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1. The new sociology of knowledge
: the life and work of Peter L. Berger
by Pfadenhauer, Michaela, 1968 and Berger, Peter L., 1929-2017
2013, 1, ISBN 1412849896, xxii, 152
Religion and sociology | Sociologists | Berger, Peter L., 1929-2017 | Knowledge, Sociology of | Sociology & Social Policy | 1929 | Biography | Berger, Peter L
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2. Full Text MLN4924, a NEDD8-activating enzyme inhibitor, is active in diffuse large B-cell lymphoma models: Rationale for treatment of NF-κB-dependent lymphoma
by Milhollen, Michael A and Traore, Tary and Adams-Duffy, Jennifer and Thomas, Michael P and Berger, Allison J and Dang, Lenny and Dick, Lawrence R and Garnsey, James J and Koenig, Erik and Langston, Steven P and Manfredi, Mark and Narayanan, Usha and Rolfe, Mark and Staudt, Louis M and Soucy, Teresa A and Yu, Jie and Zhang, Julie and Bolen, Joseph B and Smith, Peter G
Blood, ISSN 0006-4971, 09/2010, Volume 116, Issue 9, pp. 1515 - 1523
Life Sciences & Biomedicine | Hematology | Science & Technology
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3. N-Terminal Pro-B-Type Natriuretic Peptide-Guided, Intensive Patient Management in Addition to Multidisciplinary Care in Chronic Heart Failure. A 3-Arm, Prospective, Randomized Pilot Study
by Berger, Rudolf and Moertl, Deddo and Peter, Sieglinde and Ahmadi, Roozbeh and Huelsmann, Martin and Yamuti, Susan and Wagner, Brunhilde and Pacher, Richard
Journal of the American College of Cardiology, ISSN 0735-1097, 02/2010, Volume 55, Issue 7, pp. 645 - 653
nurse | chronic heart failure | natriuretic peptide | multidisciplinary care | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Office Visits - statistics & numerical data | Prospective Studies | Angiotensin II Type 1 Receptor Blockers - therapeutic use | Humans | Male | Heart Failure - blood | Furosemide - therapeutic use | Heart Failure - therapy | Austria | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Peptide Fragments - blood | Female | Cardiology | Spironolactone - therapeutic use | Length of Stay - statistics & numerical data | Natriuretic Peptide, Brain - blood | Adrenergic beta-Antagonists - therapeutic use | Heart Failure - mortality | Risk Assessment | Home Care Services, Hospital-Based | Pilot Projects | Diuretics - therapeutic use | Aged | Primary Health Care | Referral and Consultation | Specialties, Nursing | Patient Readmission - statistics & numerical data | Hypertension | Heart failure | Heart attacks | Peptides | Medical treatment | Mortality | Cardiovascular disease | Hospitalization | Heart rate | Hospitals | Rodents | Risk assessment | Nurses | Medical prognosis
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4. Full Text Effect of B-type natriuretic peptide-guided treatment of chronic heart failure on total mortality and hospitalization: an individual patient meta-analysis
by Troughton, Richard W and Frampton, Christopher M and Brunner-La Rocca, Hans-Peter and Pfisterer, Matthias and Eurlings, Luc W. M and Erntell, Hans and Persson, Hans and O'Connor, Christopher M and Moertl, Deddo and Karlström, Patric and Dahlström, Ulf and Gaggin, Hanna K and Januzzi, James L and Berger, Rudolf and Richards, A. Mark and Pinto, Yigal M and Nicholls, M. Gary
European heart journal, ISSN 0195-668X, 2014, Volume 35, Issue 23, pp. 1559 - 1567
