Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anthi Kelempisioti"'
Autor:
Erato Atsali, Dimitra Kassara, Pelagia Katsimbri, Sorina Boiu, Dimitrios T. Boumpas, Vana Papaevangelou, Olena A. Oshlyanska, Ludmila I. Omelchenko, Tatiana A. Ljudvik, Katerina Bouchalova, Marcel Schüller, Jana Franova, Jarmila Skotakova, Marie Macku, Antoni Fellas, Fiona Hawke, Derek Santos, Andrea Coda, Anthi Kelempisioti, Paula Keskitalo, Virpi Glumoff, Petri Kulmala, Paula Vahasalo, Mohammed A. Mozaffar, Asraa K. Turkistani, Samaa O. Sangoof, Vladislav Sevostyanov, Elena Zholobova, Evangelia Bountouvi, konstantinos Theodoropoulos, Renata Moutsiou, Christina Tsalapaki, Talia Diaz, Sofia Osorio, Maria Teresa Braña, Yuridiana Ramirez, Luis Aparicio, Andres Rodriguez, Enrique Faugier, Rocio Maldonado, Maria Francesca Gicchino, Carmela Granato, Giulia Macchini, Daniela Capalbo, Alma Nunzia Olivieri, Nathan Hasson, Achille Marino, Sona Narula, Melissa Lerman, Maria Amelia Muñoz Calonge, Sara Maria Murias Loza, Rosa Maria Alcobendas, Agustin Remesal, Esmeralda Núñez-Cuadros, Rocio Galindo Zavala, Gisela Díaz-Cordovés Rego, Cristina Antúnez Fernández, Yaiza García Molina, Antonio L. Urda Cardona, Nihal Sahin, Habibe S. Durmus, Ayse S. Pinarbasi, Zubeyde Gunduz, Muammer H. Poyrazoglu, Zehra F. Karaman, Turhan Oktem, Mithat Oner, Ruhan Dusunsel, Gordana Susic, Tamara Krstajic, Dragana Vujovic, Nedeljko Radlovic, Zoran Lekovic, Dusica Novakovic, Gordana Milosevski Lomic, Karina Mördrup, Gunilla Hesselstrand, Iva Sorić, Lovro Lamot, Mandica Vidovic, Mirta Lamot, Miroslav Harjacek, Eva Adank, Elvira Cannizzaro Schneider, Eiman Abdalla, Irfan Ullah, L. Jeyaseelan, Reem Abdwani, Laila A. L. Shaqsi, Ibrahim A. l. Zakwani, Antonis Fanouriakis, Mahesh Janarthanan, Dhanarathnamoorthy Vetrichelvan, P. Ramachandran, Sangeetha Geminiganesan, Dinesh Kumar, Subba Rao, Eleni-Maria Papatesta, Despoina Maritsi, Irini Eleftheriou, Maria Tsolia, Olga Vougiouka, Mustafa Çakan, Nuray Aktay Ayaz, Şerife Gül Karadağ, Gonca Keskindemirci, Vladimir Keltsev, Lyudmila Grebenkina, Kwang Nam Kim, Jong Gyun Ahn, Young Dae Kim, Maria Cristina Maggio, Rolando Cimaz, Maria Concetta Failla, Piera Dones, Mirella Collura, Giovanni Corsello, Jung-Woo Rhim, Ki-Hwan Kim, Soo-Young Lee, Seung-Beom Han, Jin-Han Kang, Jae-Hee Chung, Soo-Jung Lee, Dae-Chul Jeong, Andrei Santimov, Regina Rupp, Igor Alekseev, Natalya Plutova, Ekaterina Moskvina, Marina Kruchina, Aleksandra Tarasenko, Natalya Sokolova, Ekaterina Saveleva, Ilia Bogdanov, Dmitrii Ivanov, Tatiana Kandrina, Olga Kopanevich, Anastasiia Grafskaia, Natalia Ignateva, Daria Pulukchu, Natalia Pavlova, Olga Kalashnikova, Tatiana Kornishina, Margarita Dubko, Vyacheslav Chasnyk, Mikhail Kostik, Shama Sowdagar, Janani Sankar, Venkateswari Ramesh, Iulia E. Szabo, Claudia Sirbe, Cristina Pamfil, Laura Damian, Simona Rednic, Maria Deac, Mihaela Sparchez, Ileana Filipescu, Mirela Parvu, Dumitrita Balint, Ancuta Nicoara
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 15, Iss S2, Pp 177-191 (2017)
Externí odkaz:
https://doaj.org/article/b32aa041c31545d085e7cf12ed6ed062
Autor:
