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The 3p21.1-p21.3 Hereditary Vascular Retinopathy Locus Increases the Risk for Raynaud's Phenomenon and Migraine

Cephalalgia, 2005-12, Vol.25 (12), p.1168-1172

2005

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Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2

Neuropediatrics, 2004-10, Vol.35 (5), p.293

2004

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[P2.75]: Malformations of cortical development: Genomic analysis by high density microarrays in a large patient cohort

International journal of developmental neuroscience, 2010-12, Vol.28 (8), p.712-713

2010

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"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

Iranian journal of public health, 2003-09, Vol.32 (3)

2003

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"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

Iranian journal of public health, 2003-09, Vol.32 (3), p.47-53

2003

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Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine Gene ATP1A2

Neuropediatrics, 2004-07, Vol.35 (5), p.293-296

2004

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Recent developments in cell shipping methods

Biotechnology and bioengineering, 2022-11, Vol.119 (11), p.2985-3006

2022

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The impact of pre‐analytical variations on biochemical analytes stability: A systematic review

Journal of clinical laboratory analysis, 2020-12, Vol.34 (12), p.e23551-n/a

2020

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MicroRNAs in thyroid cancer with focus on medullary thyroid carcinoma: potential therapeutic targets and diagnostic/prognostic markers and web based tools

Oncology research, 2024, Vol.32 (6), p.1011-1019

2024

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The Cross-Talk between Polyphenols and the Target Enzymes Related to Oxidative Stress-Induced Thyroid Cancer

Oxidative medicine and cellular longevity, 2022, Vol.2022, p.2724324-20

2022

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Prediction of the CO2 emission across grassland and cropland using tower-based eddy covariance flux measurements: a machine learning approach

Environment, development and sustainability, 2023-06, Vol.25 (6), p.5495-5509

2023

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RTTN Mutations Link Primary Cilia Function to Organization of the Human Cerebral Cortex

American journal of human genetics, 2012-09, Vol.91 (3), p.533-540

2012

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Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping

American journal of human genetics, 2017-09, Vol.101 (3), p.326-339

2017

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SWI/SNF Mediates Polycomb Eviction and Epigenetic Reprogramming of the INK4b-ARF-INK4a Locus

Molecular and Cellular Biology, 2008-05, Vol.28 (10), p.3457-3464

2008

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Microcephaly with Simplified Gyration, Epilepsy, and Infantile Diabetes Linked to Inappropriate Apoptosis of Neural Progenitors

American journal of human genetics, 2011-08, Vol.89 (2), p.265-276

2011

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Human mutations in integrator complex subunits link transcriptome integrity to brain development

PLoS genetics, 2017-05, Vol.13 (5), p.e1006809-e1006809

2017

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Different Methods for Cell Viability and Proliferation Assay: Essential Tools in Pharmaceutical Studies

Anti-cancer agents in medicinal chemistry, 2022-02, Vol.22 (4), p.703-712

2022

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GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

Genes, 2022-02, Vol.13 (3), p.447

2022

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Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Haematologica (Roma), 2013-05, Vol.98 (5), p.696-704

2013

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Promoter Methylation of Tumor Suppressors in Thyroid Carcinoma: A Systematic Review

Iranian journal of public health, 2021-12, Vol.50 (12), p.2461-2472

2021

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Residual pyruvate kinase activity in PKLR‐deficient erythroid precursors of a patient suffering from severe haemolytic anaemia

European journal of haematology, 2017-06, Vol.98 (6), p.584-589

2017

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Correction: Human mutations in integrator complex subunits link transcriptome integrity to brain development

PLoS genetics, 2017-08, Vol.13 (8), p.e1006923-e1006923

2017

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A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia

Hemoglobin, 2019-03, Vol.43 (2), p.77-82

2019

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Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpoint

Genes & development, 2005-03, Vol.19 (6), p.665-670

2005

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EZH2-dependent chromatin looping controls INK4a and INK4b, but not ARF, during human progenitor cell differentiation and cellular senescence

Epigenetics & chromatin, 2009-12, Vol.2 (1), p.16-16, Article 16

2009

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The 3p21.1-p21.3 Hereditary Vascular Retinopathy Locus Increases the Risk for Raynaud's Phenomenon and Migraine

Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2

[P2.75]: Malformations of cortical development: Genomic analysis by high density microarrays in a large patient cohort

"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies"

Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine Gene ATP1A2

Recent developments in cell shipping methods

The impact of pre‐analytical variations on biochemical analytes stability: A systematic review

MicroRNAs in thyroid cancer with focus on medullary thyroid carcinoma: potential therapeutic targets and diagnostic/prognostic markers and web based tools

The Cross-Talk between Polyphenols and the Target Enzymes Related to Oxidative Stress-Induced Thyroid Cancer

Prediction of the CO2 emission across grassland and cropland using tower-based eddy covariance flux measurements: a machine learning approach

RTTN Mutations Link Primary Cilia Function to Organization of the Human Cerebral Cortex

Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping

SWI/SNF Mediates Polycomb Eviction and Epigenetic Reprogramming of the INK4b-ARF-INK4a Locus

Microcephaly with Simplified Gyration, Epilepsy, and Infantile Diabetes Linked to Inappropriate Apoptosis of Neural Progenitors

Human mutations in integrator complex subunits link transcriptome integrity to brain development

Different Methods for Cell Viability and Proliferation Assay: Essential Tools in Pharmaceutical Studies

GATA-1 Defects in Diamond-Blackfan Anemia: Phenotypic Characterization Points to a Specific Subset of Disease

Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity

Promoter Methylation of Tumor Suppressors in Thyroid Carcinoma: A Systematic Review

Residual pyruvate kinase activity in PKLR‐deficient erythroid precursors of a patient suffering from severe haemolytic anaemia

Correction: Human mutations in integrator complex subunits link transcriptome integrity to brain development

A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia

Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpoint

EZH2-dependent chromatin looping controls INK4a and INK4b, but not ARF, during human progenitor cell differentiation and cellular senescence

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