Compounds > cysteine

cysteine and Abnormality, Heart

cysteine has been researched along with Abnormality, Heart in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (83.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akdemir, ZC; Azamian, MS; Belmont, JW; Braxton, A; Chandarana, J; D'Alessandro, LC; Ding, Y; Eldomery, MK; Eng, CM; Gibbs, RA; Hanchard, NA; Harel, T; Holtzman, J; Jhangiani, SN; Kois, C; Lupski, JR; Miller, K; Muzny, DM; Rijhsinghani, A; Rosenfeld, JA; Sack, V; Shur, N; Vetrini, F; Yang, Y1
Akçaboy, MI; Atalay, S; Cengiz, FB; Inceoğlu, B; Tekin, M; Tutar, E; Uçar, T1
Blouin, JL; Bottani, A; Delavelle, J; Haenggeli, CA; Jenny, B; Kaelin, A; Radovanovic, I; Rilliet, B; Rüfenacht, D1
Calais, C; Chaventre, A; Gayet, M; Le Caignec, C; Lefevre, M; Moisan, JP; Schott, JJ1
Hiroi, Y; Hosoda, T; Ikeda, Y; Inoue, J; Ito, T; Komuro, I; Matsuo, S; Nagai, R; Sumiyoshi, T; Takano, H; Utsunomiya, T1
An, JY; Davydov, IV; Du, F; Hu, RG; Kashina, AS; Kwon, YT; Seo, JW; Varshavsky, A1

Other Studies

6 other study(ies) available for cysteine and Abnormality, Heart

ArticleYear
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
    American journal of human genetics, 2016, Oct-06, Volume: 99, Issue:4

    Topics: Alleles; Amino Acid Motifs; Amino Acid Sequence; Animals; Caenorhabditis elegans; Cysteine; Exome; Female; Fetal Diseases; Functional Laterality; Heart Defects, Congenital; Heterotaxy Syndrome; Homozygote; Humans; Infant, Newborn; Introns; Male; Membrane Proteins; Mice; Middle Aged; Models, Molecular; Mutation; Mutation, Missense; Oryzias; Pedigree; RNA Splicing; Situs Inversus

2016
The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?
    Pediatric cardiology, 2008, Volume: 29, Issue:1

    Topics: Arginine; Child; Child, Preschool; Cysteine; Double Outlet Right Ventricle; Female; Heart Defects, Congenital; Homeobox Protein Nkx-2.5; Homeodomain Proteins; Humans; Infant; Infant, Newborn; Male; Mutation, Missense; Polymorphism, Genetic; Pulmonary Atresia; Tetralogy of Fallot; Transcription Factors; Transposition of Great Vessels; Truncus Arteriosus, Persistent

2008
Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report.
    Journal of neurosurgery, 2007, Volume: 107, Issue:4 Suppl

    Topics: Adolescent; Angiography; Arginine; Cyanosis; Cysteine; Decompression, Surgical; Female; Hamartoma Syndrome, Multiple; Heart Defects, Congenital; Hemangioma; Heterozygote; Humans; Magnetic Resonance Imaging; Mutation, Missense; Paraparesis; PTEN Phosphohydrolase; Severity of Illness Index; Spinal Cord Compression; Spinal Neoplasms; Thoracic Vertebrae; Tomography, X-Ray Computed

2007
Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.
    American journal of human genetics, 2002, Volume: 71, Issue:1

    Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Arcus Senilis; Base Sequence; Calcium-Binding Proteins; Cysteine; Deafness; DNA; Female; Genes, Dominant; Heart Defects, Congenital; Humans; Intercellular Signaling Peptides and Proteins; Jagged-1 Protein; Male; Membrane Proteins; Molecular Sequence Data; Mutation; Pedigree; Protein Structure, Tertiary; Proteins; Sequence Homology, Amino Acid; Serrate-Jagged Proteins

2002
Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.
    Circulation journal : official journal of the Japanese Circulation Society, 2002, Volume: 66, Issue:6

    Topics: Cysteine; Female; Heart Defects, Congenital; Homeobox Protein Nkx-2.5; Homeodomain Proteins; Humans; Japan; Male; Pedigree; Point Mutation; Transcription Factors; Xenopus Proteins

2002
An essential role of N-terminal arginylation in cardiovascular development.
    Science (New York, N.Y.), 2002, Jul-05, Volume: 297, Issue:5578

    Topics: Alkylation; Aminoacyltransferases; Animals; Aorta; Arginine; Aspartic Acid; Blood Vessels; Cell Line; Cysteic Acid; Cysteine; Female; Glutamic Acid; Heart; Heart Defects, Congenital; Heart Septal Defects; Hypoxia-Inducible Factor 1, alpha Subunit; Male; Mice; Mice, Inbred C57BL; Neovascularization, Physiologic; Oxidation-Reduction; Proteins; Pulmonary Artery; Recombinant Proteins; RGS Proteins; Sulfinic Acids; Transcription Factors; Transfection

2002