173 related articles for article (PubMed ID: 26105184)
1. WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
Baranowska Körberg I; Hofmeister W; Markljung E; Cao J; Nilsson D; Ludwig M; Draaken M; Holmdahl G; Barker G; Reutter H; Vukojević V; Clementson Kockum C; Lundin J; Lindstrand A; Nordenskjöld A
Hum Mol Genet; 2015 Sep; 24(18):5069-78. PubMed ID: 26105184
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
Reutter H; Draaken M; Pennimpede T; Wittler L; Brockschmidt FF; Ebert AK; Bartels E; Rösch W; Boemers TM; Hirsch K; Schmiedeke E; Meesters C; Becker T; Stein R; Utsch B; Mangold E; Nordenskjöld A; Barker G; Kockum CC; Zwink N; Holmdahl G; Läckgren G; Jenetzky E; Feitz WF; Marcelis C; Wijers CH; Van Rooij IA; Gearhart JP; Herrmann BG; Ludwig M; Boyadjiev SA; Nöthen MM; Mattheisen M
Hum Mol Genet; 2014 Oct; 23(20):5536-44. PubMed ID: 24852367
[TBL] [Abstract][Full Text] [Related]
3. Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex.
Qi L; Wang M; Yagnik G; Mattheisen M; Gearhart JP; Lakshmanan Y; Ebert AK; Rösch W; Ludwig M; Draaken M; Reutter H; Boyadjiev SA
Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):759-63. PubMed ID: 23913486
[TBL] [Abstract][Full Text] [Related]
4. Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.
Draaken M; Mughal SS; Pennimpede T; Wolter S; Wittler L; Ebert AK; Rösch W; Stein R; Bartels E; Schmidt D; Boemers TM; Schmiedeke E; Hoffmann P; Moebus S; Herrmann BG; Nöthen MM; Reutter H; Ludwig M
Birth Defects Res A Clin Mol Teratol; 2013 Mar; 97(3):133-9. PubMed ID: 23359465
[TBL] [Abstract][Full Text] [Related]
5. No TAP63 promoter mutation is detected in bladder exstrophy-epispadias complex patients.
Darling T; Mahfuz I; White SJ; Cheng W
J Pediatr Surg; 2013 Dec; 48(12):2393-400. PubMed ID: 24314177
[TBL] [Abstract][Full Text] [Related]
6. PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?
Kolarova J; Bens S; Ammerpohl O; Hilger AC; Zhang R; Reutter H; Siebert R
Birth Defects Res A Clin Mol Teratol; 2016 Aug; 106(8):724-8. PubMed ID: 27223093
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide expression profiling of urinary bladder implicates desmosomal and cytoskeletal dysregulation in the bladder exstrophy-epispadias complex.
Qi L; Chen K; Hur DJ; Yagnik G; Lakshmanan Y; Kotch LE; Ashrafi GH; Martinez-Murillo F; Kowalski J; Naydenov C; Wittler L; Gearhart JP; Draaken M; Reutter H; Ludwig M; Boyadjiev SA
Int J Mol Med; 2011 Jun; 27(6):755-65. PubMed ID: 21431277
[TBL] [Abstract][Full Text] [Related]
8. De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complex.
Jelin AC; Wohler E; Martin R; Di Carlo H; Isaacs W; Ko J; Michaud J; Blakemore K; Valle D; Sobreira N; Gearhart J
Am J Med Genet A; 2024 Apr; 194(4):e63501. PubMed ID: 38082334
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular characterization of the bladder exstrophy-epispadias complex: analysis of 232 families.
Boyadjiev SA; Dodson JL; Radford CL; Ashrafi GH; Beaty TH; Mathews RI; Broman KW; Gearhart JP
BJU Int; 2004 Dec; 94(9):1337-43. PubMed ID: 15610117
[TBL] [Abstract][Full Text] [Related]
10. Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene.
