Datasets
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Additional file 1: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693295, https://springernature.figshare.com/articles/Additional_file_1_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693295
Dataset
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Additional file 1: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693295.v1, https://springernature.figshare.com/articles/Additional_file_1_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693295/1
Dataset
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Additional file 1: of Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders
Nguyen, L. S. (Creator), Fregeac, J. (Creator), Bole-Feysot, C. (Creator), Cagnard, N. (Creator), Iyer, A. (Creator), Anink, J. (Creator), Aronica, E. (Creator), Alibeu, O. (Creator), Nitschke, P. (Creator), Colleaux, L. (Creator) & Aronica, E. (Creator), Figshare, 2018
DOI: 10.6084/m9.figshare.6616259, https://springernature.figshare.com/articles/Additional_file_1_of_Role_of_miR-146a_in_neural_stem_cell_differentiation_and_neural_lineage_determination_relevance_for_neurodevelopmental_disorders/6616259
Dataset
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Additional file 1: of Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders
Nguyen, L. S. (Creator), Fregeac, J. (Creator), Bole-Feysot, C. (Creator), Cagnard, N. (Creator), Iyer, A. (Creator), Anink, J. (Creator), Aronica, E. (Creator), Alibeu, O. (Creator), Nitschke, P. (Creator), Colleaux, L. (Creator) & Aronica, E. (Creator), Figshare, 2018
DOI: 10.6084/m9.figshare.6616259.v1, https://springernature.figshare.com/articles/Additional_file_1_of_Role_of_miR-146a_in_neural_stem_cell_differentiation_and_neural_lineage_determination_relevance_for_neurodevelopmental_disorders/6616259/1
Dataset
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Additional file 10: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878860, https://springernature.figshare.com/articles/Additional_file_10_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878860
Dataset
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Additional file 10: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878860.v1, https://springernature.figshare.com/articles/Additional_file_10_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878860/1
Dataset
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Additional file 2: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693298.v1, https://springernature.figshare.com/articles/Additional_file_2_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693298/1
Dataset
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Additional file 2: of Disease progression in women with X-linked adrenoleukodystrophy is slow
Huffnagel, I. C. (Creator), Dijkgraaf, M. (Creator), Janssens, G. (Creator), van Weeghel, M. (Contributor), Van Geel, B. M. (Contributor), Poll-The, B. (Contributor), Kemp, S. (Creator), Engelen, M. (Creator) & Weeghel, M. (Creator), Figshare, 2019
DOI: 10.6084/m9.figshare.7693298, https://springernature.figshare.com/articles/Additional_file_2_of_Disease_progression_in_women_with_X-linked_adrenoleukodystrophy_is_slow/7693298
Dataset
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Additional file 2: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878881, https://springernature.figshare.com/articles/Additional_file_2_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878881
Dataset
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Additional file 2: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878881.v1, https://springernature.figshare.com/articles/Additional_file_2_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878881/1
Dataset
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Additional file 3: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878887.v1, https://springernature.figshare.com/articles/Additional_file_3_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878887/1
Dataset
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Additional file 3: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878887, https://springernature.figshare.com/articles/Additional_file_3_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878887
Dataset
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Additional file 4: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878896.v1, https://springernature.figshare.com/articles/Additional_file_4_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878896/1
Dataset
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Additional file 4: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878896, https://springernature.figshare.com/articles/Additional_file_4_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878896
Dataset
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Additional file 5: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878908, https://springernature.figshare.com/articles/Additional_file_5_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878908
Dataset
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Additional file 5: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878908.v1, https://springernature.figshare.com/articles/Additional_file_5_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878908/1
Dataset
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Additional file 7: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878920.v1, https://springernature.figshare.com/articles/Additional_file_7_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878920/1
Dataset
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Additional file 7: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878920, https://springernature.figshare.com/articles/Additional_file_7_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878920
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923.v1, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923/1
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923
Dataset
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Additional file 9: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878926, https://springernature.figshare.com/articles/Additional_file_9_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878926
Dataset
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Additional file 9: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878926.v1, https://springernature.figshare.com/articles/Additional_file_9_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878926/1
Dataset
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CpG and non-CpG Presenilin1 methylation pattern in course of neurodevelopment and neurodegeneration is associated with gene expression in human and murine brain
Monti, N. (Creator), Cavallaro, R. A. (Creator), Stoccoro, A. (Creator), Nicolia, V. (Creator), Scarpa, S. (Creator), Kovacs, G. G. (Contributor), Fiorenza, M. T. (Creator), Lucarelli, M. (Creator), Aronica, E. (Creator), Ferrer, I. (Contributor), Coppedè, F. (Creator), Troen, A. M. (Creator) & Fuso, A. (Creator), Taylor & Francis, 2020
DOI: 10.6084/m9.figshare.11806509, https://tandf.figshare.com/articles/dataset/CpG_and_non-CpG_Presenilin1_methylation_pattern_in_course_of_neurodevelopment_and_neurodegeneration_is_associated_with_gene_expression_in_human_and_murine_brain/11806509
Dataset
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CpG and non-CpG Presenilin1 methylation pattern in course of neurodevelopment and neurodegeneration is associated with gene expression in human and murine brain
Monti, N. (Creator), Cavallaro, R. A. (Creator), Stoccoro, A. (Creator), Nicolia, V. (Creator), Scarpa, S. (Creator), Kovacs, G. G. (Contributor), Fiorenza, M. T. (Creator), Lucarelli, M. (Creator), Aronica, E. (Creator), Ferrer, I. (Contributor), Coppedè, F. (Creator), Troen, A. M. (Creator) & Fuso, A. (Creator), Taylor & Francis, 2020
DOI: 10.6084/m9.figshare.11806509.v1, https://tandf.figshare.com/articles/dataset/CpG_and_non-CpG_Presenilin1_methylation_pattern_in_course_of_neurodevelopment_and_neurodegeneration_is_associated_with_gene_expression_in_human_and_murine_brain/11806509/1
Dataset
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Data from: Idiopathic inflammatory myopathy: inter-rater variability in muscle biopsy reading
Olivier, P. A. (Creator), De Paepe, B. (Creator), Aronica, E. (Creator), Berfelo, F. (Creator), Colman, R. (Creator), Amato, A. (Creator), Dimitri, D. (Creator), Gallardo, E. (Creator), Gherardi, R. (Creator), Goebel, H. (Creator), Hilton-Jones, D. (Creator), Hofer, M. (Creator), Holton, J. (Creator), Schrøder, H. D. (Creator), Selcen, D. (Creator), Stenzel, W. (Creator), de Visser, M. (Contributor), De Bleecker, J. L. (Creator), Hofer, M. (Creator) & Selcen, D. (Creator), Dryad, 9 Sept 2019
DOI: 10.5061/dryad.s9p5c79, https://datadryad.org/stash/dataset/doi:10.5061/dryad.s9p5c79
Dataset