X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (119) 119
hepatocyte nuclear factor 3-gamma (77) 77
mice (66) 66
humans (56) 56
index medicus (54) 54
hepatocyte nuclear factor 3-beta (51) 51
base sequence (47) 47
hepatocyte nuclear factor 3-alpha (47) 47
transcription factors (46) 46
biochemistry & molecular biology (44) 44
dna-binding proteins - genetics (43) 43
nuclear proteins - genetics (43) 43
molecular sequence data (41) 41
hepatocyte nuclear factor 3-gamma - metabolism (40) 40
transcription factors - genetics (40) 40
dna-binding proteins - metabolism (39) 39
rats (38) 38
hepatocyte nuclear factor 3-gamma - genetics (37) 37
nuclear proteins - metabolism (37) 37
transcription factors - metabolism (36) 36
cell biology (33) 33
liver - metabolism (30) 30
male (29) 29
binding sites (27) 27
gene expression regulation (25) 25
female (23) 23
gene expression (23) 23
promoter regions, genetic (21) 21
cell line (20) 20
expression (20) 20
research article (20) 20
transcription, genetic (20) 20
cells, cultured (19) 19
genes (19) 19
liver (18) 18
proteins (18) 18
developmental biology (17) 17
differentiation (17) 17
transcription factor (17) 17
gene-expression (16) 16
hepatocyte nuclear factor 1-beta (16) 16
hepatocyte nuclear factor 4 (16) 16
liver - cytology (16) 16
mice, inbred c57bl (16) 16
amino acid sequence (15) 15
cell differentiation (15) 15
dna - metabolism (15) 15
hepatocyte nuclear factor 1 (15) 15
hepatocyte nuclear factor 1-alpha (15) 15
transfection (15) 15
article (14) 14
dna-binding proteins - physiology (14) 14
metabolism (14) 14
mice, transgenic (14) 14
nuclear proteins - physiology (14) 14
protein binding (14) 14
genetic aspects (13) 13
research (13) 13
transcription factors - physiology (13) 13
hepatocytes - cytology (12) 12
multidisciplinary sciences (12) 12
physiological aspects (12) 12
tumor cells, cultured (12) 12
dna (11) 11
family (11) 11
forkhead transcription factors (11) 11
in-vivo (11) 11
mice, knockout (11) 11
signal transduction (11) 11
definitive endoderm (10) 10
disease models, animal (10) 10
embryonic structures (10) 10
enhancer elements, genetic (10) 10
genetics & heredity (10) 10
glucose-homeostasis (10) 10
hepatocytes - metabolism (10) 10
rodents (10) 10
analysis (9) 9
biology (9) 9
blotting, northern (9) 9
cell differentiation - genetics (9) 9
endocrinology & metabolism (9) 9
fibroblasts - cytology (9) 9
gene (9) 9
gene expression regulation, developmental (9) 9
genetic transcription (9) 9
hepatocyte nuclear factor 3-beta - metabolism (9) 9
hepatocytes (9) 9
sequence homology, amino acid (9) 9
binding (8) 8
ccaat-enhancer-binding proteins (8) 8
cells (8) 8
diabetes (8) 8
dna binding proteins (8) 8
dna-binding proteins - biosynthesis (8) 8
dna-binding proteins - chemistry (8) 8
enhancer (8) 8
fibroblasts (8) 8
fibroblasts - metabolism (8) 8
hepatocyte nuclear factor 3-gamma - physiology (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
