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1. Full Text Aldehyde dehydrogenase (ALDH) superfamily in plants: gene nomenclature and comparative genomics
by Chad Brocker and Melpomene Vasiliou and Sarah Carpenter and Christopher Carpenter and Yucheng Zhang and Xiping Wang and Simeon O. Kotchoni and Andrew J. Wood and Hans-Hubert Kirch and David Kopečný and Daniel W. Nebert and Vasilis Vasiliou
Planta, ISSN 0032-0935, 1/2013, Volume 237, Issue 1, pp. 189 - 210
Enzymes | Dehydrogenases | Terminology | Algae | Evolution | Genomes | Plants | Aldehydes | Family members | Rice | Life Sciences | ALDH | Nomenclature | Forestry | Agriculture | Ecology | Gene family | Stress response | Plant Sciences | Aldehyde dehydrogenase | Life Sciences & Biomedicine | Science & Technology | Sorghum - enzymology | Multigene Family | Arabidopsis - enzymology | Volvox - genetics | Zea mays - enzymology | Populus - genetics | Aldehydes - metabolism | Vitis - enzymology | Plants - enzymology | Bryopsida - genetics | Populus - enzymology | Chlamydomonas reinhardtii - genetics | Oryza - genetics | Plants - genetics | Plant Proteins - metabolism | Sorghum - genetics | Genomics - methods | Aldehyde Dehydrogenase - metabolism | Vitis - genetics | Zea mays - genetics | Genome, Plant - genetics | Volvox - enzymology | Terminology as Topic | Aldehyde Dehydrogenase - genetics | Chromosome Mapping | Plants - classification | Oryza - enzymology | Selaginellaceae - genetics | Arabidopsis - genetics | Plant Proteins - genetics | Animals | Chlamydomonas reinhardtii - enzymology | Bryopsida - enzymology | Chromosomes, Plant - genetics | Selaginellaceae - enzymology | Evolution, Molecular | Genes | Genomics | Plant genetics | Environmental health | Organic acids | Arabidopsis thaliana | Plant physiology | Physiological aspects | Genetic research | Universities and colleges | Comparative analysis | Index Medicus
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2. Full Text Tracking replication enzymology in vivo by genome-wide mapping of ribonucleotide incorporation
by Clausen, Anders R and Lujan, Scott A and Burkholder, Adam B and Orebaugh, Clinton D and Williams, Jessica S and Clausen, Maryam F and Malc, Ewa P and Mieczkowski, Piotr A and Fargo, David C and Smith, Duncan J and Kunkel, Thomas A
Nature structural & molecular biology, ISSN 1545-9993, 03/2015, Volume 22, Issue 3, pp. 185 - 191
Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Ribonucleotides - chemistry | Saccharomyces cerevisiae - genetics | Chromosome Mapping | Ribonucleotides - physiology | Fungal Proteins - physiology | DNA Replication - physiology | Replication Origin | DNA-Directed DNA Polymerase - physiology | High-Throughput Nucleotide Sequencing | DNA-Directed DNA Polymerase - metabolism | Sequence Analysis | DNA, Mitochondrial - chemistry | Fungal Proteins - metabolism | DNA polymerases | Physiological aspects | Ribonucleotides | Research | Structure | DNA polymerase | Enzymes | Genomes | Index Medicus | mitochondrial replication | ribonucleotide incorporation | biomarkers | replication origins | polymerase switching
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3. Full Text Telomerase mutations in smokers with severe emphysema
by Stanley, Susan E and Chen, Julian J. L and Podlevsky, Joshua D and Alder, Jonathan K and Hansel, Nadia N and Mathias, Rasika A and Qi, Xiaodong and Rafaels, Nicholas M and Wise, Robert A and Silverman, Edwin K and Barnes, Kathleen C and Armanios, Mary
The Journal of clinical investigation, ISSN 0021-9738, 02/2015, Volume 125, Issue 2, pp. 563 - 570
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Chromosome Disorders - epidemiology | Prevalence | Pneumothorax - enzymology | Humans | Middle Aged | Male | Pulmonary Fibrosis - genetics | Pulmonary Fibrosis - epidemiology | Incidence | Telomerase - genetics | Chromosome Disorders - enzymology | Pulmonary Emphysema - genetics | Adult | Female | Registries | Telomerase - metabolism | Telomere - genetics | Chromosome Disorders - pathology | alpha 1-Antitrypsin - genetics | Pneumothorax - epidemiology | Pulmonary Emphysema - pathology | Smoking - genetics | Pulmonary Fibrosis - pathology | Sex Characteristics | Smoking - metabolism | Pneumothorax - pathology | Telomere - pathology | Animals | Smoking - epidemiology | Pulmonary Fibrosis - enzymology | Telomere - enzymology | Sex Factors | Smoking - pathology | Mice | Pneumothorax - genetics | alpha 1-Antitrypsin - metabolism | Mutation | Pulmonary Emphysema - epidemiology | Chromosome Disorders - genetics | Pulmonary Emphysema - enzymology | Smokers | Gene mutations | Emphysema, Pulmonary | Genetic aspects | Telomerase | Identification and classification | Health aspects | Risk factors | Enzymes | Liver diseases | Pulmonary fibrosis | Cloning | Cell division | Chronic obstructive pulmonary disease | Emphysema | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
