X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1639) 1639
Publication (267) 267
Book Review (16) 16
Book Chapter (5) 5
Conference Proceeding (3) 3
Dissertation (2) 2
Data Set (1) 1
Newspaper Article (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1064) 1064
humans (1054) 1054
animals (859) 859
angiopoietin (617) 617
angiogenesis (595) 595
mice (593) 593
male (524) 524
female (497) 497
angiopoietins - genetics (405) 405
gene expression (332) 332
expression (328) 328
angiopoietins - metabolism (320) 320
angiopoietin-like proteins (297) 297
vascular endothelial growth factor (280) 280
angiopoietin-like 4 protein (273) 273
proteins (260) 260
cell biology (252) 252
research (248) 248
middle aged (242) 242
research article (233) 233
angiopoietins (230) 230
endothelial growth-factor (226) 226
oncology (225) 225
multidisciplinary sciences (224) 224
biochemistry & molecular biology (217) 217
medicine (209) 209
inflammation (201) 201
signal transduction (200) 200
rodents (193) 193
physiological aspects (191) 191
adult (190) 190
analysis (187) 187
genetic aspects (181) 181
science (181) 181
in-vivo (172) 172
mice, inbred c57bl (172) 172
endothelial cells (162) 162
vegf (162) 162
cells, cultured (160) 160
aged (155) 155
article (152) 152
cancer (152) 152
endothelium (146) 146
metabolism (146) 146
health aspects (143) 143
rna, messenger - metabolism (137) 137
rats (133) 133
physiology (132) 132
kinases (127) 127
metastasis (127) 127
endocrinology & metabolism (126) 126
mice, knockout (126) 126
hypoxia (125) 125
diabetes (124) 124
angiopoietin-1 (122) 122
angiopoietin-2 (122) 122
vascular endothelial growth factor a - metabolism (122) 122
angiopoietin-1 - genetics (120) 120
apoptosis (119) 119
angiopoietin-2 - genetics (116) 116
risk factors (116) 116
biology (115) 115
tie2 receptor (114) 114
vascular endothelial growth factor a - genetics (113) 113
cell line, tumor (112) 112
cells (112) 112
angiopoietin-2 - metabolism (109) 109
hematology (109) 109
lipids (109) 109
receptor, tie-2 - metabolism (109) 109
angiopoietin-1 - metabolism (108) 108
obesity (108) 108
medicine, research & experimental (107) 107
rna, messenger - genetics (107) 107
growth factors (105) 105
inhibition (105) 105
neovascularization (105) 105
tumors (105) 105
gene-expression (104) 104
cell line (103) 103
cell proliferation (103) 103
gene expression regulation (102) 102
genes (102) 102
lipoprotein-lipase (102) 102
studies (102) 102
endothelial-cells (100) 100
up-regulation (98) 98
cardiovascular system (97) 97
reverse transcriptase polymerase chain reaction (97) 97
immunohistochemistry (96) 96
genetics & heredity (95) 95
phosphorylation (95) 95
tie2 (95) 95
disease models, animal (94) 94
enzyme-linked immunosorbent assay (93) 93
immunology (92) 92
growth (91) 91
liver (91) 91
peripheral vascular disease (91) 91
receptor (91) 91
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1621) 1621
Chinese (11) 11
Japanese (6) 6
French (3) 3
Korean (2) 2
German (1) 1
Hungarian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Lipid Research, ISSN 0022-2275, 02/2011, Volume 52, Issue 2, pp. 189 - 206
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2009, Volume 284, Issue 38, pp. 25593 - 25601
Glucocorticoids are important regulators of lipid homeostasis, and chronically elevated glucocorticoid levels induce hypertriglyceridemia, hepatic steatosis,... 
