about
No association of GSTM1 null polymorphism with endometriosis in women from central and southern IranThe luteinizing hormone beta-subunit exon 3 (Gly102Ser) gene mutation and ovarian responses to controlled ovarian hyperstimulationEvaluation of glutathione S-transferase T1 deletion polymorphism on type 2 diabetes mellitus risk in Zoroastrian females in Yazd, IranEvaluation of Glutathione S-transferase T1 (GSTT1) deletion polymorphism on type 2 diabetes mellitus risk in a sample of Yazdian females in Yazd, Iran.SULF 1 gene polymorphism, rs6990375 is in significant association with fetus failure in IVF technique.Evaluation of Anxiolytic, Sedative-hypnotic and Amnesic Effects of Novel 2-phenoxy phenyl-1,3,4-oxadizole Derivatives Using Experimental Models.Association between Glutathione S-Transferase GSTM1-T1 and P1 Polymorphisms with Metabolic Syndrome in Zoroastrians in Yazd, Iran.StuI polymorphism on the androgen receptor gene is associated with recurrent spontaneous abortion.Mycobacterium tuberculosis infection in women with unexplained infertility.The association of arylendosulfatase 1 (SULF1) gene polymorphism with recurrent miscarriage.Investigating GSTT1 and GSTM1 null genotype as the risk factor of diabetes type 2 retinopathy.Case control study of the factor V Leiden and factor II G20210A mutation frequency in women with recurrent pregnancy loss.Analysis of MLH3 C2531T polymorphism in Iranian women with unexplained infertility.Congenital abnormality effect of methamphetamine on histological, cellular and chromosomal defects in fetal mice.Association between Y-chromosome AZFc region micro-deletions with recurrent miscarriage.Mosaic and partial monosomy of chromosome 21 in a case with low platelets count.An Investigation on Mitochondrial DNA Deletions and Telomere Shortening during Multiple Passages of Adult Stem Cells.Human papilloma virus and nasopharyngeal carcinoma: pathology, prognosis, recurrence and mortality of the disease.The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men.Multiplex PCR Screening of Y-chromosome microdeletions in azoospermic ICSI candidate men.Characterization of mesenchymal stem cells from human dental pulp, preapical follicle and periodontal ligamentPrevalence of dental developmental anomalies: a radiographic study.An Association Study of the SLC19A1 Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian Population.KDR gene polymorphisms and idiopathic recurrent spontaneous abortion.Sensitive determination of carbidopa through the electrochemiluminescence of luminol at graphene-modified electrodes.An inhibitory enzyme electrode for hydrogen sulfide detection.CYP2D6 Genotype and Risk of Recurrence in Tamoxifen Treated Breast Cancer Patients.Selective recognition of dysprosium(III) ions by enhanced chemiluminescence CdSe quantum dots.Serum immune reactivity against β2-Glycoprotein-I and anti-neutrophil cytoplasmic auto-antibodies by ELI-P-Complex Screening Technology in recurrent miscarriagePrognostic significance of FLT3 ITD and D835 mutations in AML patientsHigh level of microsatellite instability but not hypermethylation of mismatch repair genes in therapy-related and secondary acute myeloid leukaemia and myelodysplastic syndromeThe rs3917779 polymorphism of P-selectin's significant association with proliferative diabetic retinopathy in Yazd, IranEmerging roles of exosomal miRNAs in breast cancer drug resistanceBRCA1 and BRCA2 common mutations in iranian breast cancer patients: a meta analysis
P50
Q34176393-992008FC-6B40-41CC-AC1B-8C15EC13C4D0Q34589525-BB0CC63C-CF40-4B1A-87A2-F4F97AF1C1B4Q34878087-524FBFCE-125E-4C45-8594-FD62BBF52C8DQ35072267-16F89118-2265-4D6B-A86F-77BF2600EB6EQ35763789-8EE2014C-1567-4F06-A989-F6E7B07575A8Q35843288-AA45B746-9FFE-4102-9D5C-F10E097BFB2DQ35957345-0A7A96DD-A92B-4B52-B920-6408D88E8620Q36714838-3FC59272-1C4A-4359-A02A-9197AEC9CFAAQ36786742-CF84BD0B-21EC-4EDB-B8C3-5E7C2682818DQ37601077-9020DFB5-B92C-411F-8CAC-C2FBC6918EAFQ37607755-ADA53CE6-0BDE-48BA-9638-9984FFAE0652Q37615455-48F1530B-1A98-4184-A670-86B534BED0CDQ37615474-F0DD16B9-9E94-4ED8-A4A5-77E20275E6ECQ37615479-B8AE9016-119E-4B87-9FFC-BF26BFB40BF6Q37615573-5C470FE8-A49C-4146-98BB-125F19BC1DE0Q37692794-39B91789-CB03-479E-9361-7205187F0534Q39130410-D2B93919-C582-458F-BC75-7FD9C0524FAEQ41723299-0229F587-F72C-44A8-9244-DDF7C517ED0AQ41950200-E02615FF-286A-445C-85EB-BF879E2E33AAQ41995574-365F4A30-9B72-48EF-A353-008AEAC6CB71Q42000541-F015101E-2524-410C-A621-B2C4D6024FD6Q44555441-EAEA751E-D9DF-4AC6-ADAE-072AC798B73FQ50921546-775A6E59-D994-4FA9-B76F-D153AA571363Q52668286-184D2E41-D37A-4DA3-B6EC-566BD09AB1CFQ53471188-E888D737-222F-4611-B804-3BF9DF319306Q53757294-372344BC-9081-4F24-8A37-30828589291EQ54242495-FC2A1C21-8ABA-44CD-9967-B34533BC34E4Q54598893-6C59D4CF-F5CA-40F0-8DD5-F52FB81FFE1DQ61839218-680DE82A-42E2-4E40-A6BB-48AC75EE3048Q73263471-9A6B156E-AE8D-479B-8A7B-182A9162D0E3Q77999595-E2992B62-5238-4D7D-A128-3A060D9EC088Q86081416-BBF13106-960B-4BAA-92CA-82DA8C365C75Q92019699-79DD8FC8-7126-4C05-B4F5-0FB040A1CB79Q95621957-74200562-3213-41DA-A357-A4957076D760
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mohammad Hassan Sheikhha
@ast
Mohammad Hassan Sheikhha
@en
Mohammad Hassan Sheikhha
@es
Mohammad Hassan Sheikhha
@nl
Mohammad Hassan Sheikhha
@sl
type
label
Mohammad Hassan Sheikhha
@ast
Mohammad Hassan Sheikhha
@en
Mohammad Hassan Sheikhha
@es
Mohammad Hassan Sheikhha
@nl
Mohammad Hassan Sheikhha
@sl
prefLabel
Mohammad Hassan Sheikhha
@ast
Mohammad Hassan Sheikhha
@en
Mohammad Hassan Sheikhha
@es
Mohammad Hassan Sheikhha
@nl
Mohammad Hassan Sheikhha
@sl
P1053
Q-7643-2017
P106
P31
P3829
P496
0000-0002-3734-8970