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List of works by Francesco Pallotti

A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion.

scientific article published on 2 December 2016

A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene

scientific article published on 01 December 2018

A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck

scientific article

Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene

article

An updating of the biochemical function of coenzyme Q in mitochondria.

scientific article published on January 1994

Analysis of mtDNA deletions in muscle by in situ hybridization

scientific article published on 01 January 2000

Analysis of three screening methods for the detection of calreticulin gene mutations

scientific article published on 06 November 2019

Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase

scientific article published on 01 October 1993

Authors' Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

scientific article

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations.

scientific article published on December 2004

Biological Variation of Procalcitonin in Healthy Individuals

scientific article published on 01 October 2004

Comparison of three strategies for myocardial protection during coronary artery bypass graft surgery based on markers of cardiac damage.

scientific article published in June 2005

Decorin from different bovine tissues: study of glycosaminoglycan chain by PAGEFS

scientific article published on 15 November 2005

Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non‐synaptic mitochondria of aged rats ⬇️

scientific article published on June 30, 1997

Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.

scientific article

Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2

scientific article published on 01 May 2000

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA

scientific article published on 01 September 1999

FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy

scientific article published on 01 September 2015

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

scientific article

High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.

scientific article

Hyaluronan and human endothelial cell behavior.

scientific article

Isolation and subfractionation of mitochondria from animal cells and tissue culture lines.

scientific article published on January 2007

JAK2 mutation and atypical chronic myeloid leukemia.

scientific article

JAK2, 46/1 haplotype and chronic myelogenous leukemia: diagnostic and therapeutic potential

scientific article published on 01 December 2019

Matrix metalloproteinase 2 and tissue inhibitors of metalloproteinases regulate human aortic smooth muscle cell migration during in vitro aging

scientific article published on 01 June 2006

Mitochondrial DNA in platelets from aged subjects.

scientific article published in April 1998

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

scientific article

Mitochondrial activities of rat heart during ageing

scientific article published on 01 October 1994

Mitochondrial complex I defects in aging.

scientific article published in September 1997

Molecular cloning and characterization of UDP-glucose dehydrogenase from the amphibian Xenopus laevis and its involvement in hyaluronan synthesis.

scientific article published on 17 January 2006

New electrophoretic and chromatographic techniques for analysis of heparin and heparan sulfate.

scientific article published in August 2008

New insights into the pathobiology of Down syndrome--hyaluronan synthase-2 overexpression is regulated by collagen VI α2 chain

scientific article published on 28 March 2013

Oxidative stress, antioxidant defences and aging.

scientific article

Pathogenesis of primary defects in mitochondrial ATP synthesis.

scientific article

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

scientific article

Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene.

scientific article

Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

scientific article

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