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1. Full Text Nuclear signalling by tumour-associated antigen EpCAM
by Maetzel, Dorothea and Denzel, Sabine and Mack, Brigitte and Canis, Martin and Went, Philip and Benk, Michael and Kieu, Cuong and Papior, Peer and Baeuerle, Patrick A and Munz, Markus and Gires, Olivier
Nature Cell Biology, ISSN 1465-7392, 2009, Volume 11, Issue 2, pp. 162 - 171
EpCAM was found to be overexpressed on epithelial progenitors, carcinomas and cancer-initiating cells. The role of EpCAM in proliferation, and its association... 
BREAST-CANCER | TARGET | STEM-CELLS | ADHESION MOLECULE | DEPENDENT GAMMA-SECRETASE | EP-CAM | COLORECTAL-CANCER | C-MYC | CELL-PROLIFERATION | BETA-CATENIN | CELL BIOLOGY | ADAM17 Protein | NIH 3T3 Cells | Cell Adhesion Molecules - genetics | Colonic Neoplasms - genetics | Cell Proliferation | Active Transport, Cell Nucleus - physiology | Homeodomain Proteins - metabolism | Humans | Lymphoid Enhancer-Binding Factor 1 - genetics | Male | Presenilin-2 - metabolism | Cell Membrane - genetics | Colonic Neoplasms - metabolism | Epithelial Cell Adhesion Molecule | Cell Nucleus - metabolism | Cell Transformation, Neoplastic - genetics | Muscle Proteins - metabolism | Antigens, Neoplasm - metabolism | Cell Membrane - metabolism | Protein Structure, Tertiary | Antigens, Neoplasm - genetics | Transcription Factors - genetics | Cell Adhesion Molecules - metabolism | Cell Transformation, Neoplastic - metabolism | Lymphoid Enhancer-Binding Factor 1 - metabolism | beta Catenin - metabolism | Homeodomain Proteins - genetics | beta Catenin - genetics | Muscle Proteins - genetics | Transcription Factors - metabolism | ADAM Proteins - metabolism | Animals | Cell Nucleus - genetics | Mitosis - physiology | Carcinoma - genetics | LIM-Homeodomain Proteins | Signal Transduction - physiology | Mice | Carcinoma - metabolism | Tumor antigens | Physiological aspects | Genetic aspects | Research | Health aspects | Cell adhesion molecules | Membrane proteins
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2. Full Text Vertebrate neurogenesis is counteracted by Sox1-3 activity
by Muhr, Jonas and Novitch, Bennett G and Bylund, Magdalena and Andersson, Elisabeth
Nature Neuroscience, ISSN 1097-6256, 11/2003, Volume 6, Issue 11, pp. 1162 - 1168
The generation of neurons from stem cells involves the activity of proneural basic helix-loop-helix (bHLH) proteins, but the mechanism by which these proteins... 
VENTRAL NEURAL-TUBE | SOX2 | NERVOUS-SYSTEM | STEM-CELLS | BHLH PROTEIN | GENE-EXPRESSION | NEURONAL DIFFERENTIATION | CHICK-EMBRYO | ACHAETE-SCUTE | FATE | NEUROSCIENCES | Helix-Loop-Helix Motifs - physiology | Homeodomain Proteins - metabolism | PAX7 Transcription Factor | Phosphopyruvate Hydratase - metabolism | DNA-Binding Proteins - metabolism | Stem Cells | Tubulin - metabolism | Time Factors | Gene Expression Regulation, Developmental | Neurons - metabolism | Bromodeoxyuridine - metabolism | Membrane Glycoproteins | Spinal Cord - cytology | SOXB1 Transcription Factors | Cell Differentiation - physiology | Basic Helix-Loop-Helix Transcription Factors | DNA-Binding Proteins - physiology | HMGB Proteins | High Mobility Group Proteins - metabolism | Drosophila | Embryonic Induction | Neuropeptides - metabolism | Nuclear Proteins - metabolism | Electroporation - methods | Chick Embryo | Proto-Oncogene Proteins c-myc - metabolism | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Spinal Cord - embryology | Vertebrates | Animals | Eye Proteins - metabolism | Spinal Cord - physiology | Avian Proteins | LIM-Homeodomain Proteins | High Mobility Group Proteins - physiology | Mice | Nuclear Proteins - physiology | Neurofilament Proteins - metabolism | Physiological aspects | Research | DNA binding proteins | Neurons | Cell cycle
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3. Full Text Defective cytotoxic lymphocyte degranulation in syntaxin-11-deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
by Bryceson, Yenan T and Rudd, Eva and Zheng, Chengyun and Edner, Josefine and Ma, Daoxin and Wood, Stephanie M and Bechensteen, Anne Grete and Boelens, Jaap J and Celkan, Tiraje and Farah, Roula A and Hultenby, Kjell and Winiarski, Jacek and Roche, Paul A and Nordenskjöld, Magnus and Henter, Jan-Inge and Long, Eric O and Ljunggren, Hans-Gustaf
Blood, ISSN 0006-4971, 09/2007, Volume 110, Issue 6, pp. 1906 - 1915
Familial hemophagocytic lymphohistiocytosis (FHL) is typically an early onset, fatal disease characterized by a sepsislike illness with cytopenia,... 