by Bailey, Peter and Chang, David K and Nones, Katia and Johns, Amber L and Patch, Ann-Marie and Gingras, Marie-Claude and Miller, David K and Christ, Angelika N and Bruxner, Tim J. C and Quinn, Michael C and Nourse, Craig and Murtaugh, L. Charles and Harliwong, Ivon and Idrisoglu, Senel and Manning, Suzanne and Nourbakhsh, Ehsan and Wani, Shivangi and Fink, Lynn and Holmes, Oliver and Chin, Venessa and Anderson, Matthew J and Kazakoff, Stephen and Leonard, Conrad and Newell, Felicity and Waddell, Nick and Wood, Scott and Xu, Qinying and Wilson, Peter J and Cloonan, Nicole and Kassahn, Karin S and Taylor, Darrin and Quek, Kelly and Robertson, Alan and Pantano, Lorena and Mincarelli, Laura and Sanchez, Luis N and Evers, Lisa and Wu, Jianmin and Pinese, Mark and Cowley, Mark J and Jones, Marc D and Colvin, Emily K and Nagrial, Adnan M and Humphrey, Emily S and Chantrill, Lorraine A and Mawson, Amanda and Humphris, Jeremy and Chou, Angela and Pajic, Marina and Scarlett, Christopher J and Pinho, Andreia V and Giry-Laterriere, Marc and Rooman, Ilse and Samra, Jaswinder S and Kench, James G and Lovell, Jessica A and Merrett, Neil D and Toon, Christopher W and Epari, Krishna and Nguyen, Nam Q and Barbour, Andrew and Zeps, Nikolajs and Moran-Jones, Kim and Jamieson, Nigel B and Graham, Janet S and Duthie, Fraser and Oien, Karin and Hair, Jane and Grützmann, Robert and Maitra, Anirban and Iacobuzio-Donahue, Christine A and Wolfgang, Christopher L and Morgan, Richard A and Lawlor, Rita T and Corbo, Vincenzo and Bassi, Claudio and Rusev, Borislav and Capelli, Paola and Salvia, Roberto and Tortora, Giampaolo and Mukhopadhyay, Debabrata and Petersen, Gloria M and Munzy, Donna M and Fisher, William E and Karim, Saadia A and Eshleman, James R and Hruban, Ralph H and Pilarsky, Christian and Morton, Jennifer P and Sansom, Owen J and Scarpa, Aldo and Musgrove, Elizabeth A and Bailey, Ulla-Maja Hagbo and Hofmann, Oliver and Sutherland, Robert L and Wheeler, David A and Gill, Anthony J and Gibbs, Richard A and Pearson, John V and Waddell, Nicola and ... and Australian Pancreatic Canc Genome and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 03/2016, Volume 531, Issue 7592, pp. 47 - 52
Integrated genomic analysis of 456 pancreatic ductal adenocarcinomas identified 32 recurrently mutated genes that aggregate into 10 pathways: KRAS, TGF-beta,... 
PATHWAYS | METASTASIS | DUCTAL ADENOCARCINOMA | PACKAGE | MULTIDISCIPLINARY SCIENCES | TUMOR | MUTATIONS | DIFFERENTIATION | Pancreatic Neoplasms - metabolism | Prognosis | Hepatocyte Nuclear Factor 3-beta - genetics | Genomics | Humans | Carcinoma, Pancreatic Ductal - metabolism | Gene Expression Regulation, Neoplastic | Transcriptome | Hepatocyte Nuclear Factor 3-gamma - genetics | Gene Regulatory Networks | Histone Demethylases - genetics | Tumor Suppressor Protein p53 - genetics | Carcinoma, Pancreatic Ductal - genetics | DNA Methylation | Tumor Suppressor Proteins - genetics | Carcinoma, Pancreatic Ductal - classification | Trans-Activators - genetics | Pancreatic Neoplasms - classification | Transcription, Genetic | Nuclear Proteins - genetics | Carcinoma, Pancreatic Ductal - immunology | Genes, Neoplasm - genetics | Basic Helix-Loop-Helix Transcription Factors - genetics | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - genetics | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Carcinoma, Pancreatic Ductal - pathology | Genome, Human - genetics | Homeodomain Proteins - genetics | Animals | Pancreatic Neoplasms - immunology | Survival Analysis | Cell Line, Tumor | Mice | Physiological aspects | Pancreatic cancer | Methods | Genes | Genomes | Mutation | Gene expression | Tumors
Journal Article
Nature, ISSN 0028-0836, 07/2011, Volume 475, Issue 7356, pp. 386 - 391
The generation of functional hepatocytes independent of donor liver organs is of great therapeutic interest with regard to regenerative medicine and possible... 