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4. Full Text Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness
by Klion, Amy D and Noel, Pierre and Akin, Cem and Law, Melissa A and Gilliland, D. Gary and Cools, Jan and Metcalfe, Dean D and Nutman, Thomas B
Blood, ISSN 0006-4971, 06/2003, Volume 101, Issue 12, pp. 4660 - 4666
Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | Medical sciences | Hypereosinophilic Syndrome - drug therapy | Endomyocardial Fibrosis - enzymology | Myeloproliferative Disorders - enzymology | Prognosis | Tryptases | Humans | Middle Aged | mRNA Cleavage and Polyadenylation Factors - chemistry | Molecular Sequence Data | Male | Oncogene Proteins, Fusion | Base Sequence | Gene Deletion | Adult | Female | Endomyocardial Fibrosis - pathology | Eosinophils - pathology | Hypereosinophilic Syndrome - pathology | mRNA Cleavage and Polyadenylation Factors - genetics | Lung Diseases - enzymology | Amino Acid Sequence | Receptor, Platelet-Derived Growth Factor alpha - chemistry | Piperazines - therapeutic use | Vitamin B 12 - blood | Hypereosinophilic Syndrome - enzymology | Reverse Transcriptase Polymerase Chain Reaction | Imatinib Mesylate | Chromosomes, Human, Pair 4 | Biopsy | Pyrimidines - therapeutic use | Receptor, Platelet-Derived Growth Factor alpha - genetics | Bone Marrow - pathology | Mast Cells - pathology | Serine Endopeptidases - blood | Adolescent | Fibrosis | Splenomegaly - enzymology | Leukocytes, Mononuclear - enzymology | Aged | Mastocytosis - enzymology | Benzamides | RNA - blood | Index Medicus | Abridged Index Medicus
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5. Full Text rRNA Pseudouridylation Defects Affect Ribosomal Ligand Binding and Translational Fidelity from Yeast to Human Cells
by Jack, Karen and Bellodi, Cristian and Landry, Dori M and Niederer, Rachel O and Meskauskas, Arturas and Musalgaonkar, Sharmishtha and Kopmar, Noam and Krasnykh, Olya and Dean, Alison M and Thompson, Sunnie R and Ruggero, Davide and Dinman, Jonathan D
Molecular cell, ISSN 1097-2765, 11/2011, Volume 44, Issue 4, pp. 660 - 666
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Protein Biosynthesis | Hydro-Lyases - deficiency | Microcephaly - genetics | Microtubule-Associated Proteins - genetics | Saccharomyces cerevisiae - genetics | Humans | Ribonucleoproteins, Small Nuclear - genetics | Ribosomes - metabolism | Fetal Growth Retardation - genetics | Microcephaly - enzymology | Dyskeratosis Congenita - genetics | RNA, Ribosomal - genetics | Intellectual Disability - genetics | Nuclear Proteins - deficiency | Cell Cycle Proteins - genetics | Intellectual Disability - enzymology | RNA, Transfer - genetics | Hydro-Lyases - metabolism | Hydro-Lyases - genetics | Microtubule-Associated Proteins - deficiency | Nuclear Proteins - genetics | RNA, Transfer - chemistry | Binding Sites | Fetal Growth Retardation - enzymology | Genes, Reporter | Transduction, Genetic | Luciferases - analysis | RNA, Transfer - metabolism | RNA, Ribosomal - chemistry | Ribosomes - chemistry | RNA, Ribosomal - metabolism | Ribonucleoproteins, Small Nuclear - deficiency | Cell Cycle Proteins - deficiency | Saccharomyces cerevisiae Proteins - genetics | Dyskeratosis Congenita - enzymology | Sequence Homology, Amino Acid | Animals | Plasmids | Saccharomyces cerevisiae - enzymology | Mice | Mutation | Cricket | Chemical properties | Paralysis | Molecular genetics | Cells | Transfer RNA | Index Medicus | Dyskeratosis | Fidelity | RNA modification | Internal ribosome entry site | Translation | tRNA | rRNA | Ribosomes | X chromosome | pseudouridylation | Evolution
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6. Full Text OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome
by Uddin, Mohammed and Unda, Brianna K and Kwan, Vickie and Holzapfel, Nicholas T and White, Sean H and Chalil, Leon and Woodbury-Smith, Marc and Ho, Karen S and Harward, Erin and Murtaza, Nadeem and Dave, Biren and Pellecchia, Giovanna and D’Abate, Lia and Nalpathamkalam, Thomas and Lamoureux, Sylvia and Wei, John and Speevak, Marsha and Stavropoulos, James and Hope, Kristin J and Doble, Brad W and Nielsen, Jacob and Wassman, E. Robert and Scherer, Stephen W and Singh, Karun K
American journal of human genetics, ISSN 0002-9297, 02/2018, Volume 102, Issue 2, pp. 278 - 295