NATURAL-KILLER-CELLS | GRANULE EXOCYTOSIS | IMMUNE-SYSTEM | MEDIATED CYTOTOXICITY | NK CELLS | DENDRITIC CELLS | FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS | CLASS-I | PERFORIN GENE-MUTATIONS | INHIBITORY RECEPTORS | HEMATOLOGY | Lymphohistiocytosis, Hemophagocytic - pathology | Pore Forming Cytotoxic Proteins - genetics | Cell Proliferation | Membrane Glycoproteins - metabolism | Homeodomain Proteins - metabolism | Humans | Child, Preschool | Infant | Male | Intracellular Signaling Peptides and Proteins - metabolism | Muscle Proteins - metabolism | Qa-SNARE Proteins - genetics | Adult | Female | Membrane Proteins - metabolism | Lymphohistiocytosis, Hemophagocytic - genetics | Perforin | Intracellular Signaling Peptides and Proteins - genetics | Lymphocytes - metabolism | Pore Forming Cytotoxic Proteins - metabolism | Cytokines - metabolism | LIM Domain Proteins | Membrane Proteins - genetics | Gene Expression Regulation | Lymphocytes - cytology | Transcription Factors - genetics | Mutation - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Homeodomain Proteins - genetics | Membrane Glycoproteins - genetics | Muscle Proteins - genetics | Transcription Factors - metabolism | Killer Cells, Natural - cytology | Lymphocyte Subsets | Lymphohistiocytosis, Hemophagocytic - metabolism | Qa-SNARE Proteins - metabolism | LIM-Homeodomain Proteins | Killer Cells, Natural - metabolism | Immunobiology
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4. Full Text The Patched dependence receptor triggers apoptosis through a DRAL-caspase-9 complex
by Mille, Frédéric and Thibert, Chantal and Fombonne, Joanna and Rama, Nicolas and Guix, Catherine and Hayashi, Hideki and Corset, Véronique and Reed, John C and Mehlen, Patrick
Nature Cell Biology, ISSN 1465-7392, 2009, Volume 11, Issue 6, pp. 739 - 746
Sonic hedgehog (Shh) and its main receptor, Patched (Ptc), are implicated in both neural development and tumorigenesis(1,2). Besides its classic morphogenic... 
