Search Results - "Microarray"

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  1. 841
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    Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings by Esra Işık, Bilcağ Akgün, Tahir Atik, Ferda Özkınay, Özgür Çoğulu

    Published 2020
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  2. 842
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    Atypical teratoid rhabdoid brain tumor in an infant with ring chromosome 22 by Eun Hae Cho, Jae Bok Park, Jin Kyung Kim

    Published 2014
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  3. 843
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    Drug Dependence, Synaptic Plasticity, and Tissue Plasminogen Activator by Kiyofumi Yamada, Taku Nagai, Toshitaka Nabeshima

    Published 2005
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  4. 844
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    Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants by Nagel Bert, Gruber-Sedlmayr Ursula, Uhrig Sabine, Stöllberger Claudia, Klopocki Eva, Finsterer Josef

    Published 2012
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  5. 845
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    Differential gene repertoire in Mycobacterium ulcerans identifies candidate genes for patho-adaptation. by Michael Käser, Gerd Pluschke

    Published 2008
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  6. 846
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    Peripheral-Type Benzodiazepine Receptor Antagonist Is Effective in Relieving Neuropathic Pain in Mice by Daisuke Kondo, Hironao Saegusa, Ritsuko Yabe, Ichiro Takasaki, Takashi Kurihara, Shuqin Zong, Tsutomu Tanabe

    Published 2009
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  7. 847
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    CD26/dipeptidyl peptidase IV contributes to tumor metastasis in human lung adenocarcinoma by Lei Liu, Ming Xia Yan, Fang Yu Zhao, Jing Li, Chao Ge, Qin Geng, Miao Xin Zhu, Lei Sun, Xiang Huo He, Jin Jun Li, Ming Yao

    Published 2013
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  8. 848
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    Total Loss of MHC Class I is an Independent Indicator of Good Prognosis in Breast Cancer by Z Madjd, I Spendlove, IO Ellis, SE Pinder, LG Durrant

    Published 2005
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  9. 849
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    Dissemination of high-level mupirocin-resistant CC22-MRSA-IV in Saxony by Monecke, Stefan, Ruppelt-Lorz, Antje, Müller, Elke, Reissig, Annett, Thürmer, Alexander, Shore, Anna C., Coleman, David C., Ehricht, Ralf, Jatzwauk, Lutz

    Published 2017
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  10. 850
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    Expression of Genes Related to Germ Cell Lineage and Pluripotency in Single Cells and Colonies of Human Adult Germ Stem Cells by Sabine Conrad, Hossein Azizi, Maryam Hatami, Mikael Kubista, Michael Bonin, Jörg Hennenlotter, Karl-Dietrich Sievert, Thomas Skutella

    Published 2016
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  11. 851
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    Potential role of circulating microRNAs as early markers of preeclampsia by Blendi Ura, Giordana Feriotto, Lorenzo Monasta, Sabrine Bilel, Marina Zweyer, Claudio Celeghini

    Published 2014
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  12. 852
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    A Synopsis of Serum Biomarkers in Cutaneous Melanoma Patients by Pierre Vereecken, Frank Cornelis, Nicolas Van Baren, Valérie Vandersleyen, Jean-François Baurain

    Published 2012
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  13. 853
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    Effect of Negative Pressure Therapy on the Inflammatory Response of the Intestinal Microenvironment in a Porcine Septic Model by Kenneth C. Norbury, Mary Pat Moyer

    Published 2015
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  14. 854
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    Successful strategy of comprehensive pre-implantation genetic testing for Duchenne muscular dystrophy and chromosome balance using karyomapping and fluorescent PCR by Suchada Mongkolchaipak, Sirivipa Piyamongkol, Chutithep Teekaput, Rungthiwa Sirapat, Wanwisa Suriya, Tawiwan Pantasri, Theera Tongsong, Wirawit Piyamongkol

    Published 2021
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  15. 855
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    Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism by Naoya Kitamura, Yuki Ito, Tomoko Kawai, Hiromi Kamura, Michihiro Yamamura, Haruna Okubo, Akihiro Hasegawa, Momoko Inoue, Ken Takahashi, Michiko Miya, Hiroshi Kawame, Osamu Samura, Aikou Okamoto

    Published 2024
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  16. 856
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    IL-1β-Induced Matrix Metalloprotease-1 Promotes Mesenchymal Stem Cell Migration via PAR1 and G-Protein-Coupled Signaling Pathway by Ming-Siou Chen, Cheng-Yu Lin, Yun-Hsuan Chiu, Chie-Pein Chen, Pei-Jiun Tsai, Hwai-Shi Wang

    Published 2018
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  17. 857
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    Novel association of severe neonatal encephalopathy and Hirschsprung disease in a male with a duplication at the Xq28 region by Antiñolo Guillermo, González-Meneses Antonio, Núñez-Torres Rocío, Fernández Raquel M, Borrego Salud

    Published 2010
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  18. 858
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    Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature by Zilong Qiu, Wan-Ting Chang, Yu-Ching Chou, Kuo-Chang Wen, Yang Ziying, Kayiu Yuen, Xiongying Cai, Tung-yao Chang, Hung-Cheng Lai, Pi-Lin Sung

    Published 2022
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  19. 859
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    Multiple copy number variation in a patient with Kleefstra syndrome by Thomas Nohama Lee, Henrique El Laden Rechetello, João Batista De Arêa Lima Júnior, João Pedro Fagoti Ferraz Cornelio, Naiara Bozza Pegoraro, Salmo Raskin, Liya Regina Mikami

    Published 2023
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  20. 860
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    Genetic Testing in Neurodevelopmental Disorders by Juliann M. Savatt, Scott M. Myers

    Published 2021
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