Artykuły w czasopismach na temat „Array hybridisation analysis”
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Bachman, Kristine K., Stephanie J. DeWard, Constantinos Chrysostomou, Ricardo Munoz i Suneeta Madan-Khetarpal. "Array CGH as a first-tier test for neonates with congenital heart disease". Cardiology in the Young 25, nr 1 (6.11.2013): 115–22. http://dx.doi.org/10.1017/s1047951113001868.
Pełny tekst źródłaHightower, Hannah B., Nathaniel H. Robin, Fady M. Mikhail i Namasivayam Ambalavanan. "Array comparative genomic hybridisation testing in CHD". Cardiology in the Young 25, nr 6 (8.10.2014): 1155–72. http://dx.doi.org/10.1017/s1047951114001838.
Pełny tekst źródłaMermer, Serdar, i Derya Aydın Şahin. "Array comparative genomic hybridisation results of non-syndromic children with the conotruncal heart anomaly". Cardiology in the Young 32, nr 2 (20.01.2022): 301–6. http://dx.doi.org/10.1017/s104795112100473x.
Pełny tekst źródłaFinn, Stephen P., Paul Smyth, Esther O’Regan, Susanne Cahill, Richard Flavin, John O’Leary i Orla Sheils. "Array comparative genomic hybridisation analysis of gamma-irradiated human thyrocytes". Virchows Archiv 445, nr 4 (17.07.2004): 396–404. http://dx.doi.org/10.1007/s00428-004-1070-9.
Pełny tekst źródłaCreytens, David, Joost van Gorp, Liesbeth Ferdinande, Nadine Van Roy i Louis Libbrecht. "Array-based comparative genomic hybridisation analysis of a pleomorphic myxoid liposarcoma". Journal of Clinical Pathology 67, nr 9 (26.06.2014): 834–35. http://dx.doi.org/10.1136/jclinpath-2014-202420.
Pełny tekst źródłaBauersachs, S., S. Rehfeld, SE Ulbrich, S. Mallok, K. Prelle, H. Wenigerkind, R. Einspanier, H. Blum i E. Wolf. "Monitoring gene expression changes in bovine oviduct epithelial cells during the oestrous cycle". Journal of Molecular Endocrinology 32, nr 2 (1.04.2004): 449–66. http://dx.doi.org/10.1677/jme.0.0320449.
Pełny tekst źródłaWei, Ching Kuo, Shun Hsing Chen i Ming Chih Chen. "An empirical analysis of intention to use array-comparative genomic hybridisation method". International Journal of Biomedical Engineering and Technology 21, nr 3 (2016): 279. http://dx.doi.org/10.1504/ijbet.2016.078291.
Pełny tekst źródłaKriegshäuser, Gernot, Veronika Auner, Eva Schuster, Barbara Holzer, Christian Oberkanins, Reinhard Horvat, Paul Speiser i Robert Zeillinger. "KRAS mutation analysis in genomic DNA isolated from formalin-fixed paraffin-embedded ovarian tissue: evaluation of a strip-based reverse-hybridisation assay". Journal of Clinical Pathology 64, nr 3 (22.01.2011): 252–56. http://dx.doi.org/10.1136/jcp.2010.081414.
Pełny tekst źródłaOhguri, T. "Cytogenetic analysis of myxoid liposarcoma and myxofibrosarcoma by array-based comparative genomic hybridisation". Journal of Clinical Pathology 59, nr 9 (1.09.2006): 978–83. http://dx.doi.org/10.1136/jcp.2005.034942.
Pełny tekst źródłaLall, Meena, Pushpa Saviour, Ratna Puri, Preeti Paliwal, Surbhi Mahajan i Ishwar Verma. "Combined classical cytogenetics and array Comparative Genomic Hybridisation for genomic copy number analysis". Molecular Cytogenetics 7, Suppl 1 (2014): P3. http://dx.doi.org/10.1186/1755-8166-7-s1-p3.
