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Статті в журналах з теми "Molecular Diagnosi"
Pietravalle, Andrea, Paola Cavicchioli, Enrica Donadel, Marta Lusiani, Tommaso Malusa, Giuliana Rossi, Giovanna Contreas, and Michela Chirico. "Diagnosi precoce di diabete neonatale permanente conseguente a mutazione del gene KCNJ11." Medico e Bambino pagine elettroniche 25, no. 2 (February 28, 2022): 39–42. http://dx.doi.org/10.53126/mebxxv039.
Повний текст джерелаKutty, Dr A. V. M. "Molecular Diagnosis: A boon to healthcare." JOURNAL OF CLINICAL AND BIOMEDICAL SCIENCES 10, no. 3 (September 15, 2020): 74–75. http://dx.doi.org/10.58739/jcbs/v10i3.4.
Повний текст джерелаZhao, Sen, Yuanqiang Zhang, Weisheng Chen, Weiyu Li, Shengru Wang, Lianlei Wang, Yanxue Zhao, et al. "Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)." Journal of Medical Genetics 58, no. 1 (May 7, 2020): 41–47. http://dx.doi.org/10.1136/jmedgenet-2019-106823.
Повний текст джерелаBurboa Meza, Cinthya Y., Alexandra Zazueta Avitia, David Ramírez Alvarado, Miguel A. Segura Castruita, Paola A. Palmeros Suarez, and Juan F. Gómez-Leyva. "DIAGNÓSTICO COMPARATIVO DE BRUCELOSIS MEDIANTE MÉTODOS SEROLÓGICOS Y MOLECULARES." e-CUCBA 8, no. 16 (May 31, 2021): 50–55. http://dx.doi.org/10.32870/ecucba.vi16.198.
Повний текст джерелаGreco, F. Anthony. "Cancer of Unknown Primary Site: Improved Patient Management with Molecular and Immunohistochemical Diagnosis." American Society of Clinical Oncology Educational Book, no. 33 (May 2013): 175–81. http://dx.doi.org/10.14694/edbook_am.2013.33.175.
Повний текст джерелаFujita, Naohide, Osamu Akiyama, and Akihide Kondo. "PATH-08. THE IMPORTANCE OF RE-DIAGNOSIS OF TUMORS PREVIOUSLY CLASSIFIED AS CENTRAL NERVOUS SYSTEM PRIMITIVE NEUROECTODERMAL TUMORS." Neuro-Oncology 22, Supplement_3 (December 1, 2020): iii426. http://dx.doi.org/10.1093/neuonc/noaa222.644.
Повний текст джерелаLuk, Ho-Ming. "Angelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrative Cases." Case Reports in Genetics 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/9790169.
Повний текст джерелаERDOĞAN, Emrah, Merve YÜRÜK, Eda SİVCAN, Serkan KARACA, Orhan YILDIZ, and İzzet ŞAHİN. "Plasmodium ovale Sıtması ve Moleküler Tanısı: Relaps Olabilir mi?" Mikrobiyoloji Bulteni 53, no. 1 (January 15, 2019): 106–13. http://dx.doi.org/10.5578/mb.67713.
Повний текст джерелаPohanka, M., R. Chlibek, K. Kuca, H. Bandouchova, and J. Pikula. "Diagnosis of tularemia using biochemical, immunochemical and molecular methods: a review." Veterinární Medicína 56, No. 9 (October 6, 2011): 453–61. http://dx.doi.org/10.17221/3207-vetmed.
Повний текст джерелаEszlinger, Markus, Kurt Werner Schmid, and Ralf Paschke. "Clinical implications of molecular studies for the diagnosis of thyroid cancer." HORMONES 9, no. 1 (January 15, 2010): 51–56. http://dx.doi.org/10.14310/horm.2002.1253.
