isomethyleugenol has been researched along with Antibody Deficiency Syndrome in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (22.22) | 18.7374 |
| 1990's | 11 (61.11) | 18.2507 |
| 2000's | 2 (11.11) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (5.56) | 2.80 |
| Authors | Studies |
|---|---|
| Abolhassani, H; Aghamohammadi, A; Cheng, B; Fang, M; Hammarström, L; Jiang, C; Li, T; Lin, L; Liu, X; Luo, L; Su, Z; Wang, L; Wang, S; Wang, X; Wu, J; Zhang, W; Zhang, X | 1 |
| Carney, D; Gozani, O; Kuo, AJ; Matthews, AG; Oettinger, MA; Ramón-Maiques, S; Yang, W | 1 |
| Carney, D; Champagne, KS; Cheung, P; Ciccone, DN; Gallardo, M; Gozani, O; Han, S; Ivanov, D; Kuo, AJ; Kutateladze, TG; Matthews, AG; Oettinger, MA; Ramón-Maiques, S; Shi, Y; Utz, PJ; Walter, KL; Yang, W | 1 |
| Achatz, H; Belohradsky, BH; Hergersberg, M; Krüger, G; Meindl, A; Mittermüller, J; Murken, J; Schinzel, A; Schmucker, B; Spiegel, R | 1 |
| Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E | 1 |
| Aurias, A; Fischer, A; Jeanpierre, M; Ledeist, F; Prieur, M; Turleau, C; Viegas-Pequignot, E | 1 |
| Chen, ZY; Craig, IW; Hendriks, RW; Hinds, H; Schuurman, RK | 1 |
| Chen, ZY; Craig, IW; Hendriks, RW; Hinds, H; Kraakman, ME; Schuurman, RK | 1 |
| Abe, T; Kamachi, Y; Matsuoka, H; Torii, S; Tsuge, I | 1 |
| Bartsch, O; Belohradsky, B; Buchholz, T; Hinkel, GK; Kraft, S; Meitinger, T; Petropoulou, T; Schuffenhauer, S; Stumm, M; Wegner, RD | 1 |
| Kraakman, ME; Lambert, M; Schuurman, RK; van den Elsen, PJ; van Eggermond, MC | 1 |
| Hendriks, RW; Kraakman, ME; Mensink, RG; Schuurman, RK | 1 |
| Ernberg, I | 1 |
| Craig, IW; Espanol, T; Hendriks, RW; Kraakman, ME; Schuurman, RK | 1 |
| Ammann, AJ | 1 |
| Epplen, JT; Gahr, M; Hadam, M; Hauke, G; Hollmann, A; Peter, HH | 1 |
| Amaldi, I; Griscelli, C; Hadam, MR; Lisowska-Grospierre, B; Mach, B; Reith, W; Sanchez, CH; Satola, S | 1 |
| Goldblum, RM; Mills, GC; Schmalstieg, FC | 1 |
1 review(s) available for isomethyleugenol and Antibody Deficiency Syndrome
| Article | Year |
|---|---|
Purine nucleotide imbalance in immunodeficiency disorders.
Topics: 5'-Nucleotidase; Adenosine; Adenosine Deaminase; Adenosine Triphosphate; Autoimmune Diseases; B-Lymphocytes; Child; Child, Preschool; Cyclic AMP; Deoxyadenosines; Erythrocytes; Humans; Immunologic Deficiency Syndromes; Lymphocytes; Methylation; Nucleotidases; Phosphoribosyl Pyrophosphate; Purine Nucleotides; Purine-Nucleoside Phosphorylase; Ribonucleotide Reductases; T-Lymphocytes | 1985 |
17 other study(ies) available for isomethyleugenol and Antibody Deficiency Syndrome
| Article | Year |
|---|---|
T Cell Repertoire Abnormality in Immunodeficiency Patients with DNA Repair and Methylation Defects.
Topics: Complementarity Determining Regions; DNA Repair; Humans; Immunologic Deficiency Syndromes; Methylation; Repressor Proteins; T-Lymphocytes | 2022 |
The plant homeodomain finger of RAG2 recognizes histone H3 methylated at both lysine-4 and arginine-2.
Topics: Amino Acid Sequence; Animals; Binding Sites; Crystallography, X-Ray; DNA-Binding Proteins; Gene Rearrangement; Histone-Lysine N-Methyltransferase; Histones; Immunologic Deficiency Syndromes; Methylation; Mice; Models, Molecular; Molecular Sequence Data; Peptides; Protein Binding; Protein Conformation; Protein Interaction Mapping; Protein Processing, Post-Translational; Protein Structure, Tertiary; Sequence Alignment; Sequence Homology, Amino Acid; Zinc Fingers | 2007 |
RAG2 PHD finger couples histone H3 lysine 4 trimethylation with V(D)J recombination.
