Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Zeinab Ravesh"'
Autor:
Atta Ur Rehman, Neda Sepahi, Nicola Bedoni, Zeinab Ravesh, Arash Salmaninejad, Francesca Cancellieri, Virginie G. Peter, Mathieu Quinodoz, Majid Mojarrad, Alireza Pasdar, Ali Ghanbari Asad, Saman Ghalamkari, Mehran Piran, Mehrdad Piran, Andrea Superti-Furga, Carlo Rivolta
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Inherited retinal dystrophies (IRDs) constitute one of the most heterogeneous groups of Mendelian human disorders. Using autozygome-guided next-generation sequencing methods in 17 consanguineous pedigrees of Iranian descent with isolated or
Externí odkaz:
https://doaj.org/article/45ebab2103354052b1c5d15d59bd2b73
Autor:
Hamid A. Bakshi PhD, Hakkim L. Faruck PhD, Zeinab Ravesh PhD, Prawej Ansari PhD, J. M. A. Hannan PhD, Rina Hashimoto PhD, Kazuo Takayama PhD, Rabia Farzand PhD, Mohamed M. Nasef PhD, Adelaide Mensah PhD, Alaa A. A. Aljabali PhD, Vijay Mishra PhD, Nitin B. Charbe PhD, Rohit Goyal PhD, Poonam Negi PhD, Ángel Serrano-Aroca PhD, Bojlul Bahar PhD, Mohamed El-Tanani PhD, Aaron J. Courtenay PhD, Paul McCarron PhD, Iain G. Jack PhD, Murtaza M. Tambuwala PhD
Publikováno v:
Integrative Cancer Therapies, Vol 21 (2022)
The efficacy of chemotherapy depends on the tumor microenvironment. This microenvironment consists of a complex cellular network that can exert both stimulatory and inhibitory effects on tumor genesis. Given the increasing interest in the effectivene
Externí odkaz:
https://doaj.org/article/bed3fec6dc634b60a43684bc74c806c8
Autor:
Ali Ghanbari Asad, Alireza Pasdar, Andrea Superti-Furga, Neda Sepahi, Zeinab Ravesh, Francesca Cancellieri, Saman Ghalamkari, Mathieu Quinodoz, Mehrdad Piran, Virginie G. Peter, Arash Salmaninejad, Mehran Piran, Nicola Bedoni, Carlo Rivolta, Atta Ur Rehman, Majid Mojarrad
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports
Scientific Reports
Inherited retinal dystrophies (IRDs) constitute one of the most heterogeneous groups of Mendelian human disorders. Using autozygome-guided next-generation sequencing methods in 17 consanguineous pedigrees of Iranian descent with isolated or syndromic
Autor:
Bernd, Wissinger, Britta, Baumann, Elena, Buena-Atienza, Zeinab, Ravesh, Artur V, Cideciyan, Katarina, Stingl, Isabelle, Audo, Isabelle, Meunier, Beatrice, Bocquet, Elias I, Traboulsi, Alison J, Hardcastle, Jessica C, Gardner, Michel, Michaelides, Kari E, Branham, Thomas, Rosenberg, Sten, Andreasson, Hélène, Dollfus, David, Birch, Andrea L, Vincent, Loreto, Martorell, Jaume, Català Mora, Ulrich, Kellner, Klaus, Rüther, Birgit, Lorenz, Markus N, Preising, Emanuela, Manfredini, Yuri A, Zarate, Raymon, Vijzelaar, Eberhart, Zrenner, Samuel G, Jacobson, Susanne, Kohl
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(27)
Blue cone monochromacy (BCM) is an X-linked retinal disorder characterized by low vision, photoaversion, and poor color discrimination. BCM is due to the lack of long-wavelength-sensitive and middle-wavelength-sensitive cone photoreceptor function an
Autor:
Mohammad Miryounesi, Nasrin Alipour, Soudeh Ghafouri-Fard, Zeinab Ravesh, Masoumeh Rostami, Vahid Reza Yassaee
Publikováno v:
Gene Reports. 13:141-145
Neurodevelopmental disorders are genetically and phenotypically heterogeneous disorders encompassing wide classification of intellectual disabilities (ID) and autism spectrum disorders (ASD). In the present study, we performed whole exome sequencing
Autor:
Majid Mojarrad, Nasser Shoeibi, Carlo Rivolta, Nicola Bedoni, Zeinab Ravesh, Mathieu Quinodoz, Alireza Pasdar, Arash Salmaninejad
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Scientific Reports
Scientific Reports
Inherited retinal dystrophies (IRDs), displaying pronounced genetic and clinical heterogeneity, comprise of a broad range of diseases characterized by progressive retinal cell death and gradual loss of vision. By the combined use of whole exome seque
Autor:
Feyzollah Hashemi-Gorji, Alireza Rezayi, Vahid Reza Yassaee, Zeinab Ravesh, Fakhrolmolouk Yassaee, Shadab Salehpour, Mohammad Miryounesi
Publikováno v:
Clinica Chimica Acta. 474:88-95
This study aims to ascertain the genetic variants which contribute to the most common types of MPS in eleven Iranian families. Clinical and biochemical features were obtained during initial examination and patients were further investigated for genet
Publikováno v:
Meta Gene. 16:196-198
Lipoid congenital adrenal hyperplasia (LCAH) is the most fatal form of defects in steroid hormone biosynthesis presented with in 46,XY sex reversal and severe fatal salt-losing crisis in the infancy. The disease is caused by mutation in the steroidog
Autor:
Mohammad Hashemi, Amir Izadi, Elham Moslemi, Nasrin Alipour Olyaei, Seyed Mohammad Poorhosseini, Zeinab Ravesh, Vahid Reza Yassaee, Hamid Reza Kheiri, Feyzollah Hashemi-Gorji
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 17:155-160
Breast cancer (BC) is the second most common cancer in the world and by far the most frequent cancer among women, with an estimated 1.67 million new cancer cases diagnosed in 2012 (25% of all cancers). Polygene expression analysis is used to predict
Mutation Spectra of BRCA Genes in Iranian Women with Early Onset Breast Cancer - 15 Years Experience
Autor:
Robab Anbiaee, Azadeh Joulaee, Seyed Mohammad Poorhosseini, Ziba Soltani, Feyzollah Hashemi-Gorji, Vahid Reza Yassaee, Zeinab Ravesh
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 17:149-153
Breast cancer is the most common cancer in Iran. In the recent years an upward trend has been observed in the Iranian population. Early detection by molecular approaches may reduce breast cancer morbidity and mortality. We provided consultation to 3,