- Products [0]
- Services Marketplace [0]
- Learn More [0]
- Documents & Support [169,479]
Search unsuccessful? Go to Contact us, enter your product name, and complete the form.
Documents & Support
Citations & References
Common variants at 11p13 are associated with susceptibility to tuberculosis.
- Authors: Thye T, Owusu-Dabo E, Vannberg FO, van Crevel R, Curtis J, Sahiratmadja E, Balabanova Y, Ehmen C, Muntau B, Ruge G, Sievertsen J, Gyapong J, Nikolayevskyy V, Hill PC, Sirugo G, Drobniewski F, van de Vosse E, Newport M, Alisjahbana B, Nejentsev S, Ottenhoff TH, Hill AV, Horstmann RD, Meyer CG
- Journal: Nat Genet 2012; (44):3 257-259
- PubMed ID: 22306650
Citations & References
Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity.
- Authors: Rasmussen M, Sundström M, Göransson Kultima H, Botling J, Micke P, Birgisson H, Glimelius B, Isaksson A
- Journal: Genome Biol 2011; (12):10 R108-R108
- PubMed ID: 22023820
Citations & References
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant.
- Authors: Bolze A, Abhyankar A, Grant AV, Patel B, Yadav R, Byun M, Caillez D, Emile JF, Pastor-Anglada M, Abel L, Puel A, Govindarajan R, de Pontual L, Casanova JL
- Journal: PLoS One 2012; (7):1 e29708-e29708
- PubMed ID: 22238637
Citations & References
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
- Authors: Soemedi R, Topf A, Wilson IJ, Darlay R, Rahman T, Glen E, Hall D, Huang N, Bentham J, Bhattacharya S, Cosgrove C, Brook JD, Granados-Riveron J, Setchfield K, Bu'lock F, Thornborough C, Devriendt K, Breckpot J, Hofbeck M, Lathrop M, Rauch A, Blue GM, Winlaw DS, Hurles M, Santibanez-Koref M, Cordell HJ, Goodship JA, Keavney BD
- Journal: Hum Mol Genet 2012; (21):7 1513-1520
- PubMed ID: 22199024
Citations & References
Screening of congenital heart disease patients using multiplex ligation-dependent probe amplification: early diagnosis of syndromic patients.
- Authors: Sørensen KM, El-Segaier M, Fernlund E, Errami A, Bouvagnet P, Nehme N, Steensberg J, Hjortdal V, Soller M, Behjati M, Werge T, Kirchoff M, Schouten J, Tommerup N, Andersen PS, Larsen LA
- Journal: Am J Med Genet A 2012; (158A):4 720-725
- PubMed ID: 22383218
Citations & References
Clinical and subclinical endometritis induced alterations in bovine endometrial transcriptome and miRNome profile.
- Authors: Salilew-Wondim D, Ibrahim S, Gebremedhn S, Tesfaye D, Heppelmann M, Bollwein H, Pfarrer C, Tholen E, Neuhoff C, Schellander K, Hoelker M
- Journal: BMC Genomics 2016; (17): 218-218
- PubMed ID: 26965375
Citations & References
1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma.
- Authors: Mackintosh C, Ordóñez JL, García-Domínguez DJ, Sevillano V, Llombart-Bosch A, Szuhai K, Scotlandi K, Alberghini M, Sciot R, Sinnaeve F, Hogendoorn PC, Picci P, Knuutila S, Dirksen U, Debiec-Rychter M, Schaefer KL, de Álava E
- Journal: Oncogene 2012; (31):10 1287-1298
- PubMed ID: 21822310
Citations & References
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.
- Authors: Nakano M, Ikeda Y, Tokuda Y, Fuwa M, Omi N, Ueno M, Imai K, Adachi H, Kageyama M, Mori K, Kinoshita S, Tashiro K
- Journal: PLoS One 2012; (7):3 e33389-e33389
- PubMed ID: 22428042
Citations & References
GOexpress: an R/Bioconductor package for the identification and visualisation of robust gene ontology signatures through supervised learning of gene expression data.
- Authors: Rue-Albrecht K, McGettigan PA, Hernández B, Nalpas NC, Magee DA, Parnell AC, Gordon SV, MacHugh DE
- Journal: BMC Bioinformatics 2016; (17): 126-126
- PubMed ID: 26968614
Citations & References
High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations.
- Authors: Kühn MW, Radtke I, Bullinger L, Goorha S, Cheng J, Edelmann J, Gohlke J, Su X, Paschka P, Pounds S, Krauter J, Ganser A, Quessar A, Ribeiro R, Gaidzik VI, Shurtleff S, Krönke J, Holzmann K, Ma J, Schlenk RF, Rubnitz JE, Döhner K, Döhner H, Downing JR
- Journal: Blood 2012; (119):10 e67-e75
- PubMed ID: 22234698
Citations & References
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
- Authors: Kenny EE, Pe'er I, Karban A, Ozelius L, Mitchell AA, Ng SM, Erazo M, Ostrer H, Abraham C, Abreu MT, Atzmon G, Barzilai N, Brant SR, Bressman S, Burns ER, Chowers Y, Clark LN, Darvasi A, Doheny D, Duerr RH, Eliakim R, Giladi N, Gregersen PK, Hakonarson H, Jones MR, Marder K, McGovern DP, Mulle J, Orr-Urtreger A, Proctor DD, Pulver A, Rotter JI, Silverberg MS, Ullman T, Warren ST, Waterman M, Zhang W, Bergman A, Mayer L, Katz S, Desnick RJ, Cho JH, Peter I
- Journal: PLoS Genet 2012; (8):3 e1002559-e1002559
- PubMed ID: 22412388
Citations & References
Use of amoB as a new molecular marker for ammonia-oxidizing bacteria.
Citations & References
Facile whole mitochondrial genome resequencing from nipple aspirate fluid using MitoChip v2.0.
- Authors: Jakupciak JP, Maggrah A, Maragh S, Maki J, Reguly B, Maki K, Wittock R, Robinson K, Wagner PD, Thayer RE, Gehman K, Gehman T, Srivastava S, Ngom A, Dakubo GD, Parr RL
- Journal: BMC Cancer 2008; (8): 95-95
- PubMed ID: 18402686
Citations & References
Alteration of gene expression during nasopharyngeal carcinogenesis revealed by oligonucleotide microarray after microdissection of tumor tissue and normal epithelia from nasopharynx.
- Authors: Liu ZQ, Tian YQ, Hu YF, Li XL, Ma FR, Li GY
- Journal: Chin Med J (Engl) 2009; (122):4 437-443
- PubMed ID: 19302751
Citations & References
Meta-Analysis of Transcriptional Responses to Mastitis-Causing Escherichia coli.
- Authors: Younis S, Javed Q, Blumenberg M
- Journal: PLoS One 2016; (11):3 e0148562-e0148562
- PubMed ID: 26933871
