review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF00918012 |
P698 | PubMed publication ID | 2698397 |
P2093 | author name string | H A Erlich | |
P2860 | cites work | Genetic applications of an inverse polymerase chain reaction | Q24532247 |
A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions | Q24597783 | ||
A specific HLA-DP beta allele is associated with pauciarticular juvenile rheumatoid arthritis but not adult rheumatoid arthritis | Q24601796 | ||
Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA | Q24629757 | ||
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification | Q24633695 | ||
Targeted mutation of the Hprt gene in mouse embryonic stem cells | Q24645320 | ||
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase | Q26778389 | ||
Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer | Q27860572 | ||
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia | Q27861076 | ||
Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA | Q28119124 | ||
Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity | Q28256594 | ||
Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas | Q28269089 | ||
Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction | Q28298254 | ||
Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes | Q28307762 | ||
DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory | Q29037612 | ||
[21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction | Q29544077 | ||
HLA class II allelic variation and susceptibility to pemphigus vulgaris | Q33574546 | ||
Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations | Q33582011 | ||
An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2. | Q48344920 | ||
Detection of the molecular abnormality in chronic myeloid leukemia by use of the polymerase chain reaction. | Q53519279 | ||
Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA | Q59057758 | ||
Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes | Q59058210 | ||
Rearrangement of the breakpoint cluster region and expression of P210 BCR-ABL in a "masked" Philadelphia chromosome-positive acute myeloid leukemia | Q67947791 | ||
Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes | Q68473408 | ||
Direct cloning and sequence analysis of enzymatically amplified genomic sequences | Q68732880 | ||
Detection of minimal residual bcr/abl transcripts by a modified polymerase chain reaction | Q69038899 | ||
A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions | Q69349106 | ||
Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis | Q69761527 | ||
Simple non-invasive method to obtain DNA for gene analysis | Q69919298 | ||
Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphism | Q69920117 | ||
Guthrie spots for DNA-based carrier testing in cystic fibrosis | Q69923851 | ||
Thermostable DNA polymerase chain amplification of t(14;18) chromosome breakpoints and detection of minimal residual disease | Q33586233 | ||
Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro | Q33636924 | ||
Allelic sequence variation of the HLA-DQ loci: relationship to serology and to insulin-dependent diabetes susceptibility | Q33640310 | ||
A sensitive method for the identification of uncharacterized viruses related to known virus groups: hepadnavirus model system | Q33649323 | ||
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes | Q33829075 | ||
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma | Q34264957 | ||
Specific HLA-DQB and HLA-DRB1 alleles confer susceptibility to pemphigus vulgaris | Q34296951 | ||
Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes | Q34297073 | ||
Structural analysis of the HLA-DR, -DQ, and -DP alleles on the celiac disease-associated HLA-DR3 (DRw17) haplotype | Q34297492 | ||
Allelotype of colorectal carcinomas | Q34461209 | ||
Fidelity of DNA synthesis by the Thermus aquaticus DNA polymerase | Q34556300 | ||
Whole genome PCR: application to the identification of sequences bound by gene regulatory proteins | Q35227520 | ||
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction | Q35247229 | ||
A procedure for in vitro amplification of DNA segments that lie outside the boundaries of known sequences | Q36064468 | ||
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification | Q36191565 | ||
Detection of human papilloma virus in paraffin-embedded tissue using the polymerase chain reaction | Q36354371 | ||
Identification of human immunodeficiency virus sequences by using in vitro enzymatic amplification and oligomer cleavage detection | Q36888129 | ||
Analysis of DNA sequences in forty-year-old paraffin-embedded thin-tissue sections: a bridge between molecular biology and classical histology | Q38491382 | ||
Detection of human T-cell lymphoma/leukemia virus type I DNA and antigen in spinal fluid and blood of patients with chronic progressive myelopathy. | Q38907219 | ||
Restricted use of T cell receptor V genes in murine autoimmune encephalomyelitis raises possibilities for antibody therapy | Q39272381 | ||
DNA amplification to enhance detection of genetically engineered bacteria in environmental samples. | Q39920416 | ||
Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction. | Q40448021 | ||
Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells | Q40557488 | ||
Absence of alternative splicing in bcr-abl mRNA in chronic myeloid leukemia cell lines | Q43591465 | ||
Amplification and analysis of DNA sequences in single human sperm and diploid cells | Q43849276 | ||
Hereditary cancer, oncogenes, and antioncogenes. | Q43856656 | ||
Detection of hepatitis B virus sequences in serum by using in vitro enzymatic amplification | Q44388932 | ||
Detection of cytomegalovirus DNA in peripheral blood of patients infected with human immunodeficiency virus | Q44658783 | ||
DNA typing from single hairs | Q45283525 | ||
Mixed human immunodeficiency virus (HIV) infection in an individual: demonstration of both HIV type 1 and type 2 proviral sequences by using polymerase chain reaction | Q45834196 | ||
Detection and sequence of mutations in the factor VIII gene of haemophiliacs | Q45886057 | ||
An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. | Q45889244 | ||
Wound macrophages express TGF-alpha and other growth factors in vivo: analysis by mRNA phenotyping | Q46070830 | ||
HLA-DQ beta gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus | Q46138865 | ||
Guthrie cards for detection of point mutations in phenylketonuria | Q46372838 | ||
Limited heterogeneity of T cell receptors from lymphocytes mediating autoimmune encephalomyelitis allows specific immune intervention | Q46499427 | ||
A combination of a particular HLA-DP beta allele and an HLA-DQ heterodimer confers susceptibility to coeliac disease | Q46608878 | ||
Polymerase chain reaction with single-sided specificity: analysis of T cell receptor delta chain | Q48306084 | ||
Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase | Q48327544 | ||
A newly characterized HLA DQ beta allele associated with pemphigus vulgaris | Q48328732 | ||
P433 | issue | 6 | |
P304 | page(s) | 437-447 | |
P577 | publication date | 1989-11-01 | |
P1433 | published in | Journal of Clinical Immunology | Q6294961 |
P1476 | title | Polymerase chain reaction | |
P478 | volume | 9 |
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Q60930810 | Trichomonas vaginalis infection and the diagnostic significance of detection tests among Ghanaian outpatients | main subject | P921 |
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