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Researchgate: Majid Fardaei
Shiraz, Fars, Iran
Books & Literature
Inferior Spear-like Lens Opacity as a Sign of Keratoconus – DOAJ
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Abstract Purpose: To report 21 cases of typical inferior feather-shape lens opacity associated with keratoconus. Methods: In this cross-sectional study, we
Majid Fardaei | XanEdu Customization Platform
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Author: Majid Fardaei. Results. Expression of α2, α5 and α6 subunits of integrin in de-differentiated NIH3T3 cells by cell-free extract of embryonic stem cells.
Studies on the Molecular Mechanism Underlying Myotonic Dystrophy -...
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Studies on the Molecular Mechanism Underlying Myotonic Dystrophy. Front Cover. Majid Fardaei. University of Nottingham,
Leigh syndrome associated with a novel mutation in the ...
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by M Miryounesi · · Cited by 11 — Mohammad Miryounesi, Majid Fardaei, Seyed Mohammadbagher Tabei and Soudeh Ghafouri-Fard. From the journal Journal of Pediatric Endocrinology ... › doi › jpem › html
Related Documents
dblp: Marion G. Hamshere
dblp.dagstuhl.de
List of computer science publications by Marion G. Hamshere
In vivo co-localisation of MBNL protein with DMPK expanded-repeat...
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@article{FardaeiLBH01, title = {In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts}, author = {Majid Fardaei and Ken Larkin and J.
Majid Fardaei - Academia.edu
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Expression of [alpha]2, [alpha]5 and [alpha]6 subunits of integrin in...
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Pooneh Mokaram • Majid Fardaei • Leili Rohani •. Saeedeh Ebadat • Ahmadreza Sardarian. Received: 2 February Accepted: 25 January ...
Scientific Publications
A case report: Autosomal recessive microcephaly caused by a novel...
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Majid Fardaei b, Milad Gholami a, Mohammad Miryounesi ca Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran;
A Case Report with a Mutation in TRIOBP Gene - PubMed
pubmed.ncbi.nlm.nih.gov
by M Fardaei · · Cited by 9 — Authors. Majid Fardaei , Shaghayegh Sarrafzadeh , Soudeh Ghafouri-Fard , Mohammad Miryounesi. Affiliations. 1 Department of Medical Genetics, ... by SK Alashti · — Authors. Shayan Khalili Alashti , Jafar Fallahi , Arezoo Jokar , Majid Fardaei. Affiliations. 1 Department of Medical Genetics, Shiraz University of Medical ... › ...
MSX1 Mutation in Witkop Syndrome; A Case Report
www.ncbi.nlm.nih.gov
Faezeh Ghaderi, DDS,1 Somaye Hekmat, DDS,1 Reza Ghaderi, MD,2 and Majid Fardaei, PhD3. 1Department of Pediatric Dentistry, School of Dentistry, Shiraz ...
An immunocompetent patient with a nonsense mutation in ...bmcmedgenet.biomedcentral.com › articles
bmcmedgenet.biomedcentral.com
Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran. Majid Fardaei. Department of Medical Genetics, ...
Publications
Effects of auricular acupressure combined with low-calorie diet on...
core.ac.uk
... Mohammad Reza Parizadeh, Parisa Abbasi, Masoud Salehmoghadam, Majid Fardaei, Mohammad Hossein Dabbaghmanesh, Gordon Ferns and Pooneh Mokarram ...
Expression of α2, α5 and α6 subunits of integrin in de-differentiated...
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Generation of patient specific stem cells is among the ultimate goals in regenerative medicine. Such a cell needs to be functional when it transplants....
A new ATP7B gene mutation with severe condition in two unrelated...
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Wilson disease is associated with a defect in copper metabolism and caused by different mutations in ATP7B gene. The aim of this study was to determine...
Majid Fardaei's Research | CureHunter
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Send password reminder... Majid Fardaei Selected Research. Majid Fardaei Research Topics. Disease. 2, Hepatolenticular Degeneration (Wilson's Disease)
Reports & Statements
The genomic architecture of NLRP7 is Alu rich and predisposes to...
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NLRP7 is a major gene responsible for recurrent hydatidiform moles. Here, we report 11 novel NLRP7 protein truncating variants, of which five deletions of more...
References in Muscleblind-Like Proteins - The American ...
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Affiliations. Universite Pierre et Marie Curie, and Unite Mixt de Researche en Sante 787, Institute de Myologie, Paris, France. ,. Majid Fardaei. x. Majid Fardaei.
