Compounds > isoleucine

isoleucine and Cystic Fibrosis

isoleucine has been researched along with Cystic Fibrosis in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baskin, B; Bear, CE; Gonska, T; Huan, LJ; Janahi, IA; Molinski, SV; Ray, PN1
Cao, A; Carta, D; Coiana, A; Faa', V; Puddu, R; Rosatelli, MC1
Akcakaya, N; Apak, M; Camcioglu, Y; Cokugras, H; Gokgoz, N; Kayserili, H; Kirdar, B; Onay, T; Topaloglu, O; Tsui, LC; Zielenski, J1
Andersson, AM; Holmberg, L; Kornfält, R; Kristoffersson, AC; Lannefors, L; Schaedel, C1
Carey, WF; Morris, CP; Nelson, PV1

Other Studies

5 other study(ies) available for isoleucine and Cystic Fibrosis

ArticleYear
Genetic, cell biological, and clinical interrogation of the CFTR mutation c.3700 A>G (p.Ile1234Val) informs strategies for future medical intervention.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2014, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Aminopyridines; Animals; Benzodioxoles; Cell Line; Cricetinae; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exons; HEK293 Cells; Homozygote; Humans; Isoleucine; Male; Mutation, Missense; Qatar; RNA Splicing; Valine

2014
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
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I).
    Human genetics, 1998, Volume: 102, Issue:2

    Topics: Adenine; Amino Acid Substitution; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Cytosine; Frameshift Mutation; Humans; Isoleucine; Leucine; Methionine; Mutation; Polymorphism, Genetic; Proline; Sequence Deletion; Turkey

1998
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
Identification of a cystic fibrosis mutation: deletion of isoleucine506.
    Human genetics, 1991, Volume: 86, Issue:4

    Topics: Amino Acid Sequence; Base Sequence; Child; Chromosome Deletion; Cystic Fibrosis; Humans; Isoleucine; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Polymerase Chain Reaction

1991