Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
Celestino-Soper, Patricia B.S., Shaw, Chad A., Sanders, Stephan J., Li, Jian, Murtha, Michael T., Ercan-Sencicek, A. Gulhan, Davis, Lea, Thomson, Susanne, Gambin, Tomasz, Chinault, A. Craig, Ou, Zhishuo, German, Jennifer R., Milosavljevic, Aleksandar, Sutcliffe, James S., Cook, Edwin H., Stankiewicz, Pawel, State, Matthew W., Beaudet, Arthur L.
Published in Human molecular genetics (15.11.2011)
Published in Human molecular genetics (15.11.2011)
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Severe Depletion of CD4+ CD25+ Regulatory T Cells from the Intestinal Lamina Propria but Not Peripheral Blood or Lymph Nodes during Acute Simian Immunodeficiency Virus Infection
CHASE, Amanda J, SEDAGHAT, Ahmad R, GERMAN, Jennifer R, GAMA, Lucio, ZINK, M. Christine, CLEMENTS, Janice E, SILICIANO, Robert F
Published in Journal of Virology (01.12.2007)
Published in Journal of Virology (01.12.2007)
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Highly stable, antiviral, antibacterial cotton textiles via molecular engineering
Qian, Ji, Dong, Qi, Chun, Kayla, Zhu, Dongyang, Zhang, Xin, Mao, Yimin, Culver, James N, Tai, Sheldon, German, Jennifer R, Dean, David P, Miller, Jeffrey T, Wang, Liguang, Wu, Tianpin, Li, Tian, Brozena, Alexandra H, Briber, Robert M, Milton, Donald K, Bentley, William E, Hu, Liangbing
Published in Nature nanotechnology (01.02.2023)
Published in Nature nanotechnology (01.02.2023)
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Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
Beaudet, Arthur L, Sahoo, Trilochan, del Gaudio, Daniela, German, Jennifer R, Shinawi, Marwan, Peters, Sarika U, Person, Richard E, Garnica, Adolfo, Cheung, Sau Wai
Published in Nature genetics (01.06.2008)
Published in Nature genetics (01.06.2008)
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Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations
SAHOO, Trilochan, BACINO, Carlos A, GERMAN, Jennifer R, SHAW, Chad A, BIRD, Lynne M, KIMONIS, Virginia, ANSELM, Irinia, WAISBREN, Susan, BEAUDET, Arthur L, PETERS, Sarika U
Published in European journal of human genetics : EJHG (01.09.2007)
Published in European journal of human genetics : EJHG (01.09.2007)
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Journal Article
common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Celestino-Soper, Patrícia B. S, Violante, Sara, Crawford, Emily L, Luo, Rui, Lionel, Anath C, Delaby, Elsa, Cai, Guiqing, Sadikovic, Bekim, Lee, Kwanghyuk, Lo, Charlene, Gao, Kun, Person, Richard E, Moss, Timothy J, German, Jennifer R, Huang, Ni, Shinawi, Marwan, Treadwell-Deering, Diane, Szatmari, Peter, Roberts, Wendy, Fernandez, Bridget, Schroer, Richard J, Stevenson, Roger E, Buxbaum, Joseph D, Betancur, Catalina, Scherer, Stephen W, Sanders, Stephan J, Geschwind, Daniel H, Sutcliffe, James S, Hurles, Matthew E, Wanders, Ronald J. A, Shaw, Chad A, Leal, Suzanne M, Cook, Edwin H. Jr, Goin-Kochel, Robin P, Vaz, Frédéric M, Beaudet, Arthur L
Published in Proceedings of the National Academy of Sciences - PNAS (22.05.2012)
Published in Proceedings of the National Academy of Sciences - PNAS (22.05.2012)
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Journal Article
Severe Depletion of CD4 super(+) CD25 super(+) Regulatory T Cells from the Intestinal Lamina Propria but Not Peripheral Blood or Lymph Nodes during Acute Simian Immunodeficiency Virus Infection
Chase, Amanda J, Sedaghat, Ahmad R, German, Jennifer R, Gama, Lucio, Zink, MChristine, Clements, Janice E, Siliciano, Robert F
Published in Journal of virology (01.12.2007)
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Published in Journal of virology (01.12.2007)
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