Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Haplotype analysis")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 106

  • Page / 5
Export

Selection :

  • and

Non-syndromic Mental Retardation is not expressed in RAC1 Gene PolymorphismsTINGXI WANG; KEJIN ZHANG; ZIJIAN ZHENG et al.Neuroscience letters. 2008, Vol 437, Num 2, pp 71-75, issn 0304-3940, 5 p.Article

Neuregulin 1 and schizophreniaSTEFANSSON, Hreinn; STEINTHORSDOTTIR, Valgerdur; THORGEIRSSON, Thorgeir E et al.Annals of medicine (Helsinki). 2004, Vol 36, Num 1, pp 62-71, issn 0785-3890, 10 p.Article

Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish typeTAIRA, Makiko; ISHIURA, Hiroyuki; SAWAMURA, Hiromasa et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 237-243, issn 1364-6745, 7 p.Article

Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain)LOPEZ-LASO, Eduardo; OCHOA-SEPULVEDA, Juan José; ARTUCH, Rafael et al.Journal of neurology. 2009, Vol 256, Num 11, pp 1816-1824, issn 0340-5354, 9 p.Article

Association study between vesicle-associated membrane protein 2 gene polymorphisms and fluvoxamine response in japanese major depressive patientsSAITO, Shinichi; TAKAHASHI, Nagahide; INADA, Toshiya et al.Neuropsychobiology. 2006, Vol 54, Num 4, pp 226-230, issn 0302-282X, 5 p.Article

Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsyBUSOLIN, Giorgia; MALACRIDA, Sandro; COPPOLA, Giangennaro et al.Epilepsy research. 2011, Vol 94, Num 1-2, pp 110-116, issn 0920-1211, 7 p.Article

Promoter polymorphisms of the NOS3 gene are associated with hypnotizability-dependent vascular response to nociceptive stimulationPRESCIUTTINI, Silvano; CURCIO, Michele; CHILLEMI, Roberta et al.Neuroscience letters. 2009, Vol 467, Num 3, pp 252-255, issn 0304-3940, 4 p.Article

MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophreniaSELCH, Sandra; STROBEL, Alexander; HADERLEIN, Julia et al.Biological psychiatry (1969). 2007, Vol 61, Num 10, pp 1211-1214, issn 0006-3223, 4 p.Article

Genetic susceptibility to nickel-induced acute lung injuryPROWS, Daniel R; MCDOWELL, Susan A; ARONOW, Bruce J et al.Chemosphere (Oxford). 2003, Vol 51, Num 10, pp 1139-1148, issn 0045-6535, 10 p.Conference Paper

Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probandsDAS, Manali; DAS BHOWMIK, Aneek; BHADURI, Nipa et al.Progress in neuro-psychopharmacology & biological psychiatry. 2011, Vol 35, Num 2, pp 577-587, issn 0278-5846, 11 p.Article

Increased risk of suicide attempt in mood disorders and TPH1 genotypeGALFALVY, Hanga; HUANG, Yung-Yu; OQUENDO, Maria A et al.Journal of affective disorders. 2009, Vol 115, Num 3, pp 331-338, issn 0165-0327, 8 p.Article

16q-linked autosomal dominant cerebellar ataxia : A clinical and genetic studyOUYANG, Y; SAKOE, K; AMINO, T et al.Journal of the neurological sciences. 2006, Vol 247, Num 2, pp 180-186, issn 0022-510X, 7 p.Article

Association study of polymorphisms in the GluR7, KA1 and KA2 kainate receptor genes (GRIK3, GRIK4, GRIK5) with schizophreniaSHIBATA, Hiroki; ARAMAKI, Toshihiro; SAKAI, Mayumi et al.Psychiatry research. 2006, Vol 141, Num 1, pp 39-51, issn 0165-1781, 13 p.Article

An association study between cathechol -O -methyltransferase gene and mental retardation in the Chinese Han populationKEJIN ZHANG; JIANJUN GAO; CAIYAN AN et al.Neuroscience letters. 2007, Vol 419, Num 1, pp 83-87, issn 0304-3940, 5 p.Article

ABCB1/MDDR1 gene polymorphisms as a prognostic factor in colorectal cancerBALCERCZAK, Ewa; PANCZYK, Mariusz; PIASKOWSKI, Sylwester et al.International journal of colorectal disease (Print). 2010, Vol 25, Num 10, pp 1167-1176, issn 0179-1958, 10 p.Article

Genetic association of single nucleotide polymorphisms in endonuclease G-like 1 gene with type 2 diabetes in a Japanese populationMORITANI, M; NOMURA, K; YOSHIKAWA, T et al.Diabetologia (Berlin). 2007, Vol 50, Num 6, pp 1218-1227, issn 0012-186X, 10 p.Article

Association of GABRB3 polymorphisms with autism spectrum disorders in korean triosSOON AE KIM; JIN HEE KIM; PARK, Mira et al.Neuropsychobiology. 2006, Vol 54, Num 3, pp 160-165, issn 0302-282X, 6 p.Article

Human p53 tumor suppressor gene (TP53) and schizophrenia : Case-control and family studiesXINGQUN NI; TRAKALO, Joseph; VALENTE, Jose et al.Neuroscience letters. 2005, Vol 388, Num 3, pp 173-178, issn 0304-3940, 6 p.Article

Lack of evidence for association between the serotonin transporter gene (SLC6A4) polymorphisms and autism in the Chinese triosSUPING WU; YANQING GUO; DAI ZHANG et al.Neuroscience letters. 2005, Vol 381, Num 1-2, pp 1-5, issn 0304-3940, 5 p.Article

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyPISCIOTTA, Livia; MICCOLI, Roberto; BERTOLINI, Stefano et al.Atherosclerosis. 2003, Vol 167, Num 2, pp 335-345, issn 0021-9150, 11 p.Article

Phylogeny and phylogeography of the Tuber brumale aggrMERENYI, Zsolt; VARGA, Torda; GEML, József et al.Mycorrhiza (Berlin). 2014, Vol 24, issn 0940-6360, S101-S113, SUP1Conference Paper

ABCB1 gene polymorphisms and haplotype analysis in colorectal cancerPANCZYK, Mariusz; BALCERCZAK, Ewa; PIASKOWSKI, Sylwester et al.International journal of colorectal disease (Print). 2009, Vol 24, Num 8, pp 895-905, issn 0179-1958, 11 p.Article

Haplotype Analysis of the NADPH Oxidase p22phox Gene in Patients with Bronchial AsthmaIZAKOVICOVA HOLLA, Lydie; KANKOVA, Katerina; ZNOJIL, Vladimir et al.International archives of allergy and immunology. 2009, Vol 148, Num 1, pp 73-80, issn 1018-2438, 8 p.Article

Functional polymorphisms of the cytochrome P450 1A2 (CYP1A2) gene and prolonged QTc interval in schizophreniaTAY, Joshua K. X; CHAY HOON TAN; CHONG, Siow-Ann et al.Progress in neuro-psychopharmacology & biological psychiatry. 2007, Vol 31, Num 6, pp 1297-1302, issn 0278-5846, 6 p.Article

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patientsWANG, C. K; WU, Y. R; WANG, H. C et al.European neurology. 2004, Vol 52, Num 2, pp 96-100, issn 0014-3022, 5 p.Article

  • Page / 5