BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 34098225)

  • 21. Epigenetic Characterization of CDKN1C in Placenta Samples from Non-syndromic Intrauterine Growth Restriction.
    López-Abad M; Iglesias-Platas I; Monk D
    Front Genet; 2016; 7():62. PubMed ID: 27200075
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives.
    Cohen MM
    Pediatr Dev Pathol; 2005; 8(3):287-304. PubMed ID: 16010495
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluation of the abdominopelvic region using MRI in patients with primary amenorrhea.
    Gündoğdu E; Emekli E; Oğuzman M; Kebapçı M
    J Pediatr Endocrinol Metab; 2019 Sep; 32(9):995-1003. PubMed ID: 31369396
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Brain abnormalities in patients with Beckwith-Wiedemann syndrome.
    Gardiner K; Chitayat D; Choufani S; Shuman C; Blaser S; Terespolsky D; Farrell S; Reiss R; Wodak S; Pu S; Ray PN; Baskin B; Weksberg R
    Am J Med Genet A; 2012 Jun; 158A(6):1388-94. PubMed ID: 22585446
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation.
    Abadie C; Bernard F; Netchine I; Sanlaville D; Roque A; Rossignol S; Coupier I
    Eur J Med Genet; 2010; 53(6):400-3. PubMed ID: 20826236
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
    Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
    [TBL] [Abstract][Full Text] [Related]  

  • 28. IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies.
    Vilain E; Le Merrer M; Lecointre C; Desangles F; Kay MA; Maroteaux P; McCabe ER
    J Clin Endocrinol Metab; 1999 Dec; 84(12):4335-40. PubMed ID: 10599684
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene.
    Jurkiewicz D; Skórka A; Ciara E; Kugaudo M; Pelc M; Chrzanowska K; Krajewska-Walasek M
    Clin Dysmorphol; 2020 Jan; 29(1):28-34. PubMed ID: 31804259
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Epigenetic anomalies in childhood growth disorders.
    Netchine I; Rossignol S; Azzi S; Le Bouc Y
    Nestle Nutr Inst Workshop Ser; 2013; 71():65-73. PubMed ID: 23502140
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization.
    Brioude F; Netchine I; Praz F; Le Jule M; Calmel C; Lacombe D; Edery P; Catala M; Odent S; Isidor B; Lyonnet S; Sigaudy S; Leheup B; Audebert-Bellanger S; Burglen L; Giuliano F; Alessandri JL; Cormier-Daire V; Laffargue F; Blesson S; Coupier I; Lespinasse J; Blanchet P; Boute O; Baumann C; Polak M; Doray B; Verloes A; Viot G; Le Bouc Y; Rossignol S
    Hum Mutat; 2015 Sep; 36(9):894-902. PubMed ID: 26077438
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy.
    Goldman M; Smith A; Shuman C; Caluseriu O; Wei C; Steele L; Ray P; Sadowski P; Squire J; Weksberg R; Rosenblum ND
    J Am Soc Nephrol; 2002 Aug; 13(8):2077-84. PubMed ID: 12138139
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes.
    Netchine I; Rossignol S; Azzi S; Brioude F; Le Bouc Y
    Endocr Dev; 2012; 23():60-70. PubMed ID: 23182821
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith-Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion.
    Gripp KW; Robbins KM; Sheffield BS; Lee AF; Patel MS; Yip S; Doyle D; Stabley D; Sol-Church K
    Am J Med Genet A; 2016 Mar; 170(3):559-64. PubMed ID: 26572961
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
    Bachmann N; Crazzolara R; Bohne F; Kotzot D; Maurer K; Enklaar T; Prawitt D; Bergmann C
    Pediatr Blood Cancer; 2017 Mar; 64(3):. PubMed ID: 27650505
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome.
    Smith AC; Squire JA; Thorner P; Zielenska M; Shuman C; Grant R; Chitayat D; Nishikawa JL; Weksberg R
    Pediatr Dev Pathol; 2001; 4(6):550-8. PubMed ID: 11826361
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
    Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
    Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
    Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK
    Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A peculiar form of neonatal adrenal insufficiency: the IMAGe association. Two new cases].
    Ferey S; Merzoug V; Linglart A; Chaussain JL; Kalifa G
    J Radiol; 2003 Mar; 84(3):323-5. PubMed ID: 12736593
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
    Heide S; Chantot-Bastaraud S; Keren B; Harbison MD; Azzi S; Rossignol S; Michot C; Lackmy-Port Lys M; Demeer B; Heinrichs C; Newfield RS; Sarda P; Van Maldergem L; Trifard V; Giabicani E; Siffroi JP; Le Bouc Y; Netchine I; Brioude F
    J Med Genet; 2018 Mar; 55(3):205-213. PubMed ID: 29223973
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.