Pełny tekst źródłaKawanishi, H., T. Takahashi, M. Ito, Y. Matsui, J. Watanabe, N. Ito, T. Kamoto i in. "Genetic analysis of multifocal superficial urothelial cancers by array-based comparative genomic hybridisation". British Journal of Cancer 97, nr 2 (19.06.2007): 260–66. http://dx.doi.org/10.1038/sj.bjc.6603850.
Pełny tekst źródłaWeiss, M. M. "Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomach". Molecular Pathology 56, nr 5 (1.10.2003): 293–98. http://dx.doi.org/10.1136/mp.56.5.293.
Pełny tekst źródłaMcMahon, Colin J., Conall T. Morgan i Marie T. Greally. "Chromosome 22q11.21 microduplication in association with hypoplastic left heart syndrome with hypoplastic pulmonary arteries". Cardiology in the Young 25, nr 1 (22.01.2014): 167–70. http://dx.doi.org/10.1017/s104795111300231x.
Pełny tekst źródłaForster, T., D. Roy i P. Ghazal. "Experiments using microarray technology: limitations and standard operating procedures". Journal of Endocrinology 178, nr 2 (1.08.2003): 195–204. http://dx.doi.org/10.1677/joe.0.1780195.
Pełny tekst źródłaChua, E. W., S. Cree, M. L. Barclay, K. Doudney, K. Lehnert, A. Aitchison i M. A. Kennedy. "Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producers". Pharmacogenomics Journal 15, nr 5 (10.03.2015): 414–21. http://dx.doi.org/10.1038/tpj.2015.9.
Pełny tekst źródłaSantos, Marta, Patrícia Dias-Pereira, Christina Williams, Carlos Lopes i Matthew Breen. "Malignant canine mammary tumours: Preliminary genomic insights using oligonucleotide array comparative genomic hybridisation analysis". Veterinary Journal 222 (kwiecień 2017): 68–71. http://dx.doi.org/10.1016/j.tvjl.2017.03.005.
Pełny tekst źródłaLundén, K., M. Eklund, R. Finlay, J. Stenlid i F. O. Asiegbu. "Heterologous array analysis in Heterobasidion: Hybridisation of cDNA arrays with probe from mycelium of S, P or F-types". Journal of Microbiological Methods 75, nr 2 (październik 2008): 219–24. http://dx.doi.org/10.1016/j.mimet.2008.06.014.
Pełny tekst źródłaKarimpour-Fard, Anis, Laura Dumas, Tzulip Phang, James M. Sikela i Lawrence E. Hunter. "A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation". Human Genomics 4, nr 6 (2010): 421. http://dx.doi.org/10.1186/1479-7364-4-6-421.
Pełny tekst źródłaRobson, Stephen C., Lyn S. Chitty, Stephen Morris, Talitha Verhoef, Gareth Ambler, Diana G. Wellesley, Ruth Graham, Claire Leader, Jane Fisher i John A. Crolla. "Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation". Efficacy and Mechanism Evaluation 4, nr 1 (luty 2017): 1–104. http://dx.doi.org/10.3310/eme04010.
Pełny tekst źródłaHallor, K. H., J. Staaf, G. Jönsson, M. Heidenblad, F. Vult von Steyern, H. C. F. Bauer, M. IJszenga i in. "Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation". British Journal of Cancer 98, nr 2 (11.12.2007): 434–42. http://dx.doi.org/10.1038/sj.bjc.6604130.
Pełny tekst źródłaSirard, Marc-André, Isabelle Dufort, Maud Vallée, Lyne Massicotte, Catherine Gravel, Hélène Reghenas, Andrew J. Watson, W. Allan King i Claude Robert. "Potential and limitations of bovine-specific arrays for the analysis of mRNA levels in early development: preliminary analysis using a bovine embryonic array". Reproduction, Fertility and Development 17, nr 2 (2005): 47. http://dx.doi.org/10.1071/rd04113.
