Pages that link to "Q30761976"
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The following pages link to Chip-based genotyping by mass spectrometry (Q30761976):
Displaying 124 items.
- Analysis of chimpanzee history based on genome sequence alignments (Q21092479) (← links)
- Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene (Q21563321) (← links)
- Detecting recent positive selection in the human genome from haplotype structure (Q22122511) (← links)
- Assessing the impact of population stratification on genetic association studies (Q22337235) (← links)
- Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans (Q24288720) (← links)
- An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspeckles (Q24310786) (← links)
- A High-Density Admixture Map for Disease Gene Discovery in African Americans (Q24533390) (← links)
- Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4 (Q24538382) (← links)
- Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy (Q24643967) (← links)
- Accelerated genetic drift on chromosome X during the human dispersal out of Africa (Q24655578) (← links)
- MuPlex: multi-objective multiplex PCR assay design (Q24812244) (← links)
- Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene (Q28280022) (← links)
- The study to understand the genetics of the acute response to metformin and glipizide in humans (SUGAR-MGH): design of a pharmacogenetic resource for type 2 diabetes (Q28545045) (← links)
- TCF7L2 polymorphism, weight loss and proinsulin:insulin ratio in the diabetes prevention program (Q28742128) (← links)
- Detecting natural selection by empirical comparison to random regions of the genome (Q28750109) (← links)
- A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays (Q30651566) (← links)
- Homogeneous assays for single-nucleotide polymorphism typing using AlphaScreen (Q30662268) (← links)
- MALDI-TOF-MS analysis of protein and DNA. (Q30697312) (← links)
- Matrix-induced fragmentation of P3'-N5' phosphoramidate-containing DNA: high-throughput MALDI-TOF analysis of genomic sequence polymorphisms (Q30718506) (← links)
- Genotyping single-nucleotide polymorphisms by matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry (Q30718660) (← links)
- Sugar additives for MALDI matrices improve signal allowing the smallest nucleotide change (A:T) in a DNA sequence to be resolved (Q30725753) (← links)
- DNA sequencing using biotinylated dideoxynucleotides and mass spectrometry (Q30760911) (← links)
- Facile method for automated genotyping of single nucleotide polymorphisms by mass spectrometry (Q30818232) (← links)
- Accurate mass measurement of DNA oligonucleotide ions using high-resolution time-of-flight mass spectrometry (Q30831661) (← links)
- Solid phase capturable dideoxynucleotides for multiplex genotyping using mass spectrometry (Q30842910) (← links)
- Molecular haplotyping at high throughput. (Q30859785) (← links)
- Mass spectrometry for genotyping: an emerging tool for molecular medicine (Q30881394) (← links)
- A new MALDI-TOF based mini-sequencing assay for genotyping of SNPS. (Q30882915) (← links)
- Multiplex genotyping of the human β2-adrenergic receptor gene using solid-phase capturable dideoxynucleotides and mass spectrometry (Q30918658) (← links)
- MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging (Q30938725) (← links)
- Full flexibility genotyping of single nucleotide polymorphisms by the GOOD assay (Q30970910) (← links)
- Comparison of PrASE and Pyrosequencing for SNP Genotyping (Q33263696) (← links)
- MALDI-TOF mass spectrometry for quantitative, specific, and sensitive analysis of DNA and RNA. (Q33263722) (← links)
- Novel Plexor SNP genotyping technology: comparisons with TaqMan and homogenous MassEXTEND MALDI-TOF mass spectrometry (Q33282765) (← links)
- The impact of severity of hypertension on association of PGC-1alpha gene with blood pressure and risk of hypertension (Q33304403) (← links)
- A high-density admixture scan in 1,670 African Americans with hypertension (Q33306108) (← links)
- Discerning the ancestry of European Americans in genetic association studies (Q33315561) (← links)
- Identification and characterisation of novel SNP markers in Atlantic cod: evidence for directional selection (Q33321340) (← links)
- A comparison of SNP and STR loci for delineating population structure and performing individual genetic assignment. (Q33638564) (← links)
- Transformation of somatic cells into stem cell-like cells under a stromal niche (Q33729997) (← links)
- Lab-on-a-plate: extending the functionality of MALDI-MS and LDI-MS targets (Q33799571) (← links)
- Quantitative trait locus mapping and DNA array hybridization identify an FLM deletion as a cause for natural flowering-time variation (Q33850366) (← links)
