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 *

84 related articles for article (PubMed ID: 12565145)

  • 1. Mutation screening of the human period 2 gene in bipolar disorder.
    Shiino Y; Nakajima S; Ozeki Y; Isono T; Yamada N
    Neurosci Lett; 2003 Feb; 338(1):82-4. PubMed ID: 12565145
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome.
    Toh KL; Jones CR; He Y; Eide EJ; Hinz WA; Virshup DM; Ptácek LJ; Fu YH
    Science; 2001 Feb; 291(5506):1040-3. PubMed ID: 11232563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Positional syntenic cloning and functional characterization of the mammalian circadian mutation tau.
    Lowrey PL; Shimomura K; Antoch MP; Yamazaki S; Zemenides PD; Ralph MR; Menaker M; Takahashi JS
    Science; 2000 Apr; 288(5465):483-92. PubMed ID: 10775102
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human casein kinase Idelta phosphorylation of human circadian clock proteins period 1 and 2.
    Camacho F; Cilio M; Guo Y; Virshup DM; Patel K; Khorkova O; Styren S; Morse B; Yao Z; Keesler GA
    FEBS Lett; 2001 Feb; 489(2-3):159-65. PubMed ID: 11165242
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A length polymorphism in the circadian clock gene Per3 influences age at onset of bipolar disorder.
    Benedetti F; Dallaspezia S; Colombo C; Pirovano A; Marino E; Smeraldi E
    Neurosci Lett; 2008 Nov; 445(2):184-7. PubMed ID: 18789374
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A missense variation in human casein kinase I epsilon gene that induces functional alteration and shows an inverse association with circadian rhythm sleep disorders.
    Takano A; Uchiyama M; Kajimura N; Mishima K; Inoue Y; Kamei Y; Kitajima T; Shibui K; Katoh M; Watanabe T; Hashimotodani Y; Nakajima T; Ozeki Y; Hori T; Yamada N; Toyoshima R; Ozaki N; Okawa M; Nagai K; Takahashi K; Isojima Y; Yamauchi T; Ebisawa T
    Neuropsychopharmacology; 2004 Oct; 29(10):1901-9. PubMed ID: 15187983
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two pedigrees of familial advanced sleep phase syndrome in Japan.
    Satoh K; Mishima K; Inoue Y; Ebisawa T; Shimizu T
    Sleep; 2003 Jun; 26(4):416-7. PubMed ID: 12841366
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic association study of CSNK1E gene in bipolar disorder and circadian characteristics.
    Lee KY; Ahn YM; Kim SH; Kang HG; Joo EJ
    Nord J Psychiatry; 2018 Nov; 72(8):599-604. PubMed ID: 30445897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Modeling of a human circadian mutation yields insights into clock regulation by PER2.
    Xu Y; Toh KL; Jones CR; Shin JY; Fu YH; Ptácek LJ
    Cell; 2007 Jan; 128(1):59-70. PubMed ID: 17218255
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The GABA type A receptor alpha5 subunit gene is associated with bipolar I disorder.
    Otani K; Ujike H; Tanaka Y; Morita Y; Katsu T; Nomura A; Uchida N; Hamamura T; Fujiwara Y; Kuroda S
    Neurosci Lett; 2005 Jun 10-17; 381(1-2):108-13. PubMed ID: 15882799
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia.
    Mansour HA; Wood J; Logue T; Chowdari KV; Dayal M; Kupfer DJ; Monk TH; Devlin B; Nimgaonkar VL
    Genes Brain Behav; 2006 Mar; 5(2):150-7. PubMed ID: 16507006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association study on the DUSP6 gene, an affective disorder candidate gene on 12q23, performed by using fluorescence resonance energy transfer-based melting curve analysis on the LightCycler.
    Toyota T; Watanabe A; Shibuya H; Nankai M; Hattori E; Yamada K; Kurumaji A; Karkera JD; Detera-Wadleigh SD; Yoshikawa T
    Mol Psychiatry; 2000 Sep; 5(5):461, 489-94. PubMed ID: 11032376
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variations of human neuropsin gene and psychiatric disorders: polymorphism screening and possible association with bipolar disorder and cognitive functions.
    Izumi A; Iijima Y; Noguchi H; Numakawa T; Okada T; Hori H; Kato T; Tatsumi M; Kosuga A; Kamijima K; Asada T; Arima K; Saitoh O; Shiosaka S; Kunugi H
    Neuropsychopharmacology; 2008 Dec; 33(13):3237-45. PubMed ID: 18354391
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic variation in the 5-HT5A receptor gene in patients with bipolar disorder and major depression.
    Arias B; Collier DA; Gastó C; Pintor L; Gutiérrez B; Vallès V; Fañanás L
    Neurosci Lett; 2001 May; 303(2):111-4. PubMed ID: 11311505
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association between CLOCK 3111T/C and preferred circadian phase in Korean patients with bipolar disorder.
    Lee KY; Song JY; Kim SH; Kim SC; Joo EJ; Ahn YM; Kim YS
    Prog Neuropsychopharmacol Biol Psychiatry; 2010 Oct; 34(7):1196-201. PubMed ID: 20600471
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Functional polymorphisms in clock genes and circadian rhythm sleep disorders].
    Ebisawa T
    Nihon Shinkei Seishin Yakurigaku Zasshi; 2007 Jun; 27(3):91-4. PubMed ID: 17633519
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between bipolar I disorder and the L55M and Q192R polymorphisms of the paraoxonase 1 (PON1) gene.
    Ezzaher A; Mouhamed DH; Mechri A; Neffati F; Rejeb J; Omezzine A; Douki W; Bouslama A; Gaha L; Najjar MF
    J Affect Disord; 2012 Jun; 139(1):12-7. PubMed ID: 21783258
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Circadian rhythms. Mutant gene speeds up the human clock.
    Chicurel M
    Science; 2001 Jan; 291(5502):226-7. PubMed ID: 11253206
    [No Abstract]   [Full Text] [Related]  

  • 19. X-box binding protein 1 (XBP1) C--116G polymorphisms in bipolar disorders and age of onset.
    Hou SJ; Yen FC; Cheng CY; Tsai SJ; Hong CJ
    Neurosci Lett; 2004 Sep; 367(2):232-4. PubMed ID: 15331160
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.
    Erdmann J; Nöthen MM; Shimron-Abarbanell D; Rietschel M; Albus M; Borrmann M; Maier W; Franzek E; Körner J; Weigelt B; Fimmers R; Propping P
    Mol Psychiatry; 1996 Nov; 1(5):392-7. PubMed ID: 9154233
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.