A simple restriction endonuclease based test for the dopamine D2 receptor gene (DRD2) haplotypes: linkage disequilibrium of the haplotypes with the Taq A1 allele.
Psychiatric genetics | 1997-01-01 | PMID 9323328
Dietz G, Comings D
Genes: DRD2
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 9857 of 10600
Association analysis of the SmaI polymorphism of the dopamine D4 receptor in Japanese schizophrenics.
Psychiatric genetics | 1997-01-01 | PMID 9323329
Tani M, Koide S, Onishi H and 2 more
Phenotypically mild presentation in a patient with 2-methylacetoacetyl-coenzyme A (beta-keto)thiolase deficiency.
Journal of inherited metabolic disease | 1997-09-01 | PMID 9323571
Gibson K M, Feigenbaum A S
Carnitine-acylcarnitine translocase deficiency--a mild phenotype.
Journal of inherited metabolic disease | 1997-09-01 | PMID 9323572
Olpin S E, Bonham J R, Downing M and 4 more
Emerging Viruses: The Bunyaviridae
1997-09-01 | PMID 9323708
Spinal and cranial neural tube defects
1997-09-01 | PMID 9323786
H‐<i>ras</i> oncogene point mutations in arthritic synovium
1997-09-01 | PMID 9324018
Hereditary resistance to activated protein C: an uncommon risk factor for thromboembolic disease in lupus patients with antiphospholipid antibodies.
Arthritis and rheumatism | 1997-09-01 | PMID 9324029
Sasso E H, Suzuki L A, Thompson A R and 1 more
A novel nested-PCR strategy for the detection of rearranged immunoglobulin heavy-chain genes in B cell tumors
1997-10-01 | PMID 9324303
Complement Receptor Type 1 (CR1, CD35) Is a Receptor for C1q
1997-09-01 | PMID 9324355
Genomic Organization, Alternative Splicing, and Expression Patterns of theDSCR1(Down Syndrome Candidate Region 1) Gene
1997-09-01 | PMID 9325060
Baculoviral Display of the Green Fluorescent Protein and Rubella Virus Envelope Proteins
1997-09-01 | PMID 9325155
The Matrix Metalloproteinase-14 (MMP-14) Gene Is Structurally Distinct from Other MMP Genes and Is Co-expressed with the TIMP-2 Gene during Mouse Embryogenesis
1997-10-01 | PMID 9325265
cDNA Cloning of a Novel, Developmentally Regulated Immediate Early Gene Activated by Fibroblast Growth Factor and Encoding a Nuclear Protein
1997-10-01 | PMID 9325278
Transcription of Human ABO Histo-blood Group Genes Is Dependent upon Binding of Transcription Factor CBF/NF-Y to Minisatellite Sequence
1997-10-01 | PMID 9325321
Identification of del(6)(q21q25) as a recurring chromosomal abnormality in putative NK cell lymphoma/leukaemia
1997-09-01 | PMID 9326190
Atypical lymphocyte morphology: an adverse prognostic factor for disease progression in stage A CLL independent of trisomy 12
1997-09-01 | PMID 9326192
Fusion of TEL, the ETS-Variant Gene 6 (ETV6), to the Receptor-Associated Kinase JAK2 as a Result of t(9; 12) in a Lymphoid and t(9; 15; 12) in a Myeloid Leukemia
1997-10-01 | PMID 9326218
Interleukin-6 and the Granulocyte Colony-Stimulating Factor Receptor Are Major Independent Regulators of Granulopoiesis In Vivo But Are Not Required for Lineage Commitment or Terminal Differentiation
1997-10-01 | PMID 9326224
The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin
1997-10-01 | PMID 9326232
Semper Fidelis: What Man's Best Friend Can Teach Us about Human Biology and Disease
1997-09-01 | PMID 9326310
Identification of a Locus for Progressive Familial Intrahepatic Cholestasis PFIC2on Chromosome 2q24
1997-09-01 | PMID 9326328
Meiotic Segregation, Recombination, and Gamete Aneuploidy Assessed in a t(1;10)(p22.1;q22.3) Reciprocal Translocation Carrier by Three- and Four-Probe Multicolor FISH in Sperm
1997-09-01 | PMID 9326331
Association Mapping of Disease Loci, by Use of a Pooled DNA Genomic Screen
1997-09-01 | PMID 9326338
Activating mutations for the Met tyrosine kinase receptor in human cancer
1997-10-14 | PMID 9326629
Direct evidence to support the role of HLA-G in protecting the fetus from maternal uterine natural killer cytolysis
1997-10-14 | PMID 9326642
Targeted disruption of the mouse gene encoding steroidogenic acute regulatory protein provides insights into congenital lipoid adrenal hyperplasia
1997-10-14 | PMID 9326645
