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منو اصلی
 
صفحه اصلي > انتشارات مرکز 
 
 
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       Publication:
 

2019

1- Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia. Reports of Biochemistry & Molecular Biology, Vol.7, No.2, Jan 2019. Reports of Biochemistry and Molecular Biology 2019;(7).

2018

1-    Novel LAMA2 gene mutations associated with merosin-deficient congenital muscular dystrophy, Iranian Biomedical Journal, 22 (6): 408-414 November 2018

2- A new mutation in steroidogenic acute regulatory protein (StAR) is segregated in an Iranian family. Meta Gene. 2018;(16)196-198. 10.1016/j.mgene.2018.03.005

3- A study of CAG repeat instability of HTT gene following spermatogenesis, by single sperm analysis. Gene Reports. 2018;(12)294-298. 10.1016/j.genrep.2018.07.013

4- ACE gene rs4343 polymorphism elevates the risk of preeclampsia in pregnant women. Journal of Human Hypertension. 2018 10.1038/s41371-018-0096-4

5- Association of the Risk of Dental Caries and Polymorphism of MBL2 rs11003125 Gene in Iranian Adults. Caries Research. 2018;(14)60-64. 10.1159/000489572

6- Comparing the short-term therapeutic effects and safety profiles of rituximab therapy in pemphigus vulgaris patients either early treated or later than six months. Journal of Dermatological Treatment. 2018;(12)1-4.

7- Evaluation of caries experience in two genders and ENAM polymorphism in Iranian adults. Meta Gene. 2018;(17)78-81. 10.1016/j.mgene.2018.05.002

8- Genetic analysis of Iranian patients with familial hypercholesterolemia. Iranian Biomedical Journal. 2018;(22)117-122. 10.22034/ibj.22.2.117

9- Investigation of piwi-interacting RNA pathway genes role in idiopathic non-obstructive azoospermia. Scientific Reports. 2018;(8). 10.1038/s41598-017-17518-4

10- Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Journal of Inherited Metabolic Disease . 2018 10.1007/s10545-018-0228-6

11- Neurodegeneration with brain iron accumulation 2A: Report of four independent cases. Meta Gene. 2018;(15)87-89. 10.1016/j.mgene.2017.12.006

12- Pharmacogenetics: A strategy for personalized medicine for autoimmune diseases. Clinical Genetics. 2018;(93)481-497. 10.1111/cge.13186

13- Report of three cases with hereditary spastic paraplegia and investigation of the mutations. Meta Gene. 2018;(16)105-107. 10.1016/j.mgene.2018.02.009

14- Sixteen-year history of rituximab therapy for 1085 pemphigus vulgaris patients: A systematic review. International Immunopharmacology. 2018;(54)131-138. 10.1016/j.intimp.2017.11.005

15- The rs4846049 polymorphism in the 3?UTR region of the MTHFR gene increases the migraine susceptibility in an Iranian population. Journal of Pain Research. 2018;(11)145-149. 10.2147/JPR.S152930

16- Tofacitinib as the potent treatment for refractory pemphigus: A possible alternative treatment for pemphigus. Dermatologic therapy. 2018;(11)1-3. 10.1111/dth.12696

2017

17- A new mutation in WT1 gene associated with wilms tumor with reduced penetrance in an Iranian family. International Journal of Cancer Management. 2017;(10). 10.5812/ijcm.7500

18- Association of a novel nonsense mutation in KIAA1279 with Goldberg-Shprintzen syndrome. Iranian Journal of Child Neurology. 2017;(11)70-74.

19- Autosomal recessive polycystic kidney disorder due to two novel compound heterozygote mutations in PKHD1 gene: Case report. Tehran University Medical Journal. 2017;(74)746-749.

20- Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series. Clinica Chimica Acta. 2017;(474)88-95. 10.1016/j.cca.2017.08.017

21- Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients. Journal of inherited metabolic disorders reports. 2017;(32)7-14. 10.1007/8904_2016_572

22- Green tea in non-alcoholic fatty liver disease: A double blind randomized clinical trial. Hepatitis Monthly. 2017;(17). 10.5812/hepatmon.14993

23- Limb girdle muscular dystrophy type 2E due to a novel large deletion in SGCB gene. Iranian Journal of Child Neurology. 2017;(11)57-60. 10.22037/ijcn.v11i3.10521

24- Mental retardation due to chromosomal translocation in an Iranian consanguineous family: Report of three cases. Tehran University Medical Journal. 2017;(74)817-822.

