يعرض 1 - 10 نتائج من 40 نتيجة بحث عن '"Tord Jonson"', وقت الاستعلام: 0.92s تنقيح النتائج
  1. 1
    دورية أكاديمية
    ZMIZ1-associated neurodevelopmental disorder and Hirschsprung disease

    المؤلفون: Anders Valind, Pernilla Stenström, Sofie Samuelsson, Tord Jonson, Erik A. Eklund

    المصدر: Journal of Pediatric Surgery Case Reports, Vol 71, Iss , Pp 101889- (2021)

    مصطلحات موضوعية: Hirschsprung disease, ZMIZ1, Enteric nervous system, Pediatrics, RJ1-570, Surgery, RD1-811

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S221357662100110X; https://doaj.org/toc/2213-5766

    URL الوصول: https://doaj.org/article/57aa661ae6554ea9bd4f80ea3afdb0d4

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  2. 2
    Data from Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers

    المؤلفون: David Gisselsson, Mattias Höglund, Wiking Månsson, Sigurdur Gudjonsson, Fredrik Liedberg, Gunilla Chebil, Lena Maria Lundberg, Nina Larsson, Anna Edqvist, Tord Jonson, Olga Calcagnile, Attila Frigyesi, David Lindgren, Ylva Stewénius, Yuesheng Jin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f92ea4c7ae0bec8c841b6da206005df
    https://doi.org/10.1158/1078-0432.c.6518449

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  3. 3
    Supplementary Figure S1 from Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers

    المؤلفون: David Gisselsson, Mattias Höglund, Wiking Månsson, Sigurdur Gudjonsson, Fredrik Liedberg, Gunilla Chebil, Lena Maria Lundberg, Nina Larsson, Anna Edqvist, Tord Jonson, Olga Calcagnile, Attila Frigyesi, David Lindgren, Ylva Stewénius, Yuesheng Jin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1dec20686fdc52d9e935ff8fd399c06
    https://doi.org/10.1158/1078-0432.22441366.v1

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  4. 4
    Supplementary Tables S1-S2 from Distinct Mitotic Segregation Errors Mediate Chromosomal Instability in Aggressive Urothelial Cancers

    المؤلفون: David Gisselsson, Mattias Höglund, Wiking Månsson, Sigurdur Gudjonsson, Fredrik Liedberg, Gunilla Chebil, Lena Maria Lundberg, Nina Larsson, Anna Edqvist, Tord Jonson, Olga Calcagnile, Attila Frigyesi, David Lindgren, Ylva Stewénius, Yuesheng Jin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab470ff565b8277d609053e2a7a87d68
    https://doi.org/10.1158/1078-0432.22441363

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  5. 5
    Supplementary Table 2 from Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines

    المؤلفون: Mattias Höglund, Ad Geurts van Kessel, Joris A. Veltman, Ludmila Gorunova, Tord Jonson, Eric F. P. M. Schoenmakers, Markus Heidenblad

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1385009726f79a708a4159b498e768e8
    https://doi.org/10.1158/0008-5472.22363988

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  6. 6
    Data from Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines

    المؤلفون: Mattias Höglund, Ad Geurts van Kessel, Joris A. Veltman, Ludmila Gorunova, Tord Jonson, Eric F. P. M. Schoenmakers, Markus Heidenblad

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287568bfe8ceb34538a47bef9e76d66e
    https://doi.org/10.1158/0008-5472.c.6493973.v1

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  7. 7
    ZMIZ1-associated neurodevelopmental disorder and Hirschsprung disease

    المؤلفون: Pernilla Stenström, Sofie Samuelsson, Erik A. Eklund, Tord Jonson, Anders Valind

    المصدر: Journal of Pediatric Surgery Case Reports, Vol 71, Iss, Pp 101889-(2021)

    مصطلحات موضوعية: Genetics, ZMIZ1, Hirschsprung disease, RD1-811, business.industry, Chromosome, Disease, medicine.disease, Pediatrics, RJ1-570, 03 medical and health sciences, 0302 clinical medicine, Neurodevelopmental disorder, 030220 oncology & carcinogenesis, Pediatrics, Perinatology and Child Health, Gene expression, medicine, 030211 gastroenterology & hepatology, Enteric nervous system, Surgery, Progenitor cell, business, Gene, Transcription factor

