international

 | تاریخ ارسال: ۱۳۹۶/۷/۴ | 
 Iranian – German Collaboration

Iran Collaboration with Germany in Medicine Based on Scopus Papers from 2011 to 2017:


808 publications,   1737 person co-author with Germany,   94 institutions collaboration
Field-weighted citation impact: 3.95


 
                                                                              


 

A memorandum of understanding (MoU) has been signed in 5th of May 2017 on a joint cooperation in medical education and research between the Ministry of Health and Medical Education of Islamic Republic of Iran and the Federal Ministry of Education and Research of the Federal Republic of Germany to take necessary actions in the following areas: 

  • Support of workshops in medical sciences and health research to identify priority topics of both sides for cooperation activities. This includes joint research but also cooperation in higher education.
  • The support of cooperation activities in higher education in the field of health and medical sciences is considered as important by both sides. Joint activities should aim to support partnerships at institutional level such as joint study courses and the exchange of young researchers including PhD & early stage post-docs, or exchange of staff.
  • Support scientific collaboration including joint mobility projects (collaboration of HEIs, university hospitals, research institutes). The projects should enable researchers to connect existing national research projects to work on topics of joint interest. They include joint meetings and research stays. The exchange of young researchers within these projects should be encouraged.
  • Encourage the exchange of experiences and dissemination of information of mutual interest, particularly in the field of basic and clinical sciences.

 
Active Research Groups
 
1. Department of Anatomical Sciences, Tehran University of Medical Sciences & Institute of Neuroanatomy, RWTH Aachen University
                                    ​​     Prof. Iraj Ragerdi Kashani   (CV)                                      Prof. Cordian Beyer (CV)
                                                                                                                  
       Research interests  :
•   Amyotrophic lateral sclerosis (ALS)
•   Eating disorders/Anorexia nervosa (AN)
•   Multiple sclerosis (MS)
•   Oxidative stress
•   Spinal cord injury
•   Stroke and ischemia
•   Regenerative Medicine  
•   Cell Therapy
Publications:
  • Reprod Toxicol. 2017 Aug 14. pii: S0890-6238(17)30101-6. doi: 10.1016/j.reprotox.2017.08.006.
Role of stromal derived factor-1a (SDF-1a) for spermatogenesis of busulfan-injured rats.
Khanlarkhani N, Mortezaee K, Amidi F, Kharazinejad , Beyer C, Baazm M, Pasbakhsh P, Pazhohan A, Sobhani A, Zendedel A.
  • Int Immunopharmacol. 2017 Aug 19;51:131-139. doi: 10.1016/j.intimp.2017.08.007.
Progesterone therapy induces an M1 to M2 switch in microglia phenotype and suppresses NLRP3 inflammasome in a cuprizone-induced demyelination mouse model.
Aryanpour R, Pasbakhsh P, Zibara K, Namjoo Z, Beigi Boroujeni F, Shahbeigi S, Kashani IR, Beyer C, Zendehdel A.
  • Mol Neurobiol. 2017 Jan 27. doi: 10.1007/s12035-017-0400-2.
Estrogen Attenuates Local Inflammasome Expression and Activation after Spinal Cord Injury.
Zendedel A, Mönnink F, Hassanzadeh G, Zaminy A, Ansar MM, Habib P, Slowik A, Kipp M, Beyer C.
  • Molecular Neurobiology , July 2016, Volume 53, Issue 5, pp 3063–3075
Activation and Regulation of NLRP3 Inflammasome by Intrathecal Application of SDF-1a in a Spinal Cord Injury Model
Adib Zendedel ,Sonja Johann, Soraya Mehrabi, Mohammad-taghi Joghataei , Gholamreza Hassanzadeh, Markus Kipp, Cordian Beyer
  • Metabolic Brain Disease, April 2016, Volume 31, Issue 2, pp 425–433
Regulatory effect of triiodothyronine on brain myelination and astrogliosis after cuprizone-induced demyelination in mice
Adib Zendede, Iraj Ragerdi Kashani, Maryam Azimzadeh, Parichehr Pasbakhsh, Negar Omidi, Abolfazl Golestani, Cordian Beyer, Tim Clarner

 
2. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences & Max-Planck Institute for Molecular Genetics
 
                         ​​          Prof. Hossein Najmabadi  (CV)                                                       Prof. Hans Hilger Ropes  (CV)
                                                                                                                                                 
    
     Research interests  :
•   Genetic diagnosis of intellectual disability (ID)
•   Autosomal recessive cognitive defects
•   Molecular causes of mental retardation
•   Genetic diagnosis of Neuromuscular Disorders

Publications:
  • Am J Hum Genet. 2017 Aug 12. pii: S0002-9297(17)30288-4. doi: 10.1016/j.ajhg.2017.07.010.
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
Ivanova EL, Mau-Them FT, Riazuddin S, Kahrizi K, Laugel V, Schaefer E, de Saint Martin A, Runge K1, Iqbal Z, Spitz MA, Laura M, Drouot N, Gérard B, Deleuze JF1, de Brouwer APM, Razzaq A, Dollfus H, Assir MZ, Nitchké P, Hinckelmann MV, Ropers H, Riazuddin S, Najmabadi H, van Bokhoven H, Chelly J.
  • Hum Mutat. 2017 Jun;38(6):621-636. doi: 10.1002/humu.23205. Epub 2017 Mar 23.
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability.
Musante L, Püttmann L, Kahrizi K, Garshasbi M, Hu H1, Stehr H, Lipkowitz B, Otto S, Jensen LR, Tzschach A, Jamali P, Wienker T, Najmabadi H, Ropers HH, Kuss AW
  • Hum Mutat. 2017 Jun;38(6):621-636. doi: 10.1002/humu.23205. Epub 2017 Mar 23.
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability.
Musante L1, Püttmann L1, Kahrizi K2, Garshasbi M1, Hu H1, Stehr H3, Lipkowitz B1, Otto S1, Jensen LR4, Tzschach A1, Jamali P5, Wienker T1, Najmabadi H2, Ropers HH1, Kuss AW4.
  • PLoS Genet. 2016 May 11;12(5):e1006022. doi: 10.1371/journal.pgen.1006022. eCollection 2016 May.
BOD1 Is Required for Cognitive Function in Humans and Drosophila.
Esmaeeli-Nieh S, Fenckova M, Porter IM, Motazacker MM, Nijhof B, Castells-Nobau A, Asztalos Z, Weißmann R, Behjati F, Tzschach A, Felbor U, Scherthan H, Sayfati SM, Ropers HH, Kahrizi K, Najmabadi H, Swedlow JR, Schenck A, Kuss AW.
  • PLoS One. 2015 Aug 26;10(8):e0129631. doi: 10.1371/journal.pone.0129631. eCollection 2015.
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.
Davarniya B, Hu H, Kahrizi K, Musante L, Fattahi Z, Hosseini M, Maqsoud F, Farajollahi R, Wienker TF, Ropers HH, Najmabadi H
 

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