heiBIB: Janssen, Johannes W. G.

Janssen, Johannes W. G. Dr. rer. nat.Universität HeidelbergHeidelberg

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englisch (29)
deutsch (1)

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Publikationen in heiBIB

Ramdohr, Florian: Atypical presentation of patients with chronic myeloid leukemia in chronic phase : case report / Florian Ramdohr, Alice Fabarius, Bettina Maier, Daniela Bretschneider, Anna Jauch, Astrid Monecke, K… , 29 August 2022. - 7 S. : Illustrationen
In: Frontiers in oncology, ISSN 2234-943X. 12(2022) vom: Aug., Artikel-ID 960914, Seite 1-7
DOI: 10.3389/fonc.2022.960914
Zhong, Rujia: A preclinical study on brugada syndrome with a CACNB2 variant using human cardiomyocytes from induced pluripotent stem cells / Rujia Zhong, Theresa Schimanski, Feng Zhang, Huan Lan, Alyssa Hohn, Qiang Xu, Mengying Huang, Zhenxi… , 27 July 2022. - 17 S.
In: International journal of molecular sciences, ISSN 1422-0067. 23(2022), 15, Artikel-ID 8313, Seite 1-17
DOI: 10.3390/ijms23158313
Cristian, Flavia-Bianca: Generation of two hiPSC lines from a patient with autism spectrum disorder harboring a 120 kb deletion in SHANK2 and two control lines from each parent / Flavia-Bianca Cristian, Alexandra Köppel, Johannes Janssen, Jochen S. Utikal, Gudrun A. Rappold, Sim… , 19 September 2020. - 5 S.
In: Stem cell research, ISSN 1876-7753. 49(2020) Artikel-Nummer 102004, 5 Seiten
DOI: 10.1016/j.scr.2020.102004
Sumer, Simon: Precise correction of heterozygous SHOX2 mutations in hiPSCs derived from patients with atrial fibrillation via genome editing and sib selection / Simon Alexander Sumer, Sandra Hoffmann, Svenja Laue, Birgit Campbell, Kristin Raedecke, Viktoria Fra… , September 24, 2020. - 15 S.
In: Stem cell reports, ISSN 2213-6711. 15(2020), 4, Seite 999-1013
DOI: 10.1016/j.stemcr.2020.08.015
Kuçi, Zyrafete: Mesenchymal stromal cells from pooled mononuclear cells of multiple bone marrow donors as rescue therapy in pediatric severe steroid-refractory graft-versus-host disease : a multicenter survey / Zyrafete Kuçi, Halvard Bönig, Hermann Kreyenberg, Milica Bunos, Anna Jauch, Johannes W. G. Janssen, … , August 2016. - 10 S.
In: Haematologica, ISSN 1592-8721. 101(2016), 8, Seite 985-994
DOI: 10.3324/haematol.2015.140368
Heller, Anette: Establishment and characterization of a novel cell line, asan-paca, derived from human adenocarcinoma arising in intraductal papillary mucinous neoplasm of the pancreas / Anette Heller, PhD, Assia L. Angelova, PhD, Sonja Bauer, Svitlana P. Grekova, PhD, Marc Aprahamian, … , March 3, 2016. - 9 S.
In: Pancreas, ISSN 1536-4828. 45(2016), 10, Seite 1452-1460
DOI: 10.1097/MPA.0000000000000673
Evers, Christina: Duplication Xp11.22-p14 in females : does X-inactivation help in assessing their significance? / Christina Evers, Diana Mitter, Gertrud Strobl‐Wildemann, Ulrich Haug, Karl Hackmann, Bianca Maas, Jo… , 18 February 2015. - 10 S.
In: American journal of medical genetics, ISSN 1552-4833. 167(2015), 3, Seite 553-562
DOI: 10.1002/ajmg.a.36897
Blake, Jonathon: Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation / Jonathon Blake, Andrew Riddell, Susanne Theiss, Alexis Perez Gonzalez, Bettina Haase, Anna Jauch, Jo… , March 13, 2014
In: PLOS ONE, ISSN 1932-6203. 9(2014,3) Artikel-Nummer e90894, 11 Seiten
DOI: 10.1371/journal.pone.0090894
Kaiser, Ann-Sophie: Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia / Ann-Sophie Kaiser, Bianca Maas, Anna Wolff, Christian Sutter, Johannes WG Janssen, Katrin Hinderhofe… , 2015. - 4 S.
