Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2380) 2380
Publication (214) 214
Dissertation (12) 12
Book Chapter (10) 10
Conference Proceeding (6) 6
Book Review (3) 3
Paper (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (1868) 1868
llc-pk1 cells (1790) 1790
swine (1411) 1411
humans (687) 687
index medicus (525) 525
rats (478) 478
pharmacology & pharmacy (459) 459
cell line (452) 452
urology & nephrology (425) 425
biochemistry & molecular biology (356) 356
kidney (333) 333
male (331) 331
physiology (324) 324
kidney - metabolism (316) 316
cell biology (305) 305
expression (297) 297
llc-pk1 (297) 297
cells (278) 278
mice (271) 271
transfection (246) 246
cells, cultured (245) 245
apoptosis (242) 242
toxicology (240) 240
kidney - drug effects (214) 214
kidney - cytology (212) 212
epithelial cells - metabolism (205) 205
epithelial-cells (205) 205
kidney tubules, proximal - metabolism (197) 197
dose-response relationship, drug (195) 195
nephrotoxicity (194) 194
oxidative stress (191) 191
dogs (187) 187
llc-pk (180) 180
transport (179) 179
kinetics (177) 177
apoptosis - drug effects (166) 166
cell survival - drug effects (163) 163
kidney tubules, proximal - cytology (159) 159
phosphorylation (159) 159
epithelial cells (158) 158
kidney tubules, proximal - drug effects (157) 157
time factors (148) 148
biological transport (147) 147
epithelial cells - drug effects (145) 145
rats, sprague-dawley (138) 138
toxicity (136) 136
rat (131) 131
cell membrane - metabolism (130) 130
p-glycoprotein (130) 130
molecular sequence data (128) 128
research (126) 126
proteins (123) 123
in-vitro (115) 115
rna, messenger - metabolism (115) 115
analysis (113) 113
physiological aspects (113) 113
blotting, western (112) 112
enzyme inhibitors - pharmacology (112) 112
protein (111) 111
activation (109) 109
proximal tubule (109) 109
hydrogen-ion concentration (107) 107
cadmium (104) 104
nephrology (104) 104
biological transport - drug effects (103) 103
female (102) 102
llc-pk1 cells - drug effects (100) 100
inhibition (99) 99
rat-kidney (98) 98
gene expression (97) 97
signal transduction (96) 96
injury (95) 95
amino acid sequence (92) 92
kidney tubules - metabolism (91) 91
llc pk1 cells (90) 90
epithelium - metabolism (89) 89
kidney tubules - drug effects (88) 88
kidney - pathology (86) 86
llc-pk1 cells - metabolism (86) 86
cytotoxicity (84) 84
kidneys (83) 83
localization (83) 83
biophysics (82) 82
carrier proteins - metabolism (82) 82
article (80) 80
atp-binding cassette, sub-family b, member 1 - metabolism (80) 80
base sequence (80) 80
models, biological (80) 80
chemistry, multidisciplinary (78) 78
permeability (78) 78
calcium - metabolism (77) 77
gene-expression (77) 77
rats, wistar (77) 77
endocytosis (76) 76
kidney tubules - cytology (76) 76
line (76) 76
mechanisms (76) 76
in vitro techniques (75) 75
l-lactate dehydrogenase - metabolism (75) 75
cyclic amp - metabolism (74) 74
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2350) 2350
Japanese (20) 20
Chinese (15) 15
Korean (4) 4
German (3) 3
Portuguese (3) 3
Croatian (2) 2
Russian (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text The AP-1A and AP-1B Clathrin Adaptor Complexes Define Biochemically and Functionally Distinct Membrane Domains
by Heike Fölsch and Marc Pypaert and Sandra Maday and Laurence Pelletier and Ira Mellman
The Journal of Cell Biology, ISSN 0021-9525, 10/2003, Volume 163, Issue 2, pp. 351 - 362
Most epithelial cells contain two AP-1 clathrin adaptor complexes. AP-1A is ubiquitously expressed and involved in transport between the TGN and endosomes.... 
