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1. Full Text Risk of Pediatric Celiac Disease According to HLA Haplotype and Country
by Liu, Edwin and Lee, Hye-Seung and Aronsson, Carin A and Hagopian, William A and Koletzko, Sibylle and Rewers, Marian J and Eisenbarth, George S and Bingley, Polly J and Bonifacio, Ezio and Simell, Ville and Agardh, Daniel and TEDDY Study Grp and TEDDY Study Group
The New England journal of medicine, ISSN 0028-4793, 07/2014, Volume 371, Issue 1, pp. 42 - 49
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Biological and medical sciences | General aspects | Medical sciences | Other diseases. Semiology | Autoimmune Diseases - epidemiology | United States - epidemiology | Genetic Predisposition to Disease | Prospective Studies | Celiac Disease - genetics | Humans | Kaplan-Meier Estimate | Child, Preschool | Europe - epidemiology | Infant | Male | Risk | Transglutaminases - immunology | Autoimmune Diseases - genetics | Homozygote | HLA-DR4 Antigen - genetics | HLA-DR3 Antigen - genetics | HLA-DQ Antigens - genetics | Antibodies - blood | Female | Celiac Disease - epidemiology | Infant, Newborn | Haplotypes | Viral antibodies | Celiac disease | Histocompatibility antigens | Analysis | HLA histocompatibility antigens | Antibodies | Children | Health aspects | Risk factors | Diabetes mellitus | Heterozygotes | Environmental factors | Small intestine | Transglutaminase 2 | Children & youth | Homozygotes | Genotype & phenotype | Biopsy | Histocompatibility antigen HLA | Autoimmune diseases | Age | Genotypes | Immune system | Index Medicus | Abridged Index Medicus | Autoimmune Diseases: epidemiology | Celiac Disease: genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Europe: epidemiology | Antibodies: blood | HLA-DQ Antigens: genetics | HLA-DR3 Antigen: genetics | Klinisk medicin | Transglutaminases: immunology | United States: epidemiology | HLA-DR4 Antigen: genetics | Clinical Medicine | Endokrinologi och diabetes | Autoimmune Diseases: genetics | Celiac Disease: epidemiology | Endocrinology and Diabetes
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2. Full Text The development of a mRNA multiplex RT-PCR assay for the definitive identification of body fluids
by Fleming, Rachel I and Harbison, SallyAnn
Forensic science international : genetics, ISSN 1872-4973, 2009, Volume 4, Issue 4, pp. 244 - 256
Pathology | Forensic DNA | RT-PCR multiplex | mRNA profiling | Genetics & Heredity | Life Sciences & Biomedicine | Medicine, Legal | Legal Medicine | Science & Technology | Glucose-6-Phosphatase - genetics | Salivary Proteins and Peptides - genetics | RNA, Messenger - isolation & purification | DNA Fingerprinting | Humans | Cats - genetics | Transglutaminases - genetics | Male | Swine - genetics | Blood | Rabbits - genetics | Histatins - genetics | Chickens - genetics | Electrophoresis | Female | Transcriptional Elongation Factors - genetics | Dogs - genetics | Mice - genetics | Semen | RNA, Messenger - genetics | Glycophorin - genetics | Ubiquitin-Conjugating Enzymes - genetics | Reverse Transcriptase Polymerase Chain Reaction | DNA - genetics | DNA - isolation & purification | Animals | Matrix Metalloproteinase 11 - genetics | Protamines - genetics | Guinea Pigs - genetics | Saliva | Index Medicus
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3. Full Text Transcriptional control of transglutaminase 2 expression in mouse apoptotic thymocytes
by Sándor, Katalin and Daniel, Bence and Kiss, Bea and Kovács, Fruzsina and Szondy, Zsuzsa
Biochimica et biophysica acta. Gene regulatory mechanisms, ISSN 1874-9399, 08/2016, Volume 1859, Issue 8, pp. 964 - 974
ChIP-seq | T cells | Enhancer RNA | Transglutaminase 2 | Gene regulation | Apoptosis | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Thymocytes - metabolism | E1A-Associated p300 Protein - genetics | Transglutaminases - genetics | Apoptosis - genetics | E1A-Associated p300 Protein - metabolism | Phosphoproteins - metabolism | GTP-Binding Proteins - genetics | Receptors, Retinoic Acid - genetics | Smad4 Protein - genetics | Transcription, Genetic | Membrane Proteins - metabolism | Retinoid X Receptors - genetics | Retinoid X Receptors - metabolism | Repressor Proteins - metabolism | Tretinoin - pharmacology | Promoter Regions, Genetic | Signal Transduction | Membrane Proteins - genetics | Mice, Inbred C57BL | Gene Expression Regulation | Repressor Proteins - genetics | Receptors, Retinoic Acid - metabolism | Phosphoproteins - genetics | Smad4 Protein - metabolism | Cyclic AMP Response Element-Binding Protein - genetics | Transforming Growth Factor beta - pharmacology | Animals | Histones - genetics | Enhancer Elements, Genetic | CCCTC-Binding Factor | Transglutaminases - metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Thymocytes - cytology | Thymocytes - drug effects | Bucladesine - pharmacology | Mice | Histones - metabolism | Primary Cell Culture | GTP-Binding Proteins - metabolism | Analysis | Genomics | Bone morphogenetic proteins | Genetic aspects | Cyclic adenylic acid | Genetic transcription | Retinoids | Transforming growth factors | Protein binding
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4. Full Text RGD-independent cell adhesion via a tissue transglutaminase-fibronectin matrix promotes fibronectin fibril deposition and requires syndecan-4/2 and α5β1 integrin co-signaling
by Wang, Zhuo and Collighan, Russell J and Gross, Stephane R and Danen, Erik H. J and Orend, Gertraud and Telci, Dilek and Griffin, Martin
The Journal of biological chemistry, ISSN 0021-9258, 12/2010, Volume 285, Issue 51, pp. 40212 - 40229
RNA, Small Interfering - genetics | Integrin alpha5beta1 - genetics | Cricetulus | Protein Kinase C-alpha - metabolism | Humans | Protein Kinase C-alpha - genetics | Syndecan-4 - genetics | Actins - metabolism | Extracellular Matrix - metabolism | Transglutaminases - genetics | GTP-Binding Proteins - genetics | Heparitin Sulfate - metabolism | Actins - genetics | Extracellular Matrix - genetics | rho-Associated Kinases - metabolism | Mice, Mutant Strains | Syndecan-2 - genetics | CHO Cells | Syndecan-2 - metabolism | Cell Adhesion - genetics | Cricetinae | Syndecan-4 - metabolism | Cytoskeleton - genetics | rho-Associated Kinases - genetics | Cell Adhesion - drug effects | Fibronectins - metabolism | Animals | Signal Transduction - drug effects | Heparitin Sulfate - genetics | Transglutaminases - metabolism | Cytoskeleton - metabolism | Signal Transduction - physiology | Fibronectins - genetics | Mice | Oligopeptides - pharmacology | Integrin alpha5beta1 - metabolism | GTP-Binding Proteins - metabolism | Index Medicus | Fibronectin Deposition | Integrin | Extracellular Matrix | Signal Transduction | Cell Adhesion | Fibronectin | Syndecan | Cell Biology | Tissue Transglutaminase
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5. Full Text Defective CFTR induces aggresome formation and lung inflammation in cystic fibrosis through ROS-mediated autophagy inhibition
by Luciani, Alessandro and Villella, Valeria Rachela and Esposito, Speranza and Brunetti-Pierri, Nicola and Medina, Diego and Settembre, Carmine and Gavina, Manuela and Pulze, Laura and Giardino, Ida and Pettoello-Mantovani, Massimo and D'Apolito, Maria and Guido, Stefano and Masliah, Eliezer and Spencer, Brian and Quaratino, Sonia and Raia, Valeria and Ballabio, Andrea and Maiuri, Luigi
Nature cell biology, ISSN 1465-7392, 09/2010, Volume 12, Issue 9, pp. 863 - 875
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Reactive Oxygen Species - metabolism | Respiratory Mucosa - drug effects | Sequestosome-1 Protein | Humans | Transglutaminases - genetics | Autophagy - drug effects | Young Adult | Cystamine - therapeutic use | Inflammation - metabolism | Autophagy - genetics | Nasal Polyps - metabolism | Mice, Inbred CFTR | Respiratory Mucosa - cytology | Cystic Fibrosis - metabolism | Membrane Proteins - genetics | Mice, Transgenic | Protein Transport - genetics | Apoptosis Regulatory Proteins - metabolism | Reactive Oxygen Species - antagonists & inhibitors | Models, Biological | Cystic Fibrosis - genetics | Transglutaminases - metabolism | Adolescent | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Mice | GTP-Binding Proteins | Cystic Fibrosis - drug therapy | Protein Binding - physiology | Phosphoinositide-3 Kinase Inhibitors | Microtubule-Associated Proteins - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Salicylates - pharmacology | Epithelial Sodium Channels - genetics | Apoptosis Regulatory Proteins - genetics | Adult | Cystamine - pharmacology | Membrane Proteins - metabolism | Acetylcysteine - therapeutic use | Beclin-1 | Cystic Fibrosis Transmembrane Conductance Regulator - antagonists & inhibitors | Cell Line | Small Ubiquitin-Related Modifier Proteins - metabolism | Heat-Shock Proteins - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Antioxidants - pharmacology | Mice, Inbred Strains | Nasal Polyps - drug therapy | Antioxidants - therapeutic use | Animals | Acetylcysteine - pharmacology | Adaptor Proteins, Signal Transducing - genetics | Respiratory Mucosa - metabolism | Adaptor Proteins, Signal Transducing - metabolism | Organometallic Compounds - pharmacology | Complications and side effects | Active oxygen | Gene mutations | Lung diseases | Physiological aspects | Cystic fibrosis | Genetic aspects | Research | Health aspects | Risk factors | Index Medicus
