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1. Full Text Targetable genetic features of primary testicular and primary central nervous system lymphomas
by Chapuy, Bjoern and Roemer, Margaretha G. M and Stewart, Chip and Tan, Yuxiang and Abo, Ryan P and Zhang, Liye and Dunford, Anew J and Meredith, David M and Thorner, Aaron R and Jordanova, Ekaterina S and Liu, Gang and Feuerhake, Frieich and Ducar, Matthew D and Illerhaus, Gerald and Gusenleitner, Daniel and Linden, Erica A and Sun, Heather H and Homer, Heather and Aono, Miyuki and Pinkus, Geraldine S and Ligon, Azra H and Ligon, Keith L and Ferry, Judith A and Freeman, Gordon J and van Hummelen, Paul and Golub, Todd R and Getz, Gad and Rodig, Scott J and de Jong, Daphne and Monti, Stefano and Shipp, Margaret A
Blood, ISSN 0006-4971, 2016, Volume 127, Issue 7, pp. 869 - 881
Primary central nervous system lymphomas (PCNSLs) and primary testicular lymphomas (PTLs) are extranodal large B-cell lymphomas (LBCLs) with inferior responses... 
B-CELL LYMPHOMA | INTEGRATIVE ANALYSIS REVEALS | RECURRENT | PROLIFERATION | MUTATIONS | HEMATOLOGY | HIGH PREVALENCE | CANCER | EXPRESSION | GENOME | MYD88 | Central Nervous System Neoplasms - metabolism | Translocation, Genetic | Testicular Neoplasms - genetics | Mediastinal Neoplasms - genetics | Lymphoma, Large B-Cell, Diffuse - pathology | Central Nervous System Neoplasms - genetics | Humans | Testicular Neoplasms - metabolism | Male | Genetic Loci | Lymphoma, Large B-Cell, Diffuse - metabolism | Neoplasm Proteins - metabolism | Testicular Neoplasms - pathology | Central Nervous System Neoplasms - pathology | Mediastinal Neoplasms - pathology | Female | Mediastinal Neoplasms - metabolism | Neoplasm Proteins - genetics | Lymphoma, Large B-Cell, Diffuse - genetics | Index Medicus | Abridged Index Medicus | Lymphoid Neoplasia | 39 | 29
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2. Full Text Inhibiting DNA methylation activates cancer testis antigens and expression of the antigen processing and presentation machinery in colon and ovarian cancer cells
by Siebenkäs, Cornelia and Chiappinelli, Katherine B and Guzzetta, Angela A and Sharma, Anup and Jeschke, Jana and Vatapalli, Rajita and Baylin, Stephen B and Ahuja, Nita
PLoS ONE, ISSN 1932-6203, 06/2017, Volume 12, Issue 6, pp. e0179501 - e0179501
Innovative therapies for solid tumors are urgently needed. Recently, therapies that harness the host immune system to fight cancer cells have successfully... 
CD2 | THERAPY | IMMUNOTHERAPY | MULTIDISCIPLINARY SCIENCES | GENES | IMMUNOMODULATORY ACTION | MECHANISMS | MOLECULES | SGI-110 | Colonic Neoplasms - genetics | DNA Methylation - immunology | DNA, Neoplasm - metabolism | Humans | Antigens, Neoplasm - biosynthesis | Ovarian Neoplasms - pathology | Male | Colonic Neoplasms - metabolism | Testicular Neoplasms - pathology | Ovarian Neoplasms - genetics | Colonic Neoplasms - immunology | Female | Ovarian Neoplasms - metabolism | Caco-2 Cells | Antigens, Neoplasm - genetics | Testicular Neoplasms - genetics | Antigens, Neoplasm - immunology | Testicular Neoplasms - metabolism | Antigen Presentation - genetics | DNA Methylation - genetics | Testicular Neoplasms - immunology | Animals | Colonic Neoplasms - pathology | DNA, Neoplasm - immunology | Mice | DNA, Neoplasm - genetics | Ovarian Neoplasms - immunology | Colon cancer | Tumor antigens | Physiological aspects | Development and progression | Genetic aspects | Research | Methylation | Ovarian cancer | Therapy | Biotechnology | Animal models | Ovarian carcinoma | CD58 antigen | Antigen processing | Genomes | Tissues | Cancer therapies | Immunotherapy | Surgery | Cell cycle | DNA methylation | Inhibition | Colon | Drug dosages | Deoxyribonucleic acid--DNA | Immune system | Antigen presentation | Antigens | Tumor cells | Melanoma | Tumor cell lines | Gene expression | Ribonucleic acid--RNA | Patients | Immune systems | Medicine | Inhibitors | Epigenetics | Solid tumors | Tumors | Cancer | Index Medicus | RNA | Deoxyribonucleic acid | Ribonucleic acid | DNA
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3. Full Text The expression of HMGB1 protein and its receptor RAGE in human malignant tumors
by Kostova, Nora and Zlateva, Stanislava and Ugrinova, Iva and Pasheva, Evdokia
Molecular and Cellular Biochemistry, ISSN 0300-8177, 04/2010, Volume 337, Issue 1-2, pp. 251 - 258
High Mobility Group Box 1 (HMGB1) is a nuclear non-histone protein discovered to be released in the extracellular medium as a response to various stimuli and... 