Pełny tekst źródłaBersinger, Nick A., Markus Eisenhut, Petra Stute i Michael von Wolff. "Gonadotropin Stimulation Has Only a Limited Effect on the Concentration of Follicular Fluid Signalling Proteins: An Antibody Array Analysis". International Journal of Reproductive Medicine 2021 (27.01.2021): 1–7. http://dx.doi.org/10.1155/2021/2906164.
Pełny tekst źródłaRoberts, Ian, Stephanie A. Carter, Cinzia G. Scarpini, Konstantina Karagavriilidou, Jenny C. J. Barna, Mark Calleja i Nicholas Coleman. "A High-Throughput Computational Framework for Identifying Significant Copy Number Aberrations from Array Comparative Genomic Hybridisation Data". Advances in Bioinformatics 2012 (13.09.2012): 1–12. http://dx.doi.org/10.1155/2012/876976.
Pełny tekst źródłaNakamura, Akie, Koji Muroya, Hiroko Ogata-Kawata, Kazuhiko Nakabayashi, Keiko Matsubara, Tsutomu Ogata, Kenji Kurosawa, Maki Fukami i Masayo Kagami. "A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowth". Journal of Medical Genetics 55, nr 8 (17.02.2018): 567–70. http://dx.doi.org/10.1136/jmedgenet-2017-104986.
Pełny tekst źródłaSun, Lijuan, Qingqing Wu, Shi-Wen Jiang, Yani Yan, Xin Wang, Juan Zhang, Yan Liu, Ling Yao, Yuqing Ma i Li Wang. "Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis". BioMed Research International 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/426379.
Pełny tekst źródłaSomenzi, Elisa, Paolo Ajmone-Marsan i Mario Barbato. "Identification of Ancestry Informative Marker (AIM) Panels to Assess Hybridisation between Feral and Domestic Sheep". Animals 10, nr 4 (30.03.2020): 582. http://dx.doi.org/10.3390/ani10040582.
Pełny tekst źródłaHeyning, F. H., P. M. Jansen, P. C. W. Hogendoorn i K. Szuhai. "Array-based comparative genomic hybridisation analysis reveals recurrent chromosomal alterations in primary diffuse large B cell lymphoma of bone". Journal of Clinical Pathology 63, nr 12 (20.10.2010): 1095–100. http://dx.doi.org/10.1136/jcp.2010.078915.
Pełny tekst źródłaCui, Yushan, Yang Liu, Danyang Wang, Yuzhang Liu, Lina Liu i Baijun Fang. "Comparative Analysis of miRNA Expression Profiles of Multiple Myeloma with 1q21 Gains and Normal FISH". Acta Haematologica 139, nr 2 (2018): 96–100. http://dx.doi.org/10.1159/000486662.
Pełny tekst źródłaHillman, S., S. Pretlove, A. Coomarasamy, D. McMullan, E. Davison, E. Maher i M. Kilby. "Additional information from array comparative genomic hybridisation technology over conventional karyotyping in prenatal diagnosis-a systematic review and meta-analysis". Archives of Disease in Childhood - Fetal and Neonatal Edition 95, Supplement 1 (1.06.2010): Fa4. http://dx.doi.org/10.1136/adc.2010.192310.1.1.
Pełny tekst źródłaGuemann, Anne-Sophie, Joris Andrieux, Florence Petit, Emmanuel Halimi, Sonia Bouquillon, Sylvie Manouvrier-Hanu, Jiddeke Van De Kamp i in. "ELN gene triplication responsible for familial supravalvular aortic aneurysm". Cardiology in the Young 25, nr 4 (17.06.2014): 712–17. http://dx.doi.org/10.1017/s1047951114000766.
Pełny tekst źródłaPryor, LD, ER Williams i BV Gunn. "A morphometric analysis of Eucalyptus urophylla and related taxa with descriptions of two new species". Australian Systematic Botany 8, nr 1 (1995): 57. http://dx.doi.org/10.1071/sb9950057.