Повний текст джерелаДисертації з теми "Molecular Diagnosi"
D'AVERSA, Elisabetta. "Innovative approaches for molecular diagnosis of genetic diseases." Doctoral thesis, Università degli studi di Ferrara, 2019. http://hdl.handle.net/11392/2488091.
Повний текст джерелаLa diagnosi di patologie genetiche fetali viene effettuata a partire da materiale biologico prelevato tramite tecniche invasive, le quali presentano un elevato rischio di aborto. La diagnosi prenatale non invasiva, effettuata a partire da ccffDNA (DNA circolante fetale), isolato da sangue materno, negli ultimi anni, ha avuto una crescita esponenziale. La diagnosi del sesso, in età prenatale, permette di definire il rischio di malattie legate al cromosoma X. La prima parte della tesi ha come obbiettivo, quindi, lo sviluppo di approcci diagnostici molecolari non invasivi, rapidi e sensibili per la determinazione del sesso fetale, in particolare a settimane di gestazione precoci. Per verificare la presenza del gene SRY, sul cromosoma Y, nel ccffDNA, estratto da plasma materno, è stata impiegata, in primis, la Real Time PCR. I risultati hanno confermato il limite di rilevabilità della tecnica (9 settimane) individuato in uno studio preliminare del gruppo di ricerca. Per settimane di gestazione precoci è stata impiegata la tecnologia innovativa digital droplet PCR (ddPCR): dopo aver ottimizzato le condizioni sperimentali, sono stati analizzati campioni a settimane di gestazione comprese fra le 12 e le 4.5, e per tutti la tecnica si è dimostrata accurata al 100% nel determinare correttamente il sesso fetale. La β talassemia è una patologia autosomica recessiva associata all’assenza o riduzione delle catene β globiniche dell’emoglobina. I soggetti che presentano la forma più severa della patologia non possono sopravvivere senza trasfusioni associate a ferrochelanti. L’unico vero trattamento definitivo è il trapianto di midollo, il quale però è associato a forti rischi. Sono stati studiati, quindi, approcci terapeutici innovativi con l’obbiettivo di una terapia personalizzata. L’identificazione della specifica alterazione molecolare è, quindi, di fondamentale importanza al fine di scegliere la corretta strategia terapeutica. La seconda parte della ricerca ha, quindi, come obbiettivo lo sviluppo di approcci molecolari diagnostici pre- e postnatali rapidi, sensibili e poco costosi per l’identificazione delle più frequenti mutazioni talassemiche nel Mediterraneo (β039, β+IVSI-110, β+IVSI-6, β0IVSI-1). Per la diagnosi postnatale, è stata impiegata, in primis, la tecnologia BiacoreTM: una sonda mutata e normale sono state immobilizzate sul chip, validate e, successivamente, è stato estratto il DNA genomico di soggetti sani e pazienti omozigoti ed eterozigoti per le mutazioni considerate, ed effettuata l’analisi. Per tutti i campioni analizzati è stato possibile discriminare il diverso genotipo. Un secondo approccio ha previsto il disegno di saggi di genotipizzazione da utilizzare in Real Time PCR. Ottimizzati e validati, i saggi hanno permesso una corretta diagnosi di tutti i pazienti considerati. Lo stesso approccio, basato sui saggi di genotipizzazione, è stato utilizzato per la diagnosi prenatale delle mutazioni ereditate per via paterna. I campioni di ccffDNA sono stati preamplificati e analizzati, mostrando come questo approccio sia stato in grado di identificare il genotipo fetale a partire dalla nona settimana di gestazione. Per poter estendere la diagnosi prenatale a settimane di gestazione precoci e a mutazioni ereditate sia per via materna che da entrambi i genitori è stata utilizzata la ddPCR come approccio molecolare. I saggi di genotipizzazione per le mutazioni β039 e β+IVSI-110 sono stati ottimizzati, validati e utilizzati per l’analisi del ccffDNA. Per tutti i campioni in cui la mutazione è ereditata per via paterna, il genotipo fetale è stato correttamente individuato fino alla quinta settimana di gestazione. Per i campioni in cui solo la madre o entrambi i genitori sono portatori, è stato possibile individuare due intervalli, sulla base del rapporto fra allele mutato e normale, statisticamente separati, necessari per considerare il feto non portatore o eterozigote.
