Compounds > glutamic acid

glutamic acid and Cystic Fibrosis of Pancreas

glutamic acid has been researched along with Cystic Fibrosis of Pancreas in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's3 (33.33)29.6817
2010's5 (55.56)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cardona, ST; Kumar, B; Sorensen, JL1
Elbadawi-Sidhu, M; Fiehn, O; Gallagher, T; Gao, B; Lai, Z; Whiteson, KL; Zhang, Y1
Cesaro, L; Donella-Deana, A; Marin, O; Pinna, LA; Venerando, A1
Karamyshev, AL; Millen, L; Patrick, AE; Thomas, PJ1
Barbakadze, T; Dabrundashvili, N; Koriauli, S; Kvaratskhelia, E; Maisuradze, E; Mikeladze, DG; Natsvlishvili, N; Shanshiashvili, LV; Topuria, T; Zhuravliova, E1
Wine, JJ1
Castellani, C; Cuppens, H; De Boeck, K; Decaestecker, E; Decaestecker, K; Jaspers, M1
Casals, T; Chillón, M; Dörk, T; Estivill, X; Nunes, V; Tümmler, B1
Ambrosioni, A; Bassotti, A; Corbetta, C; Fiori, S; Giunta, A; Padoan, R; Prandoni, S; Rajnoldi, AC; Seia, M1

Other Studies

9 other study(ies) available for glutamic acid and Cystic Fibrosis of Pancreas

ArticleYear
A c-di-GMP-Modulating Protein Regulates Swimming Motility of
    Frontiers in cellular and infection microbiology, 2018, Volume: 8

    Topics: Amino Acid Sequence; Amino Acids; Arginine; Bacterial Proteins; Biofilms; Burkholderia cenocepacia; Burkholderia Infections; Cloning, Molecular; Cyclic GMP; Cystic Fibrosis; Escherichia coli Proteins; Flagellin; Gene Expression Regulation, Bacterial; Glutamic Acid; Locomotion; Lung; Mutagenesis, Insertional; Peptide Hydrolases; Phosphoric Diester Hydrolases; Phosphorus-Oxygen Lyases; Sequence Alignment; Sputum

2018
Tracking Polymicrobial Metabolism in Cystic Fibrosis Airways:
    mSphere, 2018, 04-25, Volume: 3, Issue:2

    Topics: Acetates; Carbon Radioisotopes; Coinfection; Culture Media; Cystic Fibrosis; Glutamic Acid; Humans; Lactic Acid; Metabolomics; Microbial Interactions; Micrococcaceae; Pseudomonas aeruginosa; Respiratory System

2018
A "SYDE" effect of hierarchical phosphorylation: possible relevance to the cystic fibrosis basic defect.
    Cellular and molecular life sciences : CMLS, 2014, Volume: 71, Issue:12

    Topics: Amino Acid Sequence; Aspartic Acid; Casein Kinase II; Consensus Sequence; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dictyostelium; Glutamic Acid; Humans; Molecular Sequence Data; Phosphorylation; Protein Interaction Domains and Motifs; Serine; Tyrosine

2014
Alteration of CFTR transmembrane span integration by disease-causing mutations.
    Molecular biology of the cell, 2011, Volume: 22, Issue:23

    Topics: Cell Membrane; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Endoplasmic Reticulum; Glutamic Acid; Glycine; Glycosylation; Humans; Mutation; Protein Folding; Protein Structure, Tertiary; Protein Transport; Temperature

2011
mGluR1 interacts with cystic fibrosis transmembrane conductance regulator and modulates the secretion of IL-10 in cystic fibrosis peripheral lymphocytes.
    Molecular immunology, 2012, Volume: 51, Issue:3-4

    Topics: Adolescent; Cell Membrane; Child; Child, Preschool; Chloride Channels; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Down-Regulation; Female; Glutamic Acid; Humans; Interleukin-10; Interleukin-8; Ligands; Lymphocytes; Male; Mutation; Phosphoproteins; Receptors, Metabotropic Glutamate; Sodium-Hydrogen Exchangers; T-Lymphocytes

2012
Rules of conduct for the cystic fibrosis anion channel.
    Nature medicine, 2003, Volume: 9, Issue:7

    Topics: Adenosine Triphosphate; Bicarbonates; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Glutamic Acid; Humans; Hydrolysis; Ion Channel Gating; Ion Transport; Substrate Specificity

2003
Genotype/phenotype correlation of the G85E mutation in a large cohort of cystic fibrosis patients.
    The European respiratory journal, 2004, Volume: 23, Issue:5

    Topics: Adolescent; Adult; Animals; Child; Child, Preschool; Chlorocebus aethiops; Cohort Studies; COS Cells; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pancreatic Insufficiency; Gene Deletion; Genotype; Glutamic Acid; Glycine; Heterozygote; Homozygote; Humans; Incidence; Mutation; Pancreas; Phenotype; Siblings

2004
A new missense mutation (E92K) in the first transmembrane domain of the CFTR gene causes a benign cystic fibrosis phenotype.
    Human molecular genetics, 1993, Volume: 2, Issue:1

    Topics: Base Sequence; Child; Codon; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exons; Genotype; Glutamates; Glutamic Acid; Humans; Lysine; Male; Membrane Proteins; Molecular Sequence Data; Oligodeoxyribonucleotides; Phenotype; Point Mutation; Polymerase Chain Reaction

1993
A novel missense mutation (D110E) in exon 4 of CFTR (ABCC7) in a CF infant presenting with hypochloraemic metabolic alkalosis.
    Human mutation, 2000, Volume: 15, Issue:5

    Topics: Alkalosis; Amino Acid Substitution; Aspartic Acid; Child, Preschool; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Glutamic Acid; Humans; Infant; Infant, Newborn; Male; Mutation, Missense

2000