valine and Chromosome Deletion

valine has been researched along with Chromosome Deletion in 21 studies

Research

Studies (21)

Timeframe	Studies, this research(%)	All Research%
pre-1990	8 (38.10)	18.7374
1990's	1 (4.76)	18.2507
2000's	7 (33.33)	29.6817
2010's	5 (23.81)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Carmel, M; Chen, J; Frisch, A; Gothelf, D; Kolachana, B; Law, AJ; Lipska, BK; Michaelovsky, E; Ren-Patterson, R; Weinberger, DR; Weizman, A; Zarchi, O	1
Devoto, M; Emanuel, BS; Franconi, CP; Gur, RE; McDonald-McGinn, D; McNamara, MA; Moss, E; Salmons, H; Zackai, EH	1
Girodon, F; Gisslinger, H; Hao-Shen, H; Hermouet, S; Jäger, R; Kralovics, R; Looser, R; Schaub, FX; Skoda, RC; Tichelli, A	1
Schmidt, L; Simon, TJ; Takarae, Y; Tassone, F	1
Caceres, G; Dewald, DW; List, AF; Rocha, K; Sokol, L; Stockero, KJ	1
Aguilar, JL; Baumann, T; Calvo, X; Cervantes, F; Colomer, D; Costa, D; Díaz-Beyá, M; Esteve, J; Maffioli, M; Martínez-Trillos, A; Nomdedeu, B; Nomdedeu, M; Rozman, M	1
Demant, A; El Arbi, S; Horneff, G; Kohlschmidt, N	1
Abdulsabur, N; Antshel, KM; Colgan, D; Fremont, W; Funke, B; Higgins, AM; Kates, WR; Kucherlapati, R; Shprintzen, RJ	1
Bassett, AS; Caluseriu, O; Chow, EW; Weksberg, R; Young, DA	1
O'Donovan, MC; Owen, MJ; Williams, HJ	1
Antonarakis, SE; Gothelf, D; Hallmayer, JF; Hinard, C; Hoeft, F; Morris, MA; Reiss, AL; Stoecker, JV	1
Daly, E; De Haan, L; Figee, M; Glaser, B; Linszen, DH; Morris, R; Murphy, DG; Murphy, KC; Owen, MJ; van Amelsvoort, T; Zinkstok, J	1
Blazey, DL; Burns, RO	1
Bennett, DC; Umbarger, HE	1
Kline, EL; Manross, DN; Warwick, ML	1
Achstetter, T; Findeli, A; Lemoine, Y; Merkamm, M; Nguyen-Juilleret, M	1
Bamforth, FJ; Graham, A; Kalsheker, NA; Markham, AF; Newton, CR; Powell, SJ	1
Bargmann, CI; Weinberg, RA	1
Driver, RP; Lawther, RP	1
Lawther, RP; Ortuno, MJ	1
Calvo, JM; De Felice, M; Haughn, GW; Largo, CT; Squires, CH	1

Reviews

1 review(s) available for valine and Chromosome Deletion

Article	Year
Is COMT a susceptibility gene for schizophrenia? Schizophrenia bulletin, 2007, Volume: 33, Issue:3 Topics: Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 22; Dopamine; Genetic Predisposition to Disease; Humans; Methionine; Polymorphism, Genetic; Prefrontal Cortex; Schizophrenia; Valine	2007