Soler, Aznar Maria. "Nanoplasmonic biosensors for clinical diagnosis at the point of care." Doctoral thesis, Universitat Autònoma de Barcelona, 2015. http://hdl.handle.net/10803/298172.
Повний текст джерелаThis Doctoral Thesis focuses on the development of novel analytical methodologies in optical biosensors as alternative solutions for diagnosis or therapy monitoring of relevant diseases, such as allergy, celiac disease or cancer. In particular, we propose the use of nanoplasmonic biosensors for a rapid, sensitive and label-free detection of biomarkers present in human fluids. Both the well-known Surface Plasmon Resonance (SPR) biosensor and an innovative nanoplasmonic biosensor based on gold nanodisks surfaces have been evaluated for their real application in the clinical field. The different biosensor methodologies make use of antibodies, either as biorecognition elements in immunoassays or as specific disease biomarkers for diagnostics. First, an in-depth study of two site-directed antibody immobilization strategies is presented for the direct immunoassay of protein biomarkers in biological fluids. In second place, a novel immunosensing strategy is proposed for the detection of gluten-derivative peptides in urine as a rapid and non-invasive technique for dietary control in celiac patients. On the other hand, two assays have been developed employing the nanoplasmonic biosensor to detect blood circulating antibodies as disease biomarkers. First, we have designed an alternative approach for drug allergy diagnosis (in particular for amoxicillin) based on dendrimer-based receptors, which enable the detection IgE antibodies directly in serum. And second, a new biosensing strategy is assessed to quantify specific tumor-related autoantibodies for the early diagnosis of colorectal cancer. The work in this Thesis combines the wide knowledge of the research group in the design and fabrication of powerful biosensor technology with the development of surface activation chemistry and bioanalytical techniques to overcome current challenges related to costly and time-consuming clinical analysis. Besides, the strong experience of our research group in technological transfer and the established collaborations during this doctoral work with companies as Biomedal S.L. or Protein Alternatives S.L. open up interesting opportunities to facilitate the technology-transfer process for the real implementation of Point-of-Care biosensors.
GRIONI, ANDREA. "Application of modern data science to genomics and clinical research." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2020. http://hdl.handle.net/10281/279991.
Повний текст джерелаAfter the completion of the human genome project in April 2003, the continuous flow of sequencing data and the development of new databases began to transform the field of genomics into data-driven science. Bioinformatics analyses raw experimental data with the aim to obtain information describing biological processes, thus providing a powerful tool to investigate specific molecular and genetic mechanisms. This domain knowledge in combination with genomics allows to decipher the interrelationships between genes, regulatory elements, metabolic pathways, and protein interactions. Deep learning, a subdiscipline of machine learning, has been recently applied to the field of genomics, leading to remarkable results. The two main objectives of this study were: the development and application of bioinformatic tools for the study of the genetic basis of acute lymphoblastic leukaemia, and the usage of deep learning techniques for the identification of small non-coding RNA elements in the human genome. This dissertation provides a comprehensive overview of the recent evolution of genomics as an interdisciplinary field of research strongly associated with computer science and data analysis.
Shirahata, Mitsuaki. "Gene Expression-Based Molecular Diagnostic System for Malignant Gliomas Is Superior to Histological Diagnosis." Kyoto University, 2008. http://hdl.handle.net/2433/124241.
Повний текст джерелаRamiro, Juliana. "Detecção molecular de fungos fitopatogênicos associados às sementes de soja." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/11/11135/tde-28042015-143631/.
