List of works - Haleh Akhavan-Niaki

A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population.

scientific article published on 13 April 2011

A specific haplotype in potential miRNAs binding sites of secreted frizzled-related protein 1 (SFRP1) is associated with BMD variation in osteoporosis

scientific article published on 25 July 2018

CDX1/2 and KLF5 Expression and Epigenetic Modulation of Sonic Hedgehog Signaling in Gastric Adenocarcinoma

scientific article published on 26 January 2019

CFTR haplotypes in northern Iranian population

scientific article published on 5 October 2012

Cohort profile: the Amirkola Health and Ageing Project (AHAP).

scientific article published on 5 August 2013

Cold Atmospheric Plasma Is a Potent Tool to Improve Chemotherapy in Melanoma In Vitro and In Vivo

scientific article published on 08 July 2020

Conicity Index and Waist-to-Hip Ratio Are Superior Obesity Indices in Predicting 10-Year Cardiovascular Risk Among Men and Women

scientific article published on 7 September 2015

DNA Methylation and Cancer Development: Molecular Mechanism ⬇️

scientific article published on November 1, 2013

Distribution of beta-thalassemia mutations in the northern provinces of Iran

scientific article published on 01 January 2007

Epigenetic alterations of CYLD promoter modulate its expression in gastric adenocarcinoma: A footprint of infections

scientific article published on 21 August 2018

First Report of Association Between Rare α-Thalassemia Mutation (HBA1: c.298A>T) and Hb Fontainebleau (HBA2: c.64G>C)

scientific article published on 18 June 2018

Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia

scientific article

Hedgehog signaling pathway: epigenetic regulation and role in disease and cancer development.

scientific article published on 30 January 2018

IVSII-666 of Human Beta-Globin Gene: A Polymorphic Marker Linked to Codon 8(-AA) Mutation ⬇️

scientific article published on March 31, 2011

Identification of a Rare β(0)-Thalassemia Mutation, Codon 54 (-T) (HBB: c.165delT) in an Iranian Family

scientific article published on 19 August 2015

Infection-associated epigenetic alterations in gastric cancer: New insight in cancer therapy

scientific article published on 04 August 2018

LncRNAs as potential diagnostic and prognostic biomarkers in gastric cancer: A novel approach to personalized medicine

scientific article published on 08 October 2019

Molecular insight in gastric cancer induction: an overview of cancer stemness genes.

scientific article published on April 2014

Mutation and new polymorphisms insight in introns 11 to 14a of CFTR gene of northern Iranian cystic fibrosis patients.

scientific article published on 28 March 2015

Osteoporosis: A Silent Disease with Complex Genetic Contribution.

scientific article published on 2 January 2016

PI3k/AKT signaling pathway: Erythropoiesis and beyond

scientific article published on 07 September 2018

Polypeptides from the myxomycete Physarum polycephalum interacting in vitro with microtubules

scientific article published on 01 January 1990

Purified sulforaphane from broccoli (Brassica oleracea var. italica) leads to alterations of CDX1 and CDX2 expression and changes in miR-9 and miR-326 levels in human gastric cancer cells.

scientific article published on 7 August 2018

Short exposure to collagenase and coculture with mouse embryonic pancreas improve human dermal fibroblast culture

scientific article published on 30 May 2012

Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran ⬇️

scientific article published on February 22, 2012

Targeting LA7 breast cancer stem cells of rat through repressing the genes of stemness-related transcription factors using three different biological fluids

scientific article published on 21 January 2020

Thalassemia in Iran: epidemiology, prevention, and management

scientific article published on 01 April 2007

The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population

scientific article published on 05 January 2016

The study of radiosensitivity in left handed compared to right handed healthy women