25- Multidisciplinary management of a patient with van der Woude syndrome: A case report. International Journal of Surgery Case Reports. 2017;(30)142-147. 10.1016/j.ijscr.2016.11.032

26- SOCS gene family expression profile in the blood of multiple sclerosis patients. Journal of the Neurological Sciences. 2017;(375)481-485. 10.1016/j.jns.2017.02.015

27- The role of parental microRNA alleles in recurrent pregnancy loss: an association study. Reproductive BioMedicine Online. 2017;(34)325-330. 10.1016/j.rbmo.2016.12.004

28- Towards personalized medicine for patients with autoimmune diseases: Opportunities and challenges. Immunology Letters. 2017;(190)130-138. 10.1016/j.imlet.2017.08.002

2016

29- A new nonsense mutation in CDKL5 gene in a male patient with early onset refractory epilepsy: A case report. International Journal of Pediatrics. 2016;(4)1315-1318. 10.22038/ijp.2016.6394

30- A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities. Gene. 2016;(576)379-380. 10.1016/j.gene.2015.08.039

31- A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A. Gene. 2016;(577)8-13. 10.1016/j.gene.2015.08.071

32- A novel missense mutation in CLCN1 gene in a family with autosomal recessive congenital myotonia. Iranian Journal of Medical Sciences. 2016;(41)456-458.

33- A novel nonsense mutation in PANK2 gene in two patients with pantothenate kinase-associated neurodegeneration. International Journal of Molecular and Cellular Medicine. 2016;(5)255-259. 10.22088/acadpub.BUMS.5.4.255

34- A novel splice site mutation in HPS1 gene is associated with Hermansky-Pudlak syndrome-1 (HPS1) in an Iranian family. International Journal of Molecular and Cellular Medicine. 2016;(5)192-195.

35- A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)991-993. 10.1515/jpem-2016-0032

36- Analysis of the androgen receptor CAG repeats length in Iranian patients with idiopathic non-obstructive azoospermia. Asian Pacific Journal of Reproduction. 2016;(5)71-74. 10.1016/j.apjr.2015.12.013

37- Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: Emphasizing the role of consanguinity. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)1215-1219. 10.1515/jpem-2016-0096

38- First case report of EX3del4765 mutation in PAH gene in Asian population. Iranian Red Crescent Medical Journal. 2016;(18). 10.5812/ircmj.21633

39- Functional analysis of a novel splicing mutation in the mutase gene of two unrelated pedigrees. Cell Journal. 2016;(18)397-404.

40- Gene expression profiling of the 8q22-24 position in human breast cancer: TSPYL5, MTDH, ATAD2 and CCNE2 genes are implicated in oncogenesis, while WISP1 and EXT1 genes may predict a risk of metastasis. Oncology Letters. 2016;(12)3845-3855. 10.3892/ol.2016.5218

41- Homozygosity for a Robertsonian translocation (13q;14q) In a phenotypically normal 44, XX female with a history of recurrent abortion and a normal pregnancy outcome. Journal of Reproduction and Infertility. 2016;(17)184-187.

42- Leigh syndrome associated with a novel mutation in the COX15 gene. Journal of Pediatric Endocrinology and Metabolism. 2016;(29)741-744. 10.1515/jpem-2015-0396

43- Mutation spectra of BRCA genes in Iranian women with early onset breast cancer - 15 years experience. Asian Pacific Journal of Cancer Prevention. 2016;(17)149-153. 10.7314/APJCP.2016.17.S3.149

44- Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1. Human Immunology. 2016;(77)191-195. 10.1016/j.humimm.2015.11.019

45- New gene profiling in determination of breast cancer recurrence and prognosis in Iranian women. Asian Pacific Journal of Cancer Prevention. 2016;(17)155-160. 10.7314/APJCP.2016.17.S3.155

46- Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI. Fetal and Pediatric Pathology. 2016;(35)353-358. 10.1080/15513815.2016.1191567

47- RAR-related orphan receptor A (RORA): A new susceptibility gene for multiple sclerosis. Journal of the Neurological Sciences. 2016;(369)259-262. 10.1016/j.jns.2016.08.045

48- Report of a case with trisomy 9 mosaicism. Iranian Journal of Medical Sciences. 2016;(41)249-252.

49- The study of MED12 gene mutations in uterine leiomyomas from Iranian patients. Tumor Biology. 2016;(37)1567-1571. 10.1007/s13277-015-3943-8

50- Prognosticating Metastasis Risk In Early Breast Cancer WITH EXT1 and WISP1 Genes in 8q22-24 Position. International Journal of Biology, Pharmacy and Allied Sciences (IJBPAS). 2016;(5)19962007.

2015

51- A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene. Gene. 2015;(571)149-150. 10.1016/j.gene.2015.07.058

52- A mutational and expressional analysis of DNMT3A in acute myeloid leukemia cytogenetic subgroups. Hematology. 2015;(20)397-404. 10.1179/1607845415Y.0000000001

53- A new missense mutation in the BCKDHB gene causes the classic form of maple syrup urine disease (MSUD). Journal of Pediatric Endocrinology and Metabolism. 2015;(28)673-675. 10.1515/jpem-2014-0341

54- Expression analysis of Tsga10 during in vitro differentiation of germ cells from mouse embryonic stem cell. Tehran University Medical Journal. 2015;(72)748-754.