Epithelial cells | Cell lines | Antibodies | Cell membranes | Kidney cells | Cells | Caco 2 cells | Freight | LLC PK1 cells | Endosomes | TGN | Basolateral sorting | Exocytosis | Exocyst | basolateral sorting | MDCK CELLS | COATED VESICLES | epithelial cells | BASOLATERAL PLASMA-MEMBRANE | CELL BIOLOGY | exocyst | TRANS-GOLGI NETWORK | exocytosis | POLARIZED EPITHELIAL-CELLS | SORTING SIGNALS | MANNOSE 6-PHOSPHATE RECEPTORS | GAMMA-ADAPTIN | CONTAINING PROTEIN | LIVING CELLS | Cell Polarity | Coated Pits, Cell-Membrane - ultrastructure | Humans | Protein Transport - physiology | Adaptor Protein Complex 1 - chemistry | Endosomes - metabolism | Adaptor Protein Complex 1 - metabolism | Cell Compartmentation | LLC-PK1 Cells | Epithelial Cells - physiology | trans-Golgi Network - metabolism | Swine | Endosomes - ultrastructure | Adenoviridae - genetics | Membrane Proteins - metabolism | Vesicular Transport Proteins | Caco-2 Cells | Protein Structure, Tertiary | Coated Pits, Cell-Membrane - metabolism | Membrane Proteins - genetics | Epithelial Cells - ultrastructure | Receptors, Transferrin - metabolism | Clathrin - metabolism | trans-Golgi Network - ultrastructure | Animals | Carrier Proteins - metabolism | Membrane Proteins - chemistry | Transport Vesicles - metabolism | Saccharomyces cerevisiae Proteins | Adenoviridae - metabolism | Adaptor Protein Complex mu Subunits | Cell Line, Transformed | Transport Vesicles - ultrastructure | Fungal Proteins - metabolism | Clathrin | Biochemistry | Research | Membrane proteins | epithelial cells; basolateral sorting; exocytosis; TGN; exocyst
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Isoliquiritigenin pretreatment attenuates cisplatin induced proximal tubular cells (LLC-PK1) death and enhances the toxicity induced by this drug in bladder cancer T24 cell line
by Patricia Moreno-Londoño, Angela and Bello-Alvarez, Claudia and Pedraza-Chaverri, José
Food and Chemical Toxicology, ISSN 0278-6915, 11/2017, Volume 109, Issue Pt 1, pp. 143 - 154
Cisplatin is an effective antineoplastic agent widely used in the treatment of solid tumors, however, it induces nephrotoxicity. Cisplatin-induced... 
Antioxidants | Isoliquiritigenin | Nephrotoxicity | Cisplatin | Heme oxygenase-1 | OXIDATIVE STRESS | INDUCED APOPTOSIS | FOOD SCIENCE & TECHNOLOGY | HEME OXYGENASE-1 GENE | NUCLEAR TRANSLOCATION | CARBON-MONOXIDE | PROTECTIVE ROLE | NF-E2-RELATED FACTOR-2 | TOXICOLOGY | INDUCED NEPHROTOXICITY | NF-KAPPA-B | MOLECULAR-BASIS | Heme Oxygenase-1 - metabolism | Kidney - drug effects | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Humans | Caspase 3 - metabolism | Urinary Bladder Neoplasms - drug therapy | LLC-PK1 Cells | Heme Oxygenase-1 - genetics | Kidney - metabolism | Animals | Urinary Bladder Neoplasms - genetics | Urinary Bladder Neoplasms - physiopathology | Antineoplastic Agents - adverse effects | Swine | NF-E2-Related Factor 2 - metabolism | Caspase 3 - genetics | Chalcones - pharmacology | Cisplatin - adverse effects | NF-E2-Related Factor 2 - genetics | Oxidative Stress - drug effects | Urinary Bladder Neoplasms - metabolism | Cell death | Heme | Carbon monoxide | Drug therapy | Bladder cancer | Phosphates | Superoxide | Fluorides | Bilirubin | B cells | Antineoplastic agents | Hydrochloric acid | Antimitotic agents | Surface active agents | Analysis | Lymphomas | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Shear stress-dependent regulation of apical endocytosis in renal proximal tubule cells mediated by primary cilia
by Venkatesan Raghavan and Youssef Rbaibi and Núria M. Pastor-Soler and Marcelo D. Carattino and Ora A. Weisz
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2014, Volume 111, Issue 23, pp. 8506 - 8511
The kidney has an extraordinary ability to maintain stable fractional solute and fluid reabsorption over a wide range of glomerular filtration rates (GFRs).... 
