Hasil Pencarian - Mohammad Amin Tabatabaiefar

Perbaiki Hasil
  1. 1
    Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization

    Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization oleh Asieh Amousoltani Arani, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar

    Diterbitkan 2021-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    JPX and LINC00641 ncRNAs expression in prostate tissue: a case-control study

    JPX and LINC00641 ncRNAs expression in prostate tissue: a case-control study oleh Roshanak S Sajjadi, Mohammad Hossein Modarressi, Mohammad Amin Tabatabaiefar

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Selection of optimal bioinformatic tools and proper reference for reducing the alignment error in targeted sequencing data

    Selection of optimal bioinformatic tools and proper reference for reducing the alignment error in targeted sequencing data oleh Hannane Mohammadi Nodehi, Mohammad Amin Tabatabaiefar, Mohammadreza Sehhati

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Bisulfite treatment of CG-rich track of trinucleotide repeat expansion disorder: Make the sequence less CG rich

    Bisulfite treatment of CG-rich track of trinucleotide repeat expansion disorder: Make the sequence less CG rich oleh Zahra Joz Abbasalian, Hossein Khanahmad, Mohammad Amin Tabatabaiefar

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family

    WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family oleh Mahnaz Norouzi, Mohammad Shafiei, Zeinab Abdollahi, Paniz Miar, Hamid Galehdari, Mohammad Hasan Emami, Mehrdad Zeinalian, Mohammad Amin Tabatabaiefar, Mohammad Amin Tabatabaiefar

    Diterbitkan 2021-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Implementation and Optimization of Annotation and Interpretation Step of Next-Generation Sequencing Data for Non-Syndromic Autosomal Recessive Hearing Loss

    Implementation and Optimization of Annotation and Interpretation Step of Next-Generation Sequencing Data for Non-Syndromic Autosomal Recessive Hearing Loss oleh Mehdi Shahhoseini, Newsha Molavi, Mohammad Amin Tabatabaiefar, Mohammadreza Sehhati

    Diterbitkan 2021-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    X‐linked mental retardation‐hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene

    X‐linked mental retardation‐hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene oleh Fatemeh Shakarami, Mehdi Jahani, Zahra Nouri, Mohammad Amin Tabatabaiefar

    Diterbitkan 2022-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

    Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran oleh Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI

    Diterbitkan 2017-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Using classification and K-means methods to predict breast cancer recurrence in gene expression data

    Using classification and K-means methods to predict breast cancer recurrence in gene expression data oleh Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar, Ali Haji Gholami, Mohammad Sattari

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report

    Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report oleh Mosa Arghand Dargahi, Mohammad Amin Tabatabaiefar, Shervin Taslimi, Zakaria Zakariaei

    Diterbitkan 2012-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Lynch-like Syndrome and its Molecular Approaches: A Brief Report and Literature Review

    Lynch-like Syndrome and its Molecular Approaches: A Brief Report and Literature Review oleh Zeinab Abdollahi, Mohammad Amin Tabatabaiefar, Mohammad Hassan Emami, Mehrdad Zeinalian

    Diterbitkan 2023-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report

    Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report oleh Zakaria Zakariaei, Shervin Taslimi, Mohammad Amin Tabatabaiefar, Mosa Arghand Dargahi

    Diterbitkan 2012-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    A 15;15 Translocation in a couple with Repeated Abortions: Case report

    A 15;15 Translocation in a couple with Repeated Abortions: Case report oleh Aazam Ahmadi shadmehri, Javad Tavakkoly Bazzaz, Mojtaba Darbouy, Mohammad Amin Tabatabaiefar

    Diterbitkan 2020-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science?

    Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science? oleh Zahra Mohammadi, Arezou Karamzadeh, Mohammad Amin Tabatabaiefar, Hossein Khanahmad, Laleh Shariati

    Diterbitkan 2019-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family

    Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked fa... oleh Somayeh Reiisi, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori

    Diterbitkan 2016-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

    Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent oleh Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj

    Diterbitkan 2014-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    Sequence-identification of Candida species isolated from candidemia

    Sequence-identification of Candida species isolated from candidemia oleh Naeimeh Fathi, Rasoul Mohammadi, Mohammad Amin Tabatabaiefar, Mohammad Ghahri, Seyedeh Zahra Sadrossadati

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  18. 18
    Genotyping of carbapenem resistant Acinetobacter baumannii isolated from tracheal tube discharge of hospitalized patients in intensive care units, Ahvaz, Iran

    Genotyping of carbapenem resistant Acinetobacter baumannii isolated from tracheal tube discharge of hospitalized patients in intensive care units, Ahvaz, Iran oleh Saeed Shoja, Mojtaba Moosavian, Amir Peymani, Mohammad-Amin Tabatabaiefar, Soodabeh Rostami, Nasim Ebrahimi

    Diterbitkan 2013-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  19. 19
    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

    Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsi... oleh Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

    Diterbitkan 2024-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  20. 20
    RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in two distinct Iranian families: Case report and literature review

    RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in two distinct Iranian families: Case report and literature review oleh Sajjad Biglari, Hassan Vahidnezhad, Mohammad Amin Tabatabaiefar, Hamid Reza Khorram Khorshid, Emran Esmaeilzadeh

    Diterbitkan 2024-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: