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 *

374 related articles for article (PubMed ID: 24076603)

  • 41. 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.
    Yasui DH; Scoles HA; Horike S; Meguro-Horike M; Dunaway KW; Schroeder DI; Lasalle JM
    Hum Mol Genet; 2011 Nov; 20(22):4311-23. PubMed ID: 21840925
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome.
    Ninomiya S; Yokoyama Y; Kawakami M; Une T; Maruyama H; Morishima T
    Pediatr Int; 2005 Oct; 47(5):541-5. PubMed ID: 16190961
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
    Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K
    Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109
    [TBL] [Abstract][Full Text] [Related]  

  • 44. An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
    Wu MY; Jiang M; Zhai X; Beaudet AL; Wu RC
    PLoS One; 2012; 7(4):e34348. PubMed ID: 22496793
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M; Portis T; Longnecker R; Nicholls RD
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Diagnosis of the Prader-Willi syndrome by proving the absence of the unmethylated PW71 DNA fragment.
    Lindgren AC; Grandell U; Ritzén EM; Anvret M
    Acta Paediatr; 1996 Feb; 85(2):195-8. PubMed ID: 8640049
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The Prader-Willi phenotype of fragile X syndrome.
    Nowicki ST; Tassone F; Ono MY; Ferranti J; Croquette MF; Goodlin-Jones B; Hagerman RJ
    J Dev Behav Pediatr; 2007 Apr; 28(2):133-8. PubMed ID: 17435464
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain.
    Lee S; Walker CL; Wevrick R
    Gene Expr Patterns; 2003 Oct; 3(5):599-609. PubMed ID: 12971993
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers.
    Molina O; Blanco J; Vidal F
    Mol Hum Reprod; 2010 May; 16(5):320-8. PubMed ID: 20083560
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Evaluation of Prader-Willi Syndrome gene MAGEL2 in severe childhood-onset obesity.
    O'Neill MA; Farooqi IS; Wevrick R
    Obes Res; 2005 Oct; 13(10):1841-2. PubMed ID: 16286533
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Phenotype of a child with Angelman syndrome born to a woman with Prader-Willi syndrome.
    Ostergaard JR
    Am J Med Genet A; 2015 Sep; 167A(9):2138-44. PubMed ID: 25832033
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
    Wang JC; Vaccarello-Cruz M; Ross L; Owen R; Pratt VM; Lightman K; Liu Y; Hafezi K; Cherif D; Sahoo T
    Am J Med Genet A; 2013 Jul; 161A(7):1695-701. PubMed ID: 23686718
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production.
    Chen H; Victor AK; Klein J; Tacer KF; Tai DJ; de Esch C; Nuttle A; Temirov J; Burnett LC; Rosenbaum M; Zhang Y; Ding L; Moresco JJ; Diedrich JK; Yates JR; Tillman HS; Leibel RL; Talkowski ME; Billadeau DD; Reiter LT; Potts PR
    JCI Insight; 2020 Sep; 5(17):. PubMed ID: 32879135
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
    Dittrich B; Robinson WP; Knoblauch H; Buiting K; Schmidt K; Gillessen-Kaesbach G; Horsthemke B
    Hum Genet; 1992 Nov; 90(3):313-5. PubMed ID: 1487250
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
    Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
    Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.
    Schüle B; Albalwi M; Northrop E; Francis DI; Rowell M; Slater HR; Gardner RJ; Francke U
    BMC Med Genet; 2005 May; 6():18. PubMed ID: 15877813
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Comparative analysis of autistic traits and behavioral disorders in Prader-Willi syndrome and Asperger disorder.
    Song DK; Sawada M; Yokota S; Kuroda K; Uenishi H; Kanazawa T; Ogata H; Ihara H; Nagai T; Shimoda K
    Am J Med Genet A; 2015 Jan; 167A(1):64-8. PubMed ID: 25388910
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
    Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.
    Roof E; Stone W; MacLean W; Feurer ID; Thompson T; Butler MG
    J Intellect Disabil Res; 2000 Feb; 44 ( Pt 1)(Pt 1):25-30. PubMed ID: 10711647
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.