These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 11840317)

  • 21. No evidence for linkage between schizophrenia and markers at chromosome 15q13-14.
    Curtis L; Blouin JL; Radhakrishna U; Gehrig C; Lasseter VK; Wolyniec P; Nestadt G; Dombroski B; Kazazian HH; Pulver AE; Housman D; Bertrand D; Antonarakis SE
    Am J Med Genet; 1999 Apr; 88(2):109-12. PubMed ID: 10206225
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree.
    Meyer J; Mai M; Ortega G; Mössner R; Lesch KP
    Schizophr Res; 2002 Nov; 58(1):87-91. PubMed ID: 12363395
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genomic organization and partial duplication of the human alpha7 neuronal nicotinic acetylcholine receptor gene (CHRNA7).
    Gault J; Robinson M; Berger R; Drebing C; Logel J; Hopkins J; Moore T; Jacobs S; Meriwether J; Choi MJ; Kim EJ; Walton K; Buiting K; Davis A; Breese C; Freedman R; Leonard S
    Genomics; 1998 Sep; 52(2):173-85. PubMed ID: 9782083
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.
    Stöber G; Kohlmann B; Iekiera M; Rubie C; Gawlik M; Möller-Ehrlich K; Meitinger T; Bettecken T
    BMC Psychiatry; 2005 Oct; 5():36. PubMed ID: 16225677
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Performance deficit of alpha7 nicotinic receptor knockout mice in a delayed matching-to-place task suggests a mild impairment of working/episodic-like memory.
    Fernandes C; Hoyle E; Dempster E; Schalkwyk LC; Collier DA
    Genes Brain Behav; 2006 Aug; 5(6):433-40. PubMed ID: 16923147
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy.
    Combi R; Dalprà L; Malcovati M; Oldani A; Tenchini ML; Ferini-Strambi L
    Brain Res Bull; 2004 Jun; 63(5):353-9. PubMed ID: 15245761
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Recombination in a schizophrenic proband fails to exclude CHRNA7 at chromosome 15q14.
    Leonard S; Freedman R
    Mol Psychiatry; 2003 Feb; 8(2):145-6. PubMed ID: 12610645
    [No Abstract]   [Full Text] [Related]  

  • 28. Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia.
    Leonard S; Gault J; Hopkins J; Logel J; Vianzon R; Short M; Drebing C; Berger R; Venn D; Sirota P; Zerbe G; Olincy A; Ross RG; Adler LE; Freedman R
    Arch Gen Psychiatry; 2002 Dec; 59(12):1085-96. PubMed ID: 12470124
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia.
    Selch S; Strobel A; Haderlein J; Meyer J; Jacob CP; Schmitt A; Lesch KP; Reif A
    Biol Psychiatry; 2007 May; 61(10):1211-4. PubMed ID: 17210142
    [TBL] [Abstract][Full Text] [Related]  

  • 30. No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder.
    Lohoff FW; Ferraro TN; McNabb L; Schwebel C; Dahl JP; Doyle GA; Buono RJ; Berrettini WH
    Psychiatry Res; 2005 Jun; 135(3):171-7. PubMed ID: 15996750
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular cloning and chromosomal localization of the human alpha 7-nicotinic receptor subunit gene (CHRNA7).
    Chini B; Raimond E; Elgoyhen AB; Moralli D; Balzaretti M; Heinemann S
    Genomics; 1994 Jan; 19(2):379-81. PubMed ID: 8188270
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Comparison of polymorphisms in the alpha7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects.
    Gault J; Hopkins J; Berger R; Drebing C; Logel J; Walton C; Short M; Vianzon R; Olincy A; Ross RG; Adler LE; Freedman R; Leonard S
    Am J Med Genet B Neuropsychiatr Genet; 2003 Nov; 123B(1):39-49. PubMed ID: 14582144
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Alpha7 nicotinic acetylcholine receptor gene and reduced risk of Alzheimer's disease.
    Carson R; Craig D; McGuinness B; Johnston JA; O'Neill FA; Passmore AP; Ritchie CW
    J Med Genet; 2008 Apr; 45(4):244-8. PubMed ID: 18057084
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
    Steinlein OK; Mulley JC; Propping P; Wallace RH; Phillips HA; Sutherland GR; Scheffer IE; Berkovic SF
    Nat Genet; 1995 Oct; 11(2):201-3. PubMed ID: 7550350
    [TBL] [Abstract][Full Text] [Related]  

  • 35. No missense mutation of WKL1 in a subgroup of probands with schizophrenia.
    Devaney JM; Donarum EA; Brown KM; Meyer J; Stöber G; Lesch KP; Nestadt G; Stephan DA; Pulver AE
    Mol Psychiatry; 2002; 7(4):419-23. PubMed ID: 11986987
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Possible linkage of schizophrenia and bipolar affective disorder to chromosome 3q29; a follow-up.
    Schosser A; Fuchs K; Leisch F; Bailer U; Meszaros K; Lenzinger E; Willinger U; Strobl R; Heiden A; Gebhardt C; Kasper S; Sieghart W; Hornik K; Aschauer HN
    J Psychiatr Res; 2004; 38(3):357-64. PubMed ID: 15003442
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [The transmission disequilibrium analysis between neuronal nicotinic acetylcholine receptor alpha 7 subunit gene polymorphisms and schizophrenia].
    Peng ZZ; Wan XN; Jiang TY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):154-8. PubMed ID: 18393235
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23.
    Lindholm E; Ekholm B; Balciuniene J; Johansson G; Castensson A; Koisti M; Nylander PO; Pettersson U; Adolfsson R; Jazin E
    Am J Med Genet; 1999 Aug; 88(4):369-77. PubMed ID: 10402504
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI).
    Beck C; Moulard B; Steinlein O; Guipponi M; Vallee L; Montpied P; Baldy-Moulnier M; Malafosse A
    Neurobiol Dis; 1994 Nov; 1(1-2):95-9. PubMed ID: 9216991
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype.
    Hoppman-Chaney N; Wain K; Seger PR; Superneau DW; Hodge JC
    Clin Genet; 2013 Apr; 83(4):345-51. PubMed ID: 22775350
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.