In: European journal of human genetics, ISSN 1476-5438. 23(2015), 5, Seite 704-707
DOI: 10.1038/ejhg.2014.163
Evers, Christina: Mosaic deletion of EXOC6B : further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability / Christina Evers, Bianca Maas, Karin A. Koch, Anna Jauch, Johannes W.G. Janssen, Christian Sutter, Mi… . - 7 S.
In: American journal of medical genetics, ISSN 1552-4833. 164(2014), 12, S. 3088-3094
DOI: 10.1002/ajmg.a.36770
Dikow, Nicola: 3p25.3 Microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior / Nicola Dikow, Bianca Maas, Stephanie Karch, Martin Granzow, Johannes W. G. Janssen, Anna Jauch, Katr… . - 8 S.
In: American journal of medical genetics, ISSN 1552-4833. 164(2014), 12, S. 3061-3068
DOI: 10.1002/ajmg.a.36761
Dikow, Nicola: The phenotypic spectrum of duplication 5q35.2-q35.3 encompassing NSD1 : is it really a reversed sotos syndrome? / Nicola Dikow, Bianca Maas, Harald Gaspar, Martina Kreiss‐Nachtsheim, Hartmut Engels, Alma Kuechler, … , 2 August 2013. - 9 S.
In: American journal of medical genetics, ISSN 1552-4833. 161(2013), 9, Seite 2158-2166
DOI: 10.1002/ajmg.a.36046
Bochtler, Tilmann: Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemia / Tilmann Bochtler, Friedrich Stölzel, Christoph E. Heilig, Christina Kunz, Brigitte Mohr, Anna Jauch,… , September 23, 2013. - 8 S.
In: Journal of clinical oncology, ISSN 1527-7755. 31(2013), 31, Seite 3898-3905
DOI: 10.1200/JCO.2013.50.7921
Evers, Christina: Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1 : further insights into a genetic paradox / C. Evers, M.S. Jungwirth, J. Morgenthaler, K. Hinderhofer, B. Maas, J.W.G. Janssen, A. Jauch, U. Heh… , 2014. - 6 S.
In: Clinical genetics, ISSN 1399-0004. 85(2014), 4, Seite 347-353
DOI: 10.1111/cge.12171
Evers, Christina: A small terminal deletion 11q in a boy without Jacobsen syndrome : narrowing the critical region for the 11q Jacobsen syndrome phenotype / Christina Evers, Johannes W.G. Janssen, Anna Jauch, Michael Bonin, and Ute Moog, March 2012. - 5 S.
In: American journal of medical genetics, ISSN 1552-4833. 158A(2012), 3, Seite 680-684
DOI: 10.1002/ajmg.a.34433
Behnecke, Anne: Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13) / Behnecke A, Hinderhofer K, Jauch A, Janssen JWG, Moog U, November 2012. - 5 S.
In: Clinical genetics, ISSN 1399-0004. 82(2012), 5, Seite 494-498
DOI: 10.1111/j.1399-0004.2011.01792.x
Hämmerling, Susanne Hedwig: A 15q24 microdeletion in transient myeloproliferative Disease (TMD) and acute megakaryoblastic leukaemia (AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/AMKL / Susanne Haemmerling, Wolfgang Behnisch, Tobias Doerks, Jan O. Korbel, Peer Bork, Ute Moog, Sabine He… , 1 February 2012. - 8 S.
In: British journal of haematology, ISSN 1365-2141. 157(2012), 2, Seite 180-187
DOI: 10.1111/j.1365-2141.2012.09028.x
Keller, Sascha: Body fluid derived exosomes as a novel template for clinical diagnostics / Sascha Keller, Johannes Ridinger, Anne-Kathleen Rupp, Johannes WG Janssen and Peter Altevogt, 8 June 2011. - 9 S.
In: Journal of translational medicine, ISSN 1479-5876. 9(2011), Artikel-ID 86, Seite 1-9
DOI: 10.1186/1479-5876-9-86
Evers, Christina: Pseudoautosomal inheritance of Léri-Weill syndrome : what does it mean? / C. Evers, P.H. Heidemann, D. Dunstheimer, E. Schulze, C. Haag, J.W.G. Janssen, C. Fischer, A. Jauch … , 07 April 2011. - 6 S.
In: Clinical genetics, ISSN 1399-0004. 79(2011), 5, Seite 489-494
DOI: 10.1111/j.1399-0004.2010.01488.x
