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1. Full Text Efficient production and enhanced tumor delivery of engineered extracellular vesicles
by Watson, Dionysios C and Bayik, Defne and Srivatsan, Avinash and Bergamaschi, Cristina and Valentin, Antonio and Niu, Gang and Bear, Jenifer and Monninger, Mitchell and Sun, Mei and Morales-Kastresana, Aizea and Jones, Jennifer C and Felber, Barbara K and Chen, Xiaoyuan and Gursel, Ihsan and Pavlakis, George N
Biomaterials, ISSN 0142-9612, 2016, Volume 105, pp. 195 - 205
Abstract Extracellular vesicles (EV), including exosomes and microvesicles, are nano-sized intercellular communication vehicles that participate in a multitude... 
Advanced Basic Science | Dentistry | Dextran sulfate | Scavenger receptor | Drug delivery | Reticuloendothelial system | Exosomes | Biodistribution | CLASS-A | CLEARANCE | ACTIVATION | MATERIALS SCIENCE, BIOMATERIALS | ENGINEERING, BIOMEDICAL | IL-15 | B16BL6-DERIVED EXOSOMES | INJECTION | INTERLEUKIN-15 | IL-15R-ALPHA | Neoplasms, Experimental - ultrastructure | Extracellular Vesicles - ultrastructure | Humans | Cell Fractionation - methods | Cells, Cultured | Equipment Design | Tissue Engineering - instrumentation | Macrophages - metabolism | Bioreactors | HEK293 Cells | Extracellular Vesicles - physiology | Batch Cell Culture Techniques - instrumentation | Batch Cell Culture Techniques - methods | Cell Fractionation - instrumentation | Dextran | Chemotherapy | Interleukins | Liver | Research institutes | Molecular biology | Sulfates | Health aspects | Cancer | Blood proteins | Drugs | Medical research | Drug delivery systems | Vehicles | Medicine, Experimental | Receptors | Vesicles | Cytokines | Clearances | Macrophages | Culture | Tumors
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2. Full Text Hepatocellular carcinoma mouse models: Hepatitis B virus-associated hepatocarcinogenesis and haploinsufficient tumor suppressor genes
by Teng, YC and Shen, ZQ and Kao, CH and Tsai, TF
WORLD JOURNAL OF GASTROENTEROLOGY, ISSN 1007-9327, 01/2016, Volume 22, Issue 1, pp. 300 - 325
The multifactorial and multistage pathogenesis of hepatocellular carcinoma (HCC) has fascinated a wide spectrum of scientists for decades. While a number of... 
LARGE ENVELOPE POLYPEPTIDE | SURFACE-ANTIGEN GENE | BREAKAGE SYNDROME GENE | Hepatocellular carcinoma | NONALCOHOLIC STEATOHEPATITIS | T-CELL TOLERANCE | Haploinsufficiency | S-ADENOSYLMETHIONINE | GROWTH-FACTOR-BETA | Mouse models | X PROTEIN TARGETS | Tumor suppressor genes | MOLECULAR PATHOGENESIS | Hepatitis B virus | GASTROENTEROLOGY & HEPATOLOGY | NF-KAPPA-B | Liver Neoplasms - virology | Liver Neoplasms - genetics | Hepatitis B virus - pathogenicity | Humans | Liver Neoplasms, Experimental - virology | Risk Factors | Mice, Transgenic | Carcinoma, Hepatocellular - virology | Signal Transduction - genetics | Liver Neoplasms, Experimental - ultrastructure | Cocarcinogenesis | Animals | Carcinoma, Hepatocellular - genetics | Hepatitis B virus - genetics | Liver Neoplasms, Experimental - genetics | Mice | Carcinoma, Hepatocellular - ultrastructure | Genes, Tumor Suppressor | Topic Highlight
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3. Full Text The combination effects of Shen-Ling-Bai-Zhu on promoting apoptosis of transplanted H22 hepatocellular carcinoma in mice receiving chemotherapy
by Xi, Shengyan and Peng, Ying and Peng, Yang and Minuk, Gerald Y and Shi, Mengmeng and Fu, Biqian and Yang, Jiaqi and Li, Lili and Li, Qian and Gong, Yuewen and Yue, Lifeng and Guo, Jinhua and Wang, Yanhui
Journal of Ethnopharmacology, ISSN 0378-8741, 08/2016, Volume 190, pp. 1 - 12
Shen-Ling-Bai-Zhu Powder (SLBZP) is a classic traditional Chinese medical formula that has been used for several decades in the treatment of patients with... 