Lundin J; Markljung E; Baranowska Körberg I; Hofmeister W; Cao J; Nilsson D; Holmdahl G; Barker G; Anderberg M; Vukojević V; Lindstrand A; Nordenskjöld A
Mol Genet Genomic Med; 2019 Jun; 7(6):e666. PubMed ID: 31044557
[TBL] [Abstract][Full Text] [Related]
11. Insertion/deletion polymorphisms in the ΔNp63 promoter are a risk factor for bladder exstrophy epispadias complex.
Wilkins S; Zhang KW; Mahfuz I; Quantin R; D'Cruz N; Hutson J; Ee M; Bagli D; Aitken K; Fong FN; Ng PK; Tsui SK; Fung WY; Banu T; Thakre A; Johar K; Jaureguizar E; Li L; Cheng W
PLoS Genet; 2012; 8(12):e1003070. PubMed ID: 23284286
[TBL] [Abstract][Full Text] [Related]
12. New insights into the pathogenesis of bladder exstrophy-epispadias complex.
Mahfuz I; Darling T; Wilkins S; White S; Cheng W
J Pediatr Urol; 2013 Dec; 9(6 Pt B):996-1005. PubMed ID: 23743131
[TBL] [Abstract][Full Text] [Related]
13. 22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex.
Beaman GM; Woolf AS; Cervellione RM; Keene D; Mushtaq I; Urquhart JE; Stuart HM; Newman WG
Am J Med Genet A; 2019 Mar; 179(3):404-409. PubMed ID: 30628148
[TBL] [Abstract][Full Text] [Related]
14. Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.
Draaken M; Baudisch F; Timmermann B; Kuhl H; Kerick M; Proske J; Wittler L; Pennimpede T; Ebert AK; Rösch W; Stein R; Bartels E; von Lowtzow C; Boemers TM; Herms S; Gearhart JP; Lakshmanan Y; Kockum CC; Holmdahl G; Läckgren G; Nordenskjöld A; Boyadjiev SA; Herrmann BG; Nöthen MM; Ludwig M; Reutter H
Birth Defects Res A Clin Mol Teratol; 2014 Jun; 100(6):512-7. PubMed ID: 24764164
[TBL] [Abstract][Full Text] [Related]
15. The morphogenesis of the exstrophy-epispadias complex: a new concept based on observations made in early embryonic cases of cloacal exstrophy.
Männer J; Kluth D
Anat Embryol (Berl); 2005 Aug; 210(1):51-7. PubMed ID: 16034608
[TBL] [Abstract][Full Text] [Related]
16. Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complex.
Beaman GM; Woolf AS; Lopes FM; Guo SA; Harkness JR; Cervellione RM; Keene D; Mushtaq I; Clatworthy MR; Newman WG
J Pediatr Urol; 2022 Jun; 18(3):362.e1-362.e8. PubMed ID: 35491304
[TBL] [Abstract][Full Text] [Related]
17. p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissue.
Ching BJ; Wittler L; Proske J; Yagnik G; Qi L; Draaken M; Reutter H; Gearhart JP; Ludwig M; Boyadjiev SA
Int J Mol Med; 2010 Dec; 26(6):861-7. PubMed ID: 21042780
[TBL] [Abstract][Full Text] [Related]
18. Rare exonic
Jelin AC; Sopko N; Sobreira N; Boyadjiev SA; Wohler E; Morrill C; Witmer PD; Michaud J; Valle D; Gearhart J; Dicarlo H
Front Genet; 2024; 15():1266210. PubMed ID: 38903756
[TBL] [Abstract][Full Text] [Related]
19. Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.
Reutter H; Thauvin-Robinet C; Boemers TM; Rösch WH; Ludwig M
Scand J Urol Nephrol; 2006; 40(3):221-4. PubMed ID: 16809264
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.
Reutter H; Hoischen A; Ludwig M; Stein R; Radlwimmer B; Engels H; Wolffenbuttel KP; Weber RG
BJU Int; 2007 Sep; 100(3):646-50. PubMed ID: 17669146
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
