Որոնման արդյունքները - Carissa Adams
- Ցուցադրվում են 1 - 3 արդյունքները 3
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1
Congenital microcephaly and chorioretinopathy due to de novo heterozygous <i>KIF11</i> mutations: Five novel mutations and review of the literature Ghayda Mirzaa, Laura B. Enyedi, Gretchen Parsons, Sarah Collins, Līvija Medne, Carissa Adams, Thomas Ward, Bradley V. Davitt, Alma R. Bicknese, Elaine H. Zackai, Helga V. Toriello, William B. Dobyns, Susan L. Christian
Հրապարակվել է 2014Revisão -
2
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia Laura A. Jansen, Ghayda Mirzaa, Gisele E. Ishak, Brian J. O’Roak, Joseph B. Hiatt, William H. Roden, Sonya A. Gunter, Susan L. Christian, Sarah Collins, Carissa Adams, Jean‐Baptiste Rivière, Judith St‐Onge, Jeffrey G. Ojemann, Jay Shendure, Robert F. Hevner, William B. Dobyns
Հրապարակվել է 2015Artigo -
3
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome Ghayda Mirzaa, David Parry, Andrew E. Fry, Kristin A. Giamanco, Jeremy Schwartzentruber, Megan R. Vanstone, Clare V. Logan, Nicola Roberts, Colin A. Johnson, Shawn Singh, Stanislav S. Kholmanskikh, Carissa Adams, Rebecca D. Hodge, Robert F. Hevner, David T. Bonthron, Kees P. J. Braun, Laurence Faivre, Jean‐Baptiste Rivière, Judith St‐Onge, Karen W. Gripp, Grazia M.S. Mancini, Ki Pang, Elizabeth Sweeney, Hilde Van Esch, Nienke E. Verbeek, Dagmar Wieczorek, Michelle Steinraths, Jacek Majewski, Kym M. Boycott, Daniela T. Pilz, M. Elizabeth Ross, William B. Dobyns, Eamonn Sheridan
Հրապարակվել է 2014Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Dysplasia
Epilepsy
Gene
Medicine
Megalencephaly
Neuroscience
PI3K/AKT/mTOR pathway
PTEN
Pathology
Polymicrogyria
AKT1
AKT3
Apoptosis
Audiology
Breast cancer
Cancer
Cancer research
Cell cycle
Cockayne syndrome
Cortical dysplasia
Cyclin D1
Cyclin D2
DNA repair
GSK-3
Hearing loss
Hemimegalencephaly
Intellectual disability
Internal medicine