MURINE MODEL | HEPATIC-DYSFUNCTION | PANCREAS PROGENITORS | TYROSINEMIA TYPE-I | LIVER-FUNCTION | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | FACTOR NETWORK | DIRECT CONVERSION | GENE-EXPRESSION | ENRICHED TRANSCRIPTION FACTORS | Hydrolases - genetics | Liver - enzymology | Hepatocyte Nuclear Factor 1-alpha - genetics | Tail - cytology | Liver Diseases - pathology | Gene Expression Profiling | Hepatocyte Nuclear Factor 3-gamma - genetics | Hepatocytes - metabolism | Hepatocyte Nuclear Factor 1-alpha - metabolism | Liver - physiopathology | Regenerative Medicine - methods | DNA-Binding Proteins - deficiency | Cell Differentiation - genetics | Hepatocytes - cytology | Hepatocyte Nuclear Factor 3-gamma - metabolism | Liver Diseases - enzymology | Hepatocytes - transplantation | Hepatocytes - physiology | Fibroblasts - metabolism | Cyclin-Dependent Kinase Inhibitor p16 - deficiency | GATA4 Transcription Factor - metabolism | Tissue Engineering - methods | Transduction, Genetic | Cells, Cultured | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Liver Diseases - therapy | GATA4 Transcription Factor - genetics | Survival Rate | Hydrolases - deficiency | Mice, SCID | Cell Lineage | Animals | Liver - physiology | Mice, Inbred NOD | Fibroblasts - cytology | Liver - cytology | Mice | Liver Diseases - physiopathology | Physiological aspects | Fibroblasts | Transcription factors | Research | Embryonic stem cells | Liver cells | Proteins | Gene expression | Tissue engineering | Cell adhesion & migration
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 10/2006, Volume 63, Issue 19, pp. 2317 - 2328
The Foxa subfamily of winged helix/forkhead box (Fox) transcription factors has been the subject of genetic and biochemical study for over 15 years. During... 
Life Sciences | Biochemistry, general | Transcription factors | development | Life Sciences, general | metabolism | organogenesis | diabetes | Biomedicine general | Cell Biology | Development | Diabetes | Metabolism | Organogenesis | TYROSINE AMINOTRANSFERASE GENE | ALDOLASE-B PROMOTER | transcription factors | BIOCHEMISTRY & MOLECULAR BIOLOGY | TISSUE-SPECIFIC EXPRESSION | PHOSPHOENOLPYRUVATE CARBOXYKINASE GENE | ALPHA-FETOPROTEIN GENE | GLUCOCORTICOID-RESPONSE UNIT | CELL BIOLOGY | HEPATOCYTE NUCLEAR FACTOR-3 | SYNTHETASE-I GENE | CELL-SPECIFIC ENHANCER | SECRETORY PROTEIN GENE | Protein Structure, Tertiary | Hepatocyte Nuclear Factor 3-alpha - physiology | Hepatocyte Nuclear Factor 3-beta - chemistry | Hepatocyte Nuclear Factor 3-gamma - chemistry | Multigene Family - physiology | Hepatocyte Nuclear Factor 3-beta - genetics | Gene Expression Regulation | Embryonic Development - physiology | Forkhead Transcription Factors - physiology | Hepatocyte Nuclear Factor 3-alpha - genetics | Hepatocyte Nuclear Factor 3-gamma - genetics | Forkhead Transcription Factors - genetics | Hepatocyte Nuclear Factor 3-gamma - physiology | Hepatocyte Nuclear Factor 3-beta - physiology | Animals | Hepatocyte Nuclear Factor 3-alpha - chemistry | Forkhead Transcription Factors - chemistry | Glucose - metabolism | Mice | Organogenesis - physiology | Genetics | Cell growth | Developmental biology
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2014, Volume 111, Issue 39, pp. 14289 - 14294
Aging is associated with increased adiposity and diminished thermogenesis, but the critical transcription factors influencing these metabolic changes late in... 
Adipose tissues | Obesity | Messenger RNA | White adipose tissue | Developmental biology | Brown adipose tissue | Brown adipocytes | Insulin resistance | Adipocytes | Lipid metabolism | Diabetes | PGC-1-ALPHA | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | BROWN ADIPOSE-TISSUE | GLUCOSE-HOMEOSTASIS | ENERGY-EXPENDITURE | INSULIN-RESISTANCE | FAT | NUCLEAR FACTOR 3-GAMMA | ADIPOCYTE DIFFERENTIATION | MICE | diabetes | obesity | Thermogenesis - genetics | Up-Regulation | Adipose Tissue, White - metabolism | Male | Hepatocyte Nuclear Factor 3-gamma - genetics | RNA, Messenger - metabolism | Obesity - genetics | Thermogenesis - physiology | Aging - genetics | Hepatocyte Nuclear Factor 3-gamma - metabolism | Insulin Resistance - physiology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Hepatocyte Nuclear Factor 3-gamma - deficiency | Energy Metabolism - genetics | Energy Metabolism - physiology | Promoter Regions, Genetic | RNA, Messenger - genetics | Longevity - genetics | Transcription Factors - genetics | Adiposity - genetics | Mice, Knockout | Obesity - metabolism | Transcription Factors - metabolism | Animals | Cyclic AMP Response Element-Binding Protein - metabolism | Insulin Resistance - genetics | Adipose Tissue, Brown - metabolism | Adiposity - physiology | Mice | Longevity - physiology | Aging - metabolism | Transcription factors | Analysis | Physiological aspects | Aging | Physiological research | Research | Metabolism | Protein binding | Biological Sciences
Journal Article
Journal Article
Developmental Cell, ISSN 1534-5807, 05/2012, Volume 22, Issue 5, pp. 927 - 939
During endochondral ossification, small, immature chondrocytes enlarge to form hypertrophic chondrocytes, which express collagen X. In this work, we... 
TRANSCRIPTION FACTORS | TARGETED DISRUPTION | CBFA1-DEFICIENT MICE | BONE-FORMATION | X COLLAGEN GENE | ALKALINE-PHOSPHATASE | ENHANCER | CBFA1 | NUCLEAR FACTOR 3-GAMMA | DEVELOPMENTAL BIOLOGY | EXPRESSION | CELL BIOLOGY | Chondrocytes - cytology | Hepatocyte Nuclear Factor 3-beta - genetics | Chondrogenesis - genetics | Alkaline Phosphatase - metabolism | Hepatocyte Nuclear Factor 3-gamma - genetics | Core Binding Factor Alpha 1 Subunit - metabolism | Embryo, Mammalian - metabolism | Cell Differentiation - genetics | Collagen Type X - metabolism | Hepatocyte Nuclear Factor 3-gamma - metabolism | Mice, Mutant Strains | Hepatocyte Nuclear Factor 3-gamma - deficiency | Binding Sites | Chondrocytes - metabolism | Genes, Reporter | Fibroblasts - metabolism | Hepatocyte Nuclear Factor 3-beta - metabolism | Dwarfism - embryology | Matrix Metalloproteinase 13 - genetics | Cells, Cultured | Metatarsal Bones - cytology | Myogenic Regulatory Factors - metabolism | Collagen Type X - genetics | Metatarsal Bones - metabolism | Cell Enlargement | Growth Plate - metabolism | Chick Embryo | Matrix Metalloproteinase 13 - metabolism | Dwarfism - genetics | Animals | Embryo, Mammalian - cytology | Smad1 Protein - metabolism | Fibroblasts - cytology | Mice | Hepatocyte Nuclear Factor 3-beta - deficiency | Physiological aspects | Phosphatases | Collagen | Genes | Alkaline phosphatase | Collagenase 3 | Ossification | Dwarfism | Growth plate | Enhancers | Collagen (type X) | Mineralization | Chondrocytes | Fibroblasts | Chondrogenesis | Bone (endochondral) | Hypertrophy
Journal Article
Cell Reports, ISSN 2211-1247, 01/2015, Volume 10, Issue 2, pp. 239 - 252
Journal Article
Journal Article