Carcinoma | Receptor for advanced glycation end products | Metastasis | HMGB1 protein | LOCALIZATION | DNA-BINDING | CANCER CELLS | CELL BIOLOGY | COLON-CANCER | CHROMATIN PROTEIN | AMPHOTERIN | MOBILITY GROUP BOX-1 | DIFFERENTIATION | HMG-1 | GLYCATION END-PRODUCTS | Immunohistochemistry | Neoplasms - metabolism | Humans | Male | Carcinoma, Hepatocellular - secondary | Testicular Neoplasms - pathology | Breast Neoplasms - metabolism | Neoplasm Metastasis | HMGB1 Protein - metabolism | Carcinoma, Ductal, Breast - pathology | Female | Liver Neoplasms - pathology | Carcinoma - pathology | Liver Neoplasms - secondary | Carcinoma, Ductal, Breast - metabolism | Colorectal Neoplasms - metabolism | Receptor for Advanced Glycation End Products - metabolism | Testicular Neoplasms - metabolism | Biopsy | Breast Neoplasms - pathology | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Carcinoma - metabolism | Colorectal Neoplasms - pathology | Neoplasms - pathology | Carcinoma, Hepatocellular - metabolism | Hostages | Chromosomal proteins | Cancer | Proteins | Oncology | Cellular biology | Tumors | Index Medicus
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4. Full Text Response to anti-programmed cell death protein-1 antibodies in men treated for platinum refractory germ cell cancer relapsed after high-dose chemotherapy and stem cell transplantation
by Zschäbitz, Stefanie|Lasitschka, Felix|Hadaschik, Boris|Hofheinz, Ralf-Dieter|Jentsch-Ullrich, Kathleen|Grüner, Marcus|Jäger, Dirk|Grüllich, Carsten
European Journal of Cancer, ISSN 0959-8049, 2017, Volume 76, pp. 1 - 7
Abstract Introduction Treatment options for patients with platinum refractory metastatic germ cell tumours (GCT) relapsing after high-dose chemotherapy and... 
Hematology, Oncology and Palliative Medicine | Germ cell cancer | Immunotherapy | PD-L1 | Checkpoint inhibition | Platinum refractory disease | Testicular cancer | PD-1 | LONG-TERM SURVIVAL | PD-L1 EXPRESSION | TUMORS | ONCOLOGY | NIVOLUMAB | CARCINOMA | Lung Neoplasms - drug therapy | Seminoma - diagnostic imaging | Teratoma | Endodermal Sinus Tumor - drug therapy | Compassionate Use Trials | Choriocarcinoma, Non-gestational - secondary | Humans | Middle Aged | Neoplasm Recurrence, Local - drug therapy | Antibodies, Monoclonal - therapeutic use | Male | Tomography, X-Ray Computed | Transplantation, Autologous | Testicular Neoplasms - pathology | Seminoma - metabolism | Stem Cell Transplantation | Mediastinal Neoplasms - drug therapy | Lung Neoplasms - secondary | Adult | Neoplasms, Germ Cell and Embryonal - drug therapy | Retrospective Studies | Choriocarcinoma, Non-gestational - metabolism | Endodermal Sinus Tumor - secondary | Endodermal Sinus Tumor - diagnostic imaging | Ifosfamide - therapeutic use | Antibodies, Monoclonal, Humanized - therapeutic use | Seminoma - drug therapy | Testicular Neoplasms - metabolism | Programmed Cell Death 1 Receptor - metabolism | Etoposide - therapeutic use | Neoplasms, Germ Cell and Embryonal - metabolism | Treatment Outcome | Choriocarcinoma, Non-gestational - diagnostic imaging | Endodermal Sinus Tumor - metabolism | Neoplasms, Germ Cell and Embryonal - diagnostic imaging | Cisplatin - therapeutic use | Testicular Neoplasms - drug therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Mediastinal Neoplasms - pathology | Lung Neoplasms - diagnostic imaging | Mediastinal