Повний текст джерелаSeed-born pathogenic fungi in soybean can cause serious damage to the crop, as well as direct damage by reducing seeds germination, vigor and emergence. The detection and accurate identification of plant pathogens is one of the most important strategies to initiate preventive and curative measures in the management of plant diseases. Particular attention should be taken in the detection of pathogens in seeds in order to avoid introduction and spread of pathogens in areas where they do not occur. The traditionally used methods for detection and identification of seed-born pathogenic fungi are often time consuming, laborious and require extensive knowledge of classical taxonomy. Molecular methods have been used to detect, identify and quantify a long list of plant pathogenic fungi. Quantitative real time polymerase chain reaction (qPCR) is currently considered the most efficient technique for the detection of pathogens because it does not require specialized taxonomical knowledge to interpret its results. Given the importance and implications of rapid and successful diagnosis of seed-born pathogenic fungi in soybean, this study aimed to establish a qPCR methodology to increase the detection efficiency of plant pathogenic fungi Sclerotinia sclerotiorum, Colletotrichum truncatum, Phomopsis spp. and Corynespora cassiicola, the most commonly occurring seed-born pathogenic fungi. Primers and TaqMan® hydrolysis probes were designed for these four pathogens and tested for specificity and sensitivity. Standard curves were established to quantify these pathogens, based on serial dilutions of the target DNA and specific primers and probes. Samples of naturally infected soybean seed from the states of Goiás, Minas Gerais and Paraná were subjected to detection tests using qPCR and traditional methods, for comparison purposes. From all primers and probes designed, only those for Phomopsis spp. and S. sclerotiorum showed up specificity and sensitivity, enabling their use to detect of these pathogens. Detection by traditional tests, resulted in a maximum Phomopsis spp. incidence of 2.75% in a sample from Minas Gerais and S. sclerotiorum was not detected in any of the samples. The detection and quantification of these pathogens by qPCR revealed the presence of Phomopsis spp. in all tested samples, the highest incidence level of 6.75% in a sample from Minas Gerais. S. sclerotiorum was not detected in any sample assessed by qPCR method. In comparison with traditional methods, qPCR was more sensitive in detecting Phomopsis spp. in soybean seeds.
Wang, Lei. "Molecular Probes for Pancreatic Cancer Imaging." PDXScholar, 2016. http://pdxscholar.library.pdx.edu/open_access_etds/3108.
Повний текст джерелаCATARINO, Aricléia de Moraes. "Detecção de vírus da videira por RT-PCR em tempo real e por extensão de primers alelo-específicos e caracterização molecular de isolados do Nordeste Brasileiro." Universidade Federal Rural de Pernambuco, 2015. http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/5995.
Повний текст джерелаMade available in DSpace on 2016-11-28T13:27:09Z (GMT). No. of bitstreams: 1 Aricleia de Moraes Catarino.pdf: 1031221 bytes, checksum: 5bd0ffb507daa4b9b04ebd494fd2269c (MD5) Previous issue date: 2015-02-27
The grapevine (Vitis spp.) belongs to the family of Vitaceae, being the botanical species V. vinifera L. and V. labrusca L. the most and widely cultivated, due to their products consumed as fresh fruits, jam, juices and wines. Despite the high economical importance, several factors may severely affect this crop, including the diseases caused by viruses. This study aimed to verify the incidence of virus present in commercial vineyards of two producing areas in Northeastern Brazil and evaluate the efficiency of some molecular methods for detecting and identifying viral species associated with grapevine. Materials showing or not symptoms were collected from grapevine genotypes in vineyards of Pernambuco, Paraiba, Bahia and Rio Grande do Sul, Brazil, and Locorotondo, Province of Bari, of the Puglia Region, Italy. The first part of the work was conducted at the Virology Laboratory of the Embrapa Uva e Vinho, RS, Brazil. For the identification of viral agents in the samples collected in Brazil, the extraction of total RNA was performed, cDNAs