Da Pozzo, Paola: search on Z-Library

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1

An antibody-free strategy for screening putative HDM2 inhibitors using crude bacterial lysates expressing GST-HDM2 recombinant protein

Costa, Barbara, Grillone, Agostina Francesca, Salvetti, Alessandra, Rocchiccioli, Silvia, Iacopetti, Paola, Daniele, Simona, Da Pozzo, Eleonora, Campiglia, Pietro, Novellino, Ettore, Martini, Claudia,

Journal:

Drug Testing and Analysis

Year:

2013

Language:

english

File:

PDF, 243 KB

english, 2013

2

Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?

Da Pozzo, Paola, Rubegni, Anna, Rufa, Alessandra, Cardaioli, Elena, Taglia, Ilaria, Gallus, Gian Nicola, Malandrini, Alessandro, Federico, Antonio

Journal:

Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 725 KB

english, 2015

3

Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations

Paola Da Pozzo, Elena Cardaioli, Elena Radi, Antonio Federico

Journal:

Biochemical and Biophysical Research Communications

Year:

2004

Language:

english

File:

PDF, 376 KB

english, 2004

4

New 6- and 7-heterocyclyl-1 H -indole derivatives as potent tubulin assembly and cancer cell growth inhibitors

La Regina, Giuseppe, Bai, Ruoli, Coluccia, Antonio, Naccarato, Valentina, Famiglini, Valeria, Nalli, Marianna, Masci, Domiziana, Verrico, Annalisa, Rovella, Paola, Mazzoccoli, Carmela, Da Pozzo, Eleon

Journal:

European Journal of Medicinal Chemistry

Year:

2018

Language:

english

File:

PDF, 1.10 MB

english, 2018

5

A novel heteroplasmic tRNALeu(CUN) mtDNA point mutation associated with chronic progressive external ophthalmoplegia

Elena Cardaioli, Paola Da Pozzo, Elena Radi, Maria Teresa Dotti, Antonio Federico

Journal:

Biochemical and Biophysical Research Communications

Year:

2005

Language:

english

File:

PDF, 211 KB

english, 2005

6

A newthymidine phosphorylasemutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy

Elena Cardaioli, Francesco Sicurelli, Maria Alessandra Carluccio, Gian Nicola Gallus, Paola Da Pozzo, Mauro Mondelli, Maria Antonietta Margollicci, Vanna Micheli, Antonio Federico, Maria Teresa Dotti

Journal:

Journal of Neurology

Year:

2012

Language:

english

File:

PDF, 285 KB

english, 2012

7

AM251 induces apoptosis and G2/M cell cycle arrest in A375 human melanoma cells

Carpi, Sara, Fogli, Stefano, Romanini, Antonella, Pellegrino, Mario, Adinolfi, Barbara, Podestà, Adriano, Costa, Barbara, Da Pozzo, Eleonora, Martini, Claudia, Breschi, Maria Cristina, Nieri, Paola

Journal:

Anti-Cancer Drugs

Year:

2015

Language:

english

File:

PDF, 507 KB

english, 2015

8

Replay to: Phenotypic spectrum of POLG1 mutations

Cardaioli, Elena, Da Pozzo, Paola, Federico, Antonio

Journal:

Neurological Sciences

Year:

2018

Language:

english

File:

PDF, 307 KB

english, 2018

9

A second MNGIE patient without typical mitochondrial skeletal muscle involvement

Elena Cardaioli, Paola Da Pozzo, Edoardo Malfatti, Carla Battisti, Gian Nicola Gallus, Carmen Gaudiano, Marco Macucci, Alessandro Malandrini, Maria Margollicci, Anna Rubegni, Maria Teresa Dotti, Anton

Journal:

Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 358 KB

english, 2010

10

Leber’s Hereditary Optic Neuropathy associated with cocaine, ecstasy and telithromycin consumption

Elena Cardaioli, Paola Da Pozzo, Gian Nicola Gallus, Rossella Franceschini, Alessandra Rufa, Maria Teresa Dotti, Aldo Caporossi, Antonio Federico

Journal:

Journal of Neurology

Year:

2007

Language:

english

File:

PDF, 146 KB

english, 2007

11

Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed

Mignarri, Andrea, Cenciarelli, Silvia, Da Pozzo, Paola, Cardaioli, Elena, Malandrini, Alessandro, Federico, Antonio, Dotti, Maria Teresa

Journal:

Journal of the Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 184 KB

english, 2015

12

Mitochondria, oxidative stress and neurodegeneration

Antonio Federico, Elena Cardaioli, Paola Da Pozzo, Patrizia Formichi, Gian Nicola Gallus, Elena Radi

Journal:

Journal of the Neurological Sciences

Year:

2012

Language:

english

File:

PDF, 699 KB

english, 2012

13

Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation

Elena Cardaioli, Edoardo Malfatti, Carla Battisti, Paola Da Pozzo, Anna Rubegni, Gian Nicola Gallus, Alessandro Malandrini, Antonio Federico

