Razieh Karamzadeh

发表

Comparative In Vitro Evaluation of Human Dental Pulp and Follicle Stem Cell Commitment

A. Sharifi-Zarchi, M. Baghaban Eslaminejad, Razieh Karamzadeh, 2016, Cell journal.

Isolation, characterization and comparative differentiation of human dental pulp stem cells derived from permanent teeth by using two different methods.

M. B. Eslaminejad, Razieh Karamzadeh, R. Aflatoonian, 2012, Journal of visualized experiments : JoVE.

The Dynamic Proteome of Oligodendrocyte Lineage Differentiation Features Planar Cell Polarity and Macroautophagy Pathways

V. Gupta, H. Baharvand, M. Mirzaei, 2020, GigaScience.

Machine Learning and Network Analysis of Molecular Dynamics Trajectories Reveal Two Chains of Red/Ox-specific Residue Interactions in Human Protein Disulfide Isomerase

H. Chitsaz, M. H. Karimi-Jafari, A. Moosavi-Movahedi, 2017, Scientific Reports.

Identification of a missense variant in CLDN2 in obstructive azoospermia

M. Sadeghi, M. H. Karimi-Jafari, K. McElreavey, 2019, Journal of Human Genetics.

Quantitative proteomic analysis of human testis reveals system-wide molecular and cellular pathways associated with non-obstructive azoospermia.

M. Sabbaghian, V. Gupta, H. Baharvand, 2017, Journal of proteomics.

A fresh look at the male-specific region of the human Y chromosome.

A. Goodchild, M. Sabbaghian, M. Nasr-Esfahani, 2013, Journal of proteome research.

Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity.

P. Fortina, J. Uitto, S. Zeinali, 2017, The Journal of investigative dermatology.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

Red/ox states of human protein disulfide isomerase regulate binding affinity of 17 beta-estradiol.

A. Saboury, M. H. Karimi-Jafari, A. Moosavi-Movahedi, 2017, Archives of biochemistry and biophysics.

Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis.

M. Alaei, M. Abiri, M. Noori-Daloii, 2016, Mutation research.

Type 1 Diabetes Mellitus: Cellular and Molecular Pathophysiology at A Glance

A. Shapiro, H. Baharvand, Y. Tahamtani, 2018, Cell journal.

In silico analysis of novel mutations in maple syrup urine disease patients from Iran

M. Alaei, S. Zeinali, M. Abiri, 2016, Metabolic Brain Disease.

Temporal activation of LRH‐1 and RAR‐γ in human pluripotent stem cells induces a functional naïve‐like state

H. Baharvand, T. Braun, A. Sharifi-Zarchi, 2020, EMBO reports.

Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency.

J. Uitto, J. McGrath, A. Kariminejad, 2019, Matrix biology : journal of the International Society for Matrix Biology.

Human Proteome Project and Human Pluripotent Stem Cells: Odd Bedfellows or a Perfect Match?

H. Baharvand, G. Salekdeh, M. Alikhani, 2020, Journal of proteome research.

M. B. Eslaminejad, Razieh Karamzadeh, 2013 .

Dental Pulp Polyps Contain Stem Cells Comparable to the Normal Dental Pulps

A. Attar, M. B. Eslaminejad, Razieh Karamzadeh, 2014, Journal of clinical and experimental dentistry.

Human closed and open apex premolar teeth express different toll‐like receptor

Razieh Karamzadeh, Reza Jafari, S. Aghajanpour, 2020, Molecular Genetics & Genomic Medicine.

A novel autosomal recessive GJB2‐associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma

P. Fortina, J. Uitto, A. Kariminejad, 2018, Human mutation.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

Machine Learning and Network Analysis of Molecular Dynamics Trajectories Reveal Two Chains of Red/Ox-specific Residue Interactions in Human Protein Disulfide Isomerase

H. Chitsaz, M. H. Karimi-Jafari, A. Moosavi-Movahedi, 2017, Scientific Reports.

Research Performance in Stem Cell Science and Regenerative Medicine in Iran: A National Comprehensive Observation.

H. Baharvand, Massoud Vosough, Zahra Heydari, 2019, Archives of Iranian medicine.

Molecular Dynamics Simulation of the Consequences of a PYCR1 Mutation (p.Ala189Val) in Patients with Complex Connective Tissue Disorder and Severe Intellectual Disability.

J. Uitto, M. Vasei, S. Zeinali, 2017, The Journal of investigative dermatology.

Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.

J. Casanova, P. Fortina, J. Uitto, 2019, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Identification of a missense variant in CLDN2 in obstructive azoospermia

M. Sadeghi, M. H. Karimi-Jafari, K. McElreavey, 2019, Journal of Human Genetics.

a including phenotype with abnormal anchoring and

A. Kariminejad, S. Zeinali, H. Vahidnezhad, 2018 .

Increased robustness of early embryogenesis through collective decision-making by key transcription factors

Hamidreza Chitsaz, Hossein Baharvand, Hamid Pezeshk, 2015, BMC Systems Biology.