P. D’Adamo

发表

Midlatency auditory event-related potentials in mice: comparison to midlatency auditory ERPs in humans

H. Lipp, R. Nitsch, D. Umbricht, 2004, Brain Research.

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

P. Lockhart, S. Haas, K. Hogan, 2014, American journal of human genetics.

Neural precursor cells contribute to decision-making by tuning striatal connectivity via secretion of IGFBPL-1

M. Rocca, T. Kuhlmann, G. Martino, 2020, bioRxiv.

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

F. Tamanini, M. Gulisano, B. Oostra, 1998, Nature Genetics.

Niacin‐mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination

C. Brombin, C. Taveggia, S. Previtali, 2016, EMBO molecular medicine.

39th Annual European Brain and Behaviour Society Abstracts

Maria V. Sanchez-Vives, R. C. Honey, J. L. Moore, 2007, Neural Plasticity.

Congenital, Non-inheritable Chromosomal Abnormalities Responsible for Neurological Disorders

R. Bianchi, P. D’Adamo, 2009 .

Aquaporin-8 is involved in water transport in isolated superficial colonocytes from rat proximal colon.

U. Laforenza, N. LaRusso, P. D’Adamo, 2005, The Journal of nutrition.

Mice deficient for the synaptic vesicle protein Rab3a show impaired spatial reversal learning and increased explorative activity but none of the behavioral changes shown by mice deficient for the Rab3a regulator Gdi1

H. Lipp, D. Wolfer, D. Toniolo, 2004, The European journal of neuroscience.

Down-sizing of neuronal network activity and density of presynaptic terminals by pathological acidosis are efficiently prevented by Diminazene Aceturate

G. Ferrigno, G. Comi, G. Martino, 2015, Brain, Behavior, and Immunity.

Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus

P. Gasparini, A. Filla, G. Cavaletti, 2004, Neuromuscular Disorders.

DNA variants in the human RAB3A gene are not associated with autism

E. Bacchelli, E. Maestrini, H. Lipp, 2004, Genes, brain, and behavior.

Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia

C. Cannistraci, P. Apostoli, A. Zanardi, 2017, EMBO molecular medicine.

A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome

Gilda Stefanelli, N. Landsberger, F. Antonucci, 2018, Molecular Neurobiology.

Erratum: Mutations in GDI1 are responsible for X-linked non-specific mental retardation (Nature Genetics (1998) 19 (134-139))

F. Tamanini, M. Gulisano, B. Oostra, 1998 .

X chromosome inactivation in carriers of Barth syndrome.

D. Toniolo, A. Naumova, P. Barth, 1998, American journal of human genetics.

Selective killing of spinal cord neural stem cells impairs locomotor recovery in a mouse model of spinal cord injury

G. Comi, G. Martino, P. D’Adamo, 2018, Journal of Neuroinflammation.

Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model

R. Ficarella, Emanuela Ponzi, P. D’Adamo, 2021, Human molecular genetics.

Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neurons

J. Bischofberger, L. Scorrano, J. M. Schulz, 2015, Cell Death and Differentiation.

Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains

K. Õunap, H. Esch, M. Raynaud, 2014, Human mutation.

Neural precursor cells tune striatal connectivity through the release of IGFBPL1

M. Rocca, T. Kuhlmann, G. Martino, 2022, Nature communications.

A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder

Dalila Pinto, Elena Bonora, Raffaella Tancredi, 2014, Journal of Neurodevelopmental Disorders.

Conditioned taste aversion as a learning and memory paradigm

H. Lipp, H. Welzl, P. D’Adamo, 2001, Behavioural Brain Research.

Growth defects and impaired cognitive-behavioral abilities in mice with knockout for Eif4h, a gene located in the mouse homolog of the Williams-Beuren syndrome critical region.

M. Pannese, S. Biffo, L. Politi, 2012, The American journal of pathology.

Corrigendum to “Reactive astrocytes and Wnt/β-catenin signaling link nigrostriatal injury to repair in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease” [Neurobiol. Dis. 41/2 (2011) 508–527]

G. Martino, S. Pluchino, C. Tirolo, 2011, Neurobiology of Disease.

Reactive astrocytes and Wnt/β-catenin signaling link nigrostriatal injury to repair in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease

G. Martino, S. Pluchino, C. Tirolo, 2011, Neurobiology of Disease.

Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice.

P. Chapman, H. Lipp, M. Ramsay, 2002, Human molecular genetics.

The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

R. Huganir, M. Passafaro, Francesco Raimondi, 2015, Nature Communications.

Administration of aerosolized SARS-CoV-2 to K18-hACE2 mice uncouples respiratory infection from fatal neuroinvasion

R. De Francesco, V. Broccoli, P. D’Adamo, 2021, Science Immunology.

RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour

R. Moresco, C. Bellone, P. D’Adamo, 2021, Molecular Psychiatry.

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

Andrea Menegon, Flavia Valtorta, Marina Grasso, 1998, Nature Genetics.

A novel X-linked gene, G4.5. is responsible for Barth syndrome

E. Maestrini, S. Bione, D. Toniolo, 1996, Nature Genetics.

Critical importance of RAB proteins for synaptic function

P. D’Adamo, M. Mignogna, 2017, Small GTPases.

RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions

S. Gatti, P. D’Adamo, Maila Giannandrea, 2014, Neuroscience & Biobehavioral Reviews.

Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly.

