417 results on '"Walz, Christoph"'
Search Results
52. Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency
53. Low-dose imatinib mesylate leads to rapid induction of major molecular responses and achievement of complete molecular remission in FIP1L1-PDGFRA–positive chronic eosinophilic leukemia
54. Immature Plasma Cell Myeloma Mimics Metastatic Renal Cell Carcinoma on 18F-PSMA-1007 PET/CT Due to Endothelial PSMA-Expression
55. Complete molecular remission of chronic eosinophilic leukemia complicated by CNS disease after targeted therapy with imatinib
56. DNA topoisomerase II in therapy-related acute promyelocytic leukemia
57. Activated Jak2 with the V617F Point Mutation Promotes G1/S Phase Transition
58. Novel targeted therapies to overcome imatinib mesylate resistance in chronic myeloid leukemia (CML)
59. Digital scoring of EpCAM and slug expression as prognostic markers in head and neck squamous cell carcinomas
60. Cold non‐ischemic heart preservation with continuous perfusion prevents early graft failure in orthotopic pig‐to‐baboon xenotransplantation
61. Impact of porcine cytomegalovirus on long-term orthotopic cardiac xenotransplant survival
62. The soluble transferrin receptor (TfR)-F-Index is not applicable as a test for iron status in patients with chronic lymphocytic leukemia
63. Safety and efficacy of imatinib in chronic eosinophilic leukaemia and hypereosinophilic syndrome – a phase-II study
64. Migrations- und Integrationsforschung: Jahresbericht 2014 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
65. Migrations- und Integrationsforschung: Jahresbericht 2011 der Forschungsgruppe im Bundesamt für Migration und Flüchtlinge
66. The Neurokinin-1 Receptor Is a Target in Pediatric Rhabdoid Tumors.
67. Migrations- und Integrationsforschung: Jahresbericht 2018 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
68. Pulmonary alveolar proteinosis due to heterozygous mutation in OAS1: Treatment of a novel disease with whole lung lavages and stem cell transplantation
69. BACH: Grand challenge on breast cancer histology images
70. Activation of Hedgehog Signaling in Aggressive Hepatic Hemangioma in Newborns and Infants
71. Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency
72. Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency
73. Digital scoring of EpCAM and slug expression as prognostic markers in head and neck squamous cell carcinomas.
74. Epstein–Barr Virus+ Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders
75. Epstein-Barr Virus+smooth muscle tumors as manifestation of primary immunodeficiency disorders
76. Migrations- und Integrationsforschung: Jahresbericht 2017 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
77. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases
78. Comparative proteomics reveals a diagnostic signature for pulmonary head-and-neck cancermetastasis
79. Migrations- und Integrationsforschung: Jahresbericht 2016 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
80. Migrations- und Integrationsforschung: Jahresbericht 2015 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
81. Migrations- und Integrationsforschung: Jahresbericht 2014 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
82. Rltpr Is a Central Scaffold Protein Regulating Human TCR Co-Signaling and Cytoskeletal Dynamics
83. Migrations- und Integrationsforschung: Jahresbericht 2013 des Forschungszentrums Migration, Integration und Asyl im Bundesamt für Migration und Flüchtlinge
84. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases.
85. Migrations- und Integrationsforschung: Jahresbericht 2012 der Forschungsgruppe im Bundesamt für Migration und Flüchtlinge
86. Advanced systemic mastocytosis as a mimicker of metastatic clear cell renal cell carcinoma
87. Migrations- und Integrationsforschung: Jahresbericht 2011 der Forschungsgruppe im Bundesamt für Migration und Flüchtlinge
88. Migrations- und Integrationsforschung: Jahresbericht 2010 der Forschungsgruppe im Bundesamt für Migration und Flüchtlinge
89. A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1
90. Diagnostic and Treatment Options for Severe IBD in Female X-CGD Carriers with Non-random X-inactivation
91. Response of ETV6-FLT3–positive myeloid/lymphoid neoplasm with eosinophilia to inhibitors of FMS-like tyrosine kinase 3
92. Molecular Profiling of Myeloid Progenitor Cells in Multi-Mutated Advanced Systemic Mastocytosis Identifies KIT D816V As a Distinct and Late Event
93. Adeno-Associated Viral Vector 2.9 Thymosin ß4 Application Attenuates Rejection After Heart Transplantation
94. CD52 is a molecular target in advanced systemic mastocytosis
95. Personalised analysis of cell-free circulating tumour DNA for detection of molecular residual disease and recurrence in patients with head and neck squamous cell carcinoma.
96. Mutational Complexity Is Related To Disease Severity In Systemic Mastocytosis
97. PCM1–JAK2-fusion: a potential treatment target in myelodysplastic–myeloproliferative and other hemato-lymphoid neoplasms
98. KIT D816V and JAK2 V617F Point Mutations Are Recurrently Found In Suspected Hypereosinophilic Syndrome
99. Atypical mRNA fusions inPML-RARApositive,RARA-PMLnegative acute promyelocytic leukemia
100. Novel PDGFRA Point Mutations in Hypereosinophilic Syndrome Induce Growth Factor Independence and Leukemia in Vitro and In Vivo.
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