Resultats de la cerca - James McGrath
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Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries per Dorothy M. Supp, Martina Brueckner, Michael R. Kuehn, David P. Witte, Linda A. Lowe, James McGrath, JoMichelle D. Corrales, S. Steven Potter
Publicat 1999Artigo -
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Disruption of cAMP and Prostaglandin E<sub>2</sub>Transport by Multidrug Resistance Protein 4 Deficiency Alters cAMP-Mediated Signaling and Nociceptive Response per Zhenxian Lin, Yong-Lian Zhu, Dennis R. Johnson, Kevin P. Rice, Timothy Nottoli, Bryan C. Hains, James McGrath, Stephen G. Waxman, Alan C. Sartorelli
Publicat 2007Artigo -
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Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms per Tamim H. Shaikh, Ronald J. O’Connor, Mary Ella Pierpont, James McGrath, April M. Hacker, Manjunath Nimmakayalu, Elizabeth A. Geiger, Beverly S. Emanuel, Sulagna C. Saitta
Publicat 2007Artigo -
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Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage per Pramod K. Mistry, Jun Liu, Mei Yang, Timothy Nottoli, James McGrath, Dhanpat Jain, Kate Zhang, Joan Keutzer, Wei‐Lien Chuang, Wajahat Z. Mehal, Hongyu Zhao, Aiping Lin, Shrikant Mane, Xuan Liu, Yuan Peng, Jian H. Li, Manasi Agrawal, Ling-Ling Zhu, Harry C. Blair, Lisa J. Robinson, Jameel Iqbal, Li Sun, Mone Zaidi
Publicat 2010Artigo -
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Recurrent Distal 7q11.23 Deletion Including HIP1 and YWHAG Identified in Patients with Intellectual Disabilities, Epilepsy, and Neurobehavioral Problems per Melissa B. Ramocki, Magdalena Bartnik, Przemysław Szafrański, Katarzyna Kołodziejska, Zhilian Xia, Jaclyn Bravo, G. Steve Miller, Diana L. Rodríguez, Charles A. Williams, Patricia I. Bader, Elżbieta Szczepanik, Tomasz Mazurczak, Dorota Antczak‐Marach, James G. Coldwell, Cigdem I. Akman, Karen McAlmon, Melinda Cohen, James McGrath, Elizabeth Roeder, Jennifer M. Mueller, Sung‐Hae Kang, Carlos A. Bacino, Ankita Patel, Ewa Bocian, Chad A. Shaw, Sau Wai Cheung, Tadeusz Mazurczak, Paweł Stankiewicz
Publicat 2010Artigo -
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Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability per Izak Johannes Bisschoff, Christine Zeschnigk, Denise Horn, Brigitte Wellek, Angelika Rieß, M.W. Wessels, P J Willems, Peter Bjødstrup Jensen, Andreas Busche, Jens Bekkebraten, Maya Chopra, Hanne Hove, Christina Evers, Ketil Heimdal, Ann-Sophie Kaiser, Erdmut Kunstmann, Kristina Lagerstedt‐Robinson, Maja Linné, Patricia Martín, James McGrath, Winnie Pradel, Katrina Prescott, Bernd Roesler, Goražd Rudolf, Ulrike Siebers‐Renelt, Nataliya Tyshchenko, Dagmar Wieczorek, G. Wolff, William B. Dobyns, Deborah Morris‐Rosendahl
Publicat 2012Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Cell biology
Medicine
Anatomy
Cilium
Dynein
Embryo
Embryogenesis
In vitro
Microtubule
Mutation
Neuroscience
Pathology
Phenotype
Agenesis of the corpus callosum
Andrology
Asymmetry
Biochemistry
Bioinformatics
Breakpoint
Cancer research
Cerebellar hypoplasia (non-human)
Cerebellum
Chemistry
Chromosome
Ciliopathy
Corpus callosum
DiGeorge syndrome