H22 hepatocellular carcinoma | Chemotherapy | Platelet-derived growth factor | Bcl-2, Bcl-XL | Caspase-9 | Shen-Ling-Bai-Zhu powder | Survivin | Akt | Caspase-3 | Apoptosis | Nuclear factor kappa B | H | Platelet-derivedgrowthfactor | NuclearfactorkappaB | hepatocellular carcinoma | Angiogenic Proteins - genetics | Apoptosis - drug effects | Gene Expression Regulation, Neoplastic | Drugs, Chinese Herbal - pharmacology | Male | Liver Neoplasms, Experimental - ultrastructure | RNA, Messenger - metabolism | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Dose-Response Relationship, Drug | Liver Neoplasms, Experimental - metabolism | Carcinoma, Hepatocellular - drug therapy | Time Factors | Carcinoma, Hepatocellular - genetics | Apoptosis Regulatory Proteins - genetics | Biomarkers, Tumor - metabolism | Female | Liver Neoplasms, Experimental - genetics | Carcinoma, Hepatocellular - ultrastructure | RNA, Messenger - genetics | Cisplatin - pharmacology | Apoptosis Regulatory Proteins - metabolism | Animals | Liver Neoplasms, Experimental - drug therapy | Signal Transduction - drug effects | Tumor Burden - drug effects | Cell Line, Tumor | Biomarkers, Tumor - genetics | Mice | Antineoplastic Agents, Phytogenic - pharmacology | Angiogenic Proteins - metabolism | Carcinoma, Hepatocellular - metabolism
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4. Full Text Chitosan-alginate scaffold culture system for hepatocellular carcinoma increases malignancy and drug resistance
by Leung, Matthew and Kievit, Forrest M and Florczyk, Stephen J and Veiseh, Omid and Wu, Jennifer and Park, James O and Zhang, Miqin
Pharmaceutical Research, ISSN 0724-8741, 09/2010, Volume 27, Issue 9, pp. 1939 - 1948
Purpose Hepatocellular carcinoma (HCC) is a prevalent solid malignancy. Critically needed discovery of new therapeutics has been hindered by lack of an in... 
chitosan | scaffolds | drug resistance | tumor microenvironment | hepatocellular carcinoma in vitro model | ANGIOGENESIS | PROTECTION | EFFICACY | DOXORUBICIN | CANCER | TUMORS | CHEMISTRY, MULTIDISCIPLINARY | LESIONS | GLYPICAN-3 EXPRESSION | GROWTH | PHARMACOLOGY & PHARMACY | CELL | Biocompatible Materials - chemistry | Humans | Drug Resistance, Neoplasm | Male | Liver Neoplasms, Experimental - ultrastructure | Cell Culture Techniques - methods | Neovascularization, Pathologic - pathology | Tissue Scaffolds - chemistry | Liver Neoplasms, Experimental - metabolism | Antineoplastic Agents - pharmacology | Glucuronic Acid - chemistry | Cell Survival - drug effects | Microscopy, Electron, Scanning | Liver Neoplasms, Experimental - blood supply | Hexuronic Acids - chemistry | Xenograft Model Antitumor Assays - methods | Animals | Chitosan - chemistry | Liver Neoplasms, Experimental - drug therapy | Mice, Nude | Neovascularization, Pathologic - drug therapy | Alginates - chemistry | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Neovascularization, Pathologic - metabolism | Doxorubicin - pharmacology | Liver cancer | Anthracyclines | Care and treatment | Analysis | Neovascularization | Hepatoma | Drug resistance | Cancer | Cell culture | Pharmacology | Models | Liver diseases
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5. Full Text Autophagy in Hepatocytes during Distant Tumor Growth
by Bgatova, N P and Bakhbaeva, S A and Taskaeva, Yu S and Makarova, V V and Borodin, Yu I
Bulletin of Experimental Biology and Medicine, ISSN 0007-4888, 7/2018, Volume 165, Issue 3, pp. 390 - 393
Structural changes in the liver of CBA mice were studied during the development of experimental hepatocarcinoma-29 inoculated into the hip. A decrease in the... 