Binding of high-risk human papillomavirus E6 oncoproteins to the human homologue of the <i>Drosophila</i> discs large tumor suppressor protein
1997-10-14 | PMID 9326658
Identification of a cellular receptor for subgroup E avian leukosis virus
1997-10-14 | PMID 9326659
Concordance of Genetic Alterations in Poorly Differentiated Colorectal Neuroendocrine Carcinomas and Associated Adenocarcinomas
1997-10-01 | PMID 9326914
Germline CDKN2A Mutations in Childhood Melanoma
1997-10-01 | PMID 9326917
A human compound heterozygote for two MLH1 missense mutations.
Nature genetics | 1997-10-01 | PMID 9326924
Hackman P, Tannergård P, Osei-Mensa S and 6 more
Genes: MLH1
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome
1997-10-01 | PMID 9326934
Positional cloning of the gene associated with X-linked juvenile retinoschisis
1997-10-01 | PMID 9326935
Identification of PAHX, a Refsum disease gene
1997-10-01 | PMID 9326939
Increased stress response and β–phenylethylamine in MAOB–deficient mice
1997-10-01 | PMID 9326944
Human telomeres contain two distinct Myb–related proteins, TRF1 and TRF2
1997-10-01 | PMID 9326950
Telomeric localization of TRF2, a novel human telobox protein
1997-10-01 | PMID 9326951
The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.
Heart (British Cardiac Society) | 1997-08-01 | PMID 9326982
Burn J, Camm J, Davies M J and 3 more
Altered folate and vitamin B12 metabolism in families with spina bifida offspring
1997-08-01 | PMID 9327028
Microdissection-based genetic discovery and analysis applied to cancer progression.
The cancer journal from Scientific American | 2000-01-01 | PMID 9327146
Dean-Clower E, Vortmeyer A O, Bonner R F and 3 more
ras Mutation: does it have clinical import?
The cancer journal from Scientific American | 2000-01-01 | PMID 9327149
Rosen N, Sepp-Lorenzino L
Molecular basis of inherited disorders of renal solute transport.
Current opinion in nephrology and hypertension | 1997-09-01 | PMID 9327198
López-Nieto C E, Brenner B M
Mitochondrial encephalomyopathies: gene mutation.
Neuromuscular disorders : NMD | 1997-09-01 | PMID 9327409
Potential indicators of radiosensitivity in squamous cell carcinoma of the head and neck
1997-01-01 | PMID 9327497
Interactions Between Lifestyle-Related Factors and the ApoE Polymorphism on Plasma Lipids and Apolipoproteins
1997-09-01 | PMID 9327762
Fatty Streak Formation in Fat-Fed Mice Expressing Human Copper-Zinc Superoxide Dismutase
1997-09-01 | PMID 9327771
Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystonia.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9327843
Bartholomé K, Lüdecke B
Catecholamine biosynthetic enzyme expression in neurological and psychiatric disorders.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9327844
Meloni R, Dumas S, Mallet J
Dopamine beta-hydroxylase deficiency associated with mutations in a copper transporter gene.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9327848
Kaler S G, Holmes C S, Goldstein D S
Structural diversity in the catecholamine transporter gene family: molecular cloning and characterization of an L-epinephrine transporter from bullfrog sympathetic ganglia.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9327880
Blakely R D, Apparsundaram S
Structural and functional characteristics of the dopamine D4 receptor.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9327945
Van Tol H H
The differentiation of the neurotransmitter phenotypes in chick sympathetic neurons.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9328041
Rohrer H, Ernsberger U
Genotype and phenotype in familial dysautonomia.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9328049
Axelrod F B, Goldstein D S, Holmes C and 1 more
Dopaminergic genes and substance abuse.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9328073
Uhl G R, Vandenbergh D J, Rodriguez L A and 2 more
Quantitative trait loci: mapping drug and alcohol-related genes.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9328074
Crabbe J C, Belknap J K, Metten P and 2 more
Nuclear memory: gene transcription and behavior.
