| Year |
Citation |
Score |
| 2018 |
Juriloff DM, Harris MJ. Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies. Journal of Developmental Biology. 6. PMID 30134561 DOI: 10.3390/jdb6030022 |
0.476 |
|
| 2014 |
Juriloff DM, Harris MJ, Mager DL, Gagnier L. Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 772-88. PMID 25257647 DOI: 10.1002/Bdra.23320 |
0.44 |
|
| 2012 |
Juriloff DM, Harris MJ. A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 824-40. PMID 23024041 DOI: 10.1002/Bdra.23079 |
0.481 |
|
| 2012 |
Juriloff DM, Harris MJ. Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 849-55. PMID 22753363 DOI: 10.1002/Bdra.23036 |
0.39 |
|
| 2012 |
Kooistra MK, Leduc RY, Dawe CE, Fairbridge NA, Rasmussen J, Man JH, Bujold M, Juriloff D, King-Jones K, McDermid HE. Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes. Physiological Genomics. 44: 35-46. PMID 22045912 DOI: 10.1152/Physiolgenomics.00124.2011 |
0.529 |
|
| 2012 |
Juriloff D. Planar cell polarity gene mutations in severe neural tube defects Human Mutation. 33: v-v. DOI: 10.1002/Humu.22568 |
0.389 |
|
| 2011 |
Plamondon JA, Harris MJ, Mager DL, Gagnier L, Juriloff DM. The clf2 gene has an epigenetic role in the multifactorial etiology of cleft lip and palate in the A/WySn mouse strain. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 716-27. PMID 21384535 DOI: 10.1002/Bdra.20788 |
0.425 |
|
| 2010 |
Harris MJ, Juriloff DM. An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 653-69. PMID 20740593 DOI: 10.1002/Bdra.20676 |
0.495 |
|
| 2008 |
Stoate KL, Harris MJ, Juriloff DM. Accelerated embryonic development associated with increased risk of neural tube defects induced by maternal diet in offspring of SELH/Bc mice. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 720-7. PMID 18798560 DOI: 10.1002/Bdra.20497 |
0.433 |
|
| 2008 |
Juriloff DM, Harris MJ. Mouse genetic models of cleft lip with or without cleft palate. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 63-77. PMID 18181213 DOI: 10.1002/Bdra.20430 |
0.521 |
|
| 2007 |
Harris MJ, Juriloff DM. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 79: 187-210. PMID 17177317 DOI: 10.1002/Bdra.20333 |
0.501 |
|
| 2006 |
Juriloff DM, Harris MJ, McMahon AP, Carroll TJ, Lidral AC. Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 574-9. PMID 16998816 DOI: 10.1002/Bdra.20302 |
0.523 |
|
| 2005 |
Harris MJ, Juriloff DM. Maternal diet alters exencephaly frequency in SELH/Bc strain mouse embryos. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 532-40. PMID 15968625 DOI: 10.1002/Bdra.20170 |
0.479 |
|
| 2005 |
Juriloff DM, Harris MJ, Dewell SL, Brown CJ, Mager DL, Gagnier L, Mah DG. Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 103-13. PMID 15690355 DOI: 10.1002/Bdra.20106 |
0.447 |
|
| 2005 |
Juriloff DM, Harris MJ, Mah DG. The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Genomics. 85: 139-42. PMID 15607429 DOI: 10.1016/J.Ygeno.2004.10.002 |
0.376 |
|
| 2004 |
Juriloff DM, Harris MJ, Dewell SL. A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 509-18. PMID 15329828 DOI: 10.1002/Bdra.20041 |
0.541 |
|
| 2003 |
Baust C, Gagnier L, Baillie GJ, Harris MJ, Juriloff DM, Mager DL. Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse. Journal of Virology. 77: 11448-58. PMID 14557630 DOI: 10.1128/Jvi.77.21.11448-11458.2003 |