OBESITY | PLASMA | GENE | CHROMATIN | ANGIOGENESIS | DIET | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERLIPIDEMIA | MICE | TRANSCRIPTIONAL REGULATION | PROTEIN-4 | Transcription, Genetic - drug effects | Hypertriglyceridemia - genetics | Humans | Dexamethasone - adverse effects | Receptors, Glucocorticoid - metabolism | Hepatocytes - metabolism | Fatty Liver - chemically induced | Adipose Tissue - metabolism | Angiopoietin-like 4 Protein | Dexamethasone - pharmacology | Glucocorticoids - genetics | Glucocorticoids - metabolism | Response Elements - genetics | Lipoprotein Lipase - metabolism | Glucocorticoids - adverse effects | Fatty Liver - genetics | Angiopoietins - metabolism | Fatty Liver - metabolism | Lipoprotein Lipase - genetics | Liver - metabolism | Rats | Hypertriglyceridemia - metabolism | Mice, Knockout | Triglycerides - metabolism | Adipose Tissue, White | Hypertriglyceridemia - chemically induced | Animals | Receptors, Glucocorticoid - genetics | Cell Line, Tumor | Dexamethasone - metabolism | Glucocorticoids - pharmacology | Mice | Transcription, Genetic - genetics | Triglycerides - genetics | Angiopoietins - genetics | Index Medicus | Lipids and Lipoproteins | Metabolism, Regulation, and Signaling | Transcription | Dermatologi och venereologi | Dermatology and Venereal Diseases | Dexamethasone/adverse effects/metabolism/pharmacology | Hypertriglyceridemia/chemically induced/genetics/metabolism | Receptors | Adipose Tissue/metabolism | Liver/metabolism | Tumor | Adipose Tissue | Cell Line | Fatty Liver/chemically induced/genetics/metabolism | Triglycerides/genetics/ metabolism | Response Elements/genetics | Angiopoietins/genetics/ metabolism | Knockout | Lipoprotein Lipase/genetics/metabolism | White | Hepatocytes/metabolism | Genetic/drug effects/genetics | Glucocorticoids/adverse effects/genetics/ metabolism/pharmacology | Glucocorticoid/genetics/ metabolism
Journal Article
Current Opinion in Lipidology, ISSN 0957-9672, 2014, Volume 25, Issue 3, pp. 161 - 168
Purpose of reviewSeveral mutations in the apoB, proprotein convertase subtilisin/kexin type 9 (PCSK9), and MTP genes result in low or absent levels of apoB and... 
combined hypolipidemia | angiopoietin-like 3 protein | proprotein convertase subtilisin/kexin type 9 | Abetalipoproteinemia | hypobetalipoproteinemia | kexin type 9 | proprotein convertase subtilisin | abetalipoproteinemia | BIOCHEMISTRY & MOLECULAR BIOLOGY | B GENE-MUTATIONS | TRANSFER PROTEIN | INSULIN-RESISTANCE | DENSITY-LIPOPROTEIN | IN-VIVO | ENDOCRINOLOGY & METABOLISM | FATTY LIVER | PERIPHERAL VASCULAR DISEASE | HEPATIC STEATOSIS | APOLIPOPROTEIN B-67/B-100 HETEROZYGOTES | DECREASED PRODUCTION | FAMILIAL COMBINED HYPOLIPIDEMIA | Abetalipoproteinemia - blood | Humans | Hypobetalipoproteinemia, Familial, Apolipoprotein B - blood | Apolipoproteins B - blood | Biological Transport, Active - genetics | Coronary Artery Disease - blood | Proprotein Convertases - genetics | Liver Neoplasms - blood | Angiopoietin-like Proteins | Carcinoma, Hepatocellular - genetics | Serine Endopeptidases - genetics | Cholesterol, LDL - blood | Lipid Metabolism - genetics | Carcinoma, Hepatocellular - blood | Liver Cirrhosis - genetics | Hypobetalipoproteinemia, Familial, Apolipoprotein B - genetics | Angiopoietins - metabolism | Liver Neoplasms - genetics | Proprotein Convertases - metabolism | Apolipoproteins B - genetics | Liver Cirrhosis - blood | Cholesterol, LDL - genetics | Abetalipoproteinemia - genetics | Coronary Artery Disease - genetics | Triglycerides - blood | Serine Endopeptidases - metabolism | Mutation | Triglycerides - genetics | Angiopoietins - genetics | Proprotein Convertase 9 | PCSK9 | Hypobetalipoproteinemia
Journal Article
Bone, ISSN 8756-3282, 2003, Volume 33, Issue 6, pp. 889 - 898
Distraction osteogenesis is a unique and effective way to treat limb length inequality resulting from congenital and posttraumatic skeletal defects. However,... 