PROTEIN | INHIBITION | GENE | MECHANISM | SONIC HEDGEHOG | NEURONAL DEATH | PRODUCT INDUCES APOPTOSIS | KAPPA-B | CASPASE ACTIVATION | CELL-DEATH | CELL BIOLOGY | RNA, Small Interfering - genetics | Caspase 9 - metabolism | Homeodomain Proteins - metabolism | Humans | Hedgehog Proteins - metabolism | Neoplasm Proteins - metabolism | CARD Signaling Adaptor Proteins - genetics | Multiprotein Complexes - metabolism | CARD Signaling Adaptor Proteins - metabolism | Hedgehog Proteins - genetics | Muscle Proteins - metabolism | Apoptosis Regulatory Proteins - genetics | Patched Receptors | Neoplasm Proteins - genetics | Cell Line | Receptors, Cell Surface - metabolism | Transcription Factors - genetics | Chick Embryo | Homeodomain Proteins - genetics | Apoptosis Regulatory Proteins - metabolism | Muscle Proteins - genetics | Transcription Factors - metabolism | Two-Hybrid System Techniques | Animals | Adaptor Proteins, Signal Transducing - genetics | LIM-Homeodomain Proteins | Signal Transduction - physiology | Apoptosis - physiology | Adaptor Proteins, Signal Transducing - metabolism | RNA, Small Interfering - metabolism | Receptors, Cell Surface - genetics | Causes of | Physiological aspects | Cell receptors | Research | Proteases | Apoptosis | Caspase 9 | Signal Transduction | Multiprotein Complexes | Receptors, Cell Surface | Cellular Biology | Hedgehog Proteins | Life Sciences | Muscle Proteins | Adaptor Proteins, Signal Transducing | Apoptosis Regulatory Proteins | Homeodomain Proteins | Neoplasm Proteins | CARD Signaling Adaptor Proteins | RNA, Small Interfering | Transcription Factors | Development Biology | physiology | genetics | metabolism
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5. Full Text Reduced UCP-1 content in in vitro differentiated beige/ brite adipocytes derived from preadipocytes of human subcutaneous white adipose tissues in obesity
by Carey, Andrew L and Vorlander, Camilla and Reddy-Luthmoodoo, Medini and Natoli, Alaina K and Formosa, Melissa F and Bertovic, David A and Anderson, Mitchell J and Duffy, Stephen J and Kingwell, Bronwyn A
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e91997
Introduction: Brown adipose tissue (BAT) is a potential therapeutic target to reverse obesity. The purpose of this study was to determine whether primary... 
THERMOGENESIS | ACTIVATION | MESSENGER-RNA | COLD-EXPOSURE | METABOLISM | MULTIDISCIPLINARY SCIENCES | INCREASES | ADULT HUMANS | ADIPOGENESIS | EXPRESSION | BROWN FAT | Adipocytes, Brown - metabolism | LIM-Homeodomain Proteins - metabolism | Homeodomain Proteins - metabolism | Humans | Ion Channels - genetics | Male | Mitochondrial Proteins - genetics | Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics | Fatty Acid-Binding Proteins - metabolism | PPAR gamma - metabolism | Obesity - genetics | Case-Control Studies | Subcutaneous Fat - metabolism | Mitochondrial Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Adult | Cell Differentiation | Nuclear Proteins - genetics | PPAR gamma - genetics | Biomarkers - metabolism | Adipocytes, Brown - pathology | Gene Expression | Retinoblastoma Protein - metabolism | Nuclear Proteins - metabolism | Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism | Transcription Factors - genetics | Fatty Acid-Binding Proteins - genetics | Subcutaneous Fat - pathology | Homeodomain Proteins - genetics | Obesity - metabolism | Obesity - pathology | Transcription Factors - metabolism | LIM-Homeodomain Proteins - genetics | Adipocytes, White - pathology | Ion Channels - metabolism | Retinoblastoma Protein - genetics | Primary Cell Culture | Uncoupling Protein 1 | Adipocytes, White - metabolism | Adipose tissues | Obesity | Gene expression | Health aspects | Genes | Heart | Adipose tissue | Laboratories | Adipocytes | Males | Tissues | Proteins | Uncoupling protein 1 | Rodents | Penicillin | Physiology | Cardiology | Adipose tissue (brown) | CD137 antigen | Markers | Preadipocytes | Cultures | Metabolism | Insulin | Lipolysis | Abdomen | Musculoskeletal system | Weight control | Thermogenesis | Cell lines | Stem cells | Diabetes | Peroxisome proliferator-activated receptors | Differentiation
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6. Full Text Specification of the vertebrate eye by a network of eye field transcription factors
by Michael E. Zuber and Gaia Gestri and Andrea S. Viczian and Giuseppina Barsacchi and William A. Harris
Development, ISSN 0950-1991, 11/2003, Volume 130, Issue 21, pp. 5155 - 5167
Several eye-field transcription factors (EFTFs) are expressed in the anterior region of the vertebrate neural plate and are essential for eye formation. The... 
