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 *

272 related articles for article (PubMed ID: 30003711)

  • 41. Molecular characterization of Prader-Willi syndrome by real-time PCR.
    Munce T; Simpson R; Bowling F
    Genet Test; 2008 Jun; 12(2):319-24. PubMed ID: 18554170
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
    Bittel DC; Butler MG
    Expert Rev Mol Med; 2005 Jul; 7(14):1-20. PubMed ID: 16038620
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD).
    Heseding H; Jahn K; Brändl B; Haase A; Shum IO; Kohrn T; Bleich S; Frieling H; Martin U; Müller FJ; Wunderlich S; Deest M
    Stem Cell Res; 2023 Sep; 71():103143. PubMed ID: 37343429
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.
    Toth-Fejel S; Olson S; Gunter K; Quan F; Wolford J; Popovich BW; Magenis RE
    Am J Hum Genet; 1996 May; 58(5):1008-16. PubMed ID: 8651261
    [TBL] [Abstract][Full Text] [Related]  

  • 45. From Prader-Willi syndrome to psychosis: translating parent-of-origin effects into schizophrenia research.
    Krefft M; Frydecka D; Adamowski T; Misiak B
    Epigenomics; 2014; 6(6):677-88. PubMed ID: 25531260
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
    White HE; Hall VJ; Cross NC
    Clin Chem; 2007 Nov; 53(11):1960-2. PubMed ID: 17890436
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
    Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Psychotic illness in people with Prader-Willi syndrome: a systematic review of clinical presentation, course and phenomenology.
    Aman LCS; Lester SD; Holland AJ; Fletcher PC
    Orphanet J Rare Dis; 2024 Feb; 19(1):69. PubMed ID: 38360662
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Imprinting-mutation mechanisms in Prader-Willi syndrome.
    Ohta T; Gray TA; Rogan PK; Buiting K; Gabriel JM; Saitoh S; Muralidhar B; Bilienska B; Krajewska-Walasek M; Driscoll DJ; Horsthemke B; Butler MG; Nicholls RD
    Am J Hum Genet; 1999 Feb; 64(2):397-413. PubMed ID: 9973278
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Maternal methylation imprints on human chromosome 15 are established during or after fertilization.
    El-Maarri O; Buiting K; Peery EG; Kroisel PM; Balaban B; Wagner K; Urman B; Heyd J; Lich C; Brannan CI; Walter J; Horsthemke B
    Nat Genet; 2001 Mar; 27(3):341-4. PubMed ID: 11242121
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.
    Borelina D; Engel N; Esperante S; Ferreiro V; Ferrer M; Torrado M; Goldschmidt E; Francipane L; Szijan I
    J Biochem Mol Biol; 2004 Sep; 37(5):522-6. PubMed ID: 15479613
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Comparative molecular approaches in Prader-Willi syndrome diagnosis.
    Botezatu A; Puiu M; Cucu N; Diaconu CC; Badiu C; Arsene C; Iancu IV; Plesa A; Anton G
    Gene; 2016 Jan; 575(2 Pt 1):353-8. PubMed ID: 26335514
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
    Nicholls RD; Knepper JL
    Annu Rev Genomics Hum Genet; 2001; 2():153-75. PubMed ID: 11701647
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes.
    Horsthemke B; Nazlican H; Hüsing J; Klein-Hitpass L; Claussen U; Michel S; Lich C; Gillessen-Kaesbach G; Buiting K
    Hum Mol Genet; 2003 Oct; 12(20):2723-32. PubMed ID: 12944418
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.
    Liehr T; Brude E; Gillessen-Kaesbach G; König R; Mrasek K; von Eggeling F; Starke H
    Eur J Med Genet; 2005; 48(2):175-81. PubMed ID: 16053909
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site.
    Chai JH; Locke DP; Ohta T; Greally JM; Nicholls RD
    Mamm Genome; 2001 Nov; 12(11):813-21. PubMed ID: 11845283
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome.
    Kim Y; Lee HM; Xiong Y; Sciaky N; Hulbert SW; Cao X; Everitt JI; Jin J; Roth BL; Jiang YH
    Nat Med; 2017 Feb; 23(2):213-222. PubMed ID: 28024084
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Neuronal differentiation defects in induced pluripotent stem cells derived from a Prader-Willi syndrome patient.
    Soeda S; Saito R; Fujita N; Fukuta K; Taniura H
    Neurosci Lett; 2019 Jun; 703():162-167. PubMed ID: 30902571
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
    Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.