Angiogenesis | Extracellular matrix | Bone morphogenetic protein | Distraction osteogenesis | mRNA expression | angiogenesis | STABILITY | RECEPTOR | ANGIOPOIETIN-2 | MODEL | bone morphogenetic protein | distraction osteogenesis | CARTILAGE | VASCULARIZATION | GROWTH | ENDOCRINOLOGY & METABOLISM | BONE | DIFFERENTIATION | LIGAND | extracellular matrix | Immunohistochemistry | Receptor, Fibroblast Growth Factor, Type 4 | Sialoglycoproteins - genetics | Femur - pathology | Oligonucleotide Array Sequence Analysis | Osteocalcin - genetics | Male | Gene Expression Profiling | RNA, Messenger - metabolism | Vascular Endothelial Growth Factor A - genetics | Hypoxia-Inducible Factor 1, alpha Subunit | Osteogenesis, Distraction | Fibroblast Growth Factor 2 - analysis | Angiogenesis Inducing Agents - metabolism | Receptors, Fibroblast Growth Factor - genetics | Fracture Healing - physiology | Collagen - genetics | Femur - surgery | Neuropilins - genetics | Receptors, Vascular Endothelial Growth Factor - genetics | Bone Morphogenetic Proteins - genetics | Cytokines - genetics | Transforming Growth Factor beta2 | Osteogenesis - genetics | von Willebrand Factor - analysis | Gene Expression | Femur - metabolism | Neovascularization, Physiologic - genetics | RNA, Messenger - genetics | Osteopontin | Rats | Vascular Endothelial Growth Factor A - analysis | Transcription Factors - genetics | Rats, Sprague-Dawley | Receptors, TIE - genetics | Carrier Proteins - genetics | Animals | Transforming Growth Factor beta - genetics | Fibroblast Growth Factor 2 - genetics | Vascular Endothelial Growth Factors - genetics | Fracture Healing - genetics | Angiopoietins - genetics
Journal Article
Oncogene, ISSN 0950-9232, 02/2018, Volume 37, Issue 5, pp. 673 - 686
Urothelial carcinoma (UC) carcinogenesis has been hypothesized to occur through epigenetic repression of tumor-suppressor genes (TSGs). By quantitative... 
BLADDER-CANCER | PROTEIN | METASTASIS | ANGIOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANGIOPOIETIN-LIKE 4 | VASCULAR-PERMEABILITY | LARGE GENE LISTS | CELL BIOLOGY | KAPOSIS-SARCOMA | ONCOLOGY | PROMOTES VENOUS INVASION | GENETICS & HEREDITY | EXPRESSION | Humans | Middle Aged | Tumor Microenvironment | Male | Urinary Bladder - pathology | Promoter Regions, Genetic - genetics | Case-Control Studies | Cell Movement - genetics | Urothelium - pathology | Urinary Bladder Neoplasms - genetics | Urinary Bladder Neoplasms - pathology | Aged, 80 and over | Female | Genes, Tumor Suppressor | Urinary Bladder - surgery | Gene Expression Regulation, Neoplastic - genetics | Carcinoma, Transitional Cell - genetics | Oncogenes - genetics | Cell Proliferation - genetics | Signal Transduction | Down-Regulation | Carcinogenesis - genetics | DNA Methylation - genetics | Mice, SCID | Xenograft Model Antitumor Assays | Cystectomy | Animals | Carcinoma, Transitional Cell - pathology | Epigenesis, Genetic - genetics | Angiopoietin-like 4 Protein - metabolism | Cell Line, Tumor | Mice, Inbred NOD | Aged | Mice | Carcinoma, Transitional Cell - surgery | Angiopoietin-like 4 Protein - blood | Angiopoietin-like 4 Protein - genetics | Gene silencing | Care and treatment | Development and progression | Genetic aspects | Gene expression | Health aspects | Urinary tract cancer | Cell proliferation | Immunohistochemistry | Bisulfite | Transcription | Angiopoietin | Carcinogenesis | Cell adhesion & migration | Cell activation | Cell growth | Urinary bladder | Etiology | Xenografts | DNA methylation | Urothelial carcinoma | Tumor cells | Invasiveness | Extracellular signal-regulated kinase | Tumor cell lines | Epithelium | Polymerase chain reaction | Cell lines | Epigenetics | Tumor suppressor genes | Focal adhesion kinase | Methylation | Cell migration | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 9, p. e107048
Serum Response Factor (SRF) fulfills essential roles in post-natal retinal angiogenesis and adult neovascularization. These functions have been attributed to... 
