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Neurogenetics(50)
ISSN: 1364-6745
1    
Gene expression analyses reveal molecular relationships among 20 regions of the human CNS 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:2  Page:67-80  

Roth Richard B;   Hevezi Peter;   Lee Jerry;   Willhite Dorian;   Lechner Sandra M;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:208

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2    
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan 期刊论文

NEUROGENETICS     ISSN:1364-6745  Volume:7  Issue:3  Page:133-138  

Di Fonzo A;   Wu-Chou YH;   Lu CS;   van Doeselaar M;   Simons EJ;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:170

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3    
Whole genome expression profiling of the medial and lateral substantia nigra in Parkinson's disease 期刊论文

NEUROGENETICS     ISSN:1364-6745  Volume:7  Issue:1  Page:1-11  

Moran LB;   Duke DC;   Deprez M;   Dexter DT;   Pearce RKB;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:133

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4    
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:3  Page:167-174  

Collins Ann L;   Ma Deqiong;   Whitehead Patrice L;   Martin Eden R;   Wright Harry H;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:90

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5    
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:4  Page:247-257  

Long Jeffrey M;   LaPorte Patricia;   Merscher Sandra;   Funke Birgit;   Saint-Jore Bruno;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:55

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6    
Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson's disease 期刊论文

NEUROGENETICS     ISSN:1364-6745  Volume:7  Issue:3  Page:139-148  

Duke DC;   Moran LB;   Kalaitzakis ME;   Deprez M;   Dexter DT;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:59

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7    
Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-olds 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:4  Page:239-246  

Skowronek M H;   Laucht M;   Hohm E;   Becker K;   Schmidt M H;  

来源数据库:[Web of Science, Science Citation Index Expanded, MEDLINE - Academic]         被引频次:54

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8    
Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:4  Page:269-276  

Scarciolla Oronzo;   Stuppia Liborio;   De Angelis Maria Vittoria;   Murru Stefania;   Palka Chiara;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:41

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9    
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:2  Page:105-110  

Gul Asma;   Hassan Muhammad Jawad;   Mahmood Saqib;   Chen Wenje;   Rahmani Safa;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:47

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10    
Current perspectives on the genetic causes of neural tube defects 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:4  Page:201-221  

De Marco Patrizia;   Merello Elisa;   Mascelli Samantha;   Capra Valeria;  

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:38

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11    
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:2  Page:93-103  

Mannan Ashraf U;   Boehm Johann;   Sauter Simone M;   Rauber Anne;   Byrne Paula C;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:36

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12    
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:3  Page:149-156  

Stevanin Giovanni;   Montagna Giorgia;   Azzedine Hamid;   Valente Enza Maria;   Durr Alexandra;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:34

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13    
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:1  Page:47-50  

Blair Marcia A;   Ma Shaochun;   Hedera Peter;  

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:36

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14    
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: An additional fifteen families 期刊论文

NEUROGENETICS     ISSN:1364-6745  Volume:7  Issue:4  Page:277-279  

Murrell J;   Ghetti B;   Cochran E;   Macias-Islas MA;   Medina L;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:32

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15    
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:1  Page:39-46  

Poirier K;   Lacombe D;   Gilbert-Dussardier B;   Raynaud M;   Desportes V;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:36

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16    
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease 期刊论文

NEUROGENETICS     ISSN:1364-6745  Volume:7  Issue:1  Page:27-30  

Metzger S;   Bauer P;   Tomiuk J;   Laccone F;   Didonato S;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:33

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17    
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:2  Page:111-117  

Cannelli Natalia;   Cassandrini Denise;   Bertini Enrico;   Striano Pasquale;   Fusco Lucia;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:31

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18    
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:1  Page:59-66  

Venturin Marco;   Moncini Silvia;   Villa Valentina;   Russo Silvia;   Bonati Maria Teresa;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:24

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19    
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:8  Issue:2  Page:131-135  

Chen Haijun;   von Hehn Christian;   Kaczmarek Leonard K;   Ment Laura R;   Pober Barbara R;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:13

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20    
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus 期刊论文

Neurogenetics     ISSN:1364-6745  Volume:7  Issue:4  Page:259-263  

de Wit M C. Y;   de Coo I F. M;   Julier C;   Delépine M;   Lequin M H;   ...

来源数据库:[Web of Science, Science Citation Index Expanded, Neurosciences Abstracts]         被引频次:20

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