were obtained and tested by real time RT-PCR, using primers and probes specific for the following viruses: Grapevine rupestris stem pitting-associated virus (GRSPaV), Grapevine virus A (GVA), Grapevine virus B (GVB), Grapevine leafroll-associated virus 2, 3 e 4 (GLRaV-2, -3 e -4), Grapevine fleck virus (GFkV), Grapevine rupestris vein feathering virus (GRVFV) and Grapevine fanleaf virus (GFLV). DNA fragments, products of the RT-qPCR, corresponding to the CP gene of each virus were eluted, linked to pGEM-T Easy vector (Promega) and used to transform bacteria. The plasmid DNA was extracted from transformed bacterial colonies, confirming the presence of the cloned fragments, which were sequenced. The grapevine material collected in Locorotondo was processed at the Istituto per la Protezione Sostenibile delle Piante (CNR-IPSP) and at the Dipartimento di Scienze del Suolo, della Pianta e degli Alimenti, Università degli Studi “Aldo Moro”. In order to detect in multiplex test the most relevant viruses involved in the aetiology of fanleaf degeneration and the complexes of leafroll and rugose wood of grapevine, amplification techniques based on Allele Specific Primer Extension (ASPE) were tested by using the obtained cDNAs. The results showed that the techniques aggregate some advantages, such as reduction in time and relative simplicity of implementation, completely eliminating the use of toxic reagents, such as the ethidium bromide. The use of multiplex facilitates amplification of multiple targets in a single reaction, reducing the time and cost of the analyzes.
A videira (Vitis spp.) pertence à família Vitaceae, sendo as espécies botânicas V. vinifera L. e V. labrusca L. cultivadas em maior escala devido seus produtos, consumidos na forma de frutos in natura, geleias, sucos e vinhos. Apesar da grande importância econômica, vários fatores podem comprometer a produção desta cultura, incluindo as doenças causadas por vírus. O presente trabalho teve como objetivos verificar a incidência de vírus presentes em vinhedos comerciais de duas áreas produtoras do Nordeste do Brasil e avaliar a eficiência de alguns métodos moleculares para detecção e identificação de espécies virais associadas à videira. Amostras, apresentando ou não sintomas, foram coletados de genótipos de videira em propriedades situadas em Pernambuco, Paraíba, Bahia e Rio Grande do Sul, Brasil, e em Locorotondo, Província de Bari, Região da Puglia, Itália. A primeira parte do trabalho foi conduzida no Laboratório de Virologia da Embrapa Uva e Vinho, RS, Brasil. Visando a identificação dos agentes virais, nas amostras coletadas no Brasil, foram realizadas as extrações do RNA total, obtidos os cDNAs e testados por PCR em Tempo Real, empregando-se primers e sondas, específicos para os seguintes vírus: Grapevine rupestris stem pitting-associated virus (GRSPaV), Grapevine virus A (GVA), Grapevine virus B (GVB), Grapevine leafroll-associated virus 2, 3 e 4 (GLRaV-2, -3 e -4), Grapevine fleck virus (GFkV), Grapevine rupestris vein feathering virus (GRVFV) e Grapevine fanleaf virus (GFLV). Fragmentos de DNA, produtos da RTq-PCR, correspondentes ao gene da CP de cada vírus foram eluídos, ligados ao vetor pGEM-T Easy (Promega) e utilizados na transformação de bactéria. Foi extraído o DNA plasmidial das colônias bacterianas transformadas, confirmando-se a presença dos fragmentos clonados, os quais foram sequenciados. A segunda parte, realizada com o material coletado em Locorotondo, foi processada no Istituto per la Protezione Sostenibile delle Piante (CNR-IPSP) e no Dipartimento di Scienze del Suolo, della Pianta e degli Alimenti, Università degli Studi “Aldo Moro”. Foram utilizadas, a partir de cDNAs obtidos, técnicas de amplificação baseadas na Allele Specific Primer Extension (ASPE), visando detectar em teste multiplex os vírus mais relevantes envolvidos na etiologia da degenerescência e nos complexos do enrolamento das folhas e do lenho rugoso da videira. Os resultados obtidos mostraram que as técnicas agregam algumas vantagens, como a redução no tempo e relativa simplicidade de execução, eliminando completamente o uso de reagentes tóxicos, a exemplo do brometo de etídeo. O uso de multiplex facilita a amplificação de múltiplos alvos em uma única reação, reduzindo o tempo e o custo das análises.
