serine has been researched along with Cystic Fibrosis of Pancreas in 14 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (7.14) | 18.7374 |
| 1990's | 6 (42.86) | 18.2507 |
| 2000's | 3 (21.43) | 29.6817 |
| 2010's | 4 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rimessi, A | 1 |
| Bezzerri, V | 1 |
| Salvatori, F | 1 |
| Tamanini, A | 1 |
| Nigro, F | 1 |
| Dechecchi, MC | 1 |
| Santangelo, A | 1 |
| Prandini, P | 1 |
| Munari, S | 1 |
| Provezza, L | 1 |
| Garreau de Loubresse, N | 1 |
| Muller, J | 1 |
| Ribeiro, CMP | 1 |
| Lippi, G | 1 |
| Gambari, R | 1 |
| Pinton, P | 1 |
| Cabrini, G | 1 |
| Venerando, A | 1 |
| Cesaro, L | 1 |
| Marin, O | 1 |
| Donella-Deana, A | 1 |
| Pinna, LA | 1 |
| René, C | 1 |
| Paulet, D | 1 |
| Girodon, E | 1 |
| Costa, C | 1 |
| Lalau, G | 1 |
| Leclerc, J | 1 |
| Cabet-Bey, F | 1 |
| Bienvenu, T | 2 |
| Blayau, M | 1 |
| Iron, A | 1 |
| Mittre, H | 1 |
| Feldmann, D | 1 |
| Guittard, C | 1 |
| Claustres, M | 1 |
| Georges, Md | 1 |
| McClure, M | 1 |
| DeLucas, LJ | 1 |
| Wilson, L | 1 |
| Ray, M | 1 |
| Rowe, SM | 1 |
| Wu, X | 1 |
| Dai, Q | 1 |
| Hong, JS | 1 |
| Sorscher, EJ | 1 |
| Kappes, JC | 1 |
| Barnes, S | 1 |
| Erickson, DL | 1 |
| Lines, JL | 1 |
| Pesci, EC | 1 |
| Venturi, V | 1 |
| Storey, DG | 1 |
| Kraus, C | 1 |
| Reis, A | 1 |
| Naehrlich, L | 1 |
| Dötsch, J | 1 |
| Korbmacher, C | 1 |
| Rauh, R | 1 |
| Rich, DP | 1 |
| Berger, HA | 1 |
| Cheng, SH | 1 |
| Travis, SM | 1 |
| Saxena, M | 1 |
| Smith, AE | 1 |
| Welsh, MJ | 1 |
| Schaedel, C | 1 |
| Andersson, AM | 1 |
| Kristoffersson, AC | 1 |
| Kornfält, R | 1 |
| Lannefors, L | 1 |
| Holmberg, L | 1 |
| Pasyk, EA | 1 |
| Morin, XK | 1 |
| Zeman, P | 1 |
| Garami, E | 1 |
| Galley, K | 1 |
| Huan, LJ | 1 |
| Wang, Y | 1 |
| Bear, CE | 1 |
| Cartault, F | 1 |
| Steffann, J | 1 |
| Vidaud, D | 1 |
| Bousquet, S | 1 |
| Lesure, F | 1 |
| Renouil, M | 1 |
| McDonell, N | 1 |
| Feingold, J | 1 |
| Beldjord, C | 1 |
| Monaghan, KG | 1 |
| Feldman, GL | 1 |
| Barbarotto, GM | 1 |
| Manji, S | 1 |
| Desai, TK | 1 |
| Snow, K | 1 |
| Lissens, W | 1 |
| Bonduelle, M | 1 |
| Malfroot, A | 1 |
| Dab, I | 1 |
| Liebaers, I | 1 |
| Sangiuolo, F | 1 |
| Novelli, G | 1 |
| Murru, S | 1 |
| Dallapiccola, B | 1 |
| Roussel, P | 1 |
| Lamblin, G | 1 |
| Degand, P | 1 |
| Havez, R | 1 |
14 other studies available for serine and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
PLCB3 Loss of Function Reduces Pseudomonas aeruginosa-Dependent IL-8 Release in Cystic Fibrosis.
Topics: Bronchi; Calcium Signaling; Cell Line; Computer Simulation; Cystic Fibrosis; Humans; Interleukin-8; | 2018 |
A "SYDE" effect of hierarchical phosphorylation: possible relevance to the cystic fibrosis basic defect.
Topics: Amino Acid Sequence; Aspartic Acid; Casein Kinase II; Consensus Sequence; Cystic Fibrosis; Cystic Fi | 2014 |
p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study.
Topics: Amino Acid Sequence; Arginine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; | 2011 |
Purification of CFTR for mass spectrometry analysis: identification of palmitoylation and other post-translational modifications.
Topics: Amino Acid Sequence; Binding Sites; Blotting, Western; Chromatography, Liquid; Cystic Fibrosis; Cyst | 2012 |
Pseudomonas aeruginosa relA contributes to virulence in Drosophila melanogaster.
Topics: Amino Acids; Animals; Bacterial Proteins; Cystic Fibrosis; Drosophila melanogaster; Guanosine Pentap | 2004 |
Functional characterization of a novel CFTR mutation P67S identified in a patient with atypical cystic fibrosis.
Topics: Action Potentials; Adolescent; Amino Acid Substitution; Base Sequence; Cystic Fibrosis; Cystic Fibro | 2007 |
Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.
Topics: Alanine; Amino Acid Sequence; Animals; Autoradiography; Cell Line; Chloride Channels; Cystic Fibrosi | 1993 |
Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I.
Topics: Adolescent; Adult; Age of Onset; Alleles; Amino Acid Substitution; Child; Child, Preschool; Cystic F | 1998 |
A conserved region of the R domain of cystic fibrosis transmembrane conductance regulator is important in processing and function.
Topics: Amino Acid Sequence; Animals; ATP Binding Cassette Transporter, Subfamily B, Member 1; Cell Line; Ce | 1998 |
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)
Topics: Alanine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; France; Glycine; Huma | 1998 |
Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative study.
Topics: Adolescent; Adult; Aged; Amino Acid Substitution; Arginine; Child; Child, Preschool; Cystic Fibrosis | 2000 |
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis gene.
Topics: Adenosine Triphosphate; Base Sequence; Binding Sites; Cystic Fibrosis; Cystic Fibrosis Transmembrane | 1992 |
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis.
Topics: Arginine; Base Sequence; Codon; Cystic Fibrosis; DNA; Exons; Female; Humans; Male; Molecular Sequenc | 1991 |
[Isolation of bronchial mucins secreted in cystic fibrosis].
Topics: Animals; Bronchi; Child; Chromatography, Gel; Chromatography, Ion Exchange; Cystic Fibrosis; Electro | 1972 |