105 related articles for article (PubMed ID: 17615644)
21. The zebrafish organizer requires chordino.
Schulte-Merker S; Lee KJ; McMahon AP; Hammerschmidt M
Nature; 1997 Jun; 387(6636):862-3. PubMed ID: 9202118
[No Abstract] [Full Text] [Related]
22. Association of GDF1 rs4808863 with fetal congenital heart defects: a case-control study.
Zhang J; Wu Q; Wang L; Li X; Ma Y; Yao L
BMJ Open; 2015 Dec; 5(12):e009352. PubMed ID: 26656983
[TBL] [Abstract][Full Text] [Related]
23. Screening for progranulin mutations by serum protein dosage in common neurodegenerative disorders.
Rodríguez-Rodríguez E; Vázquez-Higuera JL; Sánchez-Juan P; González-Aramburu I; Pozueta A; Mateo I; Calero M; Dobato JL; Infante J; Berciano J; Combarros O
Parkinsonism Relat Disord; 2013 Aug; 19(8):768-9. PubMed ID: 23684369
[No Abstract] [Full Text] [Related]
24. SMG9-deficiency syndrome caused by a homozygous missense variant: Expanding the genotypic and phenotypic spectrum of this developmental disorder.
Lemire G; MacDonald SK; Boycott KM
Am J Med Genet A; 2020 Jul; 182(7):1829-1831. PubMed ID: 32412169
[No Abstract] [Full Text] [Related]
25. Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome.
Vrijens K; Thys S; De Jeu MT; Postnov AA; Pfister M; Cox L; Zwijsen A; Van Hoof V; Mueller M; De Clerck NM; De Zeeuw CI; Van Camp G; Van Laer L
Neurobiol Dis; 2006 Oct; 24(1):28-40. PubMed ID: 16875832
[TBL] [Abstract][Full Text] [Related]
26. [Systems controlling limb tissue patterning].
Shiraishi Y; Kuroiwa A
Tanpakushitsu Kakusan Koso; 2005 May; 50(6 Suppl):638-43. PubMed ID: 15926493
[No Abstract] [Full Text] [Related]
27. Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis.
Lopes Floro K; Artap ST; Preis JI; Fatkin D; Chapman G; Furtado MB; Harvey RP; Hamada H; Sparrow DB; Dunwoodie SL
Hum Mol Genet; 2011 Mar; 20(6):1097-110. PubMed ID: 21224256
[TBL] [Abstract][Full Text] [Related]
28. Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.
Nagasaka M; Taniguchi-Ikeda M; Inagaki H; Ouchi Y; Kurokawa D; Yamana K; Harada R; Nozu K; Sakai Y; Mishra SK; Yamaguchi Y; Morioka I; Toda T; Kurahashi H; Iijima K
J Hum Genet; 2017 Sep; 62(9):851-855. PubMed ID: 28446798
[TBL] [Abstract][Full Text] [Related]
29. Mice with mutations in Mahogunin ring finger-1 (Mgrn1) exhibit abnormal patterning of the left-right axis.
Cota CD; Bagher P; Pelc P; Smith CO; Bodner CR; Gunn TM
Dev Dyn; 2006 Dec; 235(12):3438-47. PubMed ID: 17075880
[TBL] [Abstract][Full Text] [Related]
30. Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia.
Cerami C; Marcone A; Galimberti D; Villa C; Fenoglio C; Scarpini E; Cappa SF
J Alzheimers Dis; 2013; 36(3):415-20. PubMed ID: 23624518
[TBL] [Abstract][Full Text] [Related]
31. Genetic and Developmental Basis of Cardiovascular Malformations.
Azhar M; Ware SM
Clin Perinatol; 2016 Mar; 43(1):39-53. PubMed ID: 26876120
[TBL] [Abstract][Full Text] [Related]
32. Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects.
Debrus S; Tuffery S; Matsuoka R; Galal O; Sarda P; Sauer U; Bozio A; Tanman B; Toutain A; Claustres M; Le Paslier D; Bouvagnet P
J Mol Cell Cardiol; 1997 May; 29(5):1423-31. PubMed ID: 9201627
[TBL] [Abstract][Full Text] [Related]
33. Node and midline defects are associated with left-right development in Delta1 mutant embryos.
Przemeck GK; Heinzmann U; Beckers J; Hrabé de Angelis M
Development; 2003 Jan; 130(1):3-13. PubMed ID: 12441287
[TBL] [Abstract][Full Text] [Related]
34. From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases.
Cecchetto A; Rampazzo A; Angelini A; Bianco LD; Padalino M; Stellin G; Daliento L
Future Cardiol; 2010 May; 6(3):373-93. PubMed ID: 20462343
[TBL] [Abstract][Full Text] [Related]
35. No turning, a mouse mutation causing left-right and axial patterning defects.
Melloy PG; Ewart JL; Cohen MF; Desmond ME; Kuehn MR; Lo CW
Dev Biol; 1998 Jan; 193(1):77-89. PubMed ID: 9466889
[TBL] [Abstract][Full Text] [Related]
36. Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome.
McElhinney DB; Krantz ID; Bason L; Piccoli DA; Emerick KM; Spinner NB; Goldmuntz E
Circulation; 2002 Nov; 106(20):2567-74. PubMed ID: 12427653
[TBL] [Abstract][Full Text] [Related]
37. Knowing left from right: the molecular basis of laterality defects.
Capdevila I; Izpisúa Belmonte JC
Mol Med Today; 2000 Mar; 6(3):112-8. PubMed ID: 10689314
[TBL] [Abstract][Full Text] [Related]
38. How is developmental stability sustained in the face of genetic variation?
Whittle JR
Int J Dev Biol; 1998; 42(3):495-9. PubMed ID: 9654037
[TBL] [Abstract][Full Text] [Related]
39. Polymorphism of methionine synthase gene in nuclear families of congenital heart disease.
Zhu WL; Cheng J; Dao JJ; Zhao RB; Yan LY; Li SQ; Li Y
Biomed Environ Sci; 2004 Mar; 17(1):57-64. PubMed ID: 15202865
[TBL] [Abstract][Full Text] [Related]
40. Genomic analysis of Xenopus organizer function.
Hufton AL; Vinayagam A; Suhai S; Baker JC
BMC Dev Biol; 2006 Jun; 6():27. PubMed ID: 16756679
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