Endocytosis | Albumins | Kidneys | Epithelial cells | Cell lines | Kidney cells | Proximal tubules | Cilia | LLC PK1 cells | Glomerular filtration rate | Calcium | Ryanodine | Flow | TRANSPORT | calcium | ryanodine | COLLECTING DUCT | EPITHELIAL-CELLS | LOWE SYNDROME | KIDNEY-CELLS | MULTIDISCIPLINARY SCIENCES | MICROVILLI | OCRL1 | flow | FLOW-RATE | Cilia - physiology | Dynamins - metabolism | Calcium - metabolism | Stress, Mechanical | Adenosine Triphosphate - pharmacology | LLC-PK1 Cells | Apyrase - pharmacology | Swine | Egtazic Acid - analogs & derivatives | Madin Darby Canine Kidney Cells | Biological Transport - drug effects | Dextrans - metabolism | Cell Line | Kidney Tubules, Proximal - cytology | Albumins - metabolism | Apyrase - metabolism | Cells, Cultured | Hydrodynamics | Clathrin - metabolism | Endocytosis - physiology | Animals | Egtazic Acid - pharmacology | Signal Transduction - drug effects | Dogs | Kidney Tubules, Proximal - metabolism | Biological Transport - physiology | Kidney Tubules, Proximal - physiology | Physiological aspects | Cell research | Stress (Physiology) | Research | Cilia and ciliary motion | Biological Sciences
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination
by Planchon, Thomas A and Gao, Liang and Milkie, Daniel E and Davidson, Michael W and Galbraith, James A and Galbraith, Catherine G and Betzig, Eric
Nature Methods, ISSN 1548-7091, 05/2011, Volume 8, Issue 5, pp. 417 - 423
A key challenge when imaging living cells is how to noninvasively extract the most spatiotemporal information possible. Unlike popular wide-field and confocal... 
FLUORESCENCE MICROSCOPY | FIELD | STRUCTURED-ILLUMINATION | LIGHT | BIOCHEMICAL RESEARCH METHODS | Microscopy - methods | Mitosis | Humans | Imaging, Three-Dimensional - methods | Optical Phenomena | Microscopy, Confocal - methods | LLC-PK1 Cells | Chromosomes - ultrastructure | Animals | Microscopy - instrumentation | Swine | HeLa Cells | Luminescent Proteins | Physiological aspects | Usage | Mitochondria | Research | Cells | Fluorescence microscopy | Cellular biology | Microscopy | Scientific imaging
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Cross-species infections of cultured cells by hepatitis E virus and discovery of an infectious virus-host recombinant
by Priyanka Shukla and Hanh T. Nguyen and Udana Torian and Ronald E. Engle and Kristina Faulk and Harry R. Dalton and Richard P. Bendall and Frances E. Keane and Robert H. Purcell and Suzanne U. Emerson
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2011, Volume 108, Issue 6, pp. 2438 - 2443
The RNA virus, hepatitis E virus (HEV) is the most or second-most important cause of acute clinical hepatitis in adults throughout much of Asia, the Middle... 
Cell culture techniques | Cell lines | Viruses | Cultured cells | Infections | Kidney cells | Cellular immunity | Hepatitis E virus | Genotypes | LLC PK1 cells | Emerging virus | Zoonosis | PROTEIN | GENOMES | MULTIDISCIPLINARY SCIENCES | emerging virus | PATIENT | RELEASE | HEPATOMA | zoonosis | Caco-2 Cells | Swine Diseases - genetics | Hepatitis E - genetics | Species Specificity | Ribosomal Proteins - genetics | Humans | Middle Aged | Molecular Sequence Data | Genotype | Male | Hepatitis E virus - genetics | Hepatitis E - mortality | Pregnancy | Animals | Recombination, Genetic | Base Sequence | Deer - virology | Female | Mutagenesis, Insertional | Pregnancy Complications, Infectious - mortality | Pregnancy Complications, Infectious - genetics | Swine Diseases - mortality | Swine - virology | Hepatitis E | Disease transmission | Distribution | Physiological aspects | Causes of | Genetic aspects | Health aspects | Biological Sciences
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Cadmium (Cd2+) exposure differentially elicits both cell proliferation and cell death related responses in SK-RC-45
by Sinha, Krishnendu and Pal, Pabitra Bikash and Sil, Parames C
Toxicology in Vitro, ISSN 0887-2333, 03/2014, Volume 28, Issue 2, pp. 307 - 318
Cadmium (Cd ) is a major nephrotoxic environmental pollutant, affecting mostly proximal convoluted tubule (PCT) cells of the mammalian kidney, while... 