0.338 |
|
| 2002 |
Cunningham D, Xiao Q, Chatterjee A, Sulik K, Juriloff D, Elder F, Harrison W, Schuster G, Overbeek PA, Herman GE. exma: an X-linked insertional mutation that disrupts forebrain and eye development. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 179-85. PMID 11956759 DOI: 10.1007/S00335-001-2121-Z |
0.434 |
|
| 2001 |
Juriloff DM, Gunn TM, Harris MJ, Mah DG, Wu MK, Dewell SL. Multifactorial genetics of exencephaly in SELH/Bc mice. Teratology. 64: 189-200. PMID 11598925 DOI: 10.1002/Tera.1064 |
0.724 |
|
| 2001 |
Juriloff DM, Harris MJ, Brown CJ. Unravelling the complex genetics of cleft lip in the mouse model. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 426-35. PMID 11353389 DOI: 10.1007/S003350010284 |
0.526 |
|
| 2000 |
Juriloff DM, Harris MJ, Banks KG, Mah DG. Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 440-7. PMID 10818208 DOI: 10.1007/S003350010084 |
0.485 |
|
| 2000 |
Juriloff DM, Harris MJ. Mouse models for neural tube closure defects. Human Molecular Genetics. 9: 993-1000. PMID 10767323 DOI: 10.1093/Hmg/9.6.993 |
0.504 |
|
| 2000 |
Taylor LA, Harris MJ, Juriloff DM. Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 255-9. PMID 10754100 DOI: 10.1007/S003350010050 |
0.468 |
|
| 1999 |
Harris MJ, Juriloff DM. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice. Teratology. 60: 292-305. PMID 10525207 DOI: 10.1002/(Sici)1096-9926(199911)60:5<292::Aid-Tera10>3.0.Co;2-6 |
0.547 |
|
| 1999 |
Hofmann M, Harris M, Juriloff D, Boehm T. Spontaneous mutations in SELH/Bc mice due to insertions of early transposons: molecular characterization of null alleles at the nude and albino loci. Genomics. 52: 107-9. PMID 10348635 DOI: 10.1006/Geno.1998.5409 |
0.432 |
|
| 1999 |
Harris MJ, Juriloff DM. Nonallelic noncomplementation models in mice: the first arch and lidgap-Gates mutations. Genome. 41: 789-96. PMID 9924790 DOI: 10.1139/G98-089 |
0.397 |
|
| 1997 |
Harris MJ, Juriloff DM. Genetic landmarks for defects in mouse neural tube closure. Teratology. 56: 177-87. PMID 9358605 DOI: 10.1002/(Sici)1096-9926(199709)56:3<177::Aid-Tera1>3.0.Co;2-Z |
0.58 |
|
| 1997 |
Hall JL, Harris MJ, Juriloff DM. Effect of multifactorial genetic liability to exencephaly on the teratogenic effect of valproic acid in mice. Teratology. 55: 306-13. PMID 9261924 DOI: 10.1002/(Sici)1096-9926(199705)55:5<306::Aid-Tera2>3.0.Co;2-X |
0.439 |
|
| 1997 |
Juriloff DM, Harris MJ, Mah DG, Benson A. The lidgap-Gates (lgGa) mutation for open eyelids at birth maps to mouse chromosome 13. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 403-7. PMID 8662232 DOI: 10.1007/S003359900121 |
0.46 |
|
| 1996 |
Gunn TM, Juriloff DM, Harris MJ. Exencephaly and cleft cerebellum in SELH/Bc mouse embryos are alternative developmental consequences of the same underlying genetic defect Teratology. 54: 230-236. PMID 9035344 DOI: 10.1002/(Sici)1096-9926(199611)54:5<230::Aid-Tera3>3.0.Co;2-3 |
0.737 |
|
| 1996 |
Juriloff DM, Harris MJ, Mah DG. The clf1 gene maps to a 2- to 3-cM region of distal mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 789. PMID 8854874 DOI: 10.1007/S003359900298 |
0.319 |
|
| 1995 |
Wang KY, Juriloff DM, Diewert VM. Deficient and delayed primary palatal fusion and mesenchymal bridge formation in cleft lip-liable strains of mice. Journal of Craniofacial Genetics and Developmental Biology. 15: 99-116. PMID 8642057 |