Virpi Glumoff, Dumitrita Balint, Mustafa Çakan, Gonca Keskindemirci, Laila A. L. Shaqsi, Rocio Maldonado, Natalia Ignateva, Young Dae Kim, Ludmila I. Omelchenko, Laura Damian, Eleni-Maria Papatesta, Gunilla Hesselstrand, Dragana Vujovic, Ekaterina Saveleva, Claudia Sirbe, Melissa A. Lerman, Mahesh Janarthanan, Sara Maria Murias Loza, Andrei Santimov, Karina Mördrup, Rocio Galindo Zavala, Tatiana Kandrina, Agustin Remesal, Regina Rupp, Enrique Faugier, Rosa Alcobendas, Marina K. Kruchina, Igor Alekseev, Seung Beom Han, Mandica Vidović, Eiman Abdalla, Mihaela Sparchez, Antoni Fellas, Ayşe Seda Pınarbaşı, Marie Macku, Maria Amelia Muñoz Calonge, Katerina Bouchalova, Daniela Capalbo, Gisela Díaz-Cordovés Rego, Antonis Fanouriakis, L. Jeyaseelan, Jae-Hee Chung, Olga Vougiouka, Mikhail Kostik, Mohammed A. Mozaffar, Olga Kalashnikova, Lovro Lamot, Dae-Chul Jeong, Achille Marino, Christina Tsalapaki, Mirela Parvu, P. Ramachandran, Konstantinos C. Theodoropoulos, Tamara Krstajic, Maria Teresa Braña, Vladimir Keltsev, Iulia E. Szabo, Subba Rao, E. Zholobova, Natalya Plutova, Nathan Hasson, Janani Sankar, Zübeyde Gündüz, Mirella Collura, Dmitrii Ivanov, Nedeljko Radlovic, Cristina Antúnez Fernández, Rolando Cimaz, Zehra Filiz Karaman, Maria Cristina Maggio, Soo-Jung Lee, Maria Concetta Failla, Nuray Aktay Ayaz, Esmeralda Núñez-Cuadros, Tatiana A. Ljudvik, Simona Rednic, Cristina Pamfil, Andrea Coda, Venkateswari Ramesh, Tatiana Kornishina, Erato Atsali, Ilia Bogdanov, Zoran Lekovic, Miroslav Harjacek, Anthi Kelempisioti, Mirta Lamot, Iva Sorić, Natalia Pavlova, Ancuta Nicoara, Pelagia Katsimbri, Jin Han Kang, Habibe Selver Durmuş, Dinesh Kumar, Eva Adank, Soo Young Lee, Gordana Susic, Lyudmila Grebenkina, Talia Diaz, Ruhan Düşünsel, Andres Rodriguez, Sangeetha Geminiganesan, Irfan Ullah, Luis Aparicio, Maria Tsolia, Evangelia Bountouvi, Renata Moutsiou, Muammer Hakan Poyrazoğlu, Maria Francesca Gicchino, Marcel Schüller, Dimitra Kassara, Olga Kopanevich, Natalya Sokolova, Şerife Gül Karadağ, Fiona Hawke, Jong Gyun Ahn, Sofia Osorio, Yuridiana Ramirez, Reem Abdwani, Jung-Woo Rhim, Shama Sowdagar, Vladislav Sevostyanov, Derek Santos, Maria Deac, Turhan Oktem, Ibrahim Al Zakwani, Vana Papaevangelou, Alma Nunzia Olivieri, Dimitrios T. Boumpas, Paula Vähäsalo, Nihal Şahin, Irini Eleftheriou, Ileana Filipescu, Kwang Nam Kim, Sona Narula, Antonio L. Urda Cardona, Carmela Granato, Jarmila Skotakova, Sorina Boiu, Anastasiia Grafskaia, Elvira Cannizzaro Schneider, Margarita Dubko, Gordana Milosevski Lomic, Samaa O. Sangoof, Paula Keskitalo, Ekaterina Moskvina, Yaiza García Molina, Mithat Oner, Ki Hwan Kim, Asraa K. Turkistani, Dhanarathnamoorthy Vetrichelvan, Piera Dones, Jana Franova, Giulia Macchini, Vyacheslav Chasnyk, Giovanni Corsello, Daria Pulukchu, Olena A. Oshlyanska, Despoina Maritsi, Dusica Novakovic, Aleksandra Tarasenko, Petri Kulmala
Publikováno v:
Pediatric Rheumatology. 15
Autor:
Tomoatsu Kimura, Minna Männikkö, Pirkka Mäkelä, Tatsuya Furuichi, Yoshiharu Kawaguchi, Masahiro Nakajima, Kouichi Ozaki, Toshikazu Kubo, Atsushi Takahashi, Hiroshi Mizuta, Yuichiro Hirose, Anthi Kelempisioti, Kei Semba, Yoshiaki Toyama, Atsushi Miyake, Shiro Ikegawa, Michihiro Kamata, Tatsuki Karasugi, Jaro Karppinen, Kazuhiro Chiba, Ken Ichi Yamamura, Yasuo Mikami
