isomethyleugenol has been researched along with Bare Lymphocyte Syndrome in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 8 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benveniste, P; Cohen, A; Zhu, W | 1 |
| Berns, A; Breuer, ML; Hershfield, MS; Migchielsen, AA; Ossendorp, F; te Riele, H; Toutain, S; Valerio, D; van Roon, MA; Zurcher, C | 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 |
| Hendriks, RW; Kraakman, ME; Schuurman, RK | 2 |
| Abe, T; Ichihara, Y; Kamachi, Y; Kurosawa, Y; Matsuoka, H; Torii, S; Tsuge, I | 1 |
| Sato, T; Wakabayashi, Y | 1 |
1 review(s) available for isomethyleugenol and Bare Lymphocyte Syndrome
| Article | Year |
|---|---|
[PNP deficiency].
Topics: Deoxyguanine Nucleotides; Diagnosis, Differential; Humans; Immunity, Cellular; Methylation; Mutation; Prognosis; Purine-Nucleoside Phosphorylase; Purines; Severe Combined Immunodeficiency | 1998 |
7 other study(ies) available for isomethyleugenol and Bare Lymphocyte Syndrome
| Article | Year |
|---|---|
Interference with thymocyte differentiation by an inhibitor of S-adenosylhomocysteine hydrolase.
Topics: Adenosine Deaminase; Adenosylhomocysteinase; Animals; Apoptosis; Blotting, Northern; CD4-Positive T-Lymphocytes; CD8-Positive T-Lymphocytes; Cell Differentiation; Dideoxyadenosine; Flow Cytometry; Hydrolases; Methylation; Mice; Mice, Inbred C57BL; Receptors, Antigen, T-Cell; Severe Combined Immunodeficiency; T-Lymphocyte Subsets; Thymus Gland | 1995 |
Adenosine-deaminase-deficient mice die perinatally and exhibit liver-cell degeneration, atelectasis and small intestinal cell death.
Topics: Adenosine Deaminase; Animals; Animals, Newborn; Base Sequence; Cell Death; Disease Models, Animal; DNA Primers; Embryonic and Fetal Development; Female; Gene Targeting; Homozygote; Humans; Intestine, Small; Liver; Male; Methylation; Mice; Molecular Sequence Data; Mutation; Pregnancy; Pulmonary Atelectasis; Purines; Severe Combined Immunodeficiency; T-Lymphocyte Subsets | 1995 |
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 |
Patterns of X chromosome inactivation in haematopoietic cells of female carriers of X linked severe combined immunodeficiency.
Topics: B-Lymphocytes; Dinucleoside Phosphates; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Granulocytes; Hematopoietic System; Humans; Male; Methylation; Severe Combined Immunodeficiency; T-Lymphocytes; X Chromosome | 1993 |
The gene loci for immunoglobulin heavy chains in precursor B cell lines from a patient with severe combined immunodeficiency appear able to participate in DNA rearrangement but have a germ-line configuration.
Topics: B-Lymphocytes; Cells, Cultured; DNA-Binding Proteins; Enhancer Elements, Genetic; Gene Expression; Gene Rearrangement, B-Lymphocyte, Heavy Chain; Genes, Immunoglobulin; Homeodomain Proteins; Humans; In Vitro Techniques; Male; Methylation; Nuclear Proteins; Proteins; RNA, Messenger; Severe Combined Immunodeficiency | 1993 |
X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus.
Topics: Blotting, Southern; Cells, Cultured; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Granulocytes; Humans; Lymphocytes; Methylation; Pedigree; Restriction Mapping; Severe Combined Immunodeficiency; X Chromosome | 1992 |