Søgeresultater - Tim Morgan
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1
A Study of Caloric Restriction and Cardiovascular Aging in Cynomolgus Monkeys (Macacafascicularis): A Potential Model for Aging Research af William T. Cefalu, J. D. Wagner, Z. Q. Wang, A. D. Bell-Farrow, John R. Collins, David Haskell, R. Bechtold, Tim Morgan
Udgivet 1997Artigo -
2
Menkes disease: importance of diagnosis with molecular analysis in the neonatal period af Larissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, Vera Lúcia Jornada Krebs, Stephen P. Robertson, Tim Morgan, Rachel Sayuri Honjo, Débora Romeo Bertola, Chong Ae Kim
Udgivet 2015Artigo -
3
Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome af Kieran J. Bunn, Phil Daniel, Heleen S. Rösken, Adam C. O’Neill, Sophia Cameron‐Christie, Tim Morgan, Han G. Brunner, Angeline Lai, Henricus P. M. Kunst, David Markie, Stephen P. Robertson
Udgivet 2015Artigo -
4
12 IL28B POLYMORPHISM PREDICTS VIROLOGIC RESPONSE IN PATIENTS WITH HEPATITIS C GENOTYPE 1 TREATED WITH BOCEPREVIR (BOC) COMBINATION THERAPY af F. Poordad, J.-P. Bronowicki, Stuart C. Gordon, Stefan Zeuzem, Ira M. Jacobson, Mark Sulkowski, Thierry Poynard, Tim Morgan, Margaret Burroughs, Vilma Sniukiene, Navdeep Boparai, Clifford A. Brass, Janice K. Albrecht, Bruce R. Bacon
Udgivet 2011Artigo -
5
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration af Adam C. O’Neill, Christina Kyrousi, Johannes Klaus, Richard J. Leventer, Edwin P. Kirk, Andrew E. Fry, Daniela T. Pilz, Tim Morgan, Zandra A. Jenkins, Micha Drukker, Samuel F. Berkovic, Ingrid E. Scheffer, Renzo Guerrini, David Markie, Magdalena Götz, Silvia Cappello, Stephen P. Robertson
Udgivet 2018Artigo -
6
Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result from a Defect in the Localized Degradation of Retinoic Acid af Kathrin Laue, Hans‐Martin Pogoda, Philip B. Daniel, Arie van Haeringen, Yasemin Alanay, Simon von Ameln, Martin Rachwalski, Tim Morgan, Mary Jane Gray, Martijn H. Breuning, Gregory M. Sawyer, Andrew J. Sutherland‐Smith, Peter G. J. Nikkels, Christian Kubisch, Wilhelm Bloch, Bernd Wollnik, Matthias Hammerschmidt, Stephen P. Robertson
Udgivet 2011Artigo -
7
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype af Emma M. Wade, Zandra A. Jenkins, Philip B. Daniel, Tim Morgan, Marie Claude Addor, Lesley C. Adès, Débora Romeo Bertola, Axel Bohring, Erin Carter, Tae‐Joon Cho, Christa M. de Geus, Hans‐Christoph Duba, Elaine Fletcher, Kinga Hadzsiev, Raoul C. M. Hennekam, Chong Ae Kim, Deborah Krakow, Éva Morava, Teresa Neuhann, David O. Sillence, Andrea Superti‐Furga, Hermine E. Veenstra‐Knol, Dagmar Wieczorek, Louise C. Wilson, David Markie, Stephen P. Robertson
Udgivet 2017Artigo -
8
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A af Eyal Reinstein, Sophia Frentz, Tim Morgan, Sixto García‐Miñaúr, Richard J. Leventer, George McGillivray, Mitchel Pariani, Anthony van der Steen, Michael Pope, Muriel Holder‐Espinasse, Richard H. Scott, Elizabeth M. Thompson, Terry Robertson, Brian Coppin, Robert J. Siegel, Montserrat Bret Zurita, José Ignacio Rodrı́guez, Carmen del Rocío Monedero Morales, Yuri Blanc Rodrigues, Joaquín Arcas, Anand Saggar, Margaret A. Horton, Elaine H. Zackai, John M. Graham, David L. Rimoin, Stephen P. Robertson
Udgivet 2012Artigo -
9
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia af Emma M. Wade, Philip B. Daniel, Zandra A. Jenkins, Aideen M. McInerney‐Leo, Paul Leo, Tim Morgan, Marie Claude Addor, Lesley C. Adès, Débora Romeo Bertola, Axel Bohring, Erin Carter, Tae‐Joon Cho, Hans-Christoph Duba, Elaine Fletcher, Chong Ae Kim, Deborah Krakow, Éva Morava, Teresa Neuhann, Andrea Superti‐Furga, Irma Veenstra-Knol, Dagmar Wieczorek, Louise C. Wilson, Raoul C. M. Hennekam, Andrew J. Sutherland‐Smith, Tim M. Strom, Andrew O.M. Wilkie, Matthew A. Brown, Emma L. Duncan, David Markie, Stephen P. Robertson
Udgivet 2016Artigo -
10
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome af Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew F. Rose, Nicole M. Gilette, Pietro Artoni, Nara Sobreira, Wai‐Man Chan, Bryn D. Webb, Caroline D. Robson, Long Cheng, Carol Van Ryzin, Andres Ramirez-Martinez, Payam Mohassel, Mark Leppert, Mary Beth Scholand, Christopher Grunseich, Carlos R. Ferreira, Tyler Hartman, Ian Hayes, Tim Morgan, David Markie, Michela Fagiolini, Amy J. Swift, Peter S. Chines, Carlos E. Speck‐Martins, Francis S. Collins, Ethylin Wang Jabs, Carsten G. Bönnemann, Eric N. Olson, Caroline Andrews, Brenda J. Barry, David G. Hunter, Sarah MacKinnon, Sherin Shaaban, Mónica Erazo, Tamiesha Frempong, Ke Hao, Thomas P. Naidich, Janet C. Rucker, Zhongyang Zhang, Barbara B. Biesecker, Lori L. Bonnycastle, Carmen C. Brewer, Brian P. Brooks, John A. Butman, Wade W. Chien, Kathleen Farrell, Edmond J. FitzGibbon, Andrea Gropman, Elizabeth Hutchinson, Minal S. Jain, Kelly King, Tanya Lehky, Janice Lee, Denise K. Liberton, Narisu Narisu, Scott M. Paul, Neda Sadeghi, Joseph Snow, Beth Solomon, Angela C. Summers, Camilo Toro, Audrey Thurm, Christopher Zalewski, John C. Carey, Stephen P. Robertson, Irini Manoli, Elizabeth C. Engle
Udgivet 2017Artigo
Søgeredskaber:
Relaterede emner
Biology
Gene
Genetics
Medicine
Internal medicine
Cell biology
Phenotype
Cell
Chemistry
Cytoskeleton
FLNA
Filamin
Mutation
Pathology
Physiology
Signal transduction
Zebrafish
ATP7A
Abdominal fat
Allele
Amino acid
Anatomy
Biopsy
Boceprevir
Caloric intake
Caloric theory
Cell culture
Cell fusion
Ceruloplasmin
Chronic hepatitis