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List of works by Reza Ghassemifar

A double-embedding technique for thin tissue membranes

scientific article published on 01 November 1992

A molecular tool to assess the pathological relevance of alpha-globin DNA variants

scientific article published in June 2012

Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: laboratory diagnosis and clinical importance

scientific article published in October 2013

Alpha-smooth muscle actin expression in rat and mouse mesenteric wounds after transforming growth factor-beta1 treatment

scientific article published on 01 October 1997

Capsular contracture with textured versus smooth saline-filled implants for breast augmentation: a prospective clinical study

scientific article published on 01 June 1997

Chronic tympanic membrane perforation: a better animal model is needed.

scientific article published on July 2007

Contraction of collagen lattices by cells from Dupuytren's nodules.

scientific article published on December 1996

Experimental mast cell activation improves connective tissue repair in the perforated rat mesentery ⬇️

scientific article published on July 1, 1991

Expression of alpha-smooth muscle actin, TGF-beta 1 and TGF-beta type II receptor during connective tissue contraction

scientific article published on 01 September 1997

Fibroblast movements during contraction of collagen lattices--a quantitative study using a new three-dimensional time-lapse technique with phase-contrast laser scanning microscopy.

scientific article

Hb East Timor [β80(EF4)Asn→His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology

scientific article published on January 2010

Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype

scientific article published in January 2011

Histology of the healing tympanic membrane following perforation in rats

scientific article published on 01 October 2010

Identification and Characterization of Two Novel and Differentially Expressed Isoforms of Humanα2- andα1-Globin Genes ⬇️

scientific article published on January 1, 2012

Impaired function of postoperative macrophages from zinc‐deficient rats decreases collagen contraction ⬇️

scientific article published on 01 May 1995

Incidence of c-Cbl mutations in human acute myeloid leukaemias in an Australian patient cohort.

scientific article published on April 2011

Junctional complexes in the early mammalian embryo.

scientific article

Keratinocyte growth factor 1, fibroblast growth factor 2 and 10 in the healing tympanic membrane following perforation in rats

scientific article published on 07 December 2010

Molecular and cellular analysis of a novel HBA2 mutation (HBA2: c.94A > G) shows activation of a cryptic splice site and generation of a premature termination codon.

scientific article

Molecular and cellular analysis of three novel alpha2-globin gene promoter mutations [HBA2: c.-59C>T], [HBA2: c.-81C>A] and [HBA2: c.-91G>A] reveal varying patterns of transcriptional and translational activities.

scientific article published on January 2014

Molecular and cellular characterization of a new α-thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon

scientific article published on 23 April 2012

Society for Reproductive Biology Founders' Lecture 2003. The making of an embryo: short-term goals and long-term implications

scientific article published in January 2004

The effect of diclofenac (Voltaren) on the contraction of collagen lattices

scientific article published on 01 June 1997

The role of epidermal growth factor in the healing tympanic membrane following perforation in rats.

scientific article

Tympanic membrane wound healing in rats assessed by transcriptome profiling

scientific article published on 14 September 2011

VEGF differentially regulates transcription and translation of ZO-1alpha+ and ZO-1alpha- and mediates trans-epithelial resistance in cultured endothelial and epithelial cells

scientific article

α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of theα2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA

article

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