55- Inequality in utilization of in-patients health services in Iran. International Journal of Preventive Medicine. 2015;(2015-June)-. 10.4103/2008-7802.158169

56- MicroRNA profiling during germline differentiation of mouse embryonic stem cells. Cellular and Molecular Biology. 2015;(61)84-91. 10.14715/cmb/2015.61.3.16

57- Mutation analysis of the CYP21A2 gene in congenital adrenal hyperplasia. Cellular and Molecular Biology. 2015;(61)51-55. 10.14715/cmb/2015.61.4.9

58- Novel missense mutation in the GALNS gene in an affected patient with severe form of mucopolysaccharidosis type IVA. Clinica Chimica Acta. 2015;(450)121-124. 10.1016/j.cca.2015.08.006

59- Segregation of a novel MLH1 mutation in an Iranian Lynch syndrome family. Gene. 2015;(570)304-305. 10.1016/j.gene.2015.07.005

2014

60- A new approach for molecular diagnosis of TAR syndrome. Clinical Biochemistry. 2014;(47)835-839. 10.1016/j.clinbiochem.2014.04.018

61- A vector-based system for the differentiation of mouse embryonic stem cells toward germ-line cells. Iranian Journal of Basic Medical Sciences. 2014;(17)566-570.

62- Cloning and expression of influenza H1N1 NS1 protein in Escherichia Coli BL21. Iranian Journal of Biotechnology. 2014;(12). 10.5812/ijb.12625

63- Evaluation of in vitro spermatogenesis system effectiveness to study genes behavior: Monitoring the expression of the testis specific 10 (Tsga10) gene as a model. Archives of Iranian Medicine. 2014;(17)692-697.

64- Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro. In Vitro Cellular and Developmental Biology - Animal. 2014;(50)475-481. 10.1007/s11626-013-9722-1

65- Identifying ubiquitin D in paraffin-embedded tissues in patients with colorectal cancer. Journal of Isfahan Medical School. 2014;(32)972-981.

66- Prevalence of subclinical hypothyroidism in pregnant women in Tehran-Iran. International Journal of Fertility and Sterility. 2014;(8)163-166.

67- Single-nucleotide polymorphisms within microRNAs sequences and their 3 UTR target sites may regulate gene expression in gastrointestinal tract cancers. Iranian Red Crescent Medical Journal. 2014;(16). 10.5812/ircmj.16659

68- The effect of progesterone suppositories on threatened abortion: A randomized clinical trial. Journal of Reproduction and Infertility. 2014;(15)147-151.

69- Tuboplasty as a reversal macrosurgery for tubal ligation, is pregnancy possible? A case series. Iranian Journal of Reproductive Medicine. 2014;(12)361-364.

70- Association between  SLC4A7  and  COX11variants and breast cancer in an iranian population. European Journal of Cancer. 2014;()e45.

2013

71- MiR-520d expression analysis in breast cancer. Tehran University Medical Journal. 2013;(71)90-95.

72- Screening for genomic rearrangements at BRCA1 locus in Iranian women with breast cancer using multiplex ligation-dependent probe amplification. Journal of Genetics. 2013;(92)131-134. 10.1007/s12041-013-0223-5

2012

73- Breast cancer survival analysis: Applying the generalized gamma distribution under different conditions of the proportional hazards and accelerated failure time assumptions. International Journal of Preventive Medicine. 2012;(3)644-651.

74- Direct estimate of population attributable fraction of risk factors for cardiovascular diseases: Tehran glucose and lipid study. Iranian Journal of Epidemiology. 2012;(7)9-18.

75- Human papillomavirus infection in women with and without cervical cancer in Tehran, Iran. International Journal of Cancer. 2012;(131)E156-E161. 10.1002/ijc.26488

76- Pregnancy outcomes in women with idiopathic thrombocytopenic purpura. Iranian Journal of Reproductive Medicine. 2012;(10)489-492.

77- TAR Syndrome, a Rare Case Report with Cleft Lip/Palate. Internet Journal of Pediatrics & Neonatology. 2012;(14).

2011

78- Mutation Spectra of the AAAS Gene in Iranian Families with Allgrove Syndrome. Archives of Medical Research. 2011;(42)163-168. 10.1016/j.arcmed.2011.02.006

2010

79- A double-blind, placebo-controlled comparison of letrozole to oxandrolone effects upon growth and puberty of children with constitutional delay of puberty and idiopathic short stature. Hormone Research in Paediatrics. 2010;(74)428-435. 10.1159/000315482

80- BRCA1 and BRCA2 genetic testing in breast and/or ovarian cancer families in Iran. CELL JOURNAL. 2010;(12)329-340.

2009

81- Comparison of CEL I gene expression and mismatch-cleavage activity in some Apiaceae plants. Molecular Breeding. 2009;(24)17-24. 10.1007/s11032-009-9267-x

 
کتب
 
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دانشگاه علوم پزشکی و خدمات بهداشتی، درمانی
شهید بهشــتی
آدرس : تهران - بزرگراه شهید چمران خیابان یــمن - خیابان شهید اعــرابی جنب بیمارستان آیت الله طالقانی

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