Research articles | Human Genome Variation - Nature
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Hassan Dastsooz; Mohsen Alipour; Majid Fardaei. Article Open Access 15 Mar An unclassified variant of CHD7 activates a cryptic splice site in a ... › human genome variation
Miscellaneous
Majid Fardaei | LinkedIn
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Majid Fardaei: free download. Ebooks library. On-line books store on...
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Majid Fardaei: free download. Ebooks library. On-line books store on Z-Library | BookSC. Download books for free. Find books
怎么发音 Majid Fardaei | HowToPronounce.com
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你怎么说 Majid Fardaei 在 英语? 发音 Majid Fardaei 1 音, 更为 Majid Fardaei.
Majid fardaei mfardaei | Meaning Pronunciation Origin of Baby Name...
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Majid fardaei mfardaei : Baby Name Majid fardaei mfardaei Meaning,Pronunciation,Origin,Religion,Pronounce of Baby Name Majid fardaei mfardaei. Similar Names...
(PDF) Muscleblind-Like Proteins | Majid Fardaei - Academia.edu
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› Muscleblind_Like_Proteins
Effects of auricular acupressure combined with low-calorie ...
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Masoud Salehmoghadam,1 Majid Fardaei,7 Mohammad Hossein Dabbaghmanesh,8 Gordon Ferns,9 Pooneh Mokarram3,6 1Department of Medicine, Biochemistry and …
Mohsen; Dehghani: free download. Ebooks library. On-line books store...
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Mohsen; Dehghani: free download. Ebooks library. On-line books store on Z-Library | BookSC. Download books for free. Find books
A new missense mutation in the BCKDHB gene causes the classic form of...
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Mohammad Miryounesi, Soudeh Ghafouri-Fard, Hamedreza Goodarzi, Majid Fardaei. Journal of Pediatric Endocrinology & Metabolism: JPEM ...
Altmetric – Mutation analysis of the CTNS gene in Iranian patients...
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Forough Sadeghipour, Mitra Basiratnia, Ali Derakhshan, Majid Fardaei. Abstract. Nephropathic cystinosis is an inherited lysosomal transport disorder caused by mutations in the CTNS gene that encodes for a lysosomal membrane transporter, cystinosin. Dysfunction in this protein leads to cystine accumulation in the cells of ...
Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a...
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Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene · Majid Fardaei 1, Shaghayegh Sarrafzadeh 2, Soudeh Ghafouri-Fard *3, Mohammad Miryounesi Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran., Department of Medical Genetics, ...
Article Usage Statistics Center -- Acupuncture in Medicine
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... Mohammad Safarian, Mohammad Reza Parizadeh, Parisa Abbasi, Masoud Salehmoghadam, Majid Fardaei, Mohammad Hossein Dabbaghmanesh, Gordon ...
A new ATP7B gene mutation with severe condition in two unrelated...
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Majid Fardaei. Department of Medical Genetics and Molecular Medicine, Shiraz University of Medical Sciences, Shiraz, Iran , .ir. Bibliografia.
Abstract - Clinical Laboratorywww.clin-lab-publications.com › article
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Linkage Analysis based on Four Microsatellite Markers to Screen for Unknown Mutation in Families with Wilson Disease by Farzane Arianfar, Majid Fardaei.
[PDF] DNA Sequence Fragment Containing C to A Mutation as a...
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Hassan Dastsooz 1, Nazanin Vahedi 1, Majid Fardaei 1*. 1Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran. A R T I C L E I N F O. A B S T R A C T. Article type: Short communication. Objective(s): Denaturing high performance liquid chromatography (DHPLC) is a high throughput.
An immunocompetent patient with a nonsense Cureuswww.cureus.com › pmc_articles
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... Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi ...
A New Mutation in WT1 Gene Associated with Wilms Tumor ...
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Majid Fardaei , avatar Seyed Mohammad Bagher Tabei , avatar Soudeh Ghafouri-Fard ORCID , avatar Mohammad Miryounesi. 1 Department of Medical Genetics, ... › ijcm › articles
CrossRef TDM - Annals of Rehabilitation Medicine
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Mohammad Miryounesi, Seyed Mohammad Bagher Tabei, Mehdi Dianatpour, Majid Fardaei, Soudeh Ghafouri-Fard. Meta Gene ;16: Crossref logo. › journal › crossRefTDM
Muscleblind-Like Proteins - The American …
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Majid Fardaei. Search for articles by this author Affiliations. Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham, United Kingdom,
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