Noggin | Optx2 | Xenopus laevis | Eye field specification | Pax6 | Rx1 | Lhx2 | Tll | Neural patterning | Six3 | Transcription factor cocktails | Ectopic eye formation | Otx2 | Genetic network | ANTERIOR NEUROECTODERM | ECTOPIC EYES | noggin | CELL-PROLIFERATION | DEVELOPMENTAL BIOLOGY | genetic network | neural patterning | eye field specification | ectopic eye formation | RETINAL DEVELOPMENT | transcription factor cocktails | BRAIN-DEVELOPMENT | XENOPUS HOMOLOG | T-BOX GENES | SINE OCULIS GENE | DROSOPHILA | ET | HOMEOBOX GENE | Drosophila melanogaster - embryology | Xenopus Proteins - genetics | Xenopus laevis - anatomy & histology | Homeodomain Proteins - metabolism | Humans | Otx Transcription Factors | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | DNA-Binding Proteins - metabolism | Morphogenesis | Eye - embryology | In Situ Hybridization | Gene Expression Regulation, Developmental | Body Patterning | Trans-Activators - genetics | Xenopus laevis - genetics | Eye Proteins - genetics | Drosophila melanogaster - anatomy & histology | Repressor Proteins - metabolism | Carrier Proteins | Eye - metabolism | Xenopus laevis - embryology | Paired Box Transcription Factors | Repressor Proteins - genetics | PAX6 Transcription Factor | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Animals | Proteins - metabolism | Eye Proteins - metabolism | Xenopus laevis - metabolism | LIM-Homeodomain Proteins | Trans-Activators - metabolism | Xenopus Proteins - metabolism | Drosophila Proteins - genetics
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7. Full Text Cooperative control of striated muscle mass and metabolism by MuRF1 and MuRF2
by Labeit, Dietmar and Labeit, Siegfried and Witt, Stephanie H and Witt, Christian C and Back, Walter and Lerche, Stefanie
The EMBO Journal, ISSN 0261-4189, 01/2008, Volume 27, Issue 2, pp. 350 - 360
The muscle‐specific RING finger proteins MuRF1 and MuRF2 have been proposed to regulate protein degradation and gene expression in muscle tissues. We have... 
muscle hypertrophy and atrophy | Z‐disks | ubiquitin ligases MuRF1 and MuRF2 | striated muscle | Muscle hypertrophy and atrophy | Striated muscle | Z-disks | Ubiquitin ligases MuRF1 and MuRF2 | PROTEIN | ATROPHY | TITIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE | UBIQUITIN-LIGASE | CELL BIOLOGY | SKELETAL-MUSCLE | HYPERTROPHY | IN-VIVO | FILAMENT | GENE-EXPRESSION | Sequestosome-1 Protein | Homeodomain Proteins - metabolism | Male | Muscle, Skeletal - metabolism | Gene Expression Profiling | Muscle, Skeletal - cytology | Ubiquitin-Protein Ligases - physiology | Tripartite Motif Proteins | Heat-Shock Proteins - genetics | Myocardium - metabolism | Muscle Proteins - metabolism | Muscle, Striated - ultrastructure | Female | Muscle Proteins - physiology | Muscle, Striated - cytology | Myocardium - ultrastructure | Carps - metabolism | Microscopy, Electron, Transmission | Muscular Diseases - metabolism | Heat-Shock Proteins - metabolism | Mice, Inbred C57BL | Muscle Cells - metabolism | Muscle, Skeletal - ultrastructure | Ubiquitin-Protein Ligases - metabolism | Muscular Diseases - pathology | Signal Transduction - genetics | Transcription Factors - genetics | Mice, Inbred Strains | Blotting, Western | Homeodomain Proteins - genetics | Mice, Knockout | Muscle Cells - cytology | Myocardium - cytology | Muscle Proteins - genetics | Transcription Factors - metabolism | Animals | Adaptor Proteins, Signal Transducing - genetics | Protein Binding | LIM-Homeodomain Proteins | Signal Transduction - physiology | Mice | Muscular Diseases - genetics | Adaptor Proteins, Signal Transducing - metabolism | Muscle, Striated - metabolism | Ubiquitin-Protein Ligases - genetics | Microscopy, Fluorescence | Proteins | Cellular biology | Rodents | Muscular system | Molecular biology | Gene expression | Metabolism
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8. Full Text A regulatory pathway involving Notch1/β-catenin/Isl1 determines cardiac progenitor cell fate
by Srivastava, Deepak and Cheng, Paul and Kwon, Chulan and Nigam, Vishal and Qian, Li and Arnold, Joshua
Nature Cell Biology, ISSN 1465-7392, 08/2009, Volume 11, Issue 8, pp. 951 - 957
Regulation of multipotent cardiac progenitor cell (CPC) expansion and subsequent differentiation into cardiomyocytes, smooth muscle or endothelial cells is a... 