Pełny tekst źródłaBianco, Bianca, Denise Maria Christofolini, Gabriel Seixas Conceição i Caio Parente Barbosa. "Preimplantation genetic diagnosis associated to Duchenne muscular dystrophy". Einstein (São Paulo) 15, nr 4 (21.09.2017): 489–91. http://dx.doi.org/10.1590/s1679-45082017rc3994.
Pełny tekst źródłaUnger, Kristian, Johannes Wienberg, Andrew Riches, Ludwig Hieber, Axel Walch, Andreas Brown, Patricia C. M. O'Brien i in. "Novel gene rearrangements in transformed breast cells identified by high-resolution breakpoint analysis of chromosomal aberrations". Endocrine-Related Cancer 17, nr 1 (marzec 2010): 87–98. http://dx.doi.org/10.1677/erc-09-0065.
Pełny tekst źródłaCarvalho, Beatriz, Tineke E. Buffart, Rui M. Reis, Thomas Mons, Cátia Moutinho, Paula Silva, Nicole C. T. van Grieken i in. "Mixed Gastric Carcinomas Show Similar Chromosomal Aberrations in Both their Diffuse and Glandular Components". Analytical Cellular Pathology 28, nr 5-6 (1.01.2006): 283–94. http://dx.doi.org/10.1155/2006/650620.
Pełny tekst źródłavan Zijll de Jong, Eline, Kathryn M. Guthridge, German C. Spangenberg i John W. Forster. "Sequence Analysis of SSR-Flanking Regions Identifies Genome Affinities between Pasture Grass Fungal Endophyte Taxa". International Journal of Evolutionary Biology 2011 (12.01.2011): 1–11. http://dx.doi.org/10.4061/2011/921312.
Pełny tekst źródłaSolomon, N. M. "Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3". Journal of Medical Genetics 41, nr 9 (1.09.2004): 669–78. http://dx.doi.org/10.1136/jmg.2003.016949.
Pełny tekst źródłaSolomon, N. M., S. A. Ross, S. M. Forrest, P. Q. Thomas, T. Morgan, J. L. Belsky, F. A. Hol i in. "Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3". Journal of Medical Genetics 44, nr 4 (1.04.2007): e75-e75. http://dx.doi.org/10.1136/jmg.2007.049049.
Pełny tekst źródłaAston, E., H. Whitby, T. Maxwell, N. Glaus, B. Cowley, D. Lowry, X. L. Zhu, B. Issa, S. T. South i A. R. Brothman. "Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform". Journal of Medical Genetics 45, nr 5 (4.01.2008): 268–74. http://dx.doi.org/10.1136/jmg.2007.055319.
Pełny tekst źródłaGoh, X. Y., J. R. E. Rees, A. L. Paterson, S. F. Chin, J. C. Marioni, V. Save, M. O'Donovan i in. "Integrative analysis of array-comparative genomic hybridisation and matched gene expression profiling data reveals novel genes with prognostic significance in oesophageal adenocarcinoma". Gut 60, nr 10 (8.04.2011): 1317–26. http://dx.doi.org/10.1136/gut.2010.234179.
Pełny tekst źródłaVarma, G., R. Varma, H. Huang, A. Pryshchepava, J. Groth, D. Fleming, N. J. Nowak i in. "Array comparative genomic hybridisation (aCGH) analysis of premenopausal breast cancers from a nuclear fallout area and matched cases from Western New York". British Journal of Cancer 93, nr 6 (wrzesień 2005): 699–708. http://dx.doi.org/10.1038/sj.bjc.6602784.
Pełny tekst źródłaEsoof, Noor, Aristoteles Giagounidis, Mario Cazzola, Luca Malcovati, Carlo Aul, Andrea Pellagatti, Carrie Fidler i in. "High-Resolution Genomic Profiling of Myelodysplasia (MDS) by Microarray Comparative Genomic Hybridization (CGH)." Blood 108, nr 11 (16.11.2006): 2645. http://dx.doi.org/10.1182/blood.v108.11.2645.2645.