0.34 |
|
| 1995 |
Gunn TM, Juriloff DM, Harris MJ. Genetically determined absence of an initiation site of cranial neural tube closure is causally related to exencephaly in SELH/Bc mouse embryos Teratology. 52: 101-108. PMID 8588181 DOI: 10.1002/Tera.1420520206 |
0.729 |
|
| 1995 |
Dreger RT, Harris MJ, Peichel CL, Vogt TF, Juriloff DM. The first arch (Far) mutation in mice recombines with Hoxd and Mdk. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 662-3. PMID 8535077 DOI: 10.1007/Bf00352376 |
0.404 |
|
| 1995 |
Juriloff DM, Mah DG. The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 63-9. PMID 7767007 DOI: 10.1007/Bf00303246 |
0.441 |
|
| 1995 |
Juriloff DM. Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL(P) in the mouse is caused by two loci with epistatic interaction. Journal of Craniofacial Genetics and Developmental Biology. 15: 1-12. PMID 7601909 |
0.387 |
|
| 1994 |
Van Allen MI, Kalousek DK, Chernoff GF, Juriloff D, Harris M, McGillivray BC, Yong SL, Langlois S, MacLeod PM, Chitayat D. Evidence for multi-site closure of the neural tube in humans. American Journal of Medical Genetics. 47: 723-43. PMID 8267004 DOI: 10.1002/Ajmg.1320470528 |
0.374 |
|
| 1994 |
Harris MJ, Juriloff DM, Gunn TM, Miller JE. Development of the cerebellar defect in ataxic SELH/Bc mice. Teratology. 50: 63-73. PMID 7974256 DOI: 10.1002/Tera.1420500109 |
0.68 |
|
| 1993 |
Juriloff DM, Harris MJ. Studies of possible preventive effects of prenatal retinoic acid treatment on genetic birth defects in mice. Annals of the New York Academy of Sciences. 678: 346-7. PMID 8494281 DOI: 10.1111/J.1749-6632.1993.TB26141.X |
0.363 |
|
| 1993 |
Juriloff DM, Harris MJ, Harrod ML, Gunn TM, Miller JE. Ataxia and a cerebellar defect in the exencephaly-prone SELH/Bc mouse stock. Teratology. 47: 333-40. PMID 8322227 DOI: 10.1002/Tera.1420470410 |
0.723 |
|
| 1993 |
Gunn TM, Juriloff DM, Vogl W, Harris MJ, Miller JE. Histological study of the cranial neural folds of mice genetically liable to exencephaly. Teratology. 48: 459-71. PMID 8303615 DOI: 10.1002/Tera.1420480510 |
0.702 |
|
| 1993 |
Juriloff DM. Current status of genetic linkage studies of a major gene that causes CL(P) in mice: exclusion map. Journal of Craniofacial Genetics and Developmental Biology. 13: 223-9. PMID 8288729 |
0.359 |
|
| 1992 |
Gunn TM, Juriloff DM, Harris MJ. Further genetic studies of the cause of exencephaly in SELH mice Teratology. 45: 679-686. PMID 1412061 DOI: 10.1002/Tera.1420450613 |
0.735 |
|
| 1991 |
Tom C, Juriloff DM, Harris MJ. Studies of the effect of retinoic acid on anterior neural tube closure in mice genetically liable to exencephaly Teratology. 43: 27-40. PMID 2006470 DOI: 10.1002/Tera.1420430105 |
0.507 |
|
| 1991 |
Juriloff DM, Harris MJ. Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2. The Journal of Heredity. 82: 402-5. PMID 1940283 DOI: 10.1093/OXFORDJOURNALS.JHERED.A111111 |
0.301 |
|
| 1991 |
Juriloff DM, Harris MJ, Tom C, MacDonald KB. Normal mouse strains differ in the site of initiation of closure of the cranial neural tube Teratology. 44: 225-233. PMID 1925982 DOI: 10.1002/Tera.1420440211 |
0.508 |
|
| 1989 |
Macdonald KB, Juriloff DM, Harris MJ. Developmental study of neural tube closure in a mouse stock with a high incidence of exencephaly. Teratology. 39: 195-213. PMID 2928966 DOI: 10.1002/Tera.1420390211 |