Cadmium | Oxidative stress | NKE cell line | SK-RC-45 cell line | Antioxidative defense | HO-1 | Intrinsic and extrinsic apoptotic pathways | JNK dependent and independent apoptosis | POLY(ADP-RIBOSE) POLYMERASE | LLC-PK1 CELLS | INDUCED APOPTOSIS | KIDNEY EPITHELIAL-CELLS | KAPPA-B | IN-VITRO | REACTIVE OXYGEN | TOXICOLOGY | INDEPENDENT PATHWAYS | UP-REGULATION | NICE cell line | Cadmium Chloride - toxicity | Immunohistochemistry | Cell Survival - drug effects | Caspase 9 - metabolism | Reactive Oxygen Species - metabolism | Gene Expression - drug effects | Oxidation-Reduction | Apoptosis - drug effects | Humans | Protein Transport - drug effects | Cell Nucleus - ultrastructure | Blotting, Western | Dose-Response Relationship, Drug | Annexin A5 - metabolism | Cell Line, Tumor | Indicators and Reagents | Cell Proliferation - drug effects | Cell Death - drug effects | Cell Nucleus - drug effects | Microscopy, Fluorescence | Cell death | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text The endocannabinoid system in renal cells: regulation of Na+ transport by CB1 receptors through distinct cell signalling pathways
by Sampaio, L S and Taveira Da Silva, R and Lima, D and Sampaio, C L C and Iannotti, F A and Mazzarella, E and Di Marzo, V and Vieyra, A and Reis, R A M and Einicker‐Lamas, M
British Journal of Pharmacology, ISSN 0007-1188, 10/2015, Volume 172, Issue 19, pp. 4615 - 4625
Background and PurposeThe function of the endocannabinoid system (ECS) in renal tissue is not completely understood. Kidney function is closely related to ion... 
ACTIVATION | CANNABINOID RECEPTOR | STIMULATION | CONCISE GUIDE | PHOSPHORYLATION | PHARMACOLOGY | ANANDAMIDE | DOPAMINE | NA+,K+-ATPASE | PHARMACOLOGY & PHARMACY | PROTEIN-KINASES | Endocannabinoids - metabolism | Signal Transduction | Morpholines - pharmacology | Peptide Fragments - pharmacology | Sodium - metabolism | Naphthalenes - pharmacology | LLC-PK1 Cells | Receptor, Cannabinoid, CB1 - metabolism | Receptor, Cannabinoid, CB2 - metabolism | Sodium-Potassium-Exchanging ATPase - metabolism | TRPV Cation Channels - metabolism | Kidney - metabolism | Animals | Receptor, Cannabinoid, CB1 - agonists | Biological Transport | Piperidines - pharmacology | Swine | Benzoxazines - pharmacology | Hemoglobins - pharmacology | Receptor, Cannabinoid, CB1 - antagonists & inhibitors | Cyclic AMP - metabolism | Pyrazoles - pharmacology | Cellular signal transduction | Adenosine triphosphatase | Research Papers
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Oxalate upregulates expression of IL-2Rβ and activates IL-2R signaling in HK-2 cells, a line of human renal epithelial cells
by Koul, Sweaty and Khandrika, Lakshmipathi and Pshak, Thomas J and Iguchi, Naoko and Pal, Mintu and Steffan, Joshua J and Koul, Hari K
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 05/2014, Volume 306, Issue 9, pp. F1039 - F1046
The role of inflammation in oxalate-induced nephrolithiasis is debated. Our gene expression study indicated an increase in interleukin-2 receptor beta (IL-2R... 