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6. Full Text Coeliac disease and autoimmune disease-genetic overlap and screening
by Lundin, Knut E. A and Wijmenga, Cisca
Nature reviews. Gastroenterology & hepatology, ISSN 1759-5045, 09/2015, Volume 12, Issue 9, pp. 507 - 515
GLUTEN-FREE DIET | GLYCEMIC CONTROL | TYPE-1 DIABETES-MELLITUS | GENERAL-POPULATION COHORT | DERMATITIS-HERPETIFORMIS | ANTITISSUE TRANSGLUTAMINASE | LIVER-DISEASE | METABOLIC-CONTROL | TISSUE TRANSGLUTAMINASE | GENOME-WIDE ASSOCIATION | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Genetic Testing | Celiac Disease - genetics | Celiac Disease - immunology | Humans | Autoimmune Diseases - complications | Celiac Disease - therapy | Celiac Disease - diagnosis | Celiac disease | Care and treatment | Usage | Gluten-free diet | Diagnosis | Research | Health aspects | Genetic screening | Index Medicus
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7. Full Text Mutant huntingtin causes defective actin remodeling during stress: Defining a new role for transglutaminase 2 in neurodegenerative disease
by Munsie, Lise and Caron, Nicholas and Atwal, Randy Singh and Marsden, Ian and Wild, Edward J and Bamburg, James R and Tabrizi, Sarah J and Truant, Ray
Human molecular genetics, ISSN 0964-6906, 05/2011, Volume 20, Issue 10, pp. 1937 - 1951
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | NIH 3T3 Cells | RNA, Small Interfering - genetics | Gene Expression - genetics | Humans | Actins - metabolism | Transglutaminases - genetics | GTP-Binding Proteins - genetics | Actin Depolymerizing Factors - metabolism | Cytoskeletal Proteins - metabolism | Nuclear Proteins - genetics | Huntington Disease - enzymology | Lymphocytes - metabolism | Cell Line | Nuclear Proteins - metabolism | Hot Temperature | Mutation - genetics | Nerve Tissue Proteins - genetics | Heat-Shock Response - genetics | Protein Transport | Nerve Tissue Proteins - metabolism | Huntingtin Protein | Animals | Models, Biological | Intracellular Space - metabolism | Transglutaminases - metabolism | Huntington Disease - genetics | Protein Binding | Mice | GTP-Binding Proteins - metabolism | RNA, Small Interfering - metabolism | Index Medicus | Huntingtin | Neurodegenerative diseases | Transcription | Hyperactivity | Fluorescence | Data processing | Rods | Huntington's disease | Transglutaminase 2 | Stress | Western blotting | Computed tomography | Actin | Lymphocytes | Cofilin | Alzheimer's disease | Endoplasmic reticulum | IT15 gene
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8. Full Text Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
by Fogel, Brent L and Lee, Ji Yong and Lane, Jessica and Wahnich, Amanda and Chan, Sandy and Huang, Alden and Osborn, Greg E and Klein, Eric and Mamah, Catherine and Perlman, Susan and Geschwind, Daniel H and Coppola, Giovanni
Movement disorders, ISSN 0885-3185, 03/2012, Volume 27, Issue 3, pp. 442 - 446
dominant genetic conditions | recessive genetic conditions | cerebellar ataxia | copy number variation | spinocerebellar ataxia | Recessive genetic conditions | Dominant genetic conditions | Copy number variation | Cerebellar ataxia | Spinocerebellar ataxia | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Genetic Predisposition to Disease - genetics | Genetic Testing | Protein Precursors - genetics | Lamin Type B - genetics | Humans | Middle Aged | Transglutaminases - genetics | Male | Mutation - genetics | Nerve Tissue Proteins - genetics | Enkephalins - genetics | Heat-Shock Proteins - genetics | Magnetic Resonance Imaging | Phenotype | Cerebellar Ataxia - genetics | Databases, Bibliographic - statistics & numerical data | Adult | Female | RNA Helicases - genetics | Aged | Nuclear Proteins - genetics | Index Medicus | Spinocerebellar Ataxia | Dominant Genetic Conditions | Recessive Genetic Conditions | Cerebellar Ataxia | Copy Number Variation
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