15q13.3 microdeletion syndrome | neurodevelopmental disorder | copy-number variation | OTUD7A | dendrite | dendritic spine | synapse | schizophrenia | autism spectrum disorder | deubiquitinase | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Chromosome Deletion | Autism Spectrum Disorder - genetics | Endopeptidases - metabolism | Seizures - enzymology | Seizures - genetics | Genetic Association Studies | Humans | Male | Dendritic Spines - metabolism | Neurodevelopmental Disorders - genetics | Chromosomes, Human, Pair 15 - genetics | Intellectual Disability - genetics | Phenotype | Animals | Endopeptidases - genetics | Chromosome Disorders - enzymology | Gene Deletion | Intellectual Disability - enzymology | Female | Mice | Chromosomes, Human, Pair 15 - enzymology | Chromosome Disorders - genetics | Neurodevelopmental Disorders - enzymology | Prosencephalon - pathology | Usage | Copy number variations | Pervasive developmental disorders | Nucleotide sequencing | Research | Gene expression | Health aspects | Risk factors | DNA sequencing | Index Medicus
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7. Full Text PKM2 Regulates Chromosome Segregation and Mitosis Progression of Tumor Cells
by Jiang, Yuhui and Li, Xinjian and Yang, Weiwei and Hawke, David H and Zheng, Yanhua and Xia, Yan and Aldape, Kenneth and Wei, Chongyang and Guo, Fang and Chen, Yan and Lu, Zhimin
Molecular cell, ISSN 1097-2765, 01/2014, Volume 53, Issue 1, pp. 75 - 87
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Glioblastoma - enzymology | Mitosis | Humans | Neoplasm Proteins - metabolism | Poly-ADP-Ribose Binding Proteins | Glioblastoma - genetics | Spindle Apparatus - genetics | Cell Cycle Proteins - genetics | Membrane Proteins - metabolism | Neoplasm Proteins - genetics | Kinetochores - enzymology | Brain Neoplasms - enzymology | Chromosome Segregation | Membrane Proteins - genetics | Chromosomes, Human - genetics | Cell Cycle Proteins - metabolism | Brain Neoplasms - genetics | Chromosomes, Human - metabolism | Thyroid Hormones - genetics | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Mice, Nude | Thyroid Hormones - metabolism | Mice | HeLa Cells | Spindle Apparatus - enzymology | Genetic research | Glucose metabolism | Epidermal growth factor | Genetic transcription | Gliomas | Protein binding | Brain tumors | Chromosomes | Protein kinases | Index Medicus | spindle-assembly checkpoint | PKM2 | kinetochore | Bub3 | tumorigenesis | phosphorylation | EGFR
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8. Full Text Human Hypertension Caused by Mutations in WNK Kinases
by Frederick H. Wilson and Sandra Disse-Nicodème and Keith A. Choate and Kazuhiko Ishikawa and Carol Nelson-Williams and Isabelle Desitter and Murat Gunel and David V. Milford and Graham W. Lipkin and Jean-Michel Achard and Morgan P. Feely and Bertrand Dussol and Yvon Berland and Robert J. Unwin and Haim Mayan and David B. Simon and Zvi Farfel and Xavier Jeunemaitre and Richard P. Lifton
Science (American Association for the Advancement of Science), ISSN 0036-8075, 8/2001, Volume 293, Issue 5532, pp. 1107 - 1112
Hypertension | Polymerase chain reaction | Kidneys | Exons | Genomics | DNA | Genetic loci | Amino acids | Genetic mutation | Chromosomes | Research Article | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cardiology. Vascular system | Biological and medical sciences | Arterial hypertension. Arterial hypotension | Medical sciences | Clinical manifestations. Epidemiology. Investigative techniques. Etiology | Blood and lymphatic vessels | Sequence Deletion | Kidney Tubules, Distal - enzymology | Intercellular Junctions - enzymology | Minor Histocompatibility Antigens | Humans | Pseudohypoaldosteronism - physiopathology | Molecular Sequence Data | Male | Mutation, Missense | Phosphoproteins - metabolism | Chromosomes, Human, Pair 17 - genetics | WNK Lysine-Deficient Protein Kinase 1 | Kidney Tubules, Distal - ultrastructure | Base Sequence | Female | Kidney Tubules, Collecting - enzymology | Membrane Proteins - metabolism | Hypertension - enzymology | Hypertension - genetics | Chromosomes, Human, Pair 12 - genetics | Protein-Serine-Threonine Kinases - metabolism | Genetic Linkage | Amino Acid Sequence | Cytoplasm - enzymology | Kidney Tubules, Collecting - ultrastructure | Signal Transduction | Introns | Pseudohypoaldosteronism - genetics | Protein-Serine-Threonine Kinases - genetics | Intracellular Signaling Peptides and Proteins | Chromosome Mapping | Hypertension - physiopathology | Gene Expression Regulation, Enzymologic | Pseudohypoaldosteronism - enzymology | Zonula Occludens-1 Protein | Pedigree | Protein-Serine-Threonine Kinases - chemistry | Mutation | Microscopy, Fluorescence | Protein kinases | Genetic aspects | Proteins | Genes | WNK4 gene | WNK1 gene | pseudohypoaldosteronism (type II) | Index Medicus
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