顔鴻儀 and Hung-yee Ngan. "Molecular diagnosis of penicilliosis marneffei." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2001. http://hub.hku.hk/bib/B31970035.
Повний текст джерелаYau, Shu Ching. "Molecular diagnosis of neuromuscular disorders." Thesis, King's College London (University of London), 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.402033.
Повний текст джерелаNgan, Hung-yee. "Molecular diagnosis of penicilliosis marneffei." Hong Kong : University of Hong Kong, 2001. http://sunzi.lib.hku.hk/hkuto/record.jsp?B23595978.
Повний текст джерелаКниги з теми "Molecular Diagnosi"
W, Semmler, and Schwaiger Markus, eds. Molecular imaging. Berlin: Springer, 2008.
Знайти повний текст джерелаW, Semmler, and Schwaiger Markus, eds. Molecular imaging. Berlin: Springer, 2008.
Знайти повний текст джерелаJeffery, S. Molecular diagnosis. Oxford: BIOS Scientific, 1999.
Знайти повний текст джерелаM, Kirkwood John, ed. Molecular diagnosis and treatment of melanoma. New York: M. Dekker, 1998.
Знайти повний текст джерелаservice), ScienceDirect (Online, ed. Molecular diagnostics. 2nd ed. Amsterdam: Elsevier/Academic Press, 2010.
Знайти повний текст джерелаMolecular diagnostics of infectious diseases. Berlin: De Gruyter, 2010.
Знайти повний текст джерела1954-, Srivastava Sudhir, ed. Early detection of cancer: Molecular markers. Armonk, N.Y: Futura Pub. Co., 1994.
Знайти повний текст джерелаYousef, George M., and Serge Jothy. Molecular testing in cancer. New York: Springer, 2014.
Знайти повний текст джерелаW, Semmler, and Schwaiger Markus, eds. Impact of molecular biology and new technical developments on diagnostic imaging. Berlin: Springer, 1997.
Знайти повний текст джерелаCotter, Finbarr. Molecular Diagnosis of Cancer. New Jersey: Humana Press, 1996. http://dx.doi.org/10.1385/0896033414.
Повний текст джерелаЧастини книг з теми "Molecular Diagnosi"
García-Elorriaga, Guadalupe, and Guillermo del Rey-Pineda. "Molecular Diagnosis." In Practical and Laboratory Diagnosis of Tuberculosis, 35–53. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20478-9_4.
Повний текст джерелаHangay, George, Susan V. Gruner, F. W. Howard, John L. Capinera, Eugene J. Gerberg, Susan E. Halbert, John B. Heppner, et al. "Molecular Diagnosis." In Encyclopedia of Entomology, 2449–55. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_4659.
Повний текст джерелаWeisman, Paul, Jian-Jun Wei, and Pei Hui. "Molecular Diagnosis." In Practical Gynecologic Pathology, 417–31. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68608-6_16.
Повний текст джерелаSloan, Philip, and Max Robinson. "Promising Biomarkers for Early Diagnosis and Prognosis Prediction." In Critical Issues in Head and Neck Oncology, 3–12. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63234-2_1.
Повний текст джерелаGronthoud, Firza Alexander. "Understanding Molecular Diagnosis." In Practical Clinical Microbiology and Infectious Diseases, 75–77. First edition. | Boca Raton : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9781315194080-2-10.
