277 related articles for article (PubMed ID: 11320527)
1. A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.
Stegmann K; Boecker J; Richter B; Capra V; Finnell RH; Ngo ET; Strehl E; Ermert A; Koch MC
Teratology; 2001 May; 63(5):167-75. PubMed ID: 11320527
[TBL] [Abstract][Full Text] [Related]
2. Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?
Heil SG; Van der Put NM; Waas ET; den Heijer M; Trijbels FJ; Blom HJ
Mol Genet Metab; 2001 Jun; 73(2):164-72. PubMed ID: 11386852
[TBL] [Abstract][Full Text] [Related]
3. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
Harris MJ; Juriloff DM
Teratology; 1999 Nov; 60(5):292-305. PubMed ID: 10525207
[TBL] [Abstract][Full Text] [Related]
4. Etiology, pathogenesis and prevention of neural tube defects.
Padmanabhan R
Congenit Anom (Kyoto); 2006 Jun; 46(2):55-67. PubMed ID: 16732763
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of BMP4 and its specific inhibitor NOG as candidates in human neural tube defects (NTDs).
Felder B; Stegmann K; Schultealbert A; Geller F; Strehl E; Ermert A; Koch MC
Eur J Hum Genet; 2002 Nov; 10(11):753-6. PubMed ID: 12404109
[TBL] [Abstract][Full Text] [Related]
6. Reduced folate carrier polymorphism (80A-->G) and neural tube defects.
De Marco P; Calevo MG; Moroni A; Merello E; Raso A; Finnell RH; Zhu H; Andreussi L; Cama A; Capra V
Eur J Hum Genet; 2003 Mar; 11(3):245-52. PubMed ID: 12673279
[TBL] [Abstract][Full Text] [Related]
7. Testing for genetic associations with the PAX gene family in a spina bifida population.
Volcik KA; Blanton SH; Kruzel MC; Townsend IT; Tyerman GH; Mier RJ; Northrup H
Am J Med Genet; 2002 Jul; 110(3):195-202. PubMed ID: 12116225
[TBL] [Abstract][Full Text] [Related]
8. Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.
Barber R; Shalat S; Hendricks K; Joggerst B; Larsen R; Suarez L; Finnell R
Mol Genet Metab; 2000 May; 70(1):45-52. PubMed ID: 10833330
[TBL] [Abstract][Full Text] [Related]
9. An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.
Harris MJ; Juriloff DM
Birth Defects Res A Clin Mol Teratol; 2010 Aug; 88(8):653-69. PubMed ID: 20740593
[TBL] [Abstract][Full Text] [Related]
10. Susceptibility to spina bifida; an association study of five candidate genes.
Morrison K; Papapetrou C; Hol FA; Mariman EC; Lynch SA; Burn J; Edwards YH
Ann Hum Genet; 1998 Sep; 62(Pt 5):379-96. PubMed ID: 10088035
[TBL] [Abstract][Full Text] [Related]
11. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.
Harris MJ; Juriloff DM
Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):187-210. PubMed ID: 17177317
[TBL] [Abstract][Full Text] [Related]
12. PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.
Hol FA; Geurds MP; Chatkupt S; Shugart YY; Balling R; Schrander-Stumpel CT; Johnson WG; Hamel BC; Mariman EC
J Med Genet; 1996 Aug; 33(8):655-60. PubMed ID: 8863157
[TBL] [Abstract][Full Text] [Related]
13. Lack of association between mutations in the folate receptor-alpha gene and spina bifida.
Barber RC; Shaw GM; Lammer EJ; Greer KA; Biela TA; Lacey SW; Wasserman CR; Finnell RH
Am J Med Genet; 1998 Apr; 76(4):310-7. PubMed ID: 9545095
[TBL] [Abstract][Full Text] [Related]
14. Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.
Trembath D; Sherbondy AL; Vandyke DC; Shaw GM; Todoroff K; Lammer EJ; Finnell RH; Marker S; Lerner G; Murray JC
Teratology; 1999 May; 59(5):331-41. PubMed ID: 10332959
[TBL] [Abstract][Full Text] [Related]
15. Mutation incidence in folate metabolism genes and regulatory genes in Polish families with neural tube defects.
Gos M; Sliwerska E; Szpecht-Potocka A
J Appl Genet; 2004; 45(3):363-8. PubMed ID: 15306729
[TBL] [Abstract][Full Text] [Related]
16. Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants.
Harris MJ
Birth Defects Res A Clin Mol Teratol; 2009 Apr; 85(4):331-9. PubMed ID: 19117321
[TBL] [Abstract][Full Text] [Related]
17. Exencephaly in a subset of animals heterozygous for AP-2alpha mutation.
Kohlbecker A; Lee AE; Schorle H
Teratology; 2002 May; 65(5):213-8. PubMed ID: 11967920
[TBL] [Abstract][Full Text] [Related]
18. An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1).
Franke B; Vermeulen SH; Steegers-Theunissen RP; Coenen MJ; Schijvenaars MM; Scheffer H; den Heijer M; Blom HJ
Birth Defects Res A Clin Mol Teratol; 2009 Mar; 85(3):216-26. PubMed ID: 19161160
[TBL] [Abstract][Full Text] [Related]
19. An examination of polymorphic genes and folate metabolism in mothers affected by a spina bifida pregnancy.
Lucock M; Daskalakis I; Hinkins M; Yates Z
Mol Genet Metab; 2001 Aug; 73(4):322-32. PubMed ID: 11509014
[TBL] [Abstract][Full Text] [Related]
20. Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
Sharon D; Yamamoto H; McGee TL; Rabe V; Szerencsei RT; Winkfein RJ; Prinsen CF; Barnes CS; Andreasson S; Fishman GA; Schnetkamp PP; Berson EL; Dryja TP
Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1971-9. PubMed ID: 12037007
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