Pełny tekst źródłaZeng, Sheng, Mei-yun Zhang, Xue-jing Wang, Zheng-mao Hu, Jin-chen Li, Nan Li, Jun-ling Wang i in. "Long-read sequencing identified intronic repeat expansions inSAMD12from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy". Journal of Medical Genetics 56, nr 4 (7.09.2018): 265–70. http://dx.doi.org/10.1136/jmedgenet-2018-105484.
Pełny tekst źródłaRaghavan, Manoj, Debra Lillington, Spyros Skoulakis, Silvana Debernardi, Tracy Chaplin, Nicola J. Foot, T. Andrew Lister i Bryan D. Young. "Genome Wide SNP Analysis Reveals Frequent Uniparental Disomy (UPD) Due to Somatic Recombination in Acute Myeloid Leukemias." Blood 104, nr 11 (16.11.2004): 139. http://dx.doi.org/10.1182/blood.v104.11.139.139.
Pełny tekst źródłaSaida, Myriam, David Iles, Abdul Elnefati, Martin Brinkworth i David Miller. "Key gene regulatory sequences with distinctive ontological signatures associate with differentially endonuclease-accessible mouse sperm chromatin". REPRODUCTION 142, nr 1 (lipiec 2011): 73–86. http://dx.doi.org/10.1530/rep-10-0536.
Pełny tekst źródłaSalmela, M. T. "Upregulation of matrix metalloproteinases in a model of T cell mediated tissue injury in the gut: analysis by gene array and in situ hybridisation". Gut 51, nr 4 (1.10.2002): 540–47. http://dx.doi.org/10.1136/gut.51.4.540.
Pełny tekst źródłaDohner, Konstanze, Marianne Habdank, Frank G. Rucker, Simone Miller, Stefan Frohling, Stephen W. Scherer, Lars Bullinger i Hartmut Dohner. "Molecular Characterization of Distinct Hot Spot Regions on Chromosome 7q in Myeloid Leukemias." Blood 108, nr 11 (1.11.2006): 2349. http://dx.doi.org/10.1182/blood.v108.11.2349.2349.
Pełny tekst źródłaSchaub, Franz, Ralph Tiedt, Sylvie Hermouet, François Girodon, Robert Kralovics, André Tichelli i Radek C. Skoda. "Characterization of del20q in Peripheral Blood of MPD Patients Using Copy Number Analysis and High Resolution Oligonucleotide CGH Array". Blood 110, nr 11 (16.11.2007): 1530. http://dx.doi.org/10.1182/blood.v110.11.1530.1530.
Pełny tekst źródłaHopkins, Stephen, Jeremy Turk, Adeniyi Daramola i Marinos Kyriakopoulos. "Autism spectrum mixed neurodevelopmental disorder associated with 6q27 deletion and multiple copies within 20q11.23: a case study". Advances in Mental Health and Intellectual Disabilities 8, nr 3 (29.04.2014): 210–15. http://dx.doi.org/10.1108/amhid-07-2013-0050.
Pełny tekst źródłaCottrell, Emily, Claudia P. Cabrera, Miho Ishida, Sumana Chatterjee, James Greening, Neil Wright, Artur Bossowski i in. "Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity". European Journal of Endocrinology 183, nr 6 (grudzień 2020): 581–95. http://dx.doi.org/10.1530/eje-20-0474.
Pełny tekst źródłaRudenko, Hannah C., Monica Else, Claire Dearden, Vasantha Brito-Babapulle, Chris Jones, Tim Dexter, Kerry Fenwick i in. "Characterising the TP53-deleted subgroup of chronic lymphocytic leukemia: an analysis of additional cytogenetic abnormalities detected by interphase fluorescencein situhybridisation and array-based comparative genomic hybridisation". Leukemia & Lymphoma 49, nr 10 (styczeń 2008): 1879–86. http://dx.doi.org/10.1080/10428190802345902.
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