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Cited by in CrossRef
Number Cited Articles
Wei-Qiang Liu, Jie-Liang Li, Jian Wang, Wen-Yin He, Lip Va, Xiao-Ming Sheng, Bai-Lin Wu, Xiao-Fang Sun. Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome InactivationStem Cells and Development 2015; 24(15): 1779 doi: 10.1089/scd.2014.0463
Adelheid Woehrer, Johannes A Hainfellner. Molecular diagnostics: techniques and recommendations for 1p/19q assessmentCNS Oncology 2015; 4(5): 295 doi: 10.2217/cns.15.28
Heidi Schwarzenbach, Klaus Pantel. General Methods and Overviews, Lung Carcinoma and Prostate Carcinoma2008; 2: 481 doi: 10.1007/978-1-4020-8442-3_34
Elisa Närvä, Reija Autio, Nelly Rahkonen, Lingjia Kong, Neil Harrison, Danny Kitsberg, Lodovica Borghese, Joseph Itskovitz-Eldor, Omid Rasool, Petr Dvorak, Outi Hovatta, Timo Otonkoski, Timo Tuuri, Wei Cui, Oliver Brüstle, Duncan Baker, Edna Maltby, Harry D Moore, Nissim Benvenisty, Peter W Andrews, Olli Yli-Harja, Riitta Lahesmaa. High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosityNature Biotechnology 2010; 28(4): 371 doi: 10.1038/nbt.1615
Connie E. Kim, Kam-Meng Tchou-Wong, William N. Rom. Sputum-Based Molecular Biomarkers for the Early Detection of Lung Cancer: Limitations and PromiseCancers 2011; 3(3): 2975 doi: 10.3390/cancers3032975
Lieke van Huis-Tanja, Dinemarie Kweekel, Hans Gelderblom, Miriam Koopman, Kees Punt, Henk-Jan Guchelaar, Tahar van der Straaten. Concordance of genotype for polymorphisms in DNA isolated from peripheral blood and colorectal cancer tumor samplesPharmacogenomics 2013; 14(16): 2005 doi: 10.2217/pgs.13.169
Marieta I. Toma, Marianne Grosser, Alexander Herr, Daniela E. Aust, Axel Meye, Christian Hoefling, Susanne Fuessel, Daniela Wuttig, Manfred P. Wirth, Gustavo B. Baretton. Loss of Heterozygosity and Copy Number Abnormality in Clear Cell Renal Cell Carcinoma Discovered by High-Density Affymetrix 10K Single Nucleotide Polymorphism Mapping ArrayNeoplasia 2008; 10(7): 634 doi: 10.1593/neo.08160
Jung H. Park, Ye L. Jung, Kyungmee Lee, Changyeol Lee, Batule Bhagwan, Hyun G. Park. Emerging Areas in Bioengineering2018; : 531 doi: 10.1002/9783527803293.ch30
Takeshi Onda, Nobuharu Yamamoto, Tsukasa Kuroiwa, Akira Katakura, Nobuo Takano, Takahiko Shibahara. Aberrant expression of the ZDHHC14 gene in squamous cell carcinoma of the human tongueAsian Journal of Oral and Maxillofacial Surgery 2010; 22(4): 187 doi: 10.1016/j.ajoms.2010.09.001
Maryam Etebari, Mohsen Navari, Pier Piccaluga. SNPs Array Karyotyping in Non-Hodgkin LymphomaMicroarrays 2015; 4(4): 551 doi: 10.3390/microarrays4040551
Allison B. Chambliss, Mark A. Marzinke. Contemporary Practice in Clinical Chemistry2020; : 337 doi: 10.1016/B978-0-12-815499-1.00020-X
Ichiro Nakachi, Jessica L. Rice, Christopher D. Coldren, Michael G. Edwards, Robert S. Stearman, Steven C. Glidewell, Marileila Varella-Garcia, Wilbur A. Franklin, Robert L. Keith, Marina T. Lewis, Bifeng Gao, Daniel T. Merrick, York E. Miller, Mark W. Geraci. Application of SNP Microarrays to the Genome-Wide Analysis of Chromosomal Instability in Premalignant Airway LesionsCancer Prevention Research 2014; 7(2): 255 doi: 10.1158/1940-6207.CAPR-12-0485
Belinda J. Wagner, Sharon C. Presnell. Basic Concepts of Molecular PathologyMolecular Pathology Library 2009; 2: 97 doi: 10.1007/978-0-387-89626-7_11
Philip T. Cagle, Jaishree Jagirdar, Helmut H. Popper. Dail and Hammar’s Pulmonary Pathology2008; : 47 doi: 10.1007/978-0-387-72114-9_2
Zendee Elaba, Michael J. Murphy, Laila Mnayer. Molecular Diagnostics in Dermatology and Dermatopathology2011; : 27 doi: 10.1007/978-1-60761-171-4_3
Mohammad Ilyas. COLD-HRM: A Combination of Methods to Infer the Nature of Somatic MutationsAdvances in Cytology & Pathology 2017; 2(2) doi: 10.15406/acp.2017.02.00017
Vanessa Moreno. Kidney Biomarkers2020; : 19 doi: 10.1016/B978-0-12-815923-1.00002-X
Ana Velasco, Judit Pallares, Maria Santacana, Andre Yeramian, Xavier Dolcet, Nuria Eritja, Soraya Puente, Anabel Sorolla, Nuria Llecha, Xavier Matias-Guiu. Loss of Heterozygosity in Endometrial CarcinomaInternational Journal of Gynecological Pathology 2008; 27(3): 305 doi: 10.1097/PGP.0b013e31815daf1a