about
In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcriptsVSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran.Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.Myotonic dystrophy--a multigene disorder.Leigh syndrome associated with a novel mutation in the COX15 gene.Auricular or body acupuncture: which one is more effective in reducing abdominal fat mass in Iranian men with obesity: a randomized clinical trial.Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP GeneMultiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease.Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole.Family screening for a novel ATP7B gene mutation, c.2335T>G, in the South of Iran.Second Allele Finder Software: a Simple Approach Toward HLA Typing.Genetic variations of 21 STR markers on chromosomes 13, 18, 21, X, and Y in the south Iranian population.Expression of a2, a5 and a6 subunits of integrin in de-differentiated NIH3T3 cells by cell-free extract of embryonic stem cells.The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran.Construction of bacterial ghosts for transfer and expression of a chimeric hepatitis C virus gene in macrophages.The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.Impact of KIF6 Polymorphism rs20455 on Coronary Heart Disease Risk and Effectiveness of Statin Therapy in 100 Patients from Southern Iran.A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome.Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports.Limb Girdle Muscular Dystrophy Type 2E Due to a Novel Large Deletion in SGCB Gene.Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations.Muscleblind-like proteins: similarities and differences in normal and myotonic dystrophy muscleA Novel Missense Mutation in CLCN1 Gene in a Family with Autosomal Recessive Congenital Myotonia.MSX1 mutation in witkop syndrome; a case report.DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis.A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene.A new ATP7B gene mutation with severe condition in two unrelated Iranian families with Wilson disease.TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren-Larsson Syndrome.The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype?Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature.A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities.Linkage Analysis based on Four Microsatellite Markers to Screen for Unknown Mutation in Families with Wilson Disease.Effects of auricular acupressure combined with low-calorie diet on the leptin hormone in obese and overweight Iranian individualsSegregation of a novel MLH1 mutation in an Iranian Lynch syndrome familyThe same haplotype for two unrelated Wilson disease patients with new ATP7B mutationA new missense mutation in the BCKDHB gene causes the classic form of maple syrup urine disease (MSUD)Author's Reply
P50
Q24555640-13F30FDD-3293-4A26-8395-E25A490F3E3AQ33652581-8A98E3E9-AAF3-491A-9A15-EED76FB7D58AQ34121747-A86ECA3F-34B5-48F6-986C-4D0EA7E1D146Q34446614-5E04D5FA-D98A-4A73-AB04-E6ADD0480730Q34517478-ADAD6841-3E3D-4D07-8B79-6C95EA0F393FQ34667632-030554A7-EDC7-4C8C-A398-DF575837BCB9Q36625743-3486B636-BEB1-4A71-B931-0A7C36E1C2A8Q37121833-C2A79B60-EFD3-49FB-9859-E2204B3B3C7CQ37223063-59E97E11-AF43-4522-A0A3-08A40CE225F6Q37692789-8CA23404-51CC-4B3A-99AE-CFB57BE09384Q38977423-B688FF8A-F7F6-4EE9-8593-45DC9A0879D1Q39077445-FF731899-230F-4F48-A26C-3221812C72F2Q39399958-035A5353-38BA-4C66-91CA-1185F6BEB0D5Q39937992-2D0F46FC-33EF-4FDD-B02E-DC0BA3741743Q40368271-D7012C71-D87B-403C-B0A5-6AB31FB1180CQ41117430-00DFBDF6-A3F6-4353-9C8E-4FFF454AE420Q41118507-43F2B352-9EAC-476A-BE18-BB0ED263CABEQ41255075-F744CC34-F0A1-49CE-AEC4-ABFD8A4CD7EAQ41352478-995385E4-C29B-4931-87E3-694E87AB545AQ41460705-1B47ADF5-81C5-4B1D-9483-1FE908D49B24Q41600679-7CD949DC-6B47-4420-8B05-DF4768883EEFQ41895875-EDBC5107-3965-4AC3-A16A-0558683A2C60Q42154009-64523CF4-96AE-421C-B13C-504C8AEF08F9Q42154009-8DC51BBE-F3A6-4409-A9EE-8142CC385F0DQ42391714-B530C36C-5E55-4267-8CB1-8CBE250301C2Q42605474-BE26C1E2-19CF-43DE-B452-D16CACEE3D12Q42964324-8E80FB5E-960E-4E35-BE03-94B72FF926C3Q43702973-B8AE2E35-7619-4388-A9F3-B4380D5A29C0Q43843954-4945C0DD-E755-4ED5-BD20-158CBC4CD5FAQ47270971-C061020D-466B-4DEB-A791-213A0A5E00BBQ48155051-3A53FFB2-5AB5-4A73-A36D-45B1855E246AQ49789121-BC97A67B-640E-45D8-9FF8-747D8ED1B1B2Q49811760-99AD9EBF-25B3-4766-9681-3E1979707673Q49835961-F755358C-1810-4192-A23E-BA30A808686EQ50568405-5FFF34F4-3145-4205-876F-5D0647E4CFEEQ54129269-54A3593A-63B6-4847-8F9B-557381F64BD1Q84447673-08B6FCB7-2D90-4B03-BCB1-CCE73457B48FQ85544879-C83CC261-8BAA-4C14-A8CB-9038A8345092Q85900483-82BD09EA-74FF-45D5-85F2-2F6CCFFAEE96Q85932847-497DBEF3-3769-4EFC-A4BB-865C7F27529E
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Majid Fardaei
@ast
Majid Fardaei
@en
Majid Fardaei
@es
Majid Fardaei
@nl
type
label
Majid Fardaei
@ast
Majid Fardaei
@en
Majid Fardaei
@es
Majid Fardaei
@nl
prefLabel
Majid Fardaei
@ast
Majid Fardaei
@en
Majid Fardaei
@es
Majid Fardaei
@nl
P106
P31
P496
0000-0002-8393-0371