glutamic acid and alpha 1-Antitrypsin Deficiency

glutamic acid has been researched along with alpha 1-Antitrypsin Deficiency in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aznar, J; Carrell, RW; Corral, J; Gonzalez-Conejero, R; Huntington, JA; Miñano, A; Vayá, A; Vicente, V; Villa, P1
Chytil, A; Courtney, M; Crystal, RG; Curiel, DT1
Brantly, M; Courtney, M; Crystal, RG1

Other Studies

3 other study(ies) available for glutamic acid and alpha 1-Antitrypsin Deficiency

ArticleYear
Homozygous deficiency of heparin cofactor II: relevance of P17 glutamate residue in serpins, relationship with conformational diseases, and role in thrombosis.
    Circulation, 2004, Sep-07, Volume: 110, Issue:10

    Topics: Adult; alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Antithrombin III; Antithrombin III Deficiency; Codon, Nonsense; Codon, Terminator; Female; Genetic Predisposition to Disease; Glutamic Acid; Heparin Cofactor II; Homozygote; Humans; Liver; Models, Molecular; Point Mutation; Protein Conformation; Pulmonary Emphysema; Recurrence; Serpins; Thrombophilia; Venous Thrombosis

2004
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
Repair of the secretion defect in the Z form of alpha 1-antitrypsin by addition of a second mutation.
    Science (New York, N.Y.), 1988, Dec-23, Volume: 242, Issue:4886

    Topics: alpha 1-Antitrypsin; alpha 1-Antitrypsin Deficiency; Animals; Cell Line; Codon; DNA; Electrochemistry; Endoplasmic Reticulum; Glutamates; Glutamic Acid; Humans; Lysine; Mutation; Protein Conformation; RNA, Messenger; Structure-Activity Relationship; Transfection

1988