Advances in pharmacology (San Diego, Calif.) | 1998-01-01 | PMID 9328075
Hiroi N, Nestler E J
Identification and characterization of a DR4-restricted T cell epitope within chlamydia heat shock protein 60
1997-09-01 | PMID 9328119
An immunohistochemical study of altered immunomodulatory molecule expression in head and neck squamous cell carcinoma
1997-10-01 | PMID 9328140
Bcl-2/Bax ratios in chronic lymphocytic leukaemia and their correlation with in vitro apoptosis and clinical resistance
1997-10-01 | PMID 9328155
Apolipoprotein E genotype in familial Parkinson's disease. The French Parkinson's Disease Genetics Study Group.
Journal of neurology, neurosurgery, and psychiatry | 1997-09-01 | PMID 9328263
Genes: APOE
Bcl-2 is overexpressed and alters the threshold for apoptosis in a cholangiocarcinoma cell line
1997-10-01 | PMID 9328309
Evidence for the polyclonal nature of focal nodular hyperplasia of the liver by the study of X-chromosome inactivation
1997-10-01 | PMID 9328310
Interactions of Estrogen- and Thyroid Hormone Receptors on a Progesterone Receptor Estrogen Response Element (ERE) Sequence: a Comparison with the Vitellogenin A2 Consensus ERE
1997-10-01 | PMID 9328341
Rethinking genotype and phenotype correlations in polyglutamine expansion disorders.
Human molecular genetics | 1997-11-01 | PMID 9328463
Andrew S E, Goldberg Y P, Hayden M R
The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and Apoptosis
1997-11-01 | PMID 9328465
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10
1997-11-01 | PMID 9328471
A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A 42(43)
1997-11-01 | PMID 9328472
Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma
1997-11-01 | PMID 9328473
HLA class II peptide binding specificity and autoimmunity.
Advances in immunology | 1997-01-01 | PMID 9328640
Hammer J, Sturniolo T, Sinigaglia F
Safety and efficacy of a mutagen-attenuated Rift Valley fever virus vaccine in cattle
1997-10-01 | PMID 9328662
New insights into the metastasis-associated 67 kD laminin receptor
1997-11-01 | PMID 9328821
The Wistar-Furth rat as a model of mineralocorticoid resistance.
Kidney international. Supplement | 1997-10-01 | PMID 9328955
Ullian M E
Glucocorticoids and the Immune Function in the Human Immunodeficiency Virus Infection: A Study in Hypercortisolemic and Cortisol-Resistant Patients*
1997-10-01 | PMID 9329349
Relationship between Concentration of Serum Leptin and Fetal Growth
1997-10-01 | PMID 9329354
Tumor-Specific Decreased Expression of Calcium Sensing Receptor Messenger Ribonucleic Acid in Sporadic Primary Hyperparathyroidism<sup>1</sup>
1997-10-01 | PMID 9329389
Clinical utility of the polymerase chain reaction for diagnosis of enteroviral meningitis in infancy
1997-09-01 | PMID 9329415
Chronic hepatitis in an infant, in association with human herpesvirus-6 infection
1997-09-01 | PMID 9329433
Dendritic Translocation of RC3/Neurogranin mRNA in Normal Aging, Alzheimer Disease and Fronto-Temporal Dementia
1997-10-01 | PMID 9329454
Association between β2-adrenoceptor polymorphism and susceptibility to bronchodilator desensitisation in moderately severe stable asthmatics
1997-10-01 | PMID 9329515
A more comprehensive application of the micronucleus technique for biomonitoring of genetic damage rates in human populations—experiences from the Chernobyl catastrophe
1997-01-01 | PMID 9329635
Changes in the repair capacity of blood cells as a biomarker for chronic low-dose exposure to ionizing radiation
1997-01-01 | PMID 9329640
Use of fluorescence in situ hybridization (FISH) to assess effects of smoking, caffeine, and alcohol on aneuploidy load in sperm of healthy men
1997-01-01 | PMID 9329642
Cerebrovascular changes associated with interleukin-1 beta (IL-1 beta) and histamine (HA) levels in Alzheimer's disease.