Other Studies

20 other study(ies) available for valine and Chromosome Deletion

Article	Year
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome. Biological psychiatry, 2014, Mar-01, Volume: 75, Issue:5 Topics: Adolescent; Adult; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Chromosome Deletion; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult	2014
IQ and hemizygosity for the Val American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:8 Topics: 22q11 Deletion Syndrome; Adolescent; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; Cognition Disorders; Female; Genetic Association Studies; Genetic Predisposition to Disease; Hemizygote; Humans; Intelligence Tests; Male; Methionine; Polymorphism, Single Nucleotide; Valine; Young Adult	2016
Clonal analysis of deletions on chromosome 20q and JAK2-V617F in MPD suggests that del20q acts independently and is not one of the predisposing mutations for JAK2-V617F. Blood, 2009, Feb-26, Volume: 113, Issue:9 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Chromosome Deletion; Chromosomes, Human, Pair 20; Clone Cells; Comparative Genomic Hybridization; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Janus Kinase 2; Male; Middle Aged; Mutation; Myeloproliferative Disorders; Phenylalanine; Valine	2009
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome. Cognitive, affective & behavioral neuroscience, 2009, Volume: 9, Issue:1 Topics: Adolescent; Analysis of Variance; Attention; Case-Control Studies; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition Disorders; DiGeorge Syndrome; DNA Mutational Analysis; Female; Humans; Intelligence Tests; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Reaction Time; Valine	2009
JAK2(V617F) mutation in myelodysplastic syndrome (MDS) with del(5q) arises in genetically discordant clones. Leukemia research, 2010, Volume: 34, Issue:6 Topics: Amino Acid Substitution; Chromosome Deletion; Chromosomes, Human, Pair 5; Clone Cells; Erythroid Precursor Cells; Female; Humans; Janus Kinase 2; Middle Aged; Mutation, Missense; Myelodysplastic Syndromes; Phenylalanine; Valine	2010
Efficacy of lenalidomide in a patient with myelodysplastic syndrome with isolated del(5q) and JAK2V617F mutation. Leukemia research, 2011, Volume: 35, Issue:9 Topics: Amino Acid Substitution; Anemia, Macrocytic; Antineoplastic Agents; Chromosome Deletion; Chromosomes, Human, Pair 5; Female; Humans; Janus Kinase 2; Lenalidomide; Middle Aged; Mutation, Missense; Myelodysplastic Syndromes; Phenylalanine; Thalidomide; Treatment Outcome; Valine	2011
Infantile neuroaxonal dystrophy: a rare cause of early childhood ataxia with poor prognosis. Klinische Padiatrie, 2013, Volume: 225, Issue:1 Topics: Atrophy; Base Pairing; Cerebellum; Child, Preschool; Chromosome Deletion; Diagnosis, Differential; Disease Progression; DNA Mutational Analysis; Exons; Frontal Lobe; Gait Ataxia; Group VI Phospholipases A2; Homozygote; Humans; Magnetic Resonance Imaging; Male; Neuroaxonal Dystrophies; Temporal Lobe; Valine	2013
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome). American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2006, Apr-05, Volume: 141B, Issue:3 Topics: Abnormalities, Multiple; Adolescent; Alleles; Brain; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; DNA Mutational Analysis; Face; Female; Gene Frequency; Genotype; Heart Defects, Congenital; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Sex Factors; Syndrome; Task Performance and Analysis; Valine; Velopharyngeal Insufficiency	2006
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biological psychiatry, 2007, May-15, Volume: 61, Issue:10 Topics: Adult; Alleles; Amino Acid Substitution; Arousal; Chromosome Deletion; Chromosomes, Human, Pair 22; Female; Frontal Lobe; Gene Expression; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia; Syndrome; Valine	2007
Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome. Human brain mapping, 2007, Volume: 28, Issue:6 Topics: Adolescent; Adult; Brain Mapping; Case-Control Studies; Catechol O-Methyltransferase; Cerebral Cortex; Chromosome Deletion; Chromosomes, Human, Pair 22; Developmental Disabilities; Female; Humans; Image Processing, Computer-Assisted; Inhibition, Psychological; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Oxygen; Schizophrenia; Valine	2007
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome. Psychological medicine, 2008, Volume: 38, Issue:1 Topics: Adult; Brain; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition Disorders; DiGeorge Syndrome; Female; Gene Frequency; Humans; Hypertrophy; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Psychotic Disorders; Valine	2008
Regulation of Salmonella typhimurium ilvYC genes. Journal of bacteriology, 1984, Volume: 159, Issue:3 Topics: Base Sequence; Chromosome Deletion; Cloning, Molecular; DNA Restriction Enzymes; DNA, Recombinant; Escherichia coli; Gene Expression Regulation; Genes; Genes, Bacterial; Genotype; Isoleucine; Plasmids; Salmonella typhimurium; Transcription, Genetic; Valine	1984
Isolation and analysis of two Escherichia coli K-12 ilv attenuator deletion mutants with high-level constitutive expression of an ilv-lac fusion operon. Journal of bacteriology, 1984, Volume: 157, Issue:3 Topics: Bacteriophage lambda; Base Sequence; beta-Alanine; Chromosome Deletion; Cloning, Molecular; DNA, Recombinant; Escherichia coli; Gene Expression Regulation; Genes, Bacterial; Genes, Regulator; Isoleucine; Lac Operon; Lysogeny; Mutation; Operon; Valine	1984
Multivalent regulation of isoleucine-valine transaminase in an Escherichia coli K-12 ilvA deletion strain. Journal of bacteriology, 1977, Volume: 130, Issue:2 Topics: Chromosome Deletion; Escherichia coli; Genes; Isoleucine; Threonine Dehydratase; Transaminases; Valine	1977
A new signal peptide useful for secretion of heterologous proteins from yeast and its application for synthesis of hirudin. Gene, 1992, Jan-02, Volume: 110, Issue:1 Topics: Amino Acid Sequence; Base Sequence; Chromosome Deletion; Genes, Fungal; Genetic Variation; Genetic Vectors; Hirudins; Molecular Sequence Data; Plasmids; Protein Processing, Post-Translational; Protein Sorting Signals; Recombinant Fusion Proteins; Saccharomyces cerevisiae; Valine	1992
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
Oncogenic activation of the neu-encoded receptor protein by point mutation and deletion. The EMBO journal, 1988, Volume: 7, Issue:7 Topics: Animals; Cells, Cultured; Chromosome Deletion; ErbB Receptors; Gene Expression Regulation; Glutamates; Glutamic Acid; Mice; Mutation; Oncogenes; Plasmids; Protein-Tyrosine Kinases; Receptors, Cell Surface; Transfection; Valine	1988
Physical analysis of deletion mutations in the ilvGEDA operon of Escherichia coli K-12. Journal of bacteriology, 1985, Volume: 162, Issue:2 Topics: Chromosome Deletion; Chromosome Mapping; DNA Restriction Enzymes; Escherichia coli; Genes, Bacterial; Isoleucine; Mutation; Nucleic Acid Hybridization; Operon; Valine	1985
Effect of the deletion of upstream DNA sequences on expression from the ilvGp2 promoter of the ilvGMEDA operon of Escherichia coli K-12. Nucleic acids research, 1987, Feb-25, Volume: 15, Issue:4 Topics: Base Sequence; Chromosome Deletion; DNA, Bacterial; Escherichia coli; Genes; Genes, Regulator; Isoleucine; Operon; Plasmids; Promoter Regions, Genetic; Transcription, Genetic; Valine	1987
Unusual organization of the ilvIH promoter of Escherichia coli. Journal of bacteriology, 1985, Volume: 163, Issue:1 Topics: Base Sequence; Chromosome Deletion; Chromosome Mapping; DNA, Bacterial; Escherichia coli; Gene Expression Regulation; Isoleucine; Leucine; Molecular Sequence Data; Mutation; Operon; Promoter Regions, Genetic; RNA, Messenger; Transcription, Genetic; Valine	1985