Publikováno v:
Journal of Bone and Mineral Research. 24:1537-1543
Lumbar disc herniation (LDH) is one of the most common musculo-skeletal diseases. Recent studies have indicated that LDH has strong genetic determinants, and several susceptibility genes have been reported to associate with LDH; however, its etiology
Autor:
Anthi Kelempisioti, KL Sze, Daniel W.H. Ho, Danny Chan, Morio Matsumoto, Na Wang, Dongquan Shi, Atsushi Takahashi, Anita Yee, Qing Jiang, Paul F. O'Reilly, Pasi J. Eskola, Daisuke Togawa, Tomoatsu Kimura, Junwen Wang, Michiaki Kubo, Patrick Y. P. Kao, Yoshiaki Toyama, Masahiro Kanayama, Yoshiharu Kawaguchi, Pirkka Mäkelä, Toshikazu Kubo, You-Qiang Song, Shiro Ikegawa, Hiroshi Mizuta, Tatsuhiko Tsunoda, Cheng-ai Wu, Pak C. Sham, Kazuhiro Chiba, Stacey S. Cherny, Wei Tian, Jaro Karppinen, Keith D. K. Luk, Stefan Mundlos, John C. Y. Leong, Shea Ping Yip, Tatsuki Karasugi, Minna Männikkö, Atsushi Miyake, Marjo-Riitta Järvelin, Jin Dai, Kenneth M.C. Cheung, Kathryn S.E. Cheah, Yasuo Mikami
Publikováno v:
Europe PubMed Central
Lumbar disc degeneration (LDD) is associated with both genetic and environmental factors and affects many people worldwide. A hallmark of LDD is loss of proteoglycan and water content in the nucleus pulposus of intervertebral discs. While some geneti
Autor:
Daniel H. Geschwind, Lee Barrett, Tianxia Wu, Minakshi Poddar, Mitchell B. Max, Shad B. Smith, Lone Nikolajsen, Ze'ev Seltzer, Dmitri V. Zaykin, Yan Lu, Edith Gershon, Minna Männikkö, Andrew Allchorne, Michael Costigan, Anthi Kelempisioti, Robert S. Griffin, Clifford J. Woolf, Carly Kiselycznyk, Jessica Livneh, Giovanni Coppola, Luda Diatchenko, Inna Belfer, Enrique J. Cobos, Jaro Karppinen, David Goldman, Pei-Hong Shen, William Maixner, Feng Dai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::681322c34c688d1d8265a417ee37f584
https://europepmc.org/articles/PMC3139930/
https://europepmc.org/articles/PMC3139930/
Autor:
Michael, Costigan, Inna, Belfer, Robert S, Griffin, Feng, Dai, Lee B, Barrett, Giovanni, Coppola, Tianxia, Wu, Carly, Kiselycznyk, Minakshi, Poddar, Yan, Lu, Luda, Diatchenko, Shad, Smith, Enrique J, Cobos, Dmitri, Zaykin, Andrew, Allchorne, Edith, Gershon, Jessica, Livneh, Pei-Hong, Shen, Lone, Nikolajsen, Jaro, Karppinen, Minna, Männikkö, Anthi, Kelempisioti, David, Goldman, William, Maixner, Daniel H, Geschwind, Mitchell B, Max, Ze'ev, Seltzer, Clifford J, Woolf
Publikováno v:
Costigan, M, Belfer, I, Griffin, R S, Dai, F, Barrett, L B, Coppola, G, Wu, T, Kiselycznyk, C, Poddar, M, Lu, Y, Diatchenko, L, Smith, S, Cobos, E J, Zaykin, D, Allchorne, A, Shen, P-H, Nikolajsen, L, Karppinen, J, Männikkö, M, Kelempisioti, A, Goldman, D, Maixner, W, Geschwind, D H, Max, M B, Seltzer, Z & Woolf, C J 2010, ' Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1 ', Brain, vol. 133, pp. 2519 . https://doi.org/10.1093/brain/awq195