Neoplasms - metabolism | Platinum Compounds - administration & dosage | Seminoma - secondary | Choriocarcinoma, Non-gestational - drug therapy | Neoplasms, Germ Cell and Embryonal - secondary | Viral antibodies | Medical research | Relapse | Chemotherapy | Stem cells | Medicine, Experimental | Antibodies | Transplantation | Metastasis | Diseases | Cancer | Apoptosis | Autografts | Cell survival | PD-1 protein | Toxicity | Mortality | Clinical trials | Stem cell transplantation | Patients | Metastases | Inhibitors | Immune checkpoint | Platinum | Cell death | PD-L1 protein | Tumors | Index Medicus
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5. Full Text Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148
by Fang, J and Jia, J and Makowski, M.M and Xu, M and Jansen, P. W and Vermeulen, M and Brown, K.M and Amundadottir, L.T and al., E and PanScan Consortium and GenoMel Consortium and TRICL Consortium and GenoMEL Consortium
Nature Communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 1 - 15
Genome wide association studies (GWAS) have mapped multiple independent cancer susceptibility loci to chr5p15.33. Here, we show that fine-mapping of pancreatic... 
LUNG-CANCER | TERT-CLPTM1L LOCUS | VARIANTS | GENE | PROMOTES GROWTH | MULTIDISCIPLINARY SCIENCES | PANCREATIC-CANCER | SUSCEPTIBILITY LOCI | ZBP-89 | GENOME-WIDE ASSOCIATION | TELOMERE LENGTH | RNA, Small Interfering - genetics | Pancreatic Neoplasms - metabolism | Humans | Lung Neoplasms - metabolism | Gene Expression Regulation, Neoplastic | Lung Neoplasms - pathology | Male | Genetic Loci | Testicular Neoplasms - pathology | DNA-Binding Proteins - metabolism | Telomerase - genetics | Melanoma - genetics | Female | Telomerase - metabolism | Lung Neoplasms - genetics | Melanoma - metabolism | Skin Neoplasms - pathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Testicular Neoplasms - genetics | DNA-Binding Proteins - antagonists & inhibitors | Signal Transduction | Pancreatic Neoplasms - pathology | Testicular Neoplasms - metabolism | Pancreatic Neoplasms - genetics | Transcription Factors - antagonists & inhibitors | Chromosome Mapping | Melanoma - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Telomere Homeostasis | Chromosomes, Human, Pair 5 | Skin Neoplasms - metabolism | Transcription Factors - metabolism | Histones - genetics | Skin Neoplasms - genetics | Alleles | Cell Line, Tumor | Polymorphism, Single Nucleotide | Histones - metabolism | Telomerase - antagonists & inhibitors | RNA, Small Interfering - metabolism | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Surgery | Kirurgi
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6. Full Text Genomic evolution and chemoresistance in germ-cell tumours
by Taylor-Weiner, Amaro and Zack, Travis and O'Donnell, Elizabeth and Guerriero, Jennifer L and Bernard, Brandon and Reddy, Anita and Han, G. Celine and Aldubayan, Saud and Amin-Mansour, Ali and Schumacher, Steven E and Litchfield, Kevin and Turnbull, Clare and Gabriel, Stacey and Beroukhim, Rameen and Getz, Gad and Carter, Scott L and Hirsch, Michelle S and Letai, Anthony and Sweeney, Christopher and Van Allen, Eliezer M
Nature, ISSN 0028-0836, 11/2016, Volume 540, Issue 7631, pp. 114 - 118
Germ-cell tumours (GCTs) are derived from germ cells and occur most frequently in the testes(1,2). GCTs are histologically heterogeneous and distinctly curable... 