MAMMALIAN HEART | MYOCARDIN | SMOOTH-MUSCLE | MULTIPOTENT | GENE NKX2-5 | EMBRYONIC STEM-CELLS | SERUM RESPONSE FACTOR | DIFFERENTIATION | BETA-CATENIN | EXPRESSION | CELL BIOLOGY | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Oligonucleotide Array Sequence Analysis | Homeodomain Proteins - metabolism | Male | Gene Expression Profiling | Stem Cells - cytology | Stem Cells - metabolism | Embryo, Mammalian - metabolism | DNA-Binding Proteins - metabolism | Flow Cytometry | In Situ Hybridization | Chromatin Immunoprecipitation | RNA Interference | Gene Expression Regulation, Developmental | Myocardium - metabolism | Muscle Proteins - metabolism | Trans-Activators - genetics | Female | Cell Differentiation | Nuclear Proteins - genetics | Cells, Cultured | Nuclear Proteins - metabolism | Receptor, Notch1 - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | beta Catenin - metabolism | Blotting, Western | Homeodomain Proteins - genetics | beta Catenin - genetics | Mice, Knockout | Myocardium - cytology | Muscle Proteins - genetics | Transcription Factors - metabolism | Animals | Embryo, Mammalian - embryology | Embryo, Mammalian - cytology | LIM-Homeodomain Proteins | Trans-Activators - metabolism | Mice | Receptor, Notch1 - genetics | Myocd | β-Catenin | Notch1 | Isl1 | cardiac progenitors
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9. Full Text Lhx6 Delineates a Pathway Mediating Innate Reproductive Behaviors from the Amygdala to the Hypothalamus
by Choi, Gloria B and Dong, Hong-wei and Murphy, Andrew J and Valenzuela, David M and Yancopoulos, George D and Swanson, Larry W and Anderson, David J
Neuron, ISSN 0896-6273, 2005, Volume 46, Issue 4, pp. 647 - 660
In mammals, innate reproductive and defensive behaviors are mediated by anatomically segregated connections between the amygdala and hypothalamus. This... 
SYRIAN-HAMSTER BRAIN | INHIBIT MATERNAL-BEHAVIOR | TRANSCRIPTIONAL CODES | SEX-DISCRIMINATION | POSTERIOR PARAVENTRICULAR THALAMUS | C-FOS | DIFFERENTIAL PROJECTIONS | CENTRAL-NERVOUS-SYSTEM | CEREBRAL HEMISPHERE REGULATION | NEUROSCIENCES | MOTOR-NEURON POOL | Aggression - physiology | Homeodomain Proteins - metabolism | Male | Neural Pathways - physiology | Odorants | Behavior, Animal | Sexual Behavior, Animal - physiology | Vesicular Glutamate Transport Protein 2 | Isoenzymes - metabolism | Conflict (Psychology) | Female | Membrane Transport Proteins - metabolism | In Situ Hybridization - methods | Neural Networks (Computer) | Urine | Green Fluorescent Proteins - metabolism | Nerve Tissue Proteins - physiology | Cholera Toxin - metabolism | Hypothalamus - physiology | Mice, Inbred C57BL | Stilbamidines - pharmacokinetics | Proto-Oncogene Proteins c-fos - metabolism | Amygdala - cytology | Mice, Transgenic | Nerve Tissue Proteins - genetics | Stimulation, Chemical | Homeodomain Proteins - genetics | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Proteins - genetics | Animals | Proteins - metabolism | Hypothalamus - cytology | Glutamate Decarboxylase - metabolism | LIM-Homeodomain Proteins | Proto-Oncogene Proteins c-fos - genetics | Mice | Transcription Factors | Homeodomain Proteins - physiology | Amygdala - physiology | Proteins | Neurons | Neurosciences | Brain | Animal reproduction | Transcription factors | Odors | Animal behavior | Rodents | Control theory | Hybridization | Gene expression | Aggressiveness
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10. Full Text LIM domain-binding 1 maintains the terminally differentiated state of pancreatic β cells
by Ediger, Benjamin N and Lim, Hee-Woong and Juliana, Christine and Groff, David N and Williams, LaQueena T and Dominguez, Giselle and Liu, Jin-Hua and Taylor, Brandon L and Walp, Erik R and Kameswaran, Vasumathi and Yang, Juxiang and Liu, Chengyang and Hunter, Chad S and Kaestner, Klaus H and Naji, Ali and Li, Changhong and Sander, Maike and Stein, Roland and Sussel, Lori and Won, Kyoung-Jae and May, Catherine Lee and Stoffers, Doris A
Journal of Clinical Investigation, ISSN 0021-9738, 01/2017, Volume 127, Issue 1, pp. 215 - 229
The recognition of beta cell dedifferentiation in type 2 diabetes raises the translational relevance of mechanisms that direct and maintain beta cell identity.... 
