Hasil Pencarian - Dor-Mohammad KORDI-TAMANDANI

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  1. 1
    Analysis of IFN-γ (+874 A/T) and IL-10 (-1082 G/A) genes polymorphisms with risk of schizophrenia.

    Analysis of IFN-γ (+874 A/T) and IL-10 (-1082 G/A) genes polymorphisms with risk of schizophrenia. oleh Dor Mohammad kordi Tamandani, Azizoallah Mojahed, Maryam Najafi

    Diterbitkan 2014-01-01
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  2. 2
    Evaluation of LATS1 and LATS2 Promoter Methylation with the Risk of Pterygium Formation

    Evaluation of LATS1 and LATS2 Promoter Methylation with the Risk of Pterygium Formation oleh Maryam Najafi, Dor Mohammad Kordi-Tamandani, Mohammad Arish

    Diterbitkan 2016-01-01
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  3. 3
    Analysis of methylation and expression profile of MOB1A in blood, saliva, and tissue of patients with oral squamous cell carcinoma (OSCC) and precancerous patients

    Analysis of methylation and expression profile of MOB1A in blood, saliva, and tissue of patients with oral squamous cell carcinoma (OSCC) and precancerous patients oleh Hanieh Soleimani, Mohammad Rigi Ladez, Dor Mohammad Kordi-Tamandani

    Diterbitkan 2022-08-01
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  4. 4
    Association of miR-132 and miR-185 Genes Methylation and their Expression Profile with Risk of Congenital Factor XIII Deficiency

    Association of miR-132 and miR-185 Genes Methylation and their Expression Profile with Risk of Congenital Factor XIII Deficiency oleh Dor Mohammad Kordi-Tamandani, Zohreh Rezaei, Akbar Dorgalaleh-Mail

    Diterbitkan 2015-07-01
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  5. 5
    Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism

    Analysis of Expression Profiles of GLI3A, LATS2 and MOB1A genes in Patients with Congenital hypothyroidism oleh Sepideh Eisazaei, Maryam Nakhaee-Moghadam, Dor-Mohammad Kordi Tamandani

    Diterbitkan 2022-03-01
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  6. 6
    Strategies for whole-exome sequencing analysis in a case series study of familial male infertility

    Strategies for whole-exome sequencing analysis in a case series study of familial male infertility oleh Masomeh Askari, Dor Mohammad Kordi Tamandani, Navid Almadani, Mehdi Totonch

    Diterbitkan 2020-05-01
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  7. 7
    Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia

    Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia oleh Tahereh Dianat, Dor Mohammad Kordi Tamandani, Maryam Najafi, Ali Khajeh

    Diterbitkan 2022-12-01
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  8. 8
    Correlation between resistance to trastuzumab and miR-141 relative expression in the BT-474 human breast cancer cell line

    Correlation between resistance to trastuzumab and miR-141 relative expression in the BT-474 human breast cancer cell line oleh Zohreh Rezaei, Dor Mohammad Kordi-Tamandani, Ahmadreza Sebzari, Kazem Dastjerdi

    Diterbitkan 2017-10-01
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  9. 9
    Composition and Diversity Differences between Colon Microbiome of Colorectal Cancer Patients and Healthy Individuals by Age

    Composition and Diversity Differences between Colon Microbiome of Colorectal Cancer Patients and Healthy Individuals by Age oleh Hosseinali Abdi, Dor Mohammad Kordi-Tamandani, Milad Lagzian, Alireza Bakhshipour

    Diterbitkan 2021-10-01
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  10. 10
    Analysis of DRD1 gene expression pattern in patients with glaucoma

    Analysis of DRD1 gene expression pattern in patients with glaucoma oleh Mojtaba Reyhani, Mohammad Arish, Alireza Maleki, Shahram Banaie, Dor Mohammad Kordi-Tamandani

    Diterbitkan 2022-09-01
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  11. 11
    The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province

    The relationship between FXIII Val34Leu and PAI-1 4G/5G gene polymorphisms and recurrent miscarriage in women from Golestan province oleh Nazanin Ghaderi Nejad, Fojan saboori, Nader Mansour Samaei, Dor Mohammad Kordi-Tamandani

    Diterbitkan 2022-03-01
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  12. 12
    Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer

    Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer oleh Seyed Mohsen Miresmaeili, Dor Mohammad Kordi Tamandani, Seyed Mehdi Kalantar, Seyed Mohammad Moshtaghioun

    Diterbitkan 2016-04-01
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  13. 13
    Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients

    Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients oleh Sajad Rafiee Komachali, Zakieh Siahpoosh, Sara Rafiee Komachali, Dor Mohammad Kordi Tamandani, Mansoor Salehi

    Diterbitkan 2022-11-01
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  14. 14
    Association of Genetic Polymorphisms in GSTP1, GSTM1, and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran

    Association of Genetic Polymorphisms in GSTP1, GSTM1, and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran oleh Sima SHAHROKHZADEH, Azam SOLEIMANI, Dor-Mohammad KORDI-TAMANDANI, Mohammad Hossein SANGTARASH, Omid NEJATI, Mohsen TAHERI

    Diterbitkan 2020-06-01
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  15. 15
    Epigenetic Inactivation of Protocadherin 10 by Methylation in Colorectal Cancer

    Epigenetic Inactivation of Protocadherin 10 by Methylation in Colorectal Cancer oleh Sahar Tavakolian, Matineh Barati Bagherabad, Dor Mohammad Kordi-Tamandani, Mohammad Reza Abbaszadegan, Mohammad Amin Kerachian

    Diterbitkan 2020-02-01
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  16. 16
    Evaluation of Promoter Hypermethylation, Expression and, Oxytocin Receptor Gene (OXTR) Polymorphism with the Risk of Oral Squamous Cell Carcinoma

    Evaluation of Promoter Hypermethylation, Expression and, Oxytocin Receptor Gene (OXTR) Polymorphism with the Risk of Oral Squamous Cell Carcinoma oleh Behnaz Hassanpour, Mohammad Ayoub Rigi-Ladiz, Tayebeh Baranzehi, Mohammad Javad Ashraf, DorMohammad Kordi-Tamandani

    Diterbitkan 2021-01-01
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  17. 17
    Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

    Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis oleh Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts

    Diterbitkan 2019-02-01
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  18. 18
    A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

    A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East oleh Maryam Najafi, Maryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, Zeineb Bakey, Zeineb Bakey, Farkhondeh Behjati, Dinu Antony, Dinu Antony, Isabel Schüle, Simin Sadeghi-Bojd, Ehsan Ghayoor Karimiani, Ehsan Ghayoor Karimiani, Miriam Schmidts, Miriam Schmidts

    Diterbitkan 2019-03-01
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