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2012, 4th ed., ISBN 1936113414, 3 v. (xxxiii, 1890, 46 p.)
Book
2012, 4th ed., ISBN 1936113414, v. 2 of 3, (xxxiii, 1890, 46 p.)
Book
2012, 4th ed., ISBN 1936113414, v. 3 of 3, (xxxiii, 1890, 46 p.)
Book
2012, 4th ed., ISBN 1936113414, v. 1 of 3, (xxxiii, 1890, 46 p.)
Book
1974, ISBN 9780879691127, xi, 1028
Book
2002, ISBN 0879696257, xxiii, 712
"DNA microarray technology is a new and powerful means to analyze genomes and characterize patterns of gene expression. Its applications are widespread across... 
Laboratory manuals | DNA microarrays
Book
by Shungin, Dmitry and Winkler, Thomas W and Croteau-Chonka, Damien C and Ferreira, Teresa and Locke, Adam E and Mägi, Reedik and Strawbridge, Rona J and Pers, Tune H and Fischer, Krista and Justice, Anne E and Workalemahu, Tsegaselassie and Wu, Joseph M. W and Buchkovich, Martin L and Heard-Costa, Nancy L and Roman, Tamara S and ng, Alexander W and Song, Ci and Gustafsson, Stefan and Day, Felix R and Esko, Tonu and Fall, Tove and Kutalik, Zoltán and Luan, Jian'an and Randall, Joshua C and Scherag, Ané and Vedantam, Sailaja and Wood, Anew R and Chen, Jin and Fehrmann, Rudolf and Karjalainen, Juha and Kahali, Bratati and Liu, Ching-Ti and Schmidt, Ellen M and Absher, Devin and Amin, Najaf and Anderson, Denise and Beekman, Marian and Bragg-Gresham, Jennifer L and Buyske, Steven and Demirkan, Ayse and Ehret, Georg B and Feitosa, Mary F and Goel, Anuj and Jackson, Anne U and Johnson, Toby and Kleber, Marcus E and Kristiansson, Kati and Mangino, Massimo and Mateo Leach, Irene and Medina-Gomez, Carolina and Palmer, Cameron D and Pasko, Dorota and Pechlivanis, Sonali and Peters, Marjolein J and Prokopenko, Inga and Stančáková, Alena and Ju Sung, Yun and Tanaka, Toshiko and Teumer, Alexander and van Vliet-Ostaptchouk, Jana V and Yengo, Loïc and Zhang, Weihua and Albrecht, Eva and Ärnlöv, Johan and Arscott, Gillian M and Bandinelli, Stefania and Barrett, Amy and Bellis, Claire and Bennett, Amanda J and Berne, Christian and Blüher, Matthias and Böhringer, Stefan and Bonnet, Fabrice and Böttcher, Yvonne and Bruinenberg, Marcel and Carba, Delia B and Caspersen, Ida H and Clarke, Robert and Daw, E. Warwick and Deelen, Joris and Deelman, Ewa and Delgado, Graciela and Doney, Alex S. F and Eklund, Niina and Erdos, Michael R and Estrada, Karol and Eury, Elodie and Frieich, Nele and Garcia, Melissa E and Gieaitis, Vilmantas and Gigante, Bruna and Go, Alan S and Golay, Alain and Grallert, Harald and Grammer, Tanja B and Gräßler, Jürgen and Grewal, Jagvir and Groves, Christopher J and Haller, Toomas and Hallmans, Goran and ... and PAGE Consortium and LifeLines Cohort Study and CARDIOGRAMplusC4D Consortium and MuTHER Consortium and ICBP and ADIPOGEN Consortium and CKDGen Consortium and GEFOS Consortium and Int Endogene Consortium and GENIE Consortium and MAGIC Investigators and ReproGen Consortium and GLGC and ADIPOGen Consortium and International Endogene Consortium and The PAGE Consortium and The International Endogene Consortium and The MAGIC Investigators and The ReproGen Consortium and The CKDGen Consortium and The ADIPOGen Consortium and The ICBP and The CARDIOGRAMplusC4D Consortium and The GENIE Consortium and The GLGC and The GEFOS Consortium and The MuTHER Consortium and The LifeLines Cohort Study and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature, ISSN 0028-0836, 2015, Volume 518, Issue 7538, pp. 187 - U378
Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our... 
HUMAN HEIGHT | ABDOMINAL ADIPOSITY | MULTIDISCIPLINARY SCIENCES | COMMON SNPS | SUSCEPTIBILITY LOCI | GLYCEMIC TRAITS | FALSE DISCOVERY | MESENCHYMAL STEM-CELLS | GENOME-WIDE ASSOCIATION | ADIPOGENIC DIFFERENTIATION | SEXUAL-DIMORPHISM | Body Mass Index | Genome-Wide Association Study | Age Factors | Neovascularization, Physiologic - genetics | Epigenesis, Genetic | Humans | Male | Continental Population Groups - genetics | Sex Characteristics | Obesity - genetics | Europe - ethnology | Genome, Human - genetics | Adipose Tissue - metabolism | Insulin - metabolism | Models, Biological | Adipocytes - metabolism | Insulin Resistance - genetics | Polymorphism, Single Nucleotide - genetics | Female | Body Fat Distribution | Transcription, Genetic - genetics | Adipogenesis - genetics | Waist-Hip Ratio | Quantitative Trait Loci - genetics | Adipose tissues | Quantitative trait loci | Genetic research | Genetic aspects | Research | Metabolism | Health aspects | Studies | Body mass index | Genealogy | Body fat | Insulin resistance | Genetics | Genomes | Abdomen | Meta-analysis | Index Medicus | Life Sciences | Adipocytes/metabolism Adipogenesis/genetics Adipose Tissue/metabolism Age Factors Body Fat Distribution Body Mass Index Continental Population Groups/genetics Epigenesis, Genetic Europe/ethnology Female Genome, Human/genetics Genome-Wide Association Study Humans Insulin/metabolism Insulin Resistance/genetics Male Models, Biological Neovascularization, Physiologic/genetics Obesity/genetics Polymorphism, Single Nucleotide/genetics Quantitative Trait Loci/genetics Sex Characteristics Transcription, Genetic/genetics Waist-Hip Ratio | Clinical Medicine | Hälsa och välfärd | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Health and Welfare
Journal Article
Cold Spring Harbor protocols, ISSN 1940-3402, 10/2018, Volume 2018, Issue 10, pp. 825 - 835
Once primers and probes have been designed and obtained, it is necessary to optimize their concentration for each real-time polymerase chain reaction (PCR)... 
Polymerase chain reaction | Amplification | DNA probes | Primers | Reproducibility | Real time | Assaying | Optimization | Deoxyribonucleic acid--DNA
Journal Article
Cold Spring Harbor protocols, ISSN 1940-3402, 10/2018, Volume 2018, Issue 10, pp. 836 - 842
It is essential to prepare a standard curve for every real-time polymerase chain reaction (PCR) experiment. This protocol is used to construct a standard curve... 
Polymerase chain reaction | Construction standards | Shellfish | Real time | Toxicity | Optimization
Journal Article
Cold Spring Harbor protocols, ISSN 1940-3402, 10/2018, Volume 2018, Issue 10, pp. 769 - 777
In real-time polymerase chain reaction (PCR), also called quantitative real-time PCR [or simply quantitative PCR (qPCR)] or kinetic PCR, the amplification of... 
Data analysis | Standardization | Pollution monitoring | Fluorescence | Data processing | Quantitation | Real time | Polymerase chain reaction | Amplification | Sensitivity | Reproducibility | Reagents | Recording | Deoxyribonucleic acid--DNA
Journal Article
Cold Spring Harbor Protocols, ISSN 1940-3402, 07/2019, Issue 7
This protocol describes the generation of radiolabeled cDNA probes from poly(A)+ RNA in a random priming reaction. Probes of this type are used for... 
Poly(A) | RNA probes | DNA probes | Primers | Priming | mRNA | Probes
Journal Article
Cold Spring Harbor protocols, ISSN 1940-3402, 06/2019, Volume 2019, Issue 6, p. pdb.top095109
The polymerase chain reaction (PCR) underlies almost all of modern molecular cloning. Using PCR, a defined target sequence that occurs once within a DNA of... 
Polymerase chain reaction | Genomes | Nucleotides | Nucleotide sequence | Cloning | Deoxyribonucleic acid--DNA
Journal Article
Cold Spring Harbor protocols, ISSN 1940-3402, 06/2019, Volume 2019, Issue 6, p. pdb.prot095224
Polymerase chain reaction (PCR), rather than the more labor-intensive minipreps, is often used to screen colonies of for recombinant plasmids containing... 
Polymerase chain reaction | Amplification | Screening | Nucleotide sequence | Plasmids | Primers | Colonies | Escherichia coli | Deoxyribonucleic acid--DNA | Recombinant | Gene sequencing
Journal Article
Cold Spring Harbor Protocols, ISSN 1940-3402, 03/2019, Volume 2019, Issue 3, pp. 244 - 245
This protocol describes the setup and use of Sephadex G-50 or Bio-Gel columns for the purification of DNA. 
Column chromatography | Deoxyribonucleic acid--DNA | Purification
Journal Article
Cold Spring Harbor Protocols, ISSN 1940-3402, 03/2019, Volume 2019, Issue 3, pp. 241 - 243
Radioactive isotopes are used as tracers to monitor the progress of many reactions used to synthesize DNA and RNA. To calculate the efficiency of such... 
Trichloroacetic acid | Radioisotopes | Nucleic acids | Chemical synthesis | Computing time | Ribonucleic acid--RNA | Isotopes | Deoxyribonucleic acid--DNA | Radioactivity | Tracers
Journal Article
Cold Spring Harbor Protocols, ISSN 1940-3402, 03/2019, Volume 2019, Issue 3, pp. 188 - 191
The standard polymerase chain reaction (PCR) is easily capable of amplifying segments of DNA smaller than ∼3 kb in length-sufficient for most purposes, but not... 
Polymerase chain reaction | Amplification | Exonuclease | Proofreading | DNA-directed DNA polymerase | Deoxyribonucleic acid--DNA
Journal Article
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