TRANSCRIPTION FACTORS | MEDICINE, RESEARCH & EXPERIMENTAL | ENDOCRINE PANCREAS | GLUCOSE-CONCENTRATIONS | STEM-CELLS | STRUCTURAL BASIS | INTERNEURON IDENTITY | INSULIN-SECRETION | HOMEODOMAIN PROTEINS | GENE-EXPRESSION | MOTOR-NEURON | Hepatocyte Nuclear Factor 3-beta - genetics | LIM-Homeodomain Proteins - metabolism | Diabetes Mellitus, Type 2 - genetics | Homeodomain Proteins - metabolism | Humans | Diabetes Mellitus, Type 2 - metabolism | LIM Domain Proteins - metabolism | DNA-Binding Proteins - metabolism | Insulin-Secreting Cells - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Trans-Activators - genetics | Cell Differentiation | Hepatocyte Nuclear Factor 3-beta - metabolism | Basic Helix-Loop-Helix Transcription Factors - genetics | Mice, Transgenic | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | LIM-Homeodomain Proteins - genetics | Animals | LIM Domain Proteins - genetics | Trans-Activators - metabolism | Mice | Diabetes Mellitus, Type 2 - pathology | Insulin-Secreting Cells - pathology
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11. Full Text Wnt/β-catenin and Bmp signals control distinct sets of transcription factors in cardiac progenitor cells
by Alexandra Klaus and Marion Müller and Herbert Schulz and Yumiko Saga and James F. Martin and Walter Birchmeier
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2012, Volume 109, Issue 27, pp. 10921 - 10926
Progenitor cells of the first and second heart fields depend on cardiac-specific transcription factors for their differentiation. Using conditional mutagenesis... 
Heart | Transcription factors | Genes | Stem cells | Cellular immunity | Embryonic stem cells | In situ hybridization | Progenitor cells | Embryos | Cellular differentiation | Mesoderm patterning | Progenitor differentiation in culture | MesP1-cre | Canonical Wnt | Cardiogenesis | HEART FIELD | cardiogenesis | MULTIDISCIPLINARY SCIENCES | MOUSE | progenitor differentiation in culture | mesoderm patterning | BETA-CATENIN | CULTURE | NEGATIVE FEEDBACK LOOP | STEM | MESODERM | canonical Wnt | DIFFERENTIATION | PROTEINS | EMBRYOS | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Axin Protein - genetics | LIM-Homeodomain Proteins - metabolism | Receptors, Notch - metabolism | Homeodomain Proteins - metabolism | Wnt Signaling Pathway - physiology | Male | Bone Morphogenetic Protein 4 - metabolism | Axin Protein - metabolism | Flow Cytometry | Mice, Mutant Strains | Muscle Proteins - metabolism | Female | Cell Differentiation - physiology | Immunoglobulin J Recombination Signal Sequence-Binding Protein - genetics | Immunoglobulin J Recombination Signal Sequence-Binding Protein - metabolism | GATA4 Transcription Factor - metabolism | Chromosomal Proteins, Non-Histone - metabolism | Myocytes, Cardiac - cytology | GATA4 Transcription Factor - genetics | Transcription Factors - genetics | beta Catenin - metabolism | Homeodomain Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | Muscle Proteins - genetics | Pregnancy | Transcription Factors - metabolism | Homeobox Protein Nkx-2.5 | LIM-Homeodomain Proteins - genetics | Animals | Mice | Lac Operon | Index Medicus | Biological Sciences
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12. Full Text Androgen receptor coactivators lysine-specific histone demethylase 1 and four and a half LIM domain protein 2 predict risk of prostate cancer recurrence