Biomedicine, general | Pathology | Biomedicine | Internal Medicine | Laboratory Medicine | impaired structure of hepatocytes | distant tumor growth | Cell Biology | non-selective autophagy | MEDICINE, RESEARCH & EXPERIMENTAL | PHYSIOLOGY | LIVER | THERAPEUTIC TARGETS | MECHANISMS | CANCER | Hepatocytes - pathology | Male | Liver Neoplasms, Experimental - ultrastructure | Autophagy | Mitochondria - ultrastructure | Endoplasmic Reticulum - ultrastructure | Endoplasmic Reticulum - pathology | Lipid Droplets - ultrastructure | Mice, Inbred CBA | Lysosomes - pathology | Carcinoma, Hepatocellular - ultrastructure | Liver Neoplasms, Experimental - pathology | Lipid Droplets - pathology | Injections, Intramuscular | Mitochondria - pathology | Microscopy, Electron | Autophagosomes - pathology | Autophagosomes - ultrastructure | Lysosomes - ultrastructure | Animals | Carcinoma, Hepatocellular - pathology | Cell Line, Tumor | Hepatocytes - ultrastructure | Mice | Muscle, Skeletal | Glycogen | Tumors | Liver | Ribosomes | Homeostasis | Phagosomes | Lysosomes | Electron microscopy | Hip | Mitochondria | Hepatocytes | Intracellular | Endoplasmic reticulum | Cytoplasm | Phagocytosis
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6. Full Text Anti-tumor activities and apoptosis-regulated mechanisms of bufalin on the orthotopic transplantation tumor model of human hepatocellular carcinoma in nude mice
by Han, Ke-Qi and Huang, Guang and Gu, Wei and Su, Yong-Hua and Huang, Xue-Qiang and Ling, Chang-Quan
World Journal of Gastroenterology, ISSN 1007-9327, 06/2007, Volume 13, Issue 24, pp. 3374 - 3379
AIM: To investigate anti-tumor activities and apoptosis-regulated mechanisms of bufalin in the orthotopic transplantation tumor model of human hepatocellular... 