Not all patients with nerve injury develop neuropathic pain. The extent of nerve damage and age at the time of injury are two of the few risk factors identified to date. In addition, preclinical studies show that neuropathic pain variance is heritabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7f0bae7b36b1e05b19d7522cb9246f9
https://pure.au.dk/portal/da/publications/multiple-chronic-pain-states-are-associated-with-a-common-amino-acidchanging-allele-in-kcns1(6e12cd00-b430-11df-8c1a-000ea68e967b).html
https://pure.au.dk/portal/da/publications/multiple-chronic-pain-states-are-associated-with-a-common-amino-acidchanging-allele-in-kcns1(6e12cd00-b430-11df-8c1a-000ea68e967b).html
Autor:
Frank Reimann, Dmitri V. Zaykin, William Maixner, Feng Dai, Dustin G. Gibson, Frances A. Sanders, Tianxia Wu, Linda S. Wood, Rene H. M. te Morsche, Mitchell B. Max, Jerry Wheeler, Inna Belfer, James J. Cox, Fiona M. Gribble, Minna Männikkö, Anthi Kelempisioti, Carly Kiselycznyk, Shad B. Smith, Jaro Karppinen, Joost P.H. Drenth, C. Geoffrey Woods, Duncan McHale, Lone Nikolajsen, Minakshi Poddar, Luda Diatchenko
Publikováno v:
Reimann, F, Cox, J J, Belfer, I, Diatchenko, L, Zaykin, D V, McHale, D P, Drenth, J P H, Dai, F, Wheeler, J, Sanders, F, Wood, L, Wu, T-X, Karppinen, J, Nikolajsen, L, Männikkö, M, Max, M B, Kiselycznyk, C, Poddar, M, Te Morsche, R H M, Smith, S, Gibson, D, Kelempisioti, A, Maixner, W, Gribble, F M & Woods, C G 2010, ' Pain perception is altered by a nucleotide polymorphism in SCN9A ', Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 11, pp. 5148-5153 . https://doi.org/10.1073/pnas.0913181107
Proceedings of the National Academy of Sciences USA, 107, 11, pp. 5148-53
Proceedings of the National Academy of Sciences USA, 107, 5148-53
Proceedings of the National Academy of Sciences USA, 107, 11, pp. 5148-53
Proceedings of the National Academy of Sciences USA, 107, 5148-53
The gene SCN9A is responsible for three human pain disorders. Nonsense mutations cause a complete absence of pain, whereas activating mutations cause severe episodic pain in paroxysmal extreme pain disorder and primary erythermalgia. This led us to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e1a497d27db4d6fd3d81c6147ed56b3
https://pure.au.dk/portal/da/publications/pain-perception-is-altered-by-a-nucleotide-polymorphism-in-scn9a(bf01dd10-300e-11df-9806-000ea68e967b).html
https://pure.au.dk/portal/da/publications/pain-perception-is-altered-by-a-nucleotide-polymorphism-in-scn9a(bf01dd10-300e-11df-9806-000ea68e967b).html
Autor:
Leena Ala-Kokko, Jaro Karppinen, Jani Takatalo, Annaleena Okuloff, Jaakko Niinimäki, Minna Männikkö, Pasi J. Eskola, Anthi Kelempisioti, Svetlana Solovieva, You-Qiang Song, Osmo Tervonen, Kenneth M.C. Cheung, Marjo-Riitta Järvelin, Iita Daavittila, Roberto Blanco Sequeiros, Daniel W. Chan, Patrick Y. P. Kao, Ulla Karjalainen
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 12, Iss 1, p 153 (2011)
BMC Medical Genetics, Vol 12, Iss 1, p 153 (2011)
BACKGROUND: Disc degeneration (DD) is a common condition that progresses with aging. Although the events leading to DD are not well understood, a significant genetic influence has been found. This study was undertaken to assess the association betwee