QUANTIFICATION | MULTIDISCIPLINARY SCIENCES | DNA-DAMAGE | CISPLATIN RESISTANCE | MUTATIONS | SAMPLES | TESTICULAR-TUMORS | SEQUENCING DATA | CANCER | CARCINOMA IN-SITU | REVEALS | Proto-Oncogene Proteins p21(ras) - genetics | Genomics | Humans | Drug Resistance, Neoplasm | Male | Neoplasms, Germ Cell and Embryonal - genetics | Phylogeny | Loss of Heterozygosity | Testicular Neoplasms - pathology | Tumor Suppressor Protein p53 - genetics | Neoplasms, Germ Cell and Embryonal - drug therapy | Testicular Neoplasms - genetics | Testicular Neoplasms - metabolism | Nanog Homeobox Protein - deficiency | Neoplasms, Germ Cell and Embryonal - metabolism | Mitochondria - metabolism | Transcriptome - genetics | Disease Progression | Genome, Human - genetics | Neoplasm Metastasis - genetics | Exome - genetics | Testicular Neoplasms - drug therapy | Neoplasm Metastasis - pathology | Teratoma - genetics | Mutation | Octamer Transcription Factor-3 - deficiency | Neoplasms, Germ Cell and Embryonal - pathology | Apoptosis | Evolution, Molecular | Genetic aspects | Tumors | Chemotherapy | Cell cycle | Phylogenetics | Metastasis | Drug resistance | Chromosomes | Deoxyribonucleic acid--DNA | Cancer | Index Medicus
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7. Full Text Frequent PD-L1 expression in testicular germ cell tumors
by Fankhauser, C.D and Curioni-Fontecedro, A and Allmann, V and Beyer, J and Tischler, V and Sulser, T and Moch, H and Bode, P.K
British Journal of Cancer, ISSN 0007-0920, 07/2015, Volume 113, Issue 3, pp. 411 - 413
Background: Many testicular germ cell cancers are curable despite metastatic disease, but about 10-15% of patients fail cisplatinbased first-line treatment.... 
testicular cancer | ONCOLOGY | SAFETY | PD-L1 | Programmed cell death ligand 1 | LIGAND 1 PD-L1 | germ cell tumour | Immunohistochemistry | Testis - metabolism | Tissue Array Analysis | Humans | Middle Aged | Neoplasms, Germ Cell and Embryonal - epidemiology | Testicular Neoplasms - metabolism | Male | Neoplasms, Germ Cell and Embryonal - metabolism | Testicular Neoplasms - epidemiology | Testicular Neoplasms - pathology | Seminoma - metabolism | Young Adult | B7-H1 Antigen - metabolism | Seminoma - epidemiology | Testis - pathology | Adolescent | Aged, 80 and over | Adult | Aged | Neoplasms, Germ Cell and Embryonal - pathology | Seminoma - pathology | Index Medicus | Translational Therapeutics
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8. Full Text Glypican 3 expression in human nonneoplastic, preneoplastic, and neoplastic tissues: A tissue microarray analysis of 4,387 tissue samples
by Baumhoer, Daniel and Tornillo, Luigi and Stadlmann, Sylvia and Roncalli, Massimo and Diamantis, Eva Karamitopoulou and Terracciano, Luigi M
American Journal of Clinical Pathology, ISSN 0002-9173, 06/2008, Volume 129, Issue 6, pp. 899 - 906
Several studies have shown that gl ypican 3 (GPC3) could be a useful diagnostic marker for hepatocellular carcinoma (HCC) and for differentiating HCC from... 
GPC3 | Hepatocellular carcinoma | Tissue microarray | Glypican 3 | DIAGNOSIS | PROTEOGLYCANS | tissue microarray | MARKER | PATHOLOGY | CANCER | HEPATOCELLULAR-CARCINOMA | OVERGROWTH | GENE | BENIGN | glypican 3 | LIVER | hepatocellular carcinoma | Neoplasms - metabolism | Predictive Value of Tests | Carcinoma, Embryonal - pathology | Liver - pathology | Tissue Array Analysis | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Lung Neoplasms - metabolism | Lung Neoplasms - pathology | Male | Precancerous Conditions - metabolism | Carcinoma, Embryonal - metabolism | Glypicans - metabolism | Testicular Neoplasms - pathology | Liposarcoma - metabolism | Biomarkers, Tumor - metabolism | Female | Liver Neoplasms - pathology | Precancerous Conditions - pathology | Liposarcoma - pathology | Liver - metabolism | Testicular Neoplasms - metabolism | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Neoplasms - pathology | Carcinoma, Hepatocellular - metabolism | Index Medicus | Abridged Index Medicus
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9. Full Text STAT6 is amplified in a subset of dedifferentiated liposarcoma
by Doyle, Leona A and Tao, Derrick and Mariño-Enríquez, Adrián
Modern Pathology, ISSN 0893-3952, 01/2014, Volume 27, Issue 9, pp. 1231 - 1237
A recurrent intrachromosomal rearrangement on chromosome 12q in solitary fibrous tumor leads to the formation of a NAB2-STAT6 fusion oncogene. As a result,... 
