نتائج البحث - Saliha Yılmaz
- يعرض 1 - 3 نتائج من 3
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1
The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis حسب Mehmet Bakırcıoğlu, Ofélia P. Carvalho, Maryam Khurshid, James J. Cox, Beyhan Tüysüz, Tanyeri Barak, Saliha Yılmaz, Ahmet Okay Çağlayan, Alp Di̇nçer, Adeline K. Nicholas, Oliver Quarrell, Kelly Springell, Gulshan Karbani, Saghira Malik, Caroline Gannon, Eamonn Sheridan, Moira Crosier, Steven Lisgo, Susan Lindsay, Kaya Bilgüvar, Fanni Gergely, Murat Günel, C. Geoffrey Woods
منشور في 2011Artigo -
2
Recessive LAMC3 mutations cause malformations of occipital cortical development حسب Tanyeri Barak, Kenneth Y. Kwan, Angeliki Louvi, Veysi Demirbilek, Serap Saygı, Beyhan Tüysüz, Murim Choi, Hüseyin Boyacı, Katja Doerschner, Ying Zhu, Hande Kaymakçalan, Saliha Yılmaz, Mehmet Bakırcıoğlu, Ahmet Okay Çağlayan, Ali K. Ozturk, Katsuhito Yasuno, William J. Brunken, Ergin Atalar, Cengiz Yalçınkaya, Alp Di̇nçer, Richard A. Bronen, Shrikant Mane, Tayfun Özçelık, Richard P. Lifton, Nenad Šestan, Kaya Bilgüvar, Murat Günel
منشور في 2011Artigo -
3
Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i> حسب Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin, Jun Yin, Justin Cotney, Koray Özduman, Timuçin Avşar, Jie Li, Phillip B. Murray, Octavian Henegariu, Saliha Yılmaz, Jennifer Moliterno Günel, Geneive Carrión-Grant, Baran Yılmaz, Conor Grady, Bahattin Tanrıkulu, Mehmet Bakırcıoğlu, Hande Kaymakçalan, Ahmet Okay Çağlayan, Leman Sencar, Emre Ceyhun, Ahmet Atik, Yaşar Bayri, Hanwen Bai, Luis Kolb, Ryan Hebert, Sacit Bulent Omay, Ketu Mishra-Gorur, Murim Choi, John D. Overton, Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel
منشور في 2013Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Mutation
AKT1
Anatomy
Apoptosis
Cell biology
Cortical dysplasia
Embryonic stem cell
Epilepsy
Exome sequencing
Exon
Frameshift mutation
Growth factor
Induced pluripotent stem cell
KLF4
Lissencephaly
Medicine
Meningioma
Missense mutation
Neurogenesis
Neuroscience
Nonsense mutation
PDGFB
PI3K/AKT/mTOR pathway
Pathology
Phenotype
Platelet-derived growth factor receptor
Receptor