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Sadeq Vallian

Showing results (31-40 of 41) with videos related to

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Iranian Journal of Basic Medical Sciences|August 1, 2015
Heterozygosis deficit of polymorphic markers linked to the β-globin gene cluster region in the Iranian populationTahereh Moradi, Reihaneh Vallian, Zahra Fazeli, et al.
Scientific Reports|June 15, 2021
Meta-analysis of gene signatures and key pathways indicates suppression of JNK pathway as a regulator of chemo-resistance in AMLParastoo Modarres, Farzaneh Mohamadi Farsani, Amir Abas Nekouie, et al.
Journal of Cancer Research and Clinical Oncology|September 11, 2025
Molecular signatures of breast cancer in the Iranian population: a review of cell growth and cell cycle regulatorsZeynab Mashayekh, Jalal Vallian Broojeni, Rasool Fatehi Fard, et al.
Genetic Testing and Molecular Biomarkers|November 13, 2014
Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian populationMarjan Mojtabavi Naeini, Hamzeh Mesrian Tanha, Morteza Hashemzadeh Chaleshtori, et al.
Journal of Medical Screening|March 20, 2016
The pros and cons of the fourth revision of thalassaemia screening programme in IranAlireza Moafi, Reihaneh Vallian, Sadeq Vallian, et al.
Genetic Testing and Molecular Biomarkers|February 7, 2015
Modified tetra-primer ARMS PCR as a single-nucleotide polymorphism genotyping toolHamzeh Mesrian Tanha, Marjan Mojtabavi Naeini, Soheila Rahgozar, et al.
Iranian Journal of Biotechnology|September 30, 2017
Analysis of Promyelocytic Leukemia in Human Embryonic Carcinoma Stem Cells During Retinoic Acid-Induced Neural DifferentiationKhadijeh Karbalaie, Sadeq Vallian, Liana Lachinani, et al.
Parkinsonism & Related Disorders|March 20, 2022
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonismBarbara Garavaglia, Sadeq Vallian, Luigi M Romito, et al.
Clinical Genetics|September 3, 2025
Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype-Phenotype Correlations From 61 PatientsPegah Beheshti, Fahimeh Akbarian, Emran Esmaeilzadeh, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Iranian Journal of Basic Medical Sciences|August 1, 2015
Heterozygosis deficit of polymorphic markers linked to the β-globin gene cluster region in the Iranian populationTahereh Moradi, Reihaneh Vallian, Zahra Fazeli, et al.
Scientific Reports|June 15, 2021
Meta-analysis of gene signatures and key pathways indicates suppression of JNK pathway as a regulator of chemo-resistance in AMLParastoo Modarres, Farzaneh Mohamadi Farsani, Amir Abas Nekouie, et al.
Journal of Cancer Research and Clinical Oncology|September 11, 2025
Molecular signatures of breast cancer in the Iranian population: a review of cell growth and cell cycle regulatorsZeynab Mashayekh, Jalal Vallian Broojeni, Rasool Fatehi Fard, et al.
Genetic Testing and Molecular Biomarkers|November 13, 2014
Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian populationMarjan Mojtabavi Naeini, Hamzeh Mesrian Tanha, Morteza Hashemzadeh Chaleshtori, et al.
Journal of Medical Screening|March 20, 2016
The pros and cons of the fourth revision of thalassaemia screening programme in IranAlireza Moafi, Reihaneh Vallian, Sadeq Vallian, et al.
Genetic Testing and Molecular Biomarkers|February 7, 2015
Modified tetra-primer ARMS PCR as a single-nucleotide polymorphism genotyping toolHamzeh Mesrian Tanha, Marjan Mojtabavi Naeini, Soheila Rahgozar, et al.
Iranian Journal of Biotechnology|September 30, 2017
Analysis of Promyelocytic Leukemia in Human Embryonic Carcinoma Stem Cells During Retinoic Acid-Induced Neural DifferentiationKhadijeh Karbalaie, Sadeq Vallian, Liana Lachinani, et al.
Parkinsonism & Related Disorders|March 20, 2022
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonismBarbara Garavaglia, Sadeq Vallian, Luigi M Romito, et al.
Clinical Genetics|September 3, 2025
Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype-Phenotype Correlations From 61 PatientsPegah Beheshti, Fahimeh Akbarian, Emran Esmaeilzadeh, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Pageof 5