Compounds > glutamine

glutamine and ADPKD

glutamine has been researched along with ADPKD in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Diggs, L; Hatzivassiliou, G; Kimmelman, AC; Li, Z; Parker, SJ; Rais, R; Skolnik, EY; Slusher, BS; Somlo, S; Soomro, I; Sun, Y; Thomas, AG1
Lamnissou, K; Stefanakis, N; Trygonis, S; Ziroyiannis, P1
Badenas, C; Darnell, A; Estivill, X; Gamble, V; Harris, PC; Peral, B; Serra, E; Torra, R; Turco, AE1
Carre, A; Cledes, J; Ferec, C; Mercier, B; Perrichot, R1
Bogdanova, N; Dimitrakov, D; Dworniczak, B; Horst, J; Kalaydjieva, L; Markoff, A; McCluskey, M; Schiavello, T; Sikmann, K; Thomas, M; Todorov, V1
Angelicheva, D; Bogdanova, N; Dworniczak, B; Hantke, J; Horst, J; Hunter, M; Kalaydjieva, L; Markoff, A; McCluskey, M; Schiavello, T; Thomas, M1

Other Studies

6 other study(ies) available for glutamine and ADPKD

ArticleYear
Glutamine metabolism via glutaminase 1 in autosomal-dominant polycystic kidney disease.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2018, 08-01, Volume: 33, Issue:8

    Topics: Animals; Aquaporin 2; Benzeneacetamides; Cell Proliferation; Cells, Cultured; Female; Glutaminase; Glutamine; Humans; Male; Mice; Mice, Knockout; Polycystic Kidney, Autosomal Dominant; Receptors, Cell Surface; Signal Transduction; Thiadiazoles

2018
Modifier effect of the Glu298Asp polymorphism of endothelial nitric oxide synthase gene in autosomal-dominant polycystic kidney disease.
    Nephron. Clinical practice, 2008, Volume: 110, Issue:2

    Topics: Adult; Effect Modifier, Epidemiologic; Female; Genetic Predisposition to Disease; Glutamine; Greece; Humans; Incidence; Male; Middle Aged; Nitric Oxide Synthase Type III; Polycystic Kidney, Autosomal Dominant; Polymorphism, Single Nucleotide

2008
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families.
    Human mutation, 1998, Volume: Suppl 1

    Topics: Adolescent; Adult; Codon, Terminator; Deoxyribonucleases, Type II Site-Specific; DNA; DNA Mutational Analysis; England; Family Health; Glutamine; Humans; Italy; Male; Middle Aged; Mutation; Point Mutation; Polycystic Kidney, Autosomal Dominant; Proteins; Spain; TRPP Cation Channels

1998
Identification of 3 novel mutations (Y4236X, Q3820X, 11745+2 ins3) in autosomal dominant polycystic kidney disease 1 gene (PKD1).
    Human mutation, 2000, Volume: 15, Issue:6

    Topics: Chromosomes, Human, Pair 16; Germ-Line Mutation; Glutamine; Humans; Mutagenesis, Insertional; Polycystic Kidney, Autosomal Dominant; Proteins; TRPP Cation Channels; Tyrosine

2000
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations.
    Human mutation, 2000, Volume: 16, Issue:2

    Topics: 3' Untranslated Regions; Adult; Aged; Alternative Splicing; Amino Acid Sequence; Amino Acid Substitution; Australia; Bulgaria; Codon, Terminator; Female; Genetic Testing; Glutamine; Humans; Male; Middle Aged; Molecular Sequence Data; Mutagenesis, Insertional; Mutation; Point Mutation; Polycystic Kidney, Autosomal Dominant; Prevalence; Proteins; TRPP Cation Channels

2000
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families.
    Human mutation, 2002, Volume: 19, Issue:3

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Australia; DNA Mutational Analysis; Gene Duplication; Genetic Linkage; Glutamine; Humans; Methionine; Mice; Molecular Sequence Data; Mutation; Polycystic Kidney Diseases; Polycystic Kidney, Autosomal Dominant; Proteins; Sequence Alignment; Threonine; TRPP Cation Channels

2002