Heart failure | B-type Natriuretic peptide | Natriuretic peptides | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Biomarkers - metabolism | Sodium Potassium Chloride Symporter Inhibitors - therapeutic use | Humans | Natriuretic Peptide, Brain - metabolism | Kaplan-Meier Estimate | Hospitalization - statistics & numerical data | Male | Treatment Outcome | Ventricular Dysfunction, Left - mortality | Heart Failure - blood | Heart Failure - drug therapy | Randomized Controlled Trials as Topic | Ventricular Dysfunction, Left - therapy | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Ventricular Dysfunction, Left - blood | Female | Aged | Drug Substitution - statistics & numerical data | Angiotensin Receptor Antagonists - therapeutic use | Chronic Disease | Heart Failure - mortality | Index Medicus | Clinical Research | Medicin och hälsovetenskap
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5. General relativity and gravitation
: a centennial perspective
by Isenberg, James A., editor and MacCallum, M. A. H., editor and Berger, B. editor. (Beverly) and Ashtekar, Abhay, editor
2015, ISBN 110703731X, xxi, 674
General relativity (Physics) | Gravitation
Book
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6. Full Text A Biologic Definition of Burkitt's Lymphoma from Transcriptional and Genomic Profiling
by Hummel, Michael and Bentink, Stefan and Berger, Hilmar and Klapper, Wolfram and Wessendorf, Swen and Barth, Thomas F.E and Bernd, Heinz-Wolfram and Cogliatti, Sergio B and Dierlamm, Judith and Feller, Alfred C and Hansmann, Martin-Leo and Haralambieva, Eugenia and Harder, Lana and Hasenclever, Dirk and Kühn, Michael and Lenze, Dido and Lichter, Peter and Martin-Subero, Jose Ignacio and Möller, Peter and Müller-Hermelink, Hans-Konrad and Ott, German and Parwaresch, Reza M and Pott, Christiane and Rosenwald, Andreas and Rosolowski, Maciej and Schwaenen, Carsten and Stürzenhofecker, Benjamin and Szczepanowski, Monika and Trautmann, Heiko and Wacker, Hans-Heinrich and Spang, Rainer and Loeffler, Markus and Trümper, Lorenz and Stein, Harald and Siebert, Reiner and Molecular Mechanisms Malignant Lym and Molecular Mechanisms in Malignant Lymphomas Network Project of the Deutsche Krebshilfe
The New England journal of medicine, ISSN 0028-4793, 06/2006, Volume 354, Issue 23, pp. 2419 - 2430
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | General aspects | Medical sciences | Translocation, Genetic | Prognosis | Follow-Up Studies | Oligonucleotide Array Sequence Analysis | Humans | Lymphoma, B-Cell - diagnosis | Middle Aged | Male | Gene Expression Profiling | Genes, myc | Lymphoma, B-Cell - genetics | Burkitt Lymphoma - pathology | RNA, Neoplasm - analysis | Burkitt Lymphoma - genetics | Female | Transcription, Genetic | DNA, Neoplasm - analysis | Diagnosis, Differential | Gene Expression | Lymphoma, B-Cell - mortality | Survival Rate | Burkitt Lymphoma - diagnosis | Genes, bcl-2 | Lymphoma, B-Cell - classification | Genes, Immunoglobulin | Algorithms | Oncogene Proteins, Fusion - genetics | Genetic aspects | Genetic transcription | Research | Burkitt's lymphoma | Medical research | Chemotherapy | Gene expression | Lymphoma | Index Medicus | Abridged Index Medicus
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7. Full Text DNA-Encoded Library Screening Identifies Benzo[b][1,4]oxazepin-4-ones as Highly Potent and Monoselective Receptor Interacting Protein 1 Kinase Inhibitors