Orthotopic transplantation | Treatment | Nude mice | Model | Hepatocellular carcinoma | Bufalin | Apoptosis | PATHWAYS | treatment | ACTIVATION | LEUKEMIA U937 CELLS | apoptosis | orthotopic transplantation | CULTURE | BCL-2 | bufalin | PROSTATE-CANCER CELLS | nude mice | BAX | model | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | hepatocellular carcinoma | In Situ Nick-End Labeling | Neoplasm Transplantation | Apoptosis - drug effects | Humans | Body Weight - drug effects | Male | Transplantation, Heterologous | bcl-2-Associated X Protein - analysis | Antineoplastic Agents - therapeutic use | Liver Neoplasms, Experimental - ultrastructure | Reverse Transcriptase Polymerase Chain Reaction | Necrosis | Bufanolides - therapeutic use | Animals | Liver Neoplasms, Experimental - drug therapy | Mice, Nude | Proto-Oncogene Proteins c-bcl-2 - analysis | Mice | Mice, Inbred BALB C | Liver Neoplasms, Experimental - pathology | Proto-Oncogene Proteins c-bcl-2 - genetics | bcl-2-Associated X Protein - genetics | Rapid Communication
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7. Full Text Modulation of the unfolded protein response impedes tumor cell adaptation to proteotoxic stress: a PERK for hepatocellular carcinoma therapy
by Vandewynckel, Yves-Paul and Vandewynckel, Yves-Paul and Laukens, Debby and Laukens, Debby and Bogaerts, Eliene and Bogaerts, Eliene and Paridaens, Annelies and Paridaens, Annelies and Van den Bussche, Anja and Van den Bussche, Anja and Verhelst, Xavier and Verhelst, Xavier and Van Steenkiste, Christophe and Van Steenkiste, Christophe and Descamps, Benedicte and Descamps, Benedicte and Vanhove, Chris and Vanhove, Chris and Libbrecht, Louis and Libbrecht, Louis and De Rycke, Riet and De Rycke, Riet and Lambrecht, Bart N and Lambrecht, Bart N and Geerts, Anja and Geerts, Anja and Janssens, Sophie and Janssens, Sophie and Van Vlierberghe, Hans and Van Vlierberghe, Hans
Hepatology International, ISSN 1936-0533, 1/2015, Volume 9, Issue 1, pp. 93 - 104
Functional disturbances of the endoplasmic reticulum (ER) lead to activation of the unfolded protein response (UPR), which is involved in the consecutive steps... 
Liver neoplasm | Medicine & Public Health | Colorectal Surgery | PERK kinase | Hepatology | Surgery | HepG2 cells | Inositol-requiring enzyme-1 | Endoplasmic reticulum | Stress | ACTIVATION | KINASE | FATE | CANCER | PROTEOSTASIS | GROWTH | INHIBITOR | GASTROENTEROLOGY & HEPATOLOGY | ATF6 | Transcription Factor CHOP - genetics | Oxidative Stress | eIF-2 Kinase - metabolism | Humans | Adaptation, Physiological - drug effects | RNA, Messenger - analysis | Male | Endoplasmic Reticulum | Liver Neoplasms, Experimental - ultrastructure | Activating Transcription Factor 6 - genetics | Heat-Shock Proteins - genetics | Liver Neoplasms, Experimental - metabolism | Carcinoma, Hepatocellular - drug therapy | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Carcinoma, Hepatocellular - chemistry | Carcinoma, Hepatocellular - ultrastructure | Phosphorylation - drug effects | Cell Survival - drug effects | Unfolded Protein Response - drug effects | HSP40 Heat-Shock Proteins - genetics | Signal Transduction | Membrane Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Transcription Factor CHOP - analysis | Cell Transformation, Neoplastic - metabolism | eIF-2 Kinase - antagonists & inhibitors | Hep G2 Cells | Membrane Glycoproteins - genetics | Liver Neoplasms, Experimental - chemistry | Animals | Liver Neoplasms, Experimental - drug therapy | Membrane Proteins - antagonists & inhibitors | Protein Kinase Inhibitors - therapeutic use | Tunicamycin - pharmacology | Cell Proliferation - drug effects | Mice | Protein Kinase Inhibitors - pharmacology | Carcinoma, Hepatocellular - metabolism | Physiological aspects | Development and progression | Hepatoma | Research | Protein kinases
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8. Non-thermal effect of high-intensity focused ultrasound on ultrastructure and apoptosis in rabbit hepatic VX2 tumors
by Peng, Song and He, Wei
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, ISSN 1672-7347, 07/2015, Volume 40, Issue 7, p. 715
To observe the micromorphological changes of ultrastructure, apoptosis-related proteins expression and tumor cell apoptosis after ablation with the... 