Inflammation | Oxalate | IL-2R | p38 MAPK | Kidney stones | APOPTOSIS | PHYSIOLOGY | LLC-PK1 CELLS | PROTEIN-KINASE | TRANSDUCTION | CALCIUM-OXALATE | TRANSPORT | inflammation | PATHWAY | CRYSTALS | UROLOGY & NEPHROLOGY | oxalate | kidney stones | Up-Regulation | Phosphorylation | Epithelial Cells - metabolism | Interleukin-2 Receptor beta Subunit - drug effects | Kidney - pathology | Epithelial Cells - drug effects | Humans | Interleukin-2 Receptor beta Subunit - metabolism | Kidney - immunology | Gene Regulatory Networks | RNA, Messenger - metabolism | Janus Kinase 1 - metabolism | STAT5 Transcription Factor - metabolism | Kidney - metabolism | Nephritis - immunology | Oxalic Acid - toxicity | Time Factors | Inflammation Mediators - metabolism | Nephritis - chemically induced | p38 Mitogen-Activated Protein Kinases - metabolism | Interleukin-2 Receptor beta Subunit - genetics | Real-Time Polymerase Chain Reaction | Cell Line | Kidney - drug effects | Epithelial Cells - pathology | Gene Expression Profiling - methods | Blotting, Western | Signal Transduction - drug effects | Epithelial Cells - immunology | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Nephritis - metabolism | Protein Kinase Inhibitors - pharmacology | Enzyme Activation | Index Medicus | oxalate, p38 MAPK
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Cell surface protein disulfide isomerase regulates natriuretic peptide generation of cyclic guanosine monophosphate
by Pan, Shuchong and Chen, Horng H and Correia, Cristina and Dai, Haiming and Witt, Tyra A and Kleppe, Laurel S and Burnett, John C and Simari, Robert D
PLoS ONE, ISSN 1932-6203, 11/2014, Volume 9, Issue 11, p. e112986
Rationale: The family of natriuretic peptides (NPs), including atrial natriuretic peptide (ANP), B-type natriuretic peptide (BNP), and C-type natriuretic... 
ROTATION MECHANISM | MEMBRANE-FUSION | PATHWAYS | ACTIVATION | RECEPTOR EXTRACELLULAR DOMAIN | THIOL/DISULFIDE EXCHANGE | MULTIDISCIPLINARY SCIENCES | DISEASE | TRANSMEMBRANE SIGNAL-TRANSDUCTION | EXPRESSION | FAMILY | Diphtheria Toxin - pharmacology | Human Umbilical Vein Endothelial Cells - metabolism | Protein Disulfide-Isomerases - metabolism | Humans | Protein Disulfide-Isomerases - antagonists & inhibitors | Receptors, Guanylate Cyclase-Coupled - metabolism | Mesangial Cells - drug effects | LLC-PK1 Cells | RNA Interference | Swine | Female | Cell Membrane - metabolism | Myocytes, Smooth Muscle - drug effects | Bacitracin - pharmacology | Myocytes, Smooth Muscle - metabolism | Cell Survival - drug effects | Human Umbilical Vein Endothelial Cells - drug effects | Natriuretic Peptides - metabolism | Mice, Inbred C57BL | Cells, Cultured | Mesangial Cells - metabolism | Muscle, Smooth, Vascular - cytology | Blotting, Western | Microscopy, Confocal | Protein Disulfide-Isomerases - genetics | Animals | Cyclic GMP - metabolism | Protein Binding | Immunohistochemistry | Nurse practitioners | Public radio | Cyclic guanylic acid | Analysis | Natriuretic peptides | Disease | Peptides | Guanosine | Homeostasis | Paracrine signalling | Smooth muscle | Immunoblotting | Atrial natriuretic peptide | Kinases | Guanylate cyclase | Cell surface | Blood | Cell adhesion & migration | Proteins | Signal transduction | Receptors | Cell growth | Rodents | Cyclic GMP | Mesangial cells | Chemical bonds | Aorta | Inhibition | Autocrine signalling | C-Type natriuretic peptide | Brain natriuretic peptide | Enzymes | Disulfide bonds | Kidneys | Muscles | Endothelial cells | Studies | Protein disulfide-isomerase | Ligands | Surface plasmon resonance | In vivo methods and tests | Laboratory animals | Umbilical vein | Kidney transplantation
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Fate-Determining Mechanisms in Epithelial-Myofibroblast Transition: Major Inhibitory Role for Smad3
by András Masszi and Pam Speight and Emmanuel Charbonney and Monika Lodyga and Hiroyasu Nakano and Katalin Szászi and András Kapus
The Journal of Cell Biology, ISSN 0021-9525, 2/2010, Volume 188, Issue 3, pp. 383 - 399
Epithelial–myofibroblast (MF) transition (EMyT) is a critical process in organ fibrosis, leading to α–smooth muscle actin (SMA) expression in the epithelium.... 