TERNARY COMPLEX | ANGIOGENESIS | ACTIN | SRF | MULTIDISCIPLINARY SCIENCES | DISEASE | SERUM RESPONSE FACTOR | RETINOPATHY | MICE | NET | TRANSCRIPTION FACTOR | Proto-Oncogene Proteins c-ets - deficiency | Serum Response Factor - genetics | Retina - metabolism | Proto-Oncogene Proteins c-ets - genetics | Joint Instability - genetics | Joint Instability - pathology | Male | Retinal Neovascularization - metabolism | Arteries - metabolism | Neovascularization, Pathologic - pathology | Skin Diseases, Genetic - genetics | Retinal Vessels - pathology | Female | Retinal Neovascularization - genetics | Disease Models, Animal | Vascular Malformations - metabolism | Angiopoietins - metabolism | Joint Instability - metabolism | Retinal Vessels - metabolism | Serum Response Factor - metabolism | Mice, Inbred C57BL | Skin Diseases, Genetic - pathology | Arteries - pathology | Transcription Factors - genetics | Skin Diseases, Genetic - metabolism | Vascular Malformations - pathology | Mice, Knockout | Receptors, TIE - genetics | Transcription Factors - metabolism | Animals | Receptors, TIE - metabolism | Vascular Endothelial Growth Factors - genetics | Neovascularization, Pathologic - genetics | Signal Transduction - physiology | Vascular Endothelial Growth Factors - metabolism | Mice | Neovascularization, Pathologic - metabolism | Vascular Malformations - genetics | Angiopoietins - genetics | Retina - pathology | Retinal Neovascularization - pathology | Arteries - abnormalities | Explants | Diabetic retinopathy | Transcription factors | Angiopoietin | Cloning | Blood vessels | Retina | Kinases | Arteries | Cofactors | Vascularization | Angiogenesis | Ternary complex factors | Neurodegeneration | Cell cycle | Serum response factor | Aorta | Eye (anatomy) | Blood pressure | Adults | Molecular biology | Cardiology | Vascular endothelial growth factor
Journal Article
Lymphatic Research and Biology, ISSN 1539-6851, 02/2018, Volume 16, Issue 1, pp. 43 - 55
Background: Lymphatic endothelial cells (LECs) derived from lymphatic malformations (LMs) bear activated PIK3CA alleles yet display an inflammatory gene... 
