Pages that link to "Q33655616"
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The following pages link to Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus (Q33655616):
Displaying 50 items.
- The A3 allele of the HLA-DQA1 locus is associated with susceptibility to type 1 diabetes in Japanese (Q24299393) (← links)
- Molecular cloning and overexpression of the human FK506-binding protein FKBP (Q24302504) (← links)
- Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains (Q24305310) (← links)
- A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization (Q24308939) (← links)
- An exon-skipping mutation in the btk gene of a patient with X-linked agammaglobulinemia and isolated growth hormone deficiency (Q24312387) (← links)
- A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype (Q24323881) (← links)
- Real-time PCR in virology (Q24514920) (← links)
- Selective amplification of an mRNA and related pseudogene for a human ADP-ribosylation factor, a guanine nucleotide-dependent protein activator of cholera toxin (Q24558739) (← links)
- Phylogenetic relationships among megabats, microbats, and primates (Q24559987) (← links)
- Amino acid sequence of Fel dI, the major allergen of the domestic cat: protein sequence analysis and cDNA cloning. (Q24560053) (← links)
- A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity (Q24561532) (← links)
- Steel-Dickie mutation encodes a c-kit ligand lacking transmembrane and cytoplasmic domains (Q24561693) (← links)
- Human pancreatitis-associated protein. Messenger RNA cloning and expression in pancreatic diseases (Q24564602) (← links)
- Cloning and expression of the defective genes from a patient with delta-aminolevulinate dehydratase porphyria (Q24564883) (← links)
- (Q24564889) (← links)
- Ancient roots for polymorphism at the HLA-DQ alpha locus in primates (Q24601097) (← links)
- Mitochondrial DNA sequences in single hairs from a southern African population (Q24602206) (← links)
- Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16 (Q24604743) (← links)
- Molecular cloning, characterization, and expression of human ADP-ribosylation factors: two guanine nucleotide-dependent activators of cholera toxin (Q24609326) (← links)
- Rearrangements of the tal-1 locus as clonal markers for T cell acute lymphoblastic leukemia (Q24617887) (← links)
- Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene (Q24628731) (← links)
- Characterization of seven novel mutations of the c-erbA beta gene in unrelated kindreds with generalized thyroid hormone resistance. Evidence for two "hot spot" regions of the ligand binding domain (Q24629530) (← links)
- Apolipoprotein C-III(Lys58----Glu). Identification of an apolipoprotein C-III variant in a family with hyperalphalipoproteinemia (Q24633209) (← links)
- Molecular analysis of major histocompatibility complex alleles associated with the lupus anticoagulant (Q24633473) (← links)
- DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA (Q24643021) (← links)
- Familial case with sequence variant in the testis-determining region associated with two sex phenotypes (Q24670157) (← links)
- Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal population (Q24670184) (← links)
- Clines of nuclear DNA markers suggest a largely neolithic ancestry of the European gene pool (Q24673282) (← links)
- Flightlessness and phylogeny amongst endemic rails (Aves:Rallidae) of the New Zealand region (Q24677510) (← links)
- Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes (Q24679270) (← links)
- Improved microarray methods for profiling the Yeast Knockout strain collection (Q24815298) (← links)
- Mutations which alter the level or structure of nsP4 can affect the efficiency of Sindbis virus replication in a host-dependent manner (Q27486588) (← links)
- Discrimination of hepatitis C virus in liver tissues from different patients with hepatocellular carcinomas by direct nucleotide sequencing of amplified cDNA of the viral genome (Q27488868) (← links)
- Proliferating cell nuclear antigen (pol30) mutations suppress cdc44 mutations and identify potential regions of interaction between the two encoded proteins (Q27936355) (← links)
- DBF8, an essential gene required for efficient chromosome segregation in Saccharomyces cerevisiae (Q27937527) (← links)
- Development of Cell-SELEX Technology and Its Application in Cancer Diagnosis and Therapy (Q28080168) (← links)
- Molecular characterization of four different classes of mutations in the isovaleryl-CoA dehydrogenase gene responsible for isovaleric acidemia (Q28118842) (← links)
- Identification of two missense mutations in a dihydrolipoamide dehydrogenase-deficient patient (Q28119036) (← links)
- Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus (Q28183211) (← links)
- A case of Fabry's disease in a patient with no alpha-galactosidase A activity caused by a single amino acid substitution of Pro-40 by Ser (Q28236442) (← links)
- Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system (Q28238045) (← links)
- Differential phenotypic expression by three mutant alleles in familial lecithin:cholesterol acyltransferase deficiency (Q28249521) (← links)
- Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter (Q28270737) (← links)
- A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesis (Q28272538) (← links)
- Nonexpression of the Human Serum Amyloid A Three (SAA3) Gene (Q28305684) (← links)
- Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture (Q28324214) (← links)
- 5-Fluorouracil induces apoptosis in human colon cancer cell lines with modulation of Bcl-2 family proteins (Q28369128) (← links)
- α,β-D-constrained nucleic acids are strong terminators of thermostable DNA polymerases in polymerase chain reaction (Q28477333) (← links)
- Development of a novel DNA aptamer ligand targeting to primary cultured tumor endothelial cells by a cell-based SELEX method (Q28485460) (← links)
- Isolation of a dnaA mutant of Bacillus subtilis defective in initiation of replication: amount of DnaA protein determines cells' initiation potential (Q28488823) (← links)