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 *

74 related articles for article (PubMed ID: 7633438)

  • 1. Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.
    Robinson WP; Lalande M
    Hum Mol Genet; 1995 May; 4(5):801-6. PubMed ID: 7633438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
    Brant JO; Riva A; Resnick JL; Yang TP
    Epigenetics; 2014 Nov; 9(11):1540-56. PubMed ID: 25482058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes.
    Ubeda F
    PLoS Biol; 2008 Aug; 6(8):e208. PubMed ID: 18752349
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.
    Zhang K; Liu S; Feng B; Yang Y; Zhang H; Dong R; Liu Y; Gai Z
    PLoS One; 2016; 11(2):e0147824. PubMed ID: 26841067
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L; Chamberlain SJ
    Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.
    Chai JH; Locke DP; Greally JM; Knoll JH; Ohta T; Dunai J; Yavor A; Eichler EE; Nicholls RD
    Am J Hum Genet; 2003 Oct; 73(4):898-925. PubMed ID: 14508708
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structural Variation Shapes the Landscape of Recombination in Mouse.
    Morgan AP; Gatti DM; Najarian ML; Keane TM; Galante RJ; Pack AI; Mott R; Churchill GA; de Villena FP
    Genetics; 2017 Jun; 206(2):603-619. PubMed ID: 28592499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LDSplitDB: a database for studies of meiotic recombination hotspots in MHC using human genomic data.
    Guo J; Chen H; Yang P; Lee YT; Wu M; Przytycka TM; Kwoh CK; Zheng J
    BMC Med Genomics; 2018 Apr; 11(Suppl 2):27. PubMed ID: 29697370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Commentary.
    Butler MG
    Clin Chem; 2015 Jan; 61(1):55. PubMed ID: 25550477
    [No Abstract]   [Full Text] [Related]  

  • 10. Exploration of fine-scale recombination rate variation in the domestic horse.
    Beeson SK; Mickelson JR; McCue ME
    Genome Res; 2019 Oct; 29(10):1744-1752. PubMed ID: 31434677
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Response to vocal music in Angelman syndrome contrasts with Prader-Willi syndrome.
    Kotler J; Mehr SA; Egner A; Haig D; Krasnow MM
    Evol Hum Behav; 2019 Sep; 40(5):420-426. PubMed ID: 32655274
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Corrigendum: sleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialist.
    Gadoth N; Oksenberg A
    Front Neurol; 2015; 6():6. PubMed ID: 25675356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosomal speciation in mice: a cytogenetic analysis of recombination.
    Merico V; Giménez MD; Vasco C; Zuccotti M; Searle JB; Hauffe HC; Garagna S
    Chromosome Res; 2013 Aug; 21(5):523-33. PubMed ID: 23963733
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mammalian recombination hot spots: properties, control and evolution.
    Paigen K; Petkov P
    Nat Rev Genet; 2010 Mar; 11(3):221-33. PubMed ID: 20168297
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parental origin of chromosomes influences crossover activity within the Kcnq1 transcriptionally imprinted domain of Mus musculus.
    Ng SH; Madeira R; Parvanov ED; Petros LM; Petkov PM; Paigen K
    BMC Mol Biol; 2009 May; 10():43. PubMed ID: 19439080
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Maternally and paternally silenced imprinted genes differ in their intron content.
    Fahey ME; Mills W; Higgins DG; Moore T
    Comp Funct Genomics; 2004; 5(8):572-83. PubMed ID: 18629181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
    Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
    BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human imprinted chromosomal regions are historical hot-spots of recombination.
    Sandovici I; Kassovska-Bratinova S; Vaughan JE; Stewart R; Leppert M; Sapienza C
    PLoS Genet; 2006 Jul; 2(7):e101. PubMed ID: 16839189
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sex, not genotype, determines recombination levels in mice.
    Lynn A; Schrump S; Cherry J; Hassold T; Hunt P
    Am J Hum Genet; 2005 Oct; 77(4):670-5. PubMed ID: 16175513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosomal phenotypes and submicroscopic abnormalities.
    Devriendt K; Vermeesch JR
    Hum Genomics; 2004 Jan; 1(2):126-33. PubMed ID: 15601540
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.