Amplification | STAT6 | Dedifferentiated liposarcoma | Sarcoma | Solitary fibrous tumor | LIPOMATOUS HEMANGIOPERICYTOMA | sarcoma | MECHANISM | solitary fibrous tumor | TISSUE TUMORS | CHROMOSOMES | PATHOLOGY | amplification | dedifferentiated liposarcoma | GENE | HIGH-RESOLUTION | MDM2 | CLINICOPATHOLOGICAL ANALYSIS | Immunohistochemistry | Kidney Neoplasms - genetics | Testicular Neoplasms - genetics | Mediastinal Neoplasms - genetics | Humans | Middle Aged | Testicular Neoplasms - metabolism | In Situ Hybridization, Fluorescence | Liposarcoma - genetics | Male | Kidney Neoplasms - metabolism | STAT6 Transcription Factor - genetics | STAT6 Transcription Factor - metabolism | Cyclin-Dependent Kinase 4 - metabolism | Liposarcoma - metabolism | Gene Amplification | Biomarkers, Tumor - metabolism | Female | Aged | Biomarkers, Tumor - genetics | Mediastinal Neoplasms - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Index Medicus
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10. Full Text Embryonic stem cell transcription factor signatures in the diagnosis of primary and metastatic germ cell tumors
by Santagata, Sandro and Ligon, Keith L and Hornick, Jason L
American Journal of Surgical Pathology, ISSN 0147-5185, 06/2007, Volume 31, Issue 6, pp. 836 - 845
The core embryonic stem cell transcription factors (TFs) OCT3/4 (OCT4), NANOG, and SOX2 have shared as well as nonoverlapping roles in stem cell growth and... 
Germ cell tumor | Immunohistochemistry | Seminoma | Transcription factor | Stem cell | Embryonal carcinoma | SURGERY | transcription factor | CD30 | MARKER | ALKALINE-PHOSPHATASE | TESTICULAR CANCER | OCT4 IMMUNOHISTOCHEMISTRY | PLURIPOTENCY | embryonal carcinoma | PATHOLOGY | germ cell tumor | stem cell | NANOG | immunohistochemistry | seminoma | EXPRESSION | CARCINOMA | Embryonic Stem Cells - metabolism | Homeodomain Proteins - metabolism | Humans | Male | Carcinoma, Embryonal - metabolism | Neoplasms, Germ Cell and Embryonal - diagnosis | Retroperitoneal Neoplasms - diagnosis | Seminoma - diagnosis | DNA-Binding Proteins - metabolism | Seminoma - metabolism | Sensitivity and Specificity | HMGB Proteins - metabolism | Seminoma - classification | SOXB1 Transcription Factors | Testicular Neoplasms - classification | Testicular Neoplasms - diagnosis | Diagnosis, Differential | Nanog Homeobox Protein | Retroperitoneal Neoplasms - classification | Biomarkers, Tumor - analysis | Testicular Neoplasms - metabolism | Neoplasms, Germ Cell and Embryonal - metabolism | Retroperitoneal Neoplasms - metabolism | Transcription Factors - metabolism | Carcinoma, Embryonal - classification | Carcinoma, Embryonal - diagnosis | Octamer Transcription Factor-3 - metabolism | Neoplasms, Germ Cell and Embryonal - classification | Index Medicus
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11. Full Text Cancer/testis antigen CT45: Analysis of mRNA and protein expression in human cancer
by Chen, Yao-Tseng and Hsu, Melinda and Lee, Peishan and Shin, Sandra J and Mhawech-Fauceglia, Paulette and Odunsi, Kunle and Altorki, Nasser K and Song, Chao-Jun and Jin, Bo-Quan and Simpson, Andrew J and Old, Lloyd J
International Journal of Cancer, ISSN 0020-7136, 06/2009, Volume 124, Issue 12, pp. 2893 - 2898
CT45 is a cancer/testis gene that we previously identified by massively parallel signature sequencing. Encoded by a multigene family on chromosome X, CT45... 