Topics: Amino Acid Motifs; Animals; Binding Sites; DNA-Binding Proteins; Gene Rearrangement, B-Lymphocyte; Histones; Homeodomain Proteins; Humans; Immunologic Deficiency Syndromes; Lysine; Methylation; Mice; Models, Molecular; Protein Binding; Recombination, Genetic; Structure-Activity Relationship; Substrate Specificity; Tryptophan; VDJ Recombinases | 2007 |
A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene.
Topics: DNA; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Polymerase Chain Reaction; Receptors, Androgen; X Chromosome | 1995 |
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Base Sequence; Case-Control Studies; Centromere; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytosine; DNA, Satellite; Face; Female; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Molecular Sequence Data; Syndrome; X Chromosome | 1994 |
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
Topics: 5-Methylcytosine; Adult; Centromere; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Cytosine; DNA, Satellite; Embryo, Mammalian; Face; Female; Genetic Markers; Humans; Immunologic Deficiency Syndromes; Infant; Leukocytes; Male; Methylation; Placenta; Polymorphism, Restriction Fragment Length; Pregnancy; Repetitive Sequences, Nucleic Acid; Testis | 1993 |
Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
Topics: Agammaglobulinemia; Chromosome Mapping; Dinucleoside Phosphates; Dosage Compensation, Genetic; Exons; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Monoamine Oxidase; Polymerase Chain Reaction; Severe Combined Immunodeficiency; Wiskott-Aldrich Syndrome; X Chromosome | 1993 |
Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
Topics: Agammaglobulinemia; Chromosome Mapping; Dinucleoside Phosphates; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Repetitive Sequences, Nucleic Acid; Severe Combined Immunodeficiency; Wiskott-Aldrich Syndrome; X Chromosome | 1993 |
X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.
Topics: Adult; Agammaglobulinemia; B-Lymphocytes; Child, Preschool; Diagnosis, Differential; DNA; Dosage Compensation, Genetic; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Phosphoglycerate Kinase; Polymorphism, Genetic; X Chromosome | 1993 |
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor.
Topics: Cell Line, Transformed; Child; Child, Preschool; DNA; Female; Genetic Complementation Test; Humans; Immunologic Deficiency Syndromes; In Situ Hybridization, Fluorescence; Male; Methylation | 1995 |
The MHC class II deficiency syndrome: heterogeneity at the level of the response to 5-azadeoxycytidine.
Topics: Azacitidine; Cell Line, Transformed; Decitabine; DNA; Gene Expression Regulation; Genes, MHC Class II; HLA-D Antigens; Humans; Immunologic Deficiency Syndromes; Lymphocytes; Methylation; Promoter Regions, Genetic; Syndrome; Transcription, Genetic | 1990 |
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.
Topics: Blotting, Southern; Cells, Cultured; DNA; Dosage Compensation, Genetic; Female; Hematopoietic Stem Cells; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Repetitive Sequences, Nucleic Acid; Restriction Mapping; X Chromosome | 1991 |
Epstein-Barr virus latency and activation in vivo.
Topics: DNA, Viral; Gene Expression; Herpesvirus 4, Human; Humans; Immunologic Deficiency Syndromes; Methylation; Phenotype; Virus Activation | 1990 |
Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact.
Topics: Blotting, Southern; Clone Cells; Dosage Compensation, Genetic; Gene Rearrangement, B-Lymphocyte, Heavy Chain; Genes, Immunoglobulin; Humans; Hypergammaglobulinemia; Immunoglobulin A; Immunoglobulin G; Immunoglobulin mu-Chains; Immunologic Deficiency Syndromes; Methylation; Pedigree; Polymorphism, Restriction Fragment Length; X Chromosome | 1990 |
Predominant immunoglobulin gene rearrangements in two patients with immunodeficiency: restricted use of V gene segments and DNA hypermethylation.
Topics: Adolescent; Adult; B-Lymphocytes; Blotting, Southern; Cell Differentiation; DNA; Female; Gene Rearrangement; Genes, Immunoglobulin; Humans; Immunoglobulin Variable Region; Immunologic Deficiency Syndromes; Male; Methylation; Middle Aged | 1989 |
Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X.
Topics: B-Lymphocytes; Base Sequence; Binding, Competitive; Cell Line; Deoxyribonuclease I; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Gene Expression Regulation; Genes, MHC Class II; HLA-D Antigens; HLA-DR Antigens; Humans; Immunologic Deficiency Syndromes; Methylation; Molecular Sequence Data; Mutation; Nuclear Proteins; Promoter Regions, Genetic; Regulatory Factor X Transcription Factors; Transcription Factors; Transcription, Genetic | 1988 |
Urinary excretion of modified purines and nucleosides in immunodeficient children.
Topics: Child; Chromatography, Ion Exchange; Female; Germ-Free Life; Humans; Hydrogen-Ion Concentration; Immunologic Deficiency Syndromes; Infant; Methylation; Nucleosides; Purines; Pyrimidines | 1985 |