Compounds > valine

valine and alpha 1-Antitrypsin Deficiency

valine has been researched along with alpha 1-Antitrypsin Deficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
de la Roza, C; Jardi, R; Miravitlles, M; Rodriguez, F; Schaper, M; Vidal, R1
Cotrina, M; Jardi, R; Miravitlles, M; Pascual, C; Quer, J; Rodriguez, F; Vidal, R; Weidinger, S1
Chytil, A; Courtney, M; Crystal, RG; Curiel, DT1
Bamforth, FJ; Graham, A; Kalsheker, NA; Markham, AF; Newton, CR; Powell, SJ1

Other Studies

4 other study(ies) available for valine and alpha 1-Antitrypsin Deficiency

ArticleYear
Glutathione S-transferase P1 and lung function in patients with alpha1-antitrypsin deficiency and COPD.
    Chest, 2005, Volume: 127, Issue:5

    Topics: Aged; alpha 1-Antitrypsin Deficiency; Female; Forced Expiratory Volume; Genotype; Glutathione S-Transferase pi; Glutathione Transferase; Humans; Isoenzymes; Male; Middle Aged; Polymorphism, Genetic; Pulmonary Disease, Chronic Obstructive; Smoking; Valine

2005
Identification and molecular characterization of the new alpha-1-antitrypsin deficient allele PI Y barcelona (Asp256-->Val and Pro391-->His). Mutations in brief no. 174. Online.
    Human mutation, 1998, Volume: 12, Issue:3

    Topics: Alleles; alpha 1-Antitrypsin Deficiency; Amino Acid Substitution; Aspartic Acid; Histidine; Humans; Phenotype; Proline; Valine

1998
Serum alpha 1-antitrypsin deficiency associated with the common S-type (Glu264----Val) mutation results from intracellular degradation of alpha 1-antitrypsin prior to secretion.
    The Journal of biological chemistry, 1989, Jun-25, Volume: 264, Issue:18

    Topics: Alleles; alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Amino Acid Sequence; Animals; Base Sequence; Genes; Glutamates; Glutamic Acid; Homozygote; Humans; Mice; Molecular Sequence Data; Monocytes; Mutation; Plasmids; RNA, Messenger; Transcription, Genetic; Transfection; Valine

1989
Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys).
    Human genetics, 1989, Volume: 84, Issue:1

    Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Amino Acid Sequence; Arginine; Aspartic Acid; Base Sequence; Chromosome Deletion; Cysteine; Genes; Genetic Variation; Humans; Molecular Sequence Data; Oligonucleotide Probes; Phenylalanine; Valine

1989