Cancer/testis antigen | Cancer vaccine | Tumor antigen | NY-ESO-1 | IMMUNE-RESPONSE | cancer vaccine | HUMAN TUMOR-ANTIGENS | IDENTIFICATION | MAGE-3 PROTEIN | tumor antigen | T-CELL RESPONSES | MELANOMA | ONCOLOGY | GENES | cancer/testis antigen | ANTIBODY-RESPONSES | LYMPHOCYTES | Prognosis | Tissue Array Analysis | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | Lung Neoplasms - metabolism | Ovarian Neoplasms - pathology | Lung Neoplasms - pathology | Male | RNA, Messenger - metabolism | Testicular Neoplasms - pathology | Breast Neoplasms - metabolism | Ovarian Neoplasms - genetics | Adenocarcinoma - metabolism | Antigens, Neoplasm - metabolism | Biomarkers, Tumor - metabolism | Female | Adenocarcinoma - genetics | Ovarian Neoplasms - metabolism | Antibodies, Monoclonal - immunology | Lung Neoplasms - genetics | Recombinant Proteins - metabolism | Antigens, Neoplasm - genetics | Testicular Neoplasms - genetics | Antigens, Neoplasm - immunology | Testicular Neoplasms - metabolism | Recombinant Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Adenocarcinoma - secondary | Animals | Breast Neoplasms - genetics | Recombinant Proteins - immunology | Breast Neoplasms - pathology | Carcinoma, Squamous Cell - secondary | Biomarkers, Tumor - genetics | Mice | Mice, Inbred BALB C | Antibodies, Monoclonal - metabolism | Index Medicus
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12. Full Text The DM Domain Protein DMRT1 is a Dose-Sensitive Regulator of Fetal Germ Cell Proliferation and Pluripotency
by Anthony D. Krentz and Mark W. Murphy and Shinseog Kim and Matthew S. Cook and Blanche Capel and Rui Zhu and Angabin Mating and Aaron L. Sarver and Keith L. Parker and Michael D. Griswolds and Leendert H. J. Looijenga and Vivian J. Bardwell and David Zarkower and Judith Kimble
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2009, Volume 106, Issue 52, pp. 22232 - 22328
Dmrt1 (doublesex and mab-3 related transcription factor 1) is a conserved transcriptional regulator of male differentiation required for testicular development... 
Teratoma | Germ cells | Somatic cells | Stem cells | Cell lines | Mice | Testes | Pluripotent stem cells | Sertoli cells | Tumors | Germ cell tumor | Testicular teratoma | GDNF | Embryonal carcinoma | METHYLATION IMPRINT | TESTIS DIFFERENTIATION | testicular teratoma | 129.MOLF-CHR19 MOUSE STRAIN | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | embryonal carcinoma | germ cell tumor | TUMORS | HUMAN SPERMATOCYTIC SEMINOMAS | CONGENITAL TESTICULAR TERATOMAS | GENE | EMBRYONIC STEM-CELLS | MICE | Proto-Oncogene Proteins c-ret - metabolism | Cell Proliferation | Fetal Stem Cells - cytology | Spermatogenesis - genetics | Fetal Stem Cells - metabolism | Humans | Male | Neoplasms, Germ Cell and Embryonal - genetics | Neoplasm Proteins - metabolism | Testicular Neoplasms - pathology | Teratoma - metabolism | Cell Differentiation | Neoplasm Proteins - genetics | Genes, Tumor Suppressor | PTEN Phosphohydrolase - genetics | Gene Expression | Testicular Neoplasms - genetics | Transcription Factors - physiology | Pluripotent Stem Cells - cytology | Mice, Inbred C57BL | Testicular Neoplasms - metabolism | PTEN Phosphohydrolase - metabolism | Neoplasms, Germ Cell and Embryonal - metabolism | Gene Dosage | Transcription Factors - genetics | Mice, Knockout | Pluripotent Stem Cells - metabolism | Phenotype | Spermatogenesis - physiology | Teratoma - pathology | Animals | Teratoma - genetics | Mutation | Neoplasms, Germ Cell and Embryonal - pathology | Proto-Oncogene Proteins c-ret - genetics | Cell proliferation | Physiological aspects | Transcription factors | Genetic aspects | Research | Proteins | Chromatin | Gene expression | Rodents | Index Medicus | Biological Sciences
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