PIK3CA | endothelial cells | lymphatic malformations | MEDICINE, RESEARCH & EXPERIMENTAL | PHYSIOLOGY | PERCUTANEOUS SCLEROTHERAPY | PHOSPHORYLATION | PROTEIN-KINASE | CANCER | FAT STORAGE | PI3K | INSULIN-RESISTANCE | AMPK | MUTATIONS | LIPID DROPLETS | Interleukin-8 - genetics | Heme Oxygenase-1 - metabolism | Class I Phosphatidylinositol 3-Kinases - genetics | Vesicular Transport Proteins - metabolism | Humans | Aminoimidazole Carboxamide - pharmacology | Cyclooxygenase 2 - genetics | E-Selectin - genetics | Lipid Metabolism - genetics | Interleukin-8 - metabolism | Interleukin-6 - metabolism | Repressor Proteins - metabolism | Histone Deacetylases - genetics | Interleukin-6 - genetics | Signal Transduction | Endothelial Cells - metabolism | Membrane Proteins - genetics | Lymphoid Tissue - metabolism | Repressor Proteins - genetics | Lymphatic Abnormalities - pathology | Lymphoid Tissue - pathology | Aminoimidazole Carboxamide - analogs & derivatives | Vascular Endothelial Growth Factor C - metabolism | Angiopoietin-like 4 Protein - metabolism | Mutation | Endothelial Cells - pathology | Autophagy-Related Proteins - metabolism | AMP-Activated Protein Kinases - genetics | Angiopoietin-like 4 Protein - genetics | Lymphatic Abnormalities - genetics | AMP-Activated Protein Kinases - metabolism | Class I Phosphatidylinositol 3-Kinases - metabolism | Ribonucleotides - pharmacology | Heme Oxygenase-1 - genetics | Membrane Proteins - metabolism | Autophagy-Related Proteins - genetics | Cell Line | Vesicular Transport Proteins - genetics | Gene Expression Regulation | Lymphatic Abnormalities - metabolism | E-Selectin - metabolism | Histone Deacetylases - metabolism | Transcription Factors - genetics | Vascular Endothelial Growth Factor C - genetics | Transcription Factors - metabolism | Ankyrins - genetics | Alleles | Ankyrins - metabolism | Cyclooxygenase 2 - metabolism | Primary Cell Culture | Endothelial Cells - drug effects
Journal Article
Journal Article
by Bourcier, Romain and Le Scouarnec, Solena and Bonnaud, Stéphanie and Karakachoff, Matilde and Bourcereau, Emmanuelle and Heurtebise-Chrétien, Sandrine and Menguy, Céline and Dina, Christian and Simonet, Floriane and Moles, Alexis and Lenoble, Cédric and Lindenbaum, Pierre and Chatel, Stéphanie and Isidor, Bertrand and Génin, Emmanuelle and Deleuze, Jean-François and Schott, Jean-Jacques and Le Marec, Hervé and Desal, Hubert and Daumas-Duport, Benjamin and Connault, Jérôme and Lebranchu, Pierre and Le Tourneau, Thierry and Viarouge, Marie Pierre and Papagiannaki, Chrisanthi and Piotin, Michel and Redjem, Hocine and Mazighi, Mikael and Desilles, Jean Philippe and Naggara, Olivier and Trystram, Denis and Edjlali-Goujon, Myriam and Rodriguez, Christine and Ben Hassen, Waghi and Saleme, Suzanna and Mounayer, Charbel and Levrier, Olivier and Aguettaz, Pierre and Combaz, Xavier and Pasco, Anne and Berthier, Emeline and Bintner, Marc and Molho, Marc and Gauthier, Pascale and Chivot, Cyril and Costalat, Vincent and Darganzil, Cyril and Bonafé, Alain and Januel, Anne Christine and Michelozzi, Caterina and Cognard, Christophe and Bonneville, Fabrice and Tall, Philippe and Darcourt, Jean and Biondi, Alessandra and Iosif, Cristina and Pomero, Elisa and Ferre, Jean Christophe and Gauvrit, Jean Yves and Eugene, François and Raoult, Hélène and Gentric, Jean Christophe and Ognard, Julien and Anxionnat, René and Bracard, Serge and Derelle, Anne Laure and Tonnelet, Romain and Spelle, Laurent and Ikka, Léon and Fahed, Robert and Rouchaud, Aymeric and Ozanne, Augustin and Caroff, Jildaz and Ben Achour, Nidal and Moret, Jacques and Chabert, Emmanuel and Berge, Jérôme and Marnat, Gaultier and Barreau, Xavier and Gariel, Florent and Clarencon, Frédéric and Aggour, Mohammed and Ricolfi, Frédéric and Chavent, Adrien and Thouant, Pierre and Lebidinsky, Pablo and Lemogne, Brivael and Herbreteau, Denis and Bibi, Richard and Pierot, Laurent and Soize, Sébastien and Labeyrie, Marc Antoine and Vandendries, Christophe and Houdart, Emmanuel and Kazemi, Appoline and Leclerc, Xavier and Pruvo, Jean Pierre and Gallas, Sophie and Velasco, Stéphane and Loirand, Gervaise and ... and ICAN Study Grp and ICAN Study Group
The American Journal of Human Genetics, ISSN 0002-9297, 01/2018, Volume 102, Issue 1, pp. 133 - 141
Journal Article