0.514 |
|
| 1989 |
Harris MJ, Juriloff DM. Test of the isoallele hypothesis at the mouse first arch (far) locus. The Journal of Heredity. 80: 127-31. PMID 2926115 DOI: 10.1093/oxfordjournals.jhered.a110810 |
0.46 |
|
| 1989 |
Juriloff DM, Macdonald KB, Harris MJ. Genetic analysis of the cause of exencephaly in the SELH/Bc mouse stock. Teratology. 40: 395-405. PMID 2814901 DOI: 10.1002/Tera.1420400412 |
0.552 |
|
| 1989 |
Juriloff DM, Harris MJ. A scanning electron microscope study of fetal eyelid closure accelerated by cortisone in SWV/Bc mice. Teratology. 40: 59-66. PMID 2763210 DOI: 10.1002/Tera.1420400108 |
0.507 |
|
| 1986 |
Juriloff DM. Major genes that cause cleft lip in mice: progress in the construction of a congenic strain and in linkage mapping. Journal of Craniofacial Genetics and Developmental Biology. Supplement. 2: 55-66. PMID 3491125 |
0.319 |
|
| 1985 |
Juriloff DM, Harris MJ. Thyroxine-induced differential mortality of cleft lip mouse embryos: dose- and time-response studies of the A/WySn strain. Teratology. 31: 319-29. PMID 4040275 DOI: 10.1002/Tera.1420310302 |
0.441 |
|
| 1985 |
Juriloff DM. Prevention of the eye closure defect in lgMl/lgMl fetal mice by thyroxine. Teratology. 32: 73-86. PMID 4035594 DOI: 10.1002/Tera.1420320111 |
0.349 |
|
| 1984 |
Harris MJ, Juriloff DM, Biddle FG. Cortisone cure of the lidgap defect in fetal mice: a dose-response and time-response study. Teratology. 29: 287-95. PMID 6740513 DOI: 10.1002/Tera.1420290215 |
0.323 |
|
| 1983 |
Juriloff DM, Harris MJ, Miller JR. The lidgap defect in mice: update and hypotheses. Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie. 25: 246-54. PMID 6883178 DOI: 10.1139/g83-039 |
0.42 |
|
| 1983 |
Diewert VM, Juriloff DM. Abnormal head posture associated with induction of cleft palate by methylmercury in C57BL/6J mice. Teratology. 28: 437-47. PMID 6665742 DOI: 10.1002/Tera.1420280315 |
0.345 |
|
| 1982 |
Juriloff DM. Differences in frequency of cleft lip among the A strains of mice. Teratology. 25: 361-8. PMID 7202260 DOI: 10.1002/Tera.1420250313 |
0.431 |
|
| 1981 |
Juriloff DM. Thyroxin-induced differential mortality of mouse embryos with cleft lip. Developmental Pharmacology and Therapeutics. 2: 17-31. PMID 7249902 |
0.332 |
|
| 1980 |
Juriloff DM, Fraser FC. Genetic maternal effects on cleft lip frequency in A/J and CL/Fr mice. Teratology. 21: 167-75. PMID 7394720 DOI: 10.1002/Tera.1420210206 |
0.643 |
|
| 1980 |
Juriloff DM. Genetics of clefting in the mouse. Progress in Clinical and Biological Research. 46: 39-71. PMID 7022461 |
0.382 |
|
| 1977 |
Juriloff DM, Roberts CW. "Palatal pits"--a new trait in chickens? Poultry Science. 56: 386-388. PMID 605021 DOI: 10.3382/ps.0560386 |
0.304 |
|
| 1976 |
Juriloff DM, Trasler DG. Test of the hypothesis that embryonic face shape is a causal factor in genetic predisposition to cleft lip in mice. Teratology. 14: 35-41. PMID 960009 DOI: 10.1002/Tera.1420140106 |
0.344 |
|
| 1975 |
Juriloff DM, Roberts CW. Genetics of cleft palate in chickens and the relationship between the occurrence of the trait and maternal riboflavin deficiency Poultry Science. 54: 334-346. PMID 1178592 DOI: 10.3382/ps.0540334 |
0.335 |
|
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