Annals of the New York Academy of Sciences | 1997-09-26 | PMID 9329706
Alvarez X A, Fernández-Novoa L, Caamaño J and 5 more
APOE epsilon 4 allele frequency in Alzheimer's disease and vascular dementia in the Spanish population.
Annals of the New York Academy of Sciences | 1997-09-26 | PMID 9329722
Beyer K, Lao J I, Fernández-Novoa L and 3 more
Genes: APOE
Obesity genes and insulin resistance syndrome.
Annals of the New York Academy of Sciences | 1997-09-20 | PMID 9329740
Kahle E B, Leibel R L, Domaschko D W and 2 more
Lipid transport genes and their relation to the syndrome of insulin resistance.
Annals of the New York Academy of Sciences | 1997-09-20 | PMID 9329745
Galton D J, Zhang Q, Cavallero E and 6 more
Is a mutation of the beta 3-adrenergic receptor gene related to non-insulin-dependent diabetes mellitus and juvenile hypertension in the Czech population?
Annals of the New York Academy of Sciences | 1997-09-20 | PMID 9329748
Bendlová B, Mazura I, Vcelák J and 4 more
Phenotype and genotype comparison of hereditary hypertriglyceridemic (hHTG) and brown-Norway (BN) rats. Identification of quantitative trait loci (QTLs) for the insulin resistance syndrome.
Annals of the New York Academy of Sciences | 1997-09-20 | PMID 9329784
Kovács P, Samani N J, Seböková E and 7 more
Widely dispersed p53 mutation in respiratory epithelium. A novel mechanism for field carcinogenesis.
1997-10-15 | PMID 9329980
PfEMP1, polymorphism and pathogenesis
1997-07-01 | PMID 9329992
No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene. Biomed European Bipolar Collaborative Group.
The British journal of psychiatry : the journal of mental science | 1997-06-01 | PMID 9330018
Genes: COMT
Use of transgenic mice to eliminate retinoic acid receptor function in specific tissues.
Methods in enzymology | 1997-01-01 | PMID 9330279
Saitou M, Tanaka T, Kakizuka A
Molecular approaches to structure-function analysis of interleukin-8.
Methods in enzymology | 1997-01-01 | PMID 9330314
Fairbrother W J, Lowman H B
Biological assays for C-X-C chemokines.
Methods in enzymology | 1997-01-01 | PMID 9330316
Baly D, Gibson U, Allison D and 1 more
Characterization of quaternary structure of interleukin-8 and functional implications.
Methods in enzymology | 1997-01-01 | PMID 9330317
Rajarathnam K, Kay C M, Clark-Lewis I and 1 more
[Role of the steroidogenic acute regulatory (StAR) protein in the delivery of cholesterol to the inner mitochondrial membrane].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme | 1997-10-01 | PMID 9330574
Sugawara T
A long-sought needle in the haystack: the multiple endocrine neoplasia type 1 gene.
European journal of endocrinology | 1997-09-01 | PMID 9330583
Kopp P
The dermal—epidermal junction
1997-10-01 | PMID 9330868
The ezrin protein family: membrane-cytoskeleton interactions and disease associations
1997-10-01 | PMID 9330869