- Genomic analysis (Q33884928) (← links)
- Polymorphism, selection and tandem duplication of transferrin genes in Atlantic cod (Gadus morhua)--conserved synteny between fish monolobal and tetrapod bilobal transferrin loci (Q33911730) (← links)
- Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae) (Q33960298) (← links)
- Detection of the placental epigenetic signature of the maspin gene in maternal plasma. (Q34078379) (← links)
- Quality and completeness of SNP databases (Q34185532) (← links)
- Genetic polymorphisms in chronic hyperplastic sinusitis with nasal polyposis. (Q34187423) (← links)
- Approaches to allele frequency determination (Q34188551) (← links)
- High-throughput genotyping assay approaches (Q34189914) (← links)
- Advances in sample preparation in electromigration, chromatographic and mass spectrometric separation methods (Q34195694) (← links)
- Association between Hcy levels and the CBS844ins68 and MTHFR C677T polymorphisms with essential hypertension (Q34265348) (← links)
- PCR candidate region mismatch scanning: adaptation to quantitative, high-throughput genotyping (Q34272353) (← links)
- Single nucleotide polymorphism seeking long term association with complex disease (Q34366761) (← links)
- Genetic modulation of lipid profiles following lifestyle modification or metformin treatment: the Diabetes Prevention Program (Q34404405) (← links)
- Effects of genetic variants previously associated with fasting glucose and insulin in the Diabetes Prevention Program (Q34415887) (← links)
- Genetic polymorphisms of ATP-binding cassette (ABC) proteins, overall survival and drug toxicity in patients with Acute Myeloid Leukemia (Q34559115) (← links)
- Multiplex allele-specific target amplification based on PCR suppression (Q34590290) (← links)
- A genomewide admixture map for Latino populations (Q34628377) (← links)
- An epigenetic state associated with areas of gene duplication (Q34655383) (← links)
- Progress in high throughput SNP genotyping methods (Q34670684) (← links)
- Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program (Q34718943) (← links)
- A broad analysis of IL1 polymorphism and rheumatoid arthritis. (Q34788695) (← links)
- Functional significance of single nucleotide polymorphisms in the lactase gene in diverse US patients and evidence for a novel lactase persistence allele at -13909 in those of European ancestry (Q35020667) (← links)
- Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes (Q35041076) (← links)
- Development of reference transcriptomes for the major field insect pests of cowpea: a toolbox for insect pest management approaches in west Africa (Q35053373) (← links)
- Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men. (Q35080445) (← links)
- Temporal change in genetic integrity suggests loss of local adaptation in a wild Atlantic salmon (Salmo salar) population following introgression by farmed escapees (Q35092773) (← links)
- A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia (Q35122001) (← links)
- Analysis of sequence variations in several human genes using phosphoramidite bond DNA fragmentation and chip-based MALDI-TOF. (Q35125902) (← links)
- Development and characterization of a novel human Waldenström macroglobulinemia cell line: RPCI-WM1, Roswell Park Cancer Institute - Waldenström Macroglobulinemia 1. (Q35524194) (← links)
- TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program (Q35568877) (← links)
- Digital genotyping using molecular affinity and mass spectrometry (Q35590367) (← links)
- Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos (Q35625945) (← links)
- Genome-wide association study of antidepressant treatment-emergent suicidal ideation (Q35679930) (← links)
- The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera (Q35711211) (← links)
- Admixture mapping of an allele affecting interleukin 6 soluble receptor and interleukin 6 levels (Q35752550) (← links)
- Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology (Q35785798) (← links)
- Genetic variation in the IL-10 pathway modulates severity of acute graft-versus-host disease following hematopoietic cell transplantation: synergism between IL-10 genotype of patient and IL-10 receptor beta genotype of donor (Q35847781) (← links)
- Genome-Wide Association Study Reveals Host Genetic Factors for Liver Diseases (Q35906019) (← links)
- Combining evidence of natural selection with association analysis increases power to detect malaria-resistance variants (Q35946301) (← links)
- Miniaturization in functional genomics and proteomics (Q36148378) (← links)
