Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Alpen Ortug"'
Autor:
Tadashi Shiohama, Hideki Uchikawa, Nobuhiro Nitta, Tomozumi Takatani, Shingo Matsuda, Alpen Ortug, Emi Takahashi, Daisuke Sawada, Eiji Shimizu, Katsunori Fujii, Ichio Aoki, Hiromichi Hamada
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
Hedgehog signaling is a highly conserved pathway that plays pivotal roles in morphogenesis, tumorigenesis, osteogenesis, and wound healing. Previous investigations in patients with Gorlin syndrome found low harm avoidance traits, and increased volume
Externí odkaz:
https://doaj.org/article/3f6094d326054064a78690b38cd63dd2
Autor:
Alpen Ortug, Briana Valli, José Luis Alatorre Warren, Tadashi Shiohama, Andre van der Kouwe, Emi Takahashi
Publikováno v:
Brain Sciences, Vol 13, Iss 12, p 1655 (2023)
Lissencephaly (LIS) is a rare neurodevelopmental disorder with severe symptoms caused by abnormal neuronal migration during cortical development. It is caused by both genetic and non-genetic factors. Despite frequent studies about the cortex, compreh
Externí odkaz:
https://doaj.org/article/9bc5e57630de4b3a89130bd25e974c51
Autor:
Emi Takahashi, Nina Allan, Rafael Peres, Alpen Ortug, Andre J. W. van der Kouwe, Briana Valli, Elizabeth Ethier, Jacob Levman, Nicole Baumer, Keita Tsujimura, Nauru Idalia Vargas-Maya, Trevor A. McCracken, Rosa Lee, Alika K. Maunakea
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2023)
IntroductionAutism Spectrum Disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social interaction, communication and repetitive, restrictive behaviors, features supported by cortical activity. Given the importance of the sub
Externí odkaz:
https://doaj.org/article/aa3b78fd3832434c8d3830acc64912aa
Autor:
Yuichi Akaba, Tadashi Shiohama, Yuji Komaki, Fumiko Seki, Alpen Ortug, Daisuke Sawada, Wataru Uchida, Koji Kamagata, Keigo Shimoji, Shigeki Aoki, Satoru Takahashi, Takeshi Suzuki, Jun Natsume, Emi Takahashi, Keita Tsujimura
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Rett syndrome (RTT) is a severe progressive neurodevelopmental disorder characterized by various neurological symptoms. Almost all RTT cases are caused by mutations in the X-linked methyl-CpG-binding protein 2 (MeCP2) gene, and several mouse models h
Externí odkaz:
https://doaj.org/article/ccd0261a04494ceba7566949cb74c6ff
Autor:
Emel Hulya Yukseloglu, Alpen Ortug, Gulten Rayimoglu, Fatma Cavus Yonar, Itir Erkan, Umut Kara, Dilek Salkim Islek, Melek Ozlem Kolusayin Ozar, Kadir Dastan, Omer Karatas
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 33, Iss 1, Pp 1011-1017 (2019)
The study aimed to discover some variables influencing the risk of nicotine dependence in the Anatolian population. We examined 10 candidate genes and analysed 10 single nucleotide polymorphism (SNP) loci in 50 cases and 50 controls in a preliminary
Externí odkaz:
https://doaj.org/article/0fc9af9189fb414eb3b5ca5177aab0c6
Autor:
Alpen Ortug, Rodney Sadberry, Arthur Rezayev, Emi Takahashi, Tadashi Shiohama, Yurui Guo, Jacob Levman
Publikováno v:
Cereb Cortex
We aimed to identify symptom-related neuroimaging biomarkers for patients with dysgenesis of the corpus callosum (dCC) by summarizing neurological symptoms reported in clinical evaluations and correlating them with retrospectively collected structura
Autor:
Jose Luis Alatorre Warren, Lilit Drak, Saba Shalwani, Homoon Jung, Alpen Ortug, Emi Takahashi
Publikováno v:
The FASEB Journal. 36
Autor:
Alpen Ortug, Yurui Guo, Henry Arthur Feldman, Yangming Ou, Harrison Dieuveuil, Nicole Tara Baumer, Susan Kaminski Faja, Emi Takahashi
Publikováno v:
The FASEB Journal. 36
This study aimed to utilize high angular resolution diffusion magnetic resonance imaging (HARDI) tractography in the mapping of the pathways of the cerebellum associated with posterior fossa tumors (infratentorial neoplasms) and to determine whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f34d4f0ff264f29104fef8019cfc7131
https://hdl.handle.net/20.500.12511/10054
https://hdl.handle.net/20.500.12511/10054
Publikováno v:
The Journal of craniofacial surgery. 33(8)
Analysis of nonmetric cranial variants has been essential for identifying the human population through osteologic analysis and genetic affinities. This study aimed to examine the nonmetric cranial variants to evaluate differences among sex and side c