Повний текст джерелаLiu, Chengcheng, Xiaoting Lou, Jianxin Lyu, Jian Wang, and Yufei Xu. "Prenatal Diagnosis and Preimplantation Genetic Diagnosis." In Clinical Molecular Diagnostics, 769–800. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1037-0_43.
Повний текст джерелаKardon, Nataline, and Lisa Edelmann. "Prenatal Diagnosis." In Molecular Genetic Pathology, 441–48. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-405-6_17.
Повний текст джерелаHuang, James, Sharie B. Parks, and Richard D. Press. "Diagnostic Molecular Pathology." In Essentials of Anatomic Pathology, 3–35. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1007/978-1-60327-173-8_1.
Повний текст джерелаRichards, C. Sue, and Patricia A. Ward. "Molecular Diagnostic Testing." In Principles of Molecular Medicine, 83–88. Totowa, NJ: Humana Press, 1998. http://dx.doi.org/10.1007/978-1-59259-726-0_8.
Повний текст джерелаHuang, James, and Richard D. Press. "Molecular Diagnostic Pathology." In Essentials of Anatomic Pathology, 489–513. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6043-6_11.
Повний текст джерелаТези доповідей конференцій з теми "Molecular Diagnosi"
Litau, I. S., M. V. Alvarez Figueroa, A. A. Kazyulina, and L. V. Domotenko. "EVALUATION OF ANALYTICAL CHARACTERISTICS OF TB DIAGNOSTIC REAGENT KITS ON DOMESTIC CONTROL PANEL OF EXTERNAL QUALITY ASSESSMENT SAMPLES." In Molecular Diagnostics and Biosafety. Federal Budget Institute of Science 'Central Research Institute for Epidemiology', 2020. http://dx.doi.org/10.36233/978-5-9900432-9-9-216.
Повний текст джерелаSahu, Aditi, Ucalene Harris, Melissa Gill, Cecelia Lezcano, Allan Halpern, Anthony Rossi, Klaus Busam, et al. "PARP1 as a biomarker towards in vivo multimodal melanoma diagnosis." In Molecular-Guided Surgery: Molecules, Devices, and Applications VIII, edited by Summer L. Gibbs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2022. http://dx.doi.org/10.1117/12.2610476.
Повний текст джерелаChumachkova, Е. A., S. A. Portenko, E. S. Kazakova, O. V. Kedrova, S. A. Shcherbakova, T. L. Voznyuk, I. I. Krupinskaya, and R. N. Steshenko. "EPIDEMIOLOGICAL FEATURES OF THE COURSE OF COMMUNITY-ACQUIRED PNEUMONIA IN PATIENTS OF THE CITY OF SARATOV AND SARATOV OBLAST." In Molecular Diagnostics and Biosafety. Federal Budget Institute of Science 'Central Research Institute for Epidemiology', 2020. http://dx.doi.org/10.36233/978-5-9900432-9-9-186.
Повний текст джерелаScholler, Jules, Olivier Thouvenin, Emilie Benoit a la Guillaume, and Claude Boccara. "One hundred percent successful automatic breast cancer diagnosis using static and dynamic FFOCT images (Conference Presentation)." In Molecular-Guided Surgery: Molecules, Devices, and Applications VI, edited by Summer L. Gibbs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2020. http://dx.doi.org/10.1117/12.2544301.
Повний текст джерелаLeblond, Frédéric. "Label-free optical spectroscopy techniques for targeted, real time and informed in situ cancer diagnosis (Conference Presentation)." In Molecular-Guided Surgery: Molecules, Devices, and Applications IV, edited by Greg Biggs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2018. http://dx.doi.org/10.1117/12.2287890.
Повний текст джерелаAlbadawy, Ehab, Ashirbani Saha, Jun Zhang, Michael R. Harowicz, Maciej A. Mazurowski, and Zhe Zhu. "Breast cancer molecular subtype classification using deep features: preliminary results." In Computer-Aided Diagnosis, edited by Kensaku Mori and Nicholas Petrick. SPIE, 2018. http://dx.doi.org/10.1117/12.2295471.
