Lista de obras -

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis

scientific article published on 29 November 2018

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

scientific article published on 16 January 2019

Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility.

artículo científico publicado en 2017

Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases

article

Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of miR-200b, miR-145, and let7b in A Functional Imbalanced Epigenetic Disease

scientific article published on 20 February 2019

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation

artículo científico publicado en 2019

Generic extraction medium: From highly polar to non-polar simultaneous determination

artículo científico publicado en 2019

Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations

scientific article published on 24 June 2019

Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate

article

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

artículo científico publicado en 2019

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations

artículo científico publicado en 2019

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

scientific article published on 22 May 2019

Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations

artículo científico publicado en 2019

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

scientific article published on 18 November 2018

Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A: a first report.

artículo científico publicado en 2018

Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease

scientific article published on 27 April 2019

Therapeutic targeting of angiogenesis molecular pathways in angiogenesis-dependent diseases

artículo científico publicado en 2018

Transient expression of anti-VEFGR2 nanobody in

artículo científico publicado en 2018

Lista de obras de

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility.

Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases

Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of miR-200b, miR-145, and let7b in A Functional Imbalanced Epigenetic Disease

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation

Generic extraction medium: From highly polar to non-polar simultaneous determination

Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations

Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate

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

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations

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

Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations

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

Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A: a first report.

Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease

Therapeutic targeting of angiogenesis molecular pathways in angiogenesis-dependent diseases

Transient expression of anti-VEFGR2 nanobody in