BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 2328988)

  • 21. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
    Ungaro P; Christian SL; Fantes JA; Mutirangura A; Black S; Reynolds J; Malcolm S; Dobyns WB; Ledbetter DH
    J Med Genet; 2001 Jan; 38(1):26-34. PubMed ID: 11134237
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
    Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
    Glenn CC; Nicholls RD; Robinson WP; Saitoh S; Niikawa N; Schinzel A; Horsthemke B; Driscoll DJ
    Hum Mol Genet; 1993 Sep; 2(9):1377-82. PubMed ID: 8242060
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
    Nakao M; Sutcliffe JS; Durtschi B; Mutirangura A; Ledbetter DH; Beaudet AL
    Hum Mol Genet; 1994 Feb; 3(2):309-15. PubMed ID: 8004100
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Frequent epigenetic inactivation of the chaperone SGNE1/7B2 in human gliomas.
    Waha A; Felsberg J; Hartmann W; Hammes J; von dem Knesebeck A; Endl E; Pietsch T; Waha A
    Int J Cancer; 2012 Aug; 131(3):612-22. PubMed ID: 21901745
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE; Toth-Fejel S; Allen LJ; Black M; Brown MG; Budden S; Cohen R; Friedman JM; Kalousek D; Zonana J
    Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
    Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
    Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?
    Schinzel A; Robinson WP; Bottani A; Yagang X; Prader A
    Hum Genet; 1992 Jan; 88(3):361-2. PubMed ID: 1733842
    [No Abstract]   [Full Text] [Related]  

  • 32. Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes.
    Jauch A; Robson L; Smith A
    Hum Genet; 1995 Sep; 96(3):345-9. PubMed ID: 7649555
    [TBL] [Abstract][Full Text] [Related]  

  • 33. FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.
    Knoll JH; Sinnett D; Wagstaff J; Glatt K; Wilcox AS; Whiting PM; Wingrove P; Sikela JM; Lalande M
    Hum Mol Genet; 1993 Feb; 2(2):183-9. PubMed ID: 8388764
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. cDNA sequence of neuroendocrine protein 7B2 expressed in beta cell tumors of transgenic mice.
    Mbikay M; Grant SG; Sirois F; Tadros H; Skowronski J; Lazure C; Seidah NG; Hanahan D; Chrétien M
    Int J Pept Protein Res; 1989 Jan; 33(1):39-45. PubMed ID: 2542174
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
    Buiting K; Gross S; Ji Y; Senger G; Nicholls RD; Horsthemke B
    Cytogenet Cell Genet; 1998; 81(3-4):247-53. PubMed ID: 9730612
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Attenuation of the polypeptide 7B2, prohormone convertase PC2, and vasopressin in the hypothalamus of some Prader-Willi patients: indications for a processing defect.
    Gabreëls BA; Swaab DF; de Kleijn DP; Seidah NG; Van de Loo JW; Van de Ven WJ; Martens GJ; van Leeuwen FW
    J Clin Endocrinol Metab; 1998 Feb; 83(2):591-9. PubMed ID: 9467579
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Expression of neuroendocrine secretory protein 7B2 mRNA in the mouse and rat pituitary gland.
    Marcinkiewicz M; Touraine P; Mbikay M; Chrétien M
    Neuroendocrinology; 1993 Jul; 58(1):86-93. PubMed ID: 7505408
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.
    MacDonald HR; Wevrick R
    Hum Mol Genet; 1997 Oct; 6(11):1873-8. PubMed ID: 9302265
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
    Jay P; Rougeulle C; Massacrier A; Moncla A; Mattei MG; Malzac P; Roëckel N; Taviaux S; Lefranc JL; Cau P; Berta P; Lalande M; Muscatelli F
    Nat Genet; 1997 Nov; 17(3):357-61. PubMed ID: 9354807
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.