Neoplasms, Experimental - pathology | Neoplasms, Experimental - ultrastructure | Rabbits | Animals | Caspase 3 - metabolism | Liver Neoplasms - pathology | NF-kappa B - metabolism | Vascular Endothelial Growth Factor A - metabolism | High-Intensity Focused Ultrasound Ablation | Liver Neoplasms - ultrastructure | Apoptosis
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9. Full Text Changes in cell ultrastructure and inhibition of JAK1/STAT3 signaling pathway in CBRH-7919 cells with astaxanthin
by Song, Xiaodong and Wang, Meirong and Zhang, Lixia and Zhang, Jinjin and Wang, Xiuwen and Liu, Wenbo and Gu, Xinbin and Lv, Changjun
Toxicology Mechanisms and Methods, ISSN 1537-6516, 11/2012, Volume 22, Issue 9, pp. 679 - 686
Astaxanthin (AST), a xanthophylls carotenoid, possesses significant anticancer effects. However, to date, the molecular mechanism of anticancer remains... 
cell ultra-structure | JAK1/STAT3 signaling pathway | Astaxanthin | Cell ultra-structure | COMPLEX | DOMAIN | METASTASIS | CANCER CELLS | RAT | INITIATION | DBL-1 | HEPATOCELLULAR-CARCINOMA | NM23-H1 | MICE | TOXICOLOGY | In Situ Nick-End Labeling | Microscopy, Electron, Transmission | Microscopy, Electron, Scanning | Apoptosis - drug effects | Rats | Janus Kinase 1 - antagonists & inhibitors | Liver Neoplasms, Experimental - ultrastructure | Reverse Transcriptase Polymerase Chain Reaction | Animals | Flow Cytometry | Signal Transduction - drug effects | Fluorescent Antibody Technique | Cell Line, Tumor | Liver Neoplasms, Experimental - enzymology | Xanthophylls - pharmacology | Antineoplastic Agents - pharmacology | STAT3 Transcription Factor - antagonists & inhibitors | Microscopy, Fluorescence
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10. Full Text Cadmium chloride-induced DNA and lysosomal damage in a hepatoma cell line
by Fotakis, George and Cemeli, Eduardo and Anderson, Diana and Timbrell, John A
Toxicology in Vitro, ISSN 0887-2333, 2005, Volume 19, Issue 4, pp. 481 - 489
Cadmium is a toxic metal and no uniform mechanism of toxicity has so far been proposed. The aim of this study was to investigate the biochemical effects of... 
Lysosomes | Cadmium | Reactive oxygen species | DNA damage | AQUATIC ORGANISMS | APOPTOSIS | METALLOTHIONEIN | C-FOS | RATS | INDUCTION | STRAND BREAKS | GENOTOXICITY | EPITHELIAL-CELLS | reactive oxygen species | cadmium | lysosomes | TOXICOLOGY | EXPOSURE | Cadmium Chloride - toxicity | DNA Damage - drug effects | L-Lactate Dehydrogenase - metabolism | Lysosomes - drug effects | Reactive Oxygen Species | Glutathione - metabolism | Rats | Liver Neoplasms, Experimental - ultrastructure | Neoplasm Proteins - metabolism | Comet Assay | DNA, Neoplasm - drug effects | Lysosomes - ultrastructure | Liver Neoplasms, Experimental - metabolism | Animals | Adenosine Triphosphate - metabolism | Cadmium Poisoning - pathology | Cell Line, Tumor | Neutral Red | Cadmium Poisoning - metabolism | Cell research | Genetic research | Fluorescence | Stains and staining (Microscopy) | Lactate dehydrogenase | Mitochondrial DNA | Hepatoma | Glutathione
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11. Full Text Triacylglycerol hydrolase is localized to the endoplasmic reticulum by an unusual retrieval sequence where it participates in VLDL assembly without utilizing VLDL lipids as substrates
by Gilham, Dean and Alam, Mustafa and Gao, Wenhui and Vance, Dennis E and Lehner, Richard
Molecular Biology of the Cell, ISSN 1059-1524, 02/2005, Volume 16, Issue 2, pp. 984 - 996
The majority of hepatic intracellular triacylglycerol (TG) is mobilized by lipolysis followed by reesterification to reassemble TG before incorporation into a... 