Messenger RNA | Epithelial cells | Cell nucleus | Fibrosis | Small interfering RNA | Actins | Antibodies | Down regulation | Western blotting | LLC PK1 cells | TRANSCRIPTION FACTORS | CELL-CELL CONTACTS | SMOOTH-MUSCLE | TARGETED DISRUPTION | TGF-BETA | SERUM RESPONSE FACTOR | DOWN-REGULATION | MUSCLE ACTIN EXPRESSION | MESENCHYMAL TRANSITION | PULMONARY-FIBROSIS | CELL BIOLOGY | Cell Nucleus - immunology | Actins - biosynthesis | Epithelial Cells - metabolism | Rats | Epithelial Cells - pathology | Smad3 Protein - metabolism | Fibroblasts - pathology | Myoblasts - pathology | Actins - genetics | Smad3 Protein - genetics | Myoblasts - metabolism | Animals | Cell Nucleus - metabolism | Transforming Growth Factor beta - genetics | Cell Nucleus - genetics | Models, Biological | Swine | Response Elements - genetics | Active Transport, Cell Nucleus - genetics | Transforming Growth Factor beta - metabolism | Fibroblasts - metabolism | Fibroblasts | Research | Transforming growth factors | Properties | Myogenesis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Kidney Injury Molecule-1 Is Up-Regulated in Renal Epithelial Cells in Response to Oxalate In Vitro and in Renal Tissues in Response to Hyperoxaluria In Vivo
by Khandrika, Lakshmipathi and Koul, Sweaty and Meacham, Randall B and Koul, Hari K
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e44174
Oxalate is a metabolic end product excreted by the kidney. Mild increases in urinary oxalate are most commonly associated with Nephrolithiasis. Chronically... 
KIM-1 | CRYSTAL-FORMATION | ACTIVATED PROTEIN-KINASE | LLC-PK1 CELLS | HK-2 CELLS | MULTIDISCIPLINARY SCIENCES | LINE | DNA-SYNTHESIS | CALCIUM-OXALATE | URINARY BIOMARKER | TREATED RATS | Cell Adhesion Molecules - chemistry | Immunohistochemistry | Cell Adhesion Molecules - genetics | Epithelial Cells - metabolism | Kidney - pathology | Membrane Glycoproteins - metabolism | Rats, Wistar | Cell Adhesion Molecules - urine | Receptors, Virus - metabolism | Epithelial Cells - drug effects | Humans | Male | Receptors, Virus - genetics | RNA, Messenger - metabolism | Kidney - metabolism | Kidney Tubules - pathology | Kidney Tubules - metabolism | Oxalates - pharmacology | Protein Structure, Tertiary | Cell Line | Kidney - drug effects | Kidney Tubules - drug effects | RNA, Messenger - genetics | Crystallization | Rats | Epithelial Cells - pathology | Hepatitis A Virus Cellular Receptor 1 | Cell Adhesion Molecules - metabolism | Hyperoxaluria - pathology | Membrane Glycoproteins - genetics | Up-Regulation - drug effects | Animals | Hyperoxaluria - urine | Hyperoxaluria - genetics | Oxalates | RNA | Oxalic acid | Kidney stones | Urine | Calcification (ectopic) | Cell culture | Kidneys | Epithelial cells | Tissue culture | Exposure | Nephrolithiasis | Kinases | Gene expression | Ribonucleic acid--RNA | Cell adhesion & migration | Injury prevention | Overexpression | Rodents | Transcription activation | Animal tissues | Renal failure | Calcification | Primary hyperoxaluria | Hyperoxaluria | Ribonucleic acid
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text The Rab8 GTPase Selectively Regulates AP-1B-Dependent Basolateral Transport in Polarized Madin-Darby Canine Kidney Cells
by Agnes Lee Ang and Heike Fölsch and Ulla-Maija Koivisto and Marc Pypaert and Ira Mellman
The Journal of Cell Biology, ISSN 0021-9525, 10/2003, Volume 163, Issue 2, pp. 339 - 350
The AP-1B clathrin adaptor complex plays a key role in the recognition and intracellular transport of many membrane proteins destined for the basolateral... 