Повний текст джерелаTsourkas, Andrew, Jason Xu, and Gang Bao. "Hybridization Dynamics and Kinetics of Fret-Enhanced Molecular Beacons." In ASME 2001 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2001. http://dx.doi.org/10.1115/imece2001/bed-23163.
Повний текст джерелаHouse, Broderick J., Jasmin M. Schaefer, Connor W. Barth, Scott C. Davis, and Summer L. Gibbs. "Diagnostic performance of receptor-specific surgical specimen staining correlate with receptor expression level." In Molecular-Guided Surgery: Molecules, Devices, and Applications V, edited by Brian W. Pogue and Sylvain Gioux. SPIE, 2019. http://dx.doi.org/10.1117/12.2510625.
Повний текст джерелаGiannelli, B. F. "MOLECULAR GENETICS OF HAEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643981.
Повний текст джерелаHu, Hui, and Manoochehr Koochesfahani. "Molecular Tagging Techniques for Micro-Flow and Micro-Scale Heat Transfer Studies." In ASME 2009 Fluids Engineering Division Summer Meeting. ASMEDC, 2009. http://dx.doi.org/10.1115/fedsm2009-78059.
Повний текст джерелаЗвіти організацій з теми "Molecular Diagnosi"
Chen, Wen-Tien. Molecular Diagnosis for Breast Malignancy. Fort Belvoir, VA: Defense Technical Information Center, July 1998. http://dx.doi.org/10.21236/ada381191.
Повний текст джерелаRinchik, E. M. Workshop on molecular methods for genetic diagnosis. Final technical report. Office of Scientific and Technical Information (OSTI), July 1997. http://dx.doi.org/10.2172/501564.
Повний текст джерелаReinholz, Monica M., and Patrick C. Roche. Molecular Detection of Circulating Cancer Cells for Early Diagnosis of Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2001. http://dx.doi.org/10.21236/ada400500.
Повний текст джерелаLokshin, Anna. Integrated Development of Serum Molecular Markers for Early Diagnosis of Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, September 2006. http://dx.doi.org/10.21236/ada462774.
Повний текст джерелаLevisohn, Sharon, Maricarmen Garcia, David Yogev, and Stanley Kleven. Targeted Molecular Typing of Pathogenic Avian Mycoplasmas. United States Department of Agriculture, January 2006. http://dx.doi.org/10.32747/2006.7695853.bard.
Повний текст джерелаSvetlov, Stanislav, Ronald Hayes, and Olena Glushakova. Molecular Signatures and Diagnostic Biomarkers of Cumulative Blast-Graded Mild TBI. Fort Belvoir, VA: Defense Technical Information Center, December 2014. http://dx.doi.org/10.21236/ada612707.
Повний текст джерелаSvetlov, Stanislav. Molecular Signatures and Diagnostic Biomarkers of Cumulative, Blast-Graded Mild TBI. Fort Belvoir, VA: Defense Technical Information Center, October 2012. http://dx.doi.org/10.21236/ada582352.
Повний текст джерелаOsburn, Bennie, Marius Ianconescu, Geoffrey Akita, and Rozalia Kaufman. Rapid, Sensitive Bluetongue Virus Serogroup and Serotype Detection Using Polymerase Chain Reaction. United States Department of Agriculture, September 1995. http://dx.doi.org/10.32747/1995.7612836.bard.
Повний текст джерелаSplitter, Gary, and Menachem Banai. Microarray Analysis of Brucella melitensis Pathogenesis. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7709884.bard.
Повний текст джерелаDawson, William O., Moshe Bar-Joseph, Charles L. Niblett, Ron Gafny, Richard F. Lee, and Munir Mawassi. Citrus Tristeza Virus: Molecular Approaches to Cross Protection. United States Department of Agriculture, January 1994. http://dx.doi.org/10.32747/1994.7570551.bard.
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