MEMBRANE-FRACTION | RAT HEPATOCYTES | B-CONTAINING LIPOPROTEINS | HEPG2 CELLS | LOW-DENSITY LIPOPROTEIN | INTRACELLULAR DEGRADATION | APOLIPOPROTEIN-B | LIVER CARBOXYLESTERASES | SECRETORY PATHWAY | ACTIVE SYNTHESIS | CELL BIOLOGY | Cercopithecus aethiops | Substrate Specificity | Liver Neoplasms, Experimental - ultrastructure | Endoplasmic Reticulum - ultrastructure | Lipoproteins, VLDL - ultrastructure | Transfection | Tritium - metabolism | Gene Deletion | Lipase - analysis | Lipoproteins - metabolism | Liver Neoplasms, Experimental - pathology | Endoplasmic Reticulum - enzymology | Hydrazines | Centrifugation, Density Gradient | Oleic Acid - metabolism | Rats | Lipase - metabolism | Protein Sorting Signals | Hydrolysis | Oligopeptides - biosynthesis | Xanthenes | Microscopy, Confocal | Animals | Lipoproteins, VLDL - metabolism | Fluorescein | Cell Line, Tumor | Lipase - ultrastructure | COS Cells | Fluorescent Dyes | Lipase - genetics
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12. Full Text Changes of splenic macrophage during the process of liver cancer induced by diethylnitrosamine in rats
by ZHANG Shu LI Zong-fang PAN Dun HUANG Chen ZHOU Rui LIU Zhong-wei
中华医学杂志：英文版, ISSN 0366-6999, 2009, Volume 122, Issue 24, pp. 3043 - 3047
Background It is generally accepted that spleen plays a complex role in the tumor immunity, which would change in the different periods of cancer. In this... 
亚硝胺 | 脾脏 | 巨噬细胞 | SD大鼠 | 透射电子显微镜 | 肿瘤坏死因子-α | 二乙基 | 肝癌 | Spleen | Liver cancer | Cell function | Ultrastructure | Macrophage | cell function | PHAGOCYTOSIS | spleen | RESECTION | macrophage | SPLENECTOMY | ultrastructure | ANTITUMOR | PATHOGENESIS | SUPPRESS | MEDICINE, GENERAL & INTERNAL | HEPATOCELLULAR-CARCINOMA | IN-VITRO | COLORECTAL-CANCER | liver cancer | Diethylnitrosamine - toxicity | Liver Cirrhosis - immunology | Macrophages - ultrastructure | Microscopy, Electron, Transmission | Macrophages - pathology | Cells, Cultured | Liver Neoplasms, Experimental - chemically induced | Rats | Male | Liver Neoplasms, Experimental - immunology | Liver Neoplasms, Experimental - ultrastructure | Spleen - ultrastructure | Rats, Sprague-Dawley | Lung Neoplasms - immunology | Animals | Lung Neoplasms - secondary | Liver Neoplasms, Experimental - complications | Lung Neoplasms - ultrastructure | Liver Cirrhosis - pathology | Spleen - pathology | Disease Models, Animal
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13. Full Text The epithelial-mesenchymal transition promotes transdifferentiation of subcutaneously implanted hepatic oval cells into mesenchymal tumor tissue
by Dong, Han-Hua and Xiang, Shuai and Chen, Xiao-Ping and Liang, Hui-Fang and Zhang, Wei and Jing, Kai and Zhang, Wan-Guang and Chen, Lin
Stem Cells and Development, ISSN 1547-3287, 11/2009, Volume 18, Issue 9, pp. 1293 - 1298
Hepatic oval cells are thought to represent facultative hepatic epithelial stem cells in liver in which damage inhibits hepatocyte proliferation and liver... 
