Results
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43.
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Increased hippocampal DNA oxidation in serotonin transporter deficient mice. [electronic resource] by
- Mössner, R
- Dringen, R
- Persico, A M
- Janetzky, B
- Okladnova, O
- Albert, D
- Götz, M
- Benninghoff, J
- Schmitt, A
- Gerlach, M
- Riederer, P
- Lesch, K P
Producer: 20020806
In:
Journal of neural transmission (Vienna, Austria : 1996) vol. 109
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44.
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Differential regulation of adenosine A(1) and A(2A) receptors in serotonin transporter and monoamine oxidase A-deficient mice. [electronic resource] by
- Mössner, R
- Albert, D
- Persico, A M
- Hennig, T
- Bengel, D
- Holtmann, B
- Schmitt, A
- Keller, F
- Simantov, R
- Murphy, D
- Seif, I
- Deckert, J
- Lesch, K P
Producer: 20010208
In:
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology vol. 10
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45.
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A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs. [electronic resource] by
- Surratt, C K
- Persico, A M
- Yang, X D
- Edgar, S R
- Bird, G S
- Hawkins, A L
- Griffin, C A
- Li, X
- Jabs, E W
- Uhl, G R
Producer: 19930330
In:
FEBS letters vol. 318
Availability: No items available.
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46.
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No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder. [electronic resource] by
- Persico, A M
- Militerni, R
- Bravaccio, C
- Schneider, C
- Melmed, R
- Trillo, S
- Montecchi, F
- Palermo, M
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K L
- Conciatori, M
- Keller, F
Producer: 20020307
In:
Psychiatric genetics vol. 11
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47.
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Adenosine deaminase alleles and autistic disorder: case-control and family-based association studies. [electronic resource] by
- Persico, A M
- Militerni, R
- Bravaccio, C
- Schneider, C
- Melmed, R
- Trillo, S
- Montecchi, F
- Palermo, M T
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K L
- Conciatori, M
- Baldi, A
- Keller, F
Producer: 20001228
In:
American journal of medical genetics vol. 96
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48.
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Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. [electronic resource] by
- Persico, A M
- Pascucci, T
- Puglisi-Allegra, S
- Militerni, R
- Bravaccio, C
- Schneider, C
- Melmed, R
- Trillo, S
- Montecchi, F
- Palermo, M
- Rabinowitz, D
- Reichelt, K-L
- Conciatori, M
- Marino, R
- Keller, F
Producer: 20030225
In:
Molecular psychiatry vol. 7
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49.
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Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression. [electronic resource] by
- Lintas, C
- Sacco, R
- Garbett, K
- Mirnics, K
- Militerni, R
- Bravaccio, C
- Curatolo, P
- Manzi, B
- Schneider, C
- Melmed, R
- Elia, M
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K-L
- Persico, A M
Producer: 20090910
In:
Molecular psychiatry vol. 14
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50.
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Enhanced APOE2 transmission rates in families with autistic probands. [electronic resource] by
- Persico, A M
- D'Agruma, L
- Zelante, L
- Militerni, R
- Bravaccio, C
- Schneider, C
- Melmed, R
- Trillo, S
- Montecchi, F
- Elia, M
- Palermo, M
- Rabinowitz, D
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K-L
- Muscarella, L
- Guarnieri, V
- Melgari, J-M
- Conciatori, M
- Keller, F
Producer: 20050324
In:
Psychiatric genetics vol. 14
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51.
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Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions. [electronic resource] by
- D'Amelio, M
- Ricci, I
- Sacco, R
- Liu, X
- D'Agruma, L
- Muscarella, L A
- Guarnieri, V
- Militerni, R
- Bravaccio, C
- Elia, M
- Schneider, C
- Melmed, R
- Trillo, S
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K-L
- Macciardi, F
- Holden, J J A
- Persico, A M
Producer: 20051212
In:
Molecular psychiatry vol. 10
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52.
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Barrel pattern formation requires serotonin uptake by thalamocortical afferents, and not vesicular monoamine release. [electronic resource] by
- Persico, A M
- Mengual, E
- Moessner, R
- Hall, F S
- Revay, R S
- Sora, I
- Arellano, J
- DeFelipe, J
- Gimenez-Amaya, J M
- Conciatori, M
- Marino, R
- Baldi, A
- Cabib, S
- Pascucci, T
- Uhl, G R
- Murphy, D L
- Lesch, K P
- Keller, F
- Hall, S F
Producer: 20010920
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 21
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53.
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Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1. [electronic resource] by
- Palmieri, L
- Papaleo, V
- Porcelli, V
- Scarcia, P
- Gaita, L
- Sacco, R
- Hager, J
- Rousseau, F
- Curatolo, P
- Manzi, B
- Militerni, R
- Bravaccio, C
- Trillo, S
- Schneider, C
- Melmed, R
- Elia, M
- Lenti, C
- Saccani, M
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K-L
- Persico, A M
Producer: 20100302
In:
Molecular psychiatry vol. 15
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54.
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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. [electronic resource] by
- Persico, A M
- D'Agruma, L
- Maiorano, N
- Totaro, A
- Militerni, R
- Bravaccio, C
- Wassink, T H
- Schneider, C
- Melmed, R
- Trillo, S
- Montecchi, F
- Palermo, M
- Pascucci, T
- Puglisi-Allegra, S
- Reichelt, K L
- Conciatori, M
- Marino, R
- Quattrocchi, C C
- Baldi, A
- Zelante, L
- Gasparini, P
- Keller, F
Producer: 20010628
In:
Molecular psychiatry vol. 6
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55.
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Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum Disorder. [electronic resource] by
- Tillmann, J
- Ashwood, K
- Absoud, M
- Bölte, S
- Bonnet-Brilhault, F
- Buitelaar, J K
- Calderoni, S
- Calvo, R
- Canal-Bedia, R
- Canitano, R
- De Bildt, A
- Gomot, M
- Hoekstra, P J
- Kaale, A
- McConachie, H
- Murphy, D G
- Narzisi, A
- Oosterling, I
- Pejovic-Milovancevic, M
- Persico, A M
- Puig, O
- Roeyers, H
- Rommelse, N
- Sacco, R
- Scandurra, V
- Stanfield, A C
- Zander, E
- Charman, T
Producer: 20190701
In:
Journal of autism and developmental disorders vol. 48
Availability: No items available.
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