nature 399: 366-370, 1999.
-
(1999)
Nature
, vol.399
, pp. 366-370
-
-
Pattyn, A.1
Morin, X.2
Cremer, H.3
Goridis, C.4
Brunet, J.F.5
-
33
-
-
33750475218
-
Human fetal neuroblast and neuroblastoma transcriptome analysis confirms neuroblast origin and highlights neuroblastoma candidate genes
-
De Preter K, Vandesompele J, Heimann P, et al: Human fetal neuroblast and neuroblastoma transcriptome analysis confirms neuroblast origin and highlights neuroblastoma candidate genes. Genome Biol 7: R84, 2006.
-
(2006)
Genome Biol
, vol.7
-
-
De Preter, K.1
Vandesompele, J.2
Heimann, P.3
-
34
-
-
27644524215
-
Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2
-
Huynh TT, Pacak K, Brouwers FM, et al: Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2. Eur J Endocrinol 153: 551-563, 2005.
-
(2005)
Eur J Endocrinol
, vol.153
, pp. 551-563
-
-
Huynh, T.T.1
Pacak, K.2
Brouwers, F.M.3
-
35
-
-
33845490884
-
Can quantification of VMAT and SSTR expression be helpful for planning radionuclide therapy of malignant pheochromocytomas?
-
Kolby L, Bernhardt P, Johanson V, et al: Can quantification of VMAT and SSTR expression be helpful for planning radionuclide therapy of malignant pheochromocytomas? Ann NY Acad Sci 1073: 491-497, 2006.
-
(2006)
Ann NY Acad Sci
, vol.1073
, pp. 491-497
-
-
Kolby, L.1
Bernhardt, P.2
Johanson, V.3
-
36
-
-
0035162576
-
Differential expression of vesicular monoamine transporter (VMAT) 1 and 2 in gastrointestinal endocrine tumours
-
Jakobsen AM, Andersson P, Saglik G, et al: Differential expression of vesicular monoamine transporter (VMAT) 1 and 2 in gastrointestinal endocrine tumours. J Pathol 195: 463-472, 2001.
-
(2001)
J Pathol
, vol.195
, pp. 463-472
-
-
Jakobsen, A.M.1
Andersson, P.2
Saglik, G.3
-
37
-
-
38949115590
-
The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma
-
Revet I, Huizenga G, Chan A, et al: The MSX1 homeobox transcription factor is a downstream target of PHOX2B and activates the Delta-Notch pathway in neuroblastoma. Exp Cell Res 314: 707-719, 2008.
-
(2008)
Exp Cell Res
, vol.314
, pp. 707-719
-
-
Revet, I.1
Huizenga, G.2
Chan, A.3
-
38
-
-
0037379890
-
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
-
Amiel J, Laudier B, Attie-Bitach T, et al: Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 33: 459-461, 2003.
-
(2003)
Nat Genet
, vol.33
, pp. 459-461
-
-
Amiel, J.1
Laudier, B.2
Attie-Bitach, T.3
-
39
-
-
0344033754
-
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
-
Weese-Mayer DE, Berry-Kravis EM, Zhou L, et al: Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b. Am J Med Genet A 123: 267-278, 2003.
-
(2003)
Am J Med Genet A
, vol.123
, pp. 267-278
-
-
Weese-Mayer, D.E.1
Berry-Kravis, E.M.2
Zhou, L.3
|