Journal:

Journal of the Neurological Sciences

Year:

2012

Language:

english

File:

PDF, 559 KB

english, 2012

14

A novel point mutation in the mitochondrial tRNA(Trp) gene produces late-onset encephalomyopathy, plus additional features

Edoardo Malfatti, Elena Cardaioli, Carla Battisti, Paola Da Pozzo, Alessandro Malandrini, Alessandra Rufa, Raffaele Rocchi, Antonio Federico

Journal:

Journal of the Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 754 KB

english, 2010

15

Modulation of nurr1 gene expression in mesencephalic dopaminergic neurones

Floriana Volpicelli, Carla Perrone-Capano, Paola Da Pozzo, Luca Colucci-D'Amato, Umberto Di Porzio

Journal:

Journal of Neurochemistry

Year:

2004

File:

PDF, 30 KB

2004

16

Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNAser(UCN) gene

Elena Cardaioli, Paola Da Pozzo, Alfonso Cerase, Francesco Sicurelli, Alessandro Malandrini, Nicola De Stefano, Maria Laura Stromillo, Carla Battisti, Maria Teresa Dotti, Antonio Federico

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 332 KB

english, 2006

17

Leber Hereditary Optic Neuropathy in 2 of 4 Siblings with 11778 mtDNA Mutation: Clinical Variability or Effect of Toxic Environmental Exposure?

Rufa, Alessandra, Dotti, Maria Teresa, Cardaioli, Elena, Da Pozzo, Paola, Federico, Antonio

Journal:

European Neurology

Year:

2005

Language:

english

File:

PDF, 70 KB

english, 2005

18

Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene

Elena Cardaioli, Edoardo Malfatti, Paola Da Pozzo, Gian Nicola Gallus, Maria Alessandra Carluccio, Alessandra Rufa, Nila Volpi, Maria Teresa Dotti, Antonio Federico

Journal:

Journal of the Neurological Sciences

Year:

2011

Language:

english

File:

PDF, 711 KB

english, 2011

19

Modulation of nurr1 gene expression in mesencephalic dopaminergic neurones

Floriana Volpicelli, Carla Perrone-Capano, Paola Da Pozzo, Luca Colucci-D'Amato, Umberto Di Porzio

Journal:

Journal of Neurochemistry

Year:

2004

Language:

english

File:

PDF, 239 KB

english, 2004

20

A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss

Elena Cardaioli, Paola Da Pozzo, Gian Nicola Gallus, Alessandro Malandrini, Simona Gambelli, Carmen Gaudiano, Edoardo Malfatti, Carlo Viscomi, Enza Zicari, Gianna Berti, Giovanni Serni, Maria Teresa D

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 276 KB

english, 2007

21

Oxidative stress-induced apoptosis in peripheral blood lymphocytes from patients with POLG-related disorders

Formichi, Patrizia, Radi, Elena, Branca, Chiara, Battisti, Carla, Brunetti, Jlenia, Da Pozzo, Paola, Giannini, Fabio, Dotti, Maria Teresa, Bracci, Luisa, Federico, Antonio

Journal:

Journal of the Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 1.94 MB

english, 2016

22

A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

Da Pozzo, Paola, Cardaioli, Elena, Malfatti, Edoardo, Gallus, Gian Nicola, Malandrini, Alessandro, Gaudiano, Carmen, Berti, Gianna, Invernizzi, Federica, Zeviani, Massimo, Federico, Antonio

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 171 KB

english, 2009

23

A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia

Rubegni, Anna, Cardaioli, Elena, Chini, Elena, Da Pozzo, Paola, Battisti, Carla, Malandrini, Alessandro, Federico, Antonio

Journal:

Journal of the Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 875 KB

english, 2014

24

Epigenetic cues in midbrain dopaminergic neuron development

Carla Perrone-Capano, Paola Da Pozzo, Umberto di Porzio

Journal:

Neuroscience & Biobehavioral Reviews

Year:

2000

Language:

english

File:

PDF, 237 KB

english, 2000

25

Commentary to mitDNA research for the pathogenesis of mitochondrial disorders

Paola Da Pozzo, Antonio Federico

Journal:

Biochemical and Biophysical Research Communications

Year:

2005

Language:

english

File:

PDF, 72 KB

english, 2005

26

NovelPOLGmutations and variable clinical phenotypes in 13 Italian patients

Da Pozzo, Paola, Cardaioli, Elena, Rubegni, Anna, Gallus, Gian Nicola, Malandrini, Alessandro, Rufa, Alessandra, Battisti, Carla, Carluccio, Maria Alessandra, Rocchi, Raffaele, Giannini, Fabio, Bianch

Journal:

Neurological Sciences

Year:

2017

Language:

english

File:

PDF, 4.07 MB

english, 2017

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