by Harris, Philip A and King, Bryan W and Bandyopadhyay, Deepak and Berger, Scott B and Campobasso, Nino and Capriotti, Carol A and Cox, Julie A and Dare, Lauren and Dong, Xiaoyang and Finger, Joshua N and Grady, LaShadric C and Hoffman, Sandra J and Jeong, Jae U and Kang, James and Kasparcova, Viera and Lakdawala, Ami S and Lehr, Ruth and McNulty, Dean E and Nagilla, Rakesh and Ouellette, Michael T and Pao, Christina S and Rendina, Alan R and Schaeffer, Michelle C and Summerfield, Jennifer D and Swift, Barbara A and Totoritis, Rachel D and Ward, Paris and Zhang, Aming and Zhang, Daohua and Marquis, Robert W and Bertin, John and Gough, Peter J and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Journal of medicinal chemistry, ISSN 0022-2623, 03/2016, Volume 59, Issue 5, pp. 2163 - 2178
Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Small Molecule Libraries - pharmacology | Humans | Crystallography, X-Ray | Structure-Activity Relationship | Isoxazoles - chemical synthesis | Dose-Response Relationship, Drug | Protein Kinase Inhibitors - chemistry | Oxazepines - chemical synthesis | U937 Cells | Molecular Structure | Protein Kinase Inhibitors - chemical synthesis | Models, Molecular | Small Molecule Libraries - chemical synthesis | Isoxazoles - chemistry | Oxazepines - pharmacology | HT29 Cells | Isoxazoles - pharmacology | Small Molecule Libraries - chemistry | DNA - chemistry | Animals | Cell Line, Tumor | Mice | Protein Kinase Inhibitors - pharmacology | Receptor-Interacting Protein Serine-Threonine Kinases - antagonists & inhibitors | Oxazepines - chemistry | Index Medicus | INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY | Inhibitors | Mixtures | Solutions | BASIC BIOLOGICAL SCIENCES | Rodent models | Peptides and proteins
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8. Full Text Molecular profiling of pediatric mature B-cell lymphoma treated in population-based prospective clinical trials
by Klapper, Wolfram and Szczepanowski, Monika and Burkhardt, Birgit and Berger, Hilmar and Rosolowski, Maciej and Bentink, Stefan and Schwaenen, Carsten and Wessendorf, Swen and Spang, Rainer and Moller, Peter and Hansmann, Martin Leo and Bernd, Heinz-Wolfram and Ott, German and Hummel, Michael and Stein, Harald and Loeffler, Markus and Trumper, Lorenz and Zimmermann, Martin and Reiter, Alfred and Siebert, Reiner and Deutsche Krebshilfe and Molecular Mechanisms in Malignant Lymphomas Network Project of the Deutsche Krebshilfe
Blood, ISSN 0006-4971, 08/2008, Volume 112, Issue 4, pp. 1374 - 1381
Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | Medical sciences | Age Factors | Humans | Lymphoma, B-Cell - diagnosis | Middle Aged | Male | Treatment Outcome | Burkitt Lymphoma - diagnosis | Clinical Trials as Topic | Gene Expression Profiling | Lymphoma, B-Cell - genetics | Lymphoma, Large B-Cell, Diffuse - diagnosis | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Burkitt Lymphoma - genetics | Adult | Female | Lymphoma, Large B-Cell, Diffuse - genetics | Lymphoma, B-Cell - drug therapy | Index Medicus | Abridged Index Medicus
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9. Full Text Coaltered Ras/B-raf and TP53 Is Associated with Extremes of Survivorship and Distinct Patterns of Metastasis in Patients with Metastatic Colorectal Cancer
by Datta, Jashodeep and Smith, J. Joshua and Chatila, Walid K and McAuliffe, John C and Kandoth, Cyriac and Vakiani, Efsevia and Frankel, Timothy L and Ganesh, Karuna and Wasserman, Isaac and Lipsyc-Sharf, Marla and Guillem, Jose and Nash, Garrett M and Paty, Philip B and Weiser, Martin R and Saltz, Leonard B and Berger, Michael F and Jarnagin, William R and Balachandran, Vinod and Kingham, T. Peter and Kemeny, Nancy E and Cercek, Andrea and Garcia-Aguilar, Julio and Taylor, Barry S and Viale, Agnes and Yaeger, Rona and Solit, David B and Schultz, Nikolaus and D'Angelica, Michael
Clinical cancer research, ISSN 1078-0432, 03/2020, Volume 26, Issue 5, pp. 1077 - 1085