J. Gécz, C. Skinner, C. Schwartz, 2010, American journal of human genetics.

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.

M. Ferrari, V. Silani, B. Poletti, 2017, Parkinsonism & related disorders.

Scn1a gene reactivation after symptom onset rescues pathological phenotypes in a mouse model of Dravet syndrome

V. Broccoli, P. D’Adamo, F. Ungaro, 2022, Nature communications.

A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

M. Shy, L. Wrabetz, A. Quattrini, 2018, bioRxiv.

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

E. Haan, A. Green, S. Bione, 1997, American journal of human genetics.

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males.

J. Fryns, D. Toniolo, A. Renieri, 2000, American journal of human genetics.

Allozyme divergence and phylogenetic relationships among species of tephritid flies

G. Gasperi, P. D’Adamo, A. Malacrida, 1996, Heredity.

A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility

F. Benfenati, H. Van Esch, F. Valtorta, 2017, Human molecular genetics.

Charcot–Marie–Tooth disease type 2C: a distinct genetic entity. Clinical and molecular characterization of the first European family

L. Santoro, G. Casari, P. D’Adamo, 2002, Neuromuscular Disorders.

A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome

Gilda Stefanelli, N. Landsberger, F. Antonucci, 2018, Molecular Neurobiology.

Mouse Models of Hereditary Mental Retardation

H. Lipp, D. Wolfer, H. Welzl, 2006 .

Hyperactivity and novelty-induced hyperreactivity in mice lacking Rac3

N. Berardi, P. D’Adamo, C. Braschi, 2008, Behavioural Brain Research.

Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2−/y Mice

M. Passafaro, M. Francolini, A. Falqui, 2017, Cerebral cortex.

Accelerated extinction of conditioned taste aversion in P301L tau transgenic mice

R. Nitsch, H. Welzl, J. Götz, 2004, Neurobiology of Disease.

Increased neuroplasticity and hippocampal microglia activation in a mice model of rapid antidepressant treatment

G. Martino, Lorenza Calcaterra, F. Benedetti, 2016, Behavioural Brain Research.

X‐linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies

K. Devriendt, S. Claes, J. Fryns, 1997, Clinical genetics.

Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity.

D. Centonze, J. García-Verdugo, L. Leocani, 2012, Brain : a journal of neurology.

2-Deoxy-d-Glucose Ameliorates PKD Progression.

A. Boletta, I. Rowe, G. Quilici, 2016, Journal of the American Society of Nephrology : JASN.

Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patients

L. Leocani, G. Comi, C. Baldoli, 2017, Scientific Reports.

Controlled administration of aerosolized SARS-CoV-2 to K18-hACE2 transgenic mice uncouples respiratory infection and anosmia from fatal neuroinvasion

R. De Francesco, V. Broccoli, P. D’Adamo, 2021, bioRxiv.

Disruption of ArhGAP15 results in hyperactive Rac1, affects the architecture and function of hippocampal inhibitory neurons and causes cognitive deficits

M. Passafaro, G. Merlo, A. Mauro, 2016, Scientific Reports.

A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder

D. Pinto, E. Bacchelli, A. Battaglia, 2014, Journal of Neurodevelopmental Disorders.

Selective killing of spinal cord neural stem cells impairs locomotor recovery in a mouse model of spinal cord injury

G. Comi, G. Martino, P. D’Adamo, 2018, Journal of Neuroinflammation.

Altered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability

E. Fedele, A. Bruns, S. Taverna, 2017, Neuroscience.

Temporal gene expression profile of the hippocampus following trace fear conditioning

M. Pelizzola, M. Mayhaus, P. Ricciardi-Castagnoli, 2010, Brain Research.

Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks

L. Leocani, M. Cursi, G. Biella, 2015, Cerebral cortex.

Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training.

F. Benfenati, H. Lipp, V. Meskenaite, 2009, Human molecular genetics.

Impaired αGDI Function in the X-Linked Intellectual Disability: The Impact on Astroglia Vesicle Dynamics

M. Kreft, R. Zorec, P. D’Adamo, 2016, Molecular Neurobiology.

Inhibiting glycolysis rescues memory impairment in an intellectual disability Gdi1-null mouse

M. Kreft, R. Zorec, J. Velebit, 2020, Metabolism: clinical and experimental.

X-linked non-specific mental retardation.

D. Toniolo, P. D’Adamo, 2000, Current opinion in genetics & development.

Forebrain Deletion of αGDI in Adult Mice Worsens the Pre-Synaptic Deficit at Cortico-Lateral Amygdala Synaptic Connections

Y. Humeau, D. Toniolo, P. D’Adamo, 2012, PloS one.

Increased neuroplasticity and hippocampal microglia activation in a mice model of rapid antidepressant treatment

G. Martino, Lorenza Calcaterra, F. Benedetti, 2016, Behavioural Brain Research.

RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions

S. Gatti, P. D’Adamo, Maila Giannandrea, 2014, Neuroscience & Biobehavioral Reviews.

Reactive astrocytes and Wnt/β-catenin signaling link nigrostriatal injury to repair in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease

G. Martino, S. Pluchino, C. Tirolo, 2011, Neurobiology of Disease.