D. Juriloff

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Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain.

M. J. Harris, D. Mager, D. Juriloff, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Mouse models for neural tube closure defects.

M. J. Harris, D. Juriloff, D M Juriloff, 2000, Human molecular genetics.

Hemifacial deficiency induced by a shift in dominance of the mouse mutation far: a possible genetic model for hemifacial microsomia.

M. J. Harris, U. Froster-Iskenius, D. Juriloff, 1987, Journal of craniofacial genetics and developmental biology.

Development of the cerebellar defect in ataxic SELH/Bc mice.

M. J. Harris, D. Juriloff, T. Gunn, 1994, Teratology.

Ataxia and a cerebellar defect in the exencephaly-prone SELH/Bc mouse stock.

M. J. Harris, D. Juriloff, T. Gunn, 1993, Teratology.

Effect of multifactorial genetic liability to exencephaly on the teratogenic effect of valproic acid in mice.

M. J. Harris, J. Hall, D. Juriloff, 1997, Teratology.

The clf2 gene has an epigenetic role in the multifactorial etiology of cleft lip and palate in the A/WySn mouse strain.

M. J. Harris, D. Mager, D. Juriloff, 2011, Birth defects research. Part A, Clinical and molecular teratology.

exma: an X-linked insertional mutation that disrupts forebrain and eye development

G. Herman, P. Overbeek, K. Sulik, 2002, Mammalian Genome.

Differences in frequency of cleft lip among the A strains of mice.

D. Juriloff, 1982, Teratology.

Nonallelic noncomplementation models in mice: the first arch and lidgap-Gates mutations.

M. J. Harris, D. Juriloff, 1998, Genome.

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.

M. J. Harris, A. McMahon, D. Juriloff, 2006, Birth defects research. Part A, Clinical and molecular teratology.

Spontaneous mutations