MEDICINE, RESEARCH & EXPERIMENTAL | REGULATORS SNAIL | E-CADHERIN EXPRESSION | BONE-MARROW | TRANSCRIPTION FACTOR SNAIL | CANCER | CELL & TISSUE ENGINEERING | TRANSPLANTATION | NEURAL STEM-CELLS | IN-VIVO | GENE-EXPRESSION | DIFFERENTIATION | HEMATOLOGY | CARCINOMA | Mesenchymoma - ultrastructure | Cadherins - metabolism | Vimentin - metabolism | Male | Transplantation, Heterologous | Neoplasms, Experimental - pathology | Cell Transdifferentiation | Female | Snail Family Transcription Factors | Neoplasms, Experimental - ultrastructure | Mesenchymoma - metabolism | Microscopy, Electron, Transmission | Epithelium - pathology | Mesenchymoma - pathology | Cells, Cultured | Rats | In Situ Hybridization, Fluorescence | Rats, Sprague-Dawley | Blotting, Western | Transcription Factors - metabolism | Animals | Mice, Nude | Liver - cytology | Mice | Mice, Inbred BALB C | Neoplasms, Experimental - metabolism | Mesoderm - pathology | Cell Transplantation - methods | Physiological aspects | Research | Cell differentiation | Liver cells | Stem cells | Original Research Reports
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14. Full Text Organ-specificity of the extravasation process: An ultrastructural study
by Paku, Sándor and Döme, Balázs and Tóth, Réka and Timár, József
Clinical and Experimental Metastasis, ISSN 0262-0898, 10/2000, Volume 18, Issue 6, pp. 481 - 492
The process of extravasation of the high metastatic Lewis lung carcinoma line was examined in different organs. Four of the five organs (liver, lungs, brain... 
endothelium | extravasation | Lewis lung carcinoma | basement membrane | Medicine & Public Health | Hematology | Cancer Research | Oncology | ultrastructure | Surgical Oncology | Ultrastructure | Extravasation | Basement membrane | Endothelium | Liver Neoplasms, Experimental - secondary | Kidney Neoplasms - ultrastructure | Mice, Inbred C57BL | Lung Neoplasms - pathology | Brain Neoplasms - blood supply | Liver Neoplasms, Experimental - blood supply | Liver Neoplasms, Experimental - ultrastructure | Organ Specificity | Carcinoma, Lewis Lung - blood supply | Adrenal Gland Neoplasms - ultrastructure | Brain Neoplasms - secondary | Neoplasm Metastasis | Animals | Adrenal Gland Neoplasms - blood supply | Lung Neoplasms - ultrastructure | Carcinoma, Lewis Lung - pathology | Adrenal Gland Neoplasms - secondary | Mice | Brain Neoplasms - ultrastructure | Carcinoma, Lewis Lung - ultrastructure | Kidney Neoplasms - secondary | Kidney Neoplasms - blood supply | Lung Neoplasms - blood supply
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15. Full Text Association of myosin I alpha with endosomes and lysosomes in mammalian cells
by Raposo, Graça and Cordonnier, Marie-Neige and Tenza, Danièle and Menichi, Bernadette and Dürrbach, Antoine and Louvard, Daniel and Coudrier, Evelyne
Molecular Biology of the Cell, ISSN 1059-1524, 1999, Volume 10, Issue 5, pp. 1477 - 1494
Myosin Is, which constitute a ubiquitous monomeric subclass of myosins with actin-based motor properties, are associated with plasma membrane and intracellular... 
ORGANIZATION | LOCALIZATION | TRANSPORT | ACTIN | NERVE GROWTH CONES | VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | UNCONVENTIONAL MYOSIN | MEMBRANE-PROTEINS | IDENTIFICATION | PLASMA-MEMBRANE | CELL BIOLOGY
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