serine has been researched along with Cystic Fibrosis 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.
Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
| 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
| 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 |