threonine and Cystic Fibrosis

threonine has been researched along with Cystic Fibrosis in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cao, A; Carta, D; Coiana, A; Faa', V; Puddu, R; Rosatelli, MC1
Amos, J; Grosso, LE; Hajianpour, A; Lyon, E; Millson, A; Schaefer, FV; Sebastian, S; Spitzer, SG; Stenzel, TT; Taylor, AK; Wolff, DJ1
Andersson, AM; Holmberg, L; Kornfält, R; Kristoffersson, AC; Lannefors, L; Schaedel, C1
Degand, P; Havez, R; Lamblin, G; Roussel, P1

Other Studies

4 other study(ies) available for threonine and Cystic Fibrosis

ArticleYear
Preconceptional identification of cystic fibrosis carriers in the Sardinian population: A pilot screening program.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2011, Volume: 10, Issue:3

    Topics: Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Gene Deletion; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Genetic Testing; Homozygote; Humans; Isoleucine; Italy; Male; Mutation; Phenylalanine; Pilot Projects; Threonine

2011
Multicenter characterization and validation of the intron-8 poly(T) tract (IVS8-T) status in 25 Coriell cell repository cystic fibrosis reference cell lines for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation assays.
    Clinical chemistry, 2004, Volume: 50, Issue:1

    Topics: Cell Line; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Humans; Introns; Mutation; Polymorphism, Genetic; Reference Standards; Threonine

2004
Mild cystic fibrosis mutations in Southern Sweden with special reference to S549I and T338I.
    Clinical genetics, 1998, Volume: 53, Issue:5

    Topics: Adolescent; Adult; Age of Onset; Alleles; Amino Acid Substitution; Child; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Female; Forced Expiratory Volume; Genotype; Humans; Infant; Isoleucine; Lung; Male; Mutation; Pancreas; Polymorphism, Genetic; Pseudomonas aeruginosa; Serine; Sweden; Threonine; Vital Capacity

1998
[Isolation of bronchial mucins secreted in cystic fibrosis].
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 36, Issue:2

    Topics: Animals; Bronchi; Child; Chromatography, Gel; Chromatography, Ion Exchange; Cystic Fibrosis; Electrophoresis; Fucose; Galactose; Hexosamines; Humans; Hydrogen-Ion Concentration; Immunoelectrophoresis; Mucins; Mucus; Neuraminic Acids; Rabbits; Serine; Sputum; Sulfuric Acids; Threonine

1972