Lista de obras - Francesco Pallotti - Dominio Público Uruguay

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

artículo científico publicado en 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

artículo científico publicado en 2014

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.

artículo científico publicado en 1994

Analysis of mtDNA deletions in muscle by in situ hybridization

artículo científico publicado en 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.

artículo científico publicado en 2015

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

artículo científico publicado en 2004

Biological Variation of Procalcitonin in Healthy Individuals

artículo científico publicado en 2004

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

artículo científico publicado en 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 ⬇️

artículo científico publicado el 30 de junio de 1997

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

artículo científico publicado en 2007

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

artículo científico publicado en 2000

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

artículo científico publicado en 1999

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

artículo científico publicado en 2015

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

artículo científico publicado en 2006

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

artículo científico publicado en 2010

Hyaluronan and human endothelial cell behavior.

artículo científico publicado en 2008

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

artículo científico publicado en 2007

JAK2 mutation and atypical chronic myeloid leukemia.

artículo científico publicado en 2009

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

artículo científico publicado en 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.

artículo científico publicado en 1998

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

artículo científico publicado en 2002

Mitochondrial activities of rat heart during ageing

artículo científico publicado en 1994

Mitochondrial complex I defects in aging.

artículo científico publicado en 1997

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

artículo científico publicado en 2006

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

artículo científico publicado en 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.

artículo científico publicado en 1998

Pathogenesis of primary defects in mitochondrial ATP synthesis.

artículo científico publicado en 2001

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

artículo científico publicado en 2002

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

artículo científico publicado en 2016

Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

artículo científico publicado en 2015

The Fate of Human Sperm-Derived mtDNA in Somatic Cells ⬇️

artículo científico publicado el 1 de octubre de 1997

Lista de obras de Francesco Pallotti

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

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

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

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

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

Analysis of mtDNA deletions in muscle by in situ hybridization

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

Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase

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

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

Biological Variation of Procalcitonin in Healthy Individuals

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

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

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

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

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

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

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

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

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

Hyaluronan and human endothelial cell behavior.

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

JAK2 mutation and atypical chronic myeloid leukemia.

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

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

Mitochondrial DNA in platelets from aged subjects.

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

Mitochondrial activities of rat heart during ageing

Mitochondrial complex I defects in aging.

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

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

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

Oxidative stress, antioxidant defences and aging.

Pathogenesis of primary defects in mitochondrial ATP synthesis.

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

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

Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia.

The Fate of Human Sperm-Derived mtDNA in Somatic Cells ⬇️