Heilig, Christoph E.: Chromosomal instability correlates with poor outcome in patients with myelodysplastic syndromes irrespectively of the cytogenetic risk group / Christoph E. Heilig, Harald Löffler, Ulrich Mahlknecht, Johannes W.G. Janssen, Anthony D. Ho, Anna J… , [April 2010]. - 8 S. : Illustrationen
In: Journal of cellular and molecular medicine, ISSN 1582-4934. 14(2010), 4 vom: Apr., Seite 895-902
DOI: 10.1111/j.1582-4934.2009.00905.x
Schaaf, Christian P.: Novel interaction partners of the TPR/MET tyrosine kinase / Christian P. Schaaf ... Claus R. Bartram ; Johannes W. G. Janssen. - 3 S.
In: The FASEB journal, ISSN 0892-6638. 19(2005), S. 267-269
Nakao, Makoto: Rapid and reliable quantification of minimal residual disease in acute lymphoblastic leukemia using rearranged immunoglobulin and T-cell receptor loci by LightCycler technology / Makoto Nakao ; Johannes W. G. Janssen ... Claus R. Bartram. - 9 S.
In: Cancer research, ISSN 0008-5472. 60(2000), S. 3281-3289
Janssen, Johannes W. G.: Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32) / Johannes W. G. Janssen ... Anna Jauch ... Claus R. Bartram .... - 18 S.
In: Blood, ISSN 0006-4971. 95(2000), S. 2691-2698
Janssen, Johannes W. G.: Funktionelle Charakterisierung von Onkogenen des Menschen nach Isolation mittels DNA Transfektion / vorgelegt von Johannes W. G. Janssen, 1999 [ersch.] 2000. - Getr. Zählung : Ill.
Janssen, Johannes W. G.: An oncogenic fusion product of the phosphatidylinositol 3-kinase p85β subunit and HUMORF8, a putative deubiquitinating enzyme / Johannes WG Janssen, Lothar Schleithoff, Claus R. Bartram, Ansgar S. Schulz, 23 April 1998. - 6 S.
In: Oncogene, ISSN 1476-5594. 16(1998), 13, Seite 1767-1772
DOI: 10.1038/sj.onc.1201695
Rieder, Harald: High rate of chromosome abnormalities detected by fluorescence in situ hybridization using BCR and ABL probes in adult acute lymphoblastic leukemia / H. Rieder, C. Bonwetsch, L.A.J. Janssen, J. Maurer, J.W.G. Janssen, S. Schwartz, W.-D. Ludwig, W. Ga… , 02 September 1998. - 9 S.
In: Leukemia, ISSN 1476-5551. 12(1998), 9, Seite 1473-1481
DOI: 10.1038/sj.leu.2401127
Hansen-Hagge, Thomas E.: An evolutionarily conserved gene on human chromosome 5q33-q34,UBH1, encodes a novel deubiquitinating enzyme / Thomas E. Hansen-Hagge, Johannes W.G. Janssen, Horst Hameister, Feroz R. Papa, Ulrich Zechner, Taku … , 1 May 1998. - 8 S.
In: Genomics, ISSN 1089-8646. 49(1998), 3, Seite 411-418
DOI: 10.1006/geno.1998.5275
Braunger, Jürgen: Intracellular signaling of the Ufo/Axl receptor tyrosine kinase is mediated mainly by a multisubstrate docking-site / Jürgen Braunger ... Claus R. Bartram ; Johannes W. G. Janssen. - 13 S.
In: Oncogene, ISSN 0950-9232. 14(1997), S. 2619-2631
Schlieben, Sigrid: Incidence and clinical outcome of children with BCR/ABL-positive acute lymphoblastic leukemia (ALL). A prospective RT-PCR study based on 673 patients enrolled in the German pediatric multicenter therapy trials ALL-BFM-90 and CoALL-05-92 / Schlieben S, Borkhardt A, Reinisch I, Ritterbach J, Janssen JW, Ratei R, Schrappe M, Repp R, Zimmerm… , 1996. - 7 S.
In: Leukemia, ISSN 0887-6924. 10(1996), 6, Seite 957-963
Janssen, Johannes W. G.: Pre-pre-B acute lymphoblastic leukemia : high frequency of alternatively spliced ALL1-AF4 transcripts and absence of minimal residual disease during complete remission / Johannes W. G. Janssen ... Claus R. Bartram. - 8 S.
In: Blood, ISSN 0006-4971. 84(1994), S. 3835-3842

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