BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 26114957)

  • 41. Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations.
    Kearney HM; Kearney JB; Conlin LK
    Clin Lab Med; 2011 Dec; 31(4):595-613, ix. PubMed ID: 22118739
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Epigenetic inheritance associated with human chromosome 14.
    Kamnasaran D
    Clin Invest Med; 2001 Jun; 24(3):138-46. PubMed ID: 11437065
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.
    Nakabayashi K; Trujillo AM; Tayama C; Camprubi C; Yoshida W; Lapunzina P; Sanchez A; Soejima H; Aburatani H; Nagae G; Ogata T; Hata K; Monk D
    Hum Mol Genet; 2011 Aug; 20(16):3188-97. PubMed ID: 21593219
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.
    Flotho C; Steinemann D; Mullighan CG; Neale G; Mayer K; Kratz CP; Schlegelberger B; Downing JR; Niemeyer CM
    Oncogene; 2007 Aug; 26(39):5816-21. PubMed ID: 17353900
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Soft tissue sarcoma subtypes exhibit distinct patterns of acquired uniparental disomy.
    Tuna M; Ju Z; Amos CI; Mills GB
    BMC Med Genomics; 2012 Dec; 5():60. PubMed ID: 23217126
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
    Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms.
    Prasasya R; Grotheer KV; Siracusa LD; Bartolomei MS
    Hum Mol Genet; 2020 Sep; 29(R1):R107-R116. PubMed ID: 32592473
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient.
    Kawashima-Goto S; Imamura T; Seki M; Kato M; Yoshida K; Sugimoto A; Kaneda D; Fujiki A; Miyachi M; Nakatani T; Osone S; Ishida H; Taki T; Takita J; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Ogawa S; Hosoi H
    Int J Hematol; 2015 Apr; 101(4):411-6. PubMed ID: 25430085
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
    Bullman H; Lever M; Robinson DO; Mackay DJ; Holder SE; Wakeling EL
    J Med Genet; 2008 Jun; 45(6):396-9. PubMed ID: 18474587
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy.
    Niida Y; Kuroda M; Mitani Y; Yokoi A; Ozaki M
    J Hum Genet; 2012 Oct; 57(10):687-90. PubMed ID: 22854541
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prognostic value of acquired uniparental disomy (aUPD) in primary breast cancer.
    Tuna M; Smid M; Martens JW; Foekens JA
    Breast Cancer Res Treat; 2012 Feb; 132(1):189-96. PubMed ID: 21604015
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H; Higashimoto K
    J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.
    Kotzot D
    Ann Genet; 2004; 47(3):251-60. PubMed ID: 15337470
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A fascination with chromosome rescue in uniparental disomy: Mendelian recessive outlaws and imprinting copyrights infringements.
    Engel E
    Eur J Hum Genet; 2006 Nov; 14(11):1158-69. PubMed ID: 16724013
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Early embryonic failure associated with uniparental disomy for human chromosome 21.
    Henderson DJ; Sherman LS; Loughna SC; Bennett PR; Moore GE
    Hum Mol Genet; 1994 Aug; 3(8):1373-6. PubMed ID: 7987317
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders.
    Xiao P; Liu P; Weber JL; Papasian CJ; Recker RR; Deng HW
    Hum Mutat; 2006 Feb; 27(2):133-7. PubMed ID: 16429396
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Uniparental disomies 7 and 14.
    Hoffmann K; Heller R
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):77-100. PubMed ID: 21396576
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia.
    Gupta M; Raghavan M; Gale RE; Chelala C; Allen C; Molloy G; Chaplin T; Linch DC; Cazier JB; Young BD
    Genes Chromosomes Cancer; 2008 Sep; 47(9):729-39. PubMed ID: 18506749
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.
    Papenhausen PR; Mueller OT; Johnson VP; Sutcliffe M; Diamond TM; Kousseff BG
    Am J Med Genet; 1995 Nov; 59(3):271-5. PubMed ID: 8599348
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Large heterozygous deletion and uniparental disomy masquerading as homozygosity in CHKB gene.
    Wu T; Zhang C; He F; Yang L; Yin F; Peng J
    Mol Genet Genomic Med; 2023 Jul; 11(7):e2162. PubMed ID: 36896673
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.