Life Sciences & Biomedicine | Oncology | Science & Technology | Index Medicus
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10. Full Text RIPK1 ensures intestinal homeostasis by protecting the epithelium against apoptosis
by Takahashi, Nozomi and Vereecke, Lars and Bertrand, Mathieu J M and Duprez, Linde and Berger, Scott B and Divert, Tatyana and Gonçalves, Amanda and Sze, Mozes and Gilbert, Barbara and Kourula, Stephanie and Goossens, Vera and Lefebvre, Sylvie and Günther, Claudia and Becker, Christoph and Bertin, John and Gough, Peter J and Declercq, Wim and van Loo, Geert and Vandenabeele, Peter
Nature (London), ISSN 0028-0836, 2014, Volume 513, Issue 7516, pp. 95 - 99
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Intestines - drug effects | Protein Kinases - metabolism | Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Inflammation - pathology | Epithelial Cells - metabolism | Apoptosis - drug effects | Epithelial Cells - drug effects | Caspase 8 - metabolism | Male | NF-kappa B - metabolism | Intestines - metabolism | Organoids - enzymology | Necrosis | Caspase 8 - genetics | Receptors, Tumor Necrosis Factor, Type I - deficiency | Inflammation - metabolism | Gene Deletion | Organoids - metabolism | Female | Homeostasis - drug effects | Epithelial Cells - cytology | Tumor Necrosis Factors - pharmacology | Cell Survival - drug effects | Epithelium - drug effects | Epithelium - pathology | Intestines - pathology | Epithelium - metabolism | Organoids - cytology | Epithelial Cells - pathology | Mice, Knockout | Receptor-Interacting Protein Serine-Threonine Kinases - genetics | Animals | Myeloid Differentiation Factor 88 - deficiency | Organoids - drug effects | Survival Analysis | Anti-Bacterial Agents - pharmacology | Mice | Receptor-Interacting Protein Serine-Threonine Kinases - deficiency | Intestines - cytology | Protein research | Physiological aspects | Homeostasis | Research | Epithelium | Protein kinases | Apoptosis | Proteins | Genotype & phenotype | Antibiotics | Transgenic animals | Rodents | Ligands | Colon | Kinases | Index Medicus
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11. Full Text Autophagy mediates degradation of nuclear lamina
by Dou, Zhixun and Xu, Caiyue and Donahue, Greg and Shimi, Takeshi and Pan, Ji-An and Zhu, Jiajun and Ivanov, Andrejs and Capell, Brian C and Drake, Adam M and Shah, Parisha P and Catanzaro, Joseph M and Ricketts, M. Daniel and Lamark, Trond and Adam, Stephen A and Marmorstein, Ronen and Zong, Wei-Xing and Johansen, Terje and Goldman, Robert D and Adams, Peter D and Berger, Shelley L
Nature (London), ISSN 0028-0836, 11/2015, Volume 527, Issue 7576, pp. 105 - 109
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Chromatin - metabolism | Lamin Type B - genetics | Microtubule-Associated Proteins - metabolism | Humans | Cells, Cultured | Cytoplasm - metabolism | Autophagy | Lamin Type B - metabolism | Oncogene Protein p21(ras) - metabolism | Autophagy-Related Protein 8 Family | Animals | Lysosomes - metabolism | Nuclear Lamina - metabolism | Cell Transformation, Neoplastic | Cellular Senescence | Proteolysis | HEK293 Cells | Fibroblasts | Protein Binding | Mice | Microfilament Proteins - metabolism | Adaptor Proteins, Signal Transducing - metabolism | Chromatin - chemistry | Autophagy (Cytology) | Cellular proteins | Genetic aspects | Disease susceptibility | Properties | Health aspects | Carcinogenesis | Proteins | Studies | Cell growth | Senescence | Peptides | Gene expression | Index Medicus
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