Complementary DNA | Epithelial cells | Neurons | Antibodies | Cell membranes | Recycling | Cells | Freight | LLC PK1 cells | Endosomes | Polarity | Rab8 | MDCK | AP-1 | Sorting | CYTOPLASMIC DOMAIN | ADAPTER COMPLEXES | MDCK CELLS | LDL RECEPTOR | PLASMA-MEMBRANE | CELL BIOLOGY | EPITHELIAL-CELLS | GOLGI NETWORK | sorting | SORTING SIGNALS | MANNOSE 6-PHOSPHATE RECEPTORS | GAMMA-ADAPTIN | polarity | rab GTP-Binding Proteins - metabolism | Cell Line | Gene Expression | Adaptor Protein Complex gamma Subunits - metabolism | cdc42 GTP-Binding Protein - metabolism | rab GTP-Binding Proteins - genetics | GTP Phosphohydrolases - ultrastructure | Kidney - cytology | Endosomes - metabolism | Adaptor Protein Complex 1 - metabolism | trans-Golgi Network - ultrastructure | trans-Golgi Network - metabolism | Animals | GTP Phosphohydrolases - metabolism | Biological Transport | rab GTP-Binding Proteins - ultrastructure | Dogs | Adenoviridae - genetics | Biomarkers | Cell Polarity - physiology | Transferrin - pharmacokinetics | Adenoviridae - metabolism | Enzyme Activation | Mutation | Clathrin | Chemical properties | Research | Membrane proteins | Rab8; AP-1; sorting; polarity; MDCK
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text KIM-1-mediated phagocytosis reduces acute injury to the kidney
by Yang, Li and Brooks, Craig R and Xiao, Sheng and Sabbisetti, Venkata and Yeung, Melissa Y and Hsiao, Li-Li and Ichimura, Takaharu and Kuchroo, Vijay and Bonventre, Joseph V
Journal of Clinical Investigation, ISSN 0021-9738, 04/2015, Volume 125, Issue 4, pp. 1620 - 1636
Kidney injury molecule 1 (KIM-1, also known as TIM-1) is markedly upregulated in the proximal tubule after injury and is maladaptive when chronically... 
ISCHEMIA-REPERFUSION INJURY | B-CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | ISCHEMIA/REPERFUSION INJURY | MOLECULE-1 KIM-1 | EPITHELIAL-CELLS | APOPTOTIC CELLS | INNATE IMMUNE-RESPONSE | T-CELL IG | ACUTE-RENAL-FAILURE | URINARY BIOMARKER | Epithelial Cells - metabolism | Kidney - blood supply | Macrophage Activation - genetics | Apoptosis - drug effects | Intercellular Signaling Peptides and Proteins - biosynthesis | Male | NF-kappa B - metabolism | LLC-PK1 Cells | Epithelial Cells - secretion | Cisplatin - toxicity | Extracellular Matrix Proteins | Membrane Proteins - physiology | Swine | Kidney Tubules, Proximal - secretion | Acute Kidney Injury - chemically induced | Intercellular Signaling Peptides and Proteins - secretion | Acute Kidney Injury - etiology | Macrophage Activation - physiology | Protein Structure, Tertiary | Membrane Proteins - genetics | Mice, Inbred C57BL | Cytokines - secretion | Gene Expression Regulation | Phagocytosis - physiology | Inflammation | Radiation Chimera | Hepatitis A Virus Cellular Receptor 1 | Immunity, Innate | Acute Kidney Injury - prevention & control | Homeodomain Proteins - genetics | Mice, Knockout | Animals | Reperfusion Injury - prevention & control | Membrane Proteins - chemistry | Kidney Tubules, Proximal - metabolism | Phosphatidylinositol 3-Kinases - physiology | Mice | Apoptosis - physiology | Cytokines - biosynthesis | Kidneys | Immune response | Genetic research | Genetic aspects | Research | Gene expression | Injuries | Proteins | Phosphorylation | Hospitals | Laboratories | Mortality | Rodents | Acidification | Kinases | Apoptosis | Nephrology | Cell Biology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights