BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 20605837)

  • 1. Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.
    Weber S; Landwehr C; Renkert M; Hoischen A; Wühl E; Denecke J; Radlwimmer B; Haffner D; Schaefer F; Weber RG
    Nephrol Dial Transplant; 2011 Jan; 26(1):136-43. PubMed ID: 20605837
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy-number variation analysis in familial nonsyndromic congenital anomalies of the kidney and urinary tract: Evidence for the causative role of a transposable element-associated genomic rearrangement.
    Siomou E; Mitsioni AG; Giapros V; Bouba I; Noutsopoulos D; Georgiou I
    Mol Med Rep; 2017 Jun; 15(6):3631-3636. PubMed ID: 28440405
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DNA copy number changes in alveolar soft part sarcoma: a comparative genomic hybridization study.
    Kiuru-Kuhlefelt S; El-Rifai W; Sarlomo-Rikala M; Knuutila S; Miettinen M
    Mod Pathol; 1998 Mar; 11(3):227-31. PubMed ID: 9521467
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparative genomic hybridization of squamous cell carcinoma of the esophagus: the possible involvement of the DPI gene in the 13q34 amplicon.
    Shinomiya T; Mori T; Ariyama Y; Sakabe T; Fukuda Y; Murakami Y; Nakamura Y; Inazawa J
    Genes Chromosomes Cancer; 1999 Apr; 24(4):337-44. PubMed ID: 10092132
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Solving the puzzle: case examples of array comparative genomic hybridization as a tool to end the diagnostic odyssey.
    Mroch AR; Flanagan JD; Stein QP
    Curr Probl Pediatr Adolesc Health Care; 2012 Mar; 42(3):74-8. PubMed ID: 22325475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic basis for malformation-associated uropathy and renal dysplasia].
    Oppezzo C; Barberis V; Edefonti A; Cusi D; Marra G
    G Ital Nefrol; 2003; 20(2):120-6. PubMed ID: 12746796
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Profile of chromosomal imbalances in 10 cases of primary alveolar rhabdomyosarcoma analyzed by comparative genomic hybridization].
    Li QX; Li F; Zhang W; Liu X; Ma YQ; Shi XL; Miao N
    Zhonghua Zhong Liu Za Zhi; 2009 Aug; 31(8):571-6. PubMed ID: 20021942
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital anomalies of the kidney and urinary tract--role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene.
    Pope JC; Brock JW; Adams MC; Miyazaki Y; Stephens FD; Ichikawa I
    J Urol; 2001 Jan; 165(1):196-202. PubMed ID: 11125405
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression profiling of the AT2R mRNA in affected tissue from children with CAKUT.
    Stanković A; Zivković M; Kostić M; Atanacković J; Krstić Z; Alavantić D
    Clin Biochem; 2010 Jan; 43(1-2):71-5. PubMed ID: 19781541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
    Young TA; Burgess BL; Rao NP; Gorin MB; Straatsma BR
    Mol Vis; 2007 Dec; 13():2328-33. PubMed ID: 18199974
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic imbalances in endometrial hyperplasia and endometrioid carcinoma detected by comparative genomic hybridization.
    Muslumanoglu HM; Oner U; Ozalp S; Acikalin MF; Yalcin OT; Ozdemir M; Artan S
    Eur J Obstet Gynecol Reprod Biol; 2005 May; 120(1):107-14. PubMed ID: 15866096
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Prenatal diagnosis of fetal urinary abnormalities and microdeletion on chromosome 1q21.1].
    Fu F; Huang YH; Liao C; Li R; Feng SH; Mai QJ; Li WK
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):505-9. PubMed ID: 23042382
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).
    Yoshimura-Furuhata M; Nishimura-Tadaki A; Amano Y; Ehara T; Hamasaki Y; Muramatsu M; Shishido S; Aikawa A; Hamada R; Ishikura K; Hataya H; Hidaka Y; Noda S; Koike K; Wakui K; Fukushima Y; Matsumoto N; Awazu M; Miyake N; Kosho T
    Am J Med Genet A; 2015 Mar; 167A(3):592-601. PubMed ID: 25691411
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT).
    Combes P; Planche V; Eymard-Pierre E; Sarret C; Rodriguez D; Boespflug-Tanguy O; Vaurs-Barriere C
    Ann Hum Genet; 2012 May; 76(3):261-7. PubMed ID: 22348788
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
    Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
    Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital anomalies of the kidney and urinary tract: an embryogenetic review.
    dos Santos Junior AC; de Miranda DM; Simões e Silva AC
    Birth Defects Res C Embryo Today; 2014 Dec; 102(4):374-81. PubMed ID: 25420794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
    van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
    Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH.
    Mercer CL; Browne CE; Barber JC; Maloney VK; Huang S; Thomas NS; Foulds N; MacLachlan N
    Cytogenet Genome Res; 2009; 124(2):179-86. PubMed ID: 19420931
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: evidence of locus on chromosome 13q.
    Vats AN; Ishwad C; Vats KR; Moritz M; Ellis D; Mueller C; Surti U; Parizhskaya MZ; Meza MP; Burke L; Schneck FX; Saxena M; Ferrell R
    Kidney Int; 2003 Jul; 64(1):17-24. PubMed ID: 12787391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents.
    Houcinat N; Llanas B; Moutton S; Toutain J; Cailley D; Arveiler B; Combe C; Lacombe D; Rooryck C
    Am J Med Genet A; 2015 Nov; 167A(11):2714-9. PubMed ID: 26114937
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.