- The C allele of ATM rs11212617 does not associate with metformin response in the Diabetes Prevention Program (Q36181390) (← links)
- Molecular engineering approaches for DNA sequencing and analysis (Q36252216) (← links)
- The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA. (Q36326943) (← links)
- Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications (Q36424760) (← links)
- Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program (Q36496759) (← links)
- Screen for Footprints of Selection during Domestication/Captive Breeding of Atlantic Salmon (Q36530054) (← links)
- Association of fatty-acid synthase polymorphisms and expression with outcomes after radical prostatectomy (Q36570819) (← links)
- SNP panel identification assay (SPIA): a genetic-based assay for the identification of cell lines (Q36633219) (← links)
- A genomic selection component analysis characterizes migration-selection balance (Q36639668) (← links)
- A linkage map of the Atlantic salmon (Salmo salar) based on EST-derived SNP markers (Q36688544) (← links)
- Arrayed identification of DNA signatures (Q36691728) (← links)
- Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program (Q36842653) (← links)
- Association studies of common variants in 10 hypogonadotropic hypogonadism genes with age at menarche (Q36971993) (← links)
- MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. (Q36986986) (← links)
- Obesity polymorphisms identified in genome-wide association studies interact with n-3 polyunsaturated fatty acid intake and modify the genetic association with adiposity phenotypes in Yup'ik people (Q37126358) (← links)
- Association testing of TCF7L2 polymorphisms with type 2 diabetes in multi-ethnic youth. (Q37154128) (← links)
- Triplet repeat length bias and variation in the human transcriptome (Q37351751) (← links)
- CDKAL1 and HHEX are associated with type 2 diabetes-related traits among Yup'ik people. (Q37660145) (← links)
- Expressed sequences and polymorphisms in rohu carp (Labeo rohita, Hamilton) revealed by mRNA-seq. (Q38328085) (← links)
- Sequential DEXAS: a method for obtaining DNA sequences from genomic DNA and blood in one reaction (Q39982185) (← links)
- Monoallelic expression and asynchronous replication of p120 catenin in mouse and human cells (Q40496560) (← links)
- Association between mitochondrial DNA haplogroup and myelodysplastic syndromes. (Q40778773) (← links)
- A single major QTL controls expression of larval Cry1F resistance trait in Ostrinia nubilalis (Lepidoptera: Crambidae) and is independent of midgut receptor genes (Q42016316) (← links)
- Multiple regions within 8q24 independently affect risk for prostate cancer (Q42038345) (← links)
- Embryonic stem cell-like cells established by culture of adult ovarian cells in mice (Q42287444) (← links)
- Correlation between polymorphisms of the reduced folate carrier gene (SLC19A1) and survival after pemetrexed-based therapy in non-small cell lung cancer: a North Central Cancer Treatment Group-based exploratory study. (Q42961795) (← links)
- Polymorphisms in stearoyl coa desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup'ik people. (Q43750703) (← links)
- Screening genetic variability at the CNR1 gene in both major depression etiology and clinical response to citalopram treatment (Q45754167) (← links)
- Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression (Q46174250) (← links)
- A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility (Q46279618) (← links)
- Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism (Q48440447) (← links)
- Unique features of mutations revealed by sequentially reprogrammed induced pluripotent stem cells (Q50600342) (← links)
- A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis. (Q51171205) (← links)
- Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes (Q57040429) (← links)
- Correlation of interleukin-10 gene haplotype with hepatocellular carcinoma in Taiwan (Q57205363) (← links)
- Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes (Q57251858) (← links)
- Conservation genomics of Atlantic salmon: SNPs associated with QTLs for adaptive traits in parr from four trans-Atlantic backcrosses (Q60567774) (← links)
- Rapid genotyping by MALDI-monitored nuclease selection from probe libraries (Q73150375) (← links)
- Current awareness on comparative and functional genomics [bibliography] (Q73748101) (← links)
- A commented dictionary of techniques for genotyping (Q73892756) (← links)
- Screening of PAH Common Mutations in Chinese Phenylketonuria Patients Using iPLEX MALDI-TOF MS (Q89623790) (← links)
- Upgrading SELEX technology by using lambda exonuclease digestion for single-stranded DNA generation (Q95779812) (← links)