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e2094c341830e4582787c2a1e3ba1f4
    http://www.sciencedirect.com/science/article/pii/S221357662100110X

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  8. 8
    Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation

    المؤلفون: Johanna Elander, Tove Ullmark, Hans Ehrencrona, Tord Jonson, Paul Piccinelli, Sofie Samuelsson, Karolina Löwgren, Karolina Falkenius-Schmidt, Johannes Ehinger, Karin Stenfeldt, Maria Värendh

    المصدر: International Journal of Pediatric Otorhinolaryngology. 159:111218

    مصطلحات موضوعية: Hearing Loss, Bilateral, Male, Otorhinolaryngology, Hearing Loss, Sensorineural, Pediatrics, Perinatology and Child Health, Humans, Female, Pilot Projects, Prospective Studies, General Medicine, Child, Cochlear Implantation

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6b72caf910aa8ec948291151879862a
    https://doi.org/10.1016/j.ijporl.2022.111218

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  9. 9
    Dysregulated gene expression throughTP53promoter swapping in osteosarcoma

    المؤلفون: Karim H. Saba, Valeria Difilippo, Michal Kovac, Louise Cornmark, Linda Magnusson, Jenny Nilsson, Hilda van den Bos, Diana C. J. Spierings, Mahtab Bidgoli, Tord Jonson, Vaiyapuri P. Sumathi, Otte Brosjö, Johan Staaf, Floris Foijer, Emelie Styring, Michaela Nathrath, Daniel Baumhoer, Karolin H. Nord

    مصطلحات موضوعية: Transcriptome, medicine.anatomical_structure, Tumor suppressor gene, Cell, Cancer cell, medicine, Cancer research, Osteosarcoma, Promoter, Biology, medicine.disease, Gene, Loss function

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::729097b5658da80fb7d3a15f1ea6a3ba
    https://doi.org/10.1101/2020.04.20.050252

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  10. 10
    Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism

    المؤلفون: Maria Elfving, Torbjörn Backman, Henrik Thybo Christesen, Henrik Petersen, Tord Jonson, Lars Kjærsgaard Hansen, Klaus Brusgaard, Lene Gaarsmand Christensen, Annette Rønholt Larsen, Åsa Löfgren, Sönke Detlefsen, Karen Grønskov, Johan Svensson, Sofie Samuelsson, Lars S. Rasmussen, Karen Brøndum-Nielsen

    المصدر: Christesen, H T, Christensen, L G, Löfgren, Å M, Brøndum-Nielsen, K, Svensson, J, Brusgaard, K, Samuelsson, S, Elfving, M, Jonson, T, Grønskov, K, Rasmussen, L, Backman, T, Hansen, L K, Larsen, A R, Petersen, H & Detlefsen, S 2020, ' Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism ', European Journal of Medical Genetics, vol. 63, no. 1, 103632 . https://doi.org/10.1016/j.ejmg.2019.02.004

    مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Beckwith-Wiedemann Syndrome, medicine.medical_treatment, Beckwith–Wiedemann syndrome, Pancreatoblastoma, 030105 genetics & heredity, Genome-wide uniparental disomy, Polymorphism, Single Nucleotide, 03 medical and health sciences, Genomic Imprinting, Angelman syndrome, Genetics, medicine, Chromosomes, Human, Humans, Genetic Predisposition to Disease, Genetics (clinical), medicine.diagnostic_test, business.industry, Genome, Human, Mosaicism, Focal nodular hyperplasia, General Medicine, Congenital hyperinsulinism, DNA Methylation, Uniparental Disomy, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, Phenotype, Organ Specificity, Liver biopsy, Child, Preschool, Pancreatectomy, Beckwith-Wiedemann syndrome, Congenital Hyperinsulinism, Female, business, Pancreas

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946f689bcc2d3bd2f76ac1c08ef087c0
    https://findresearcher.sdu.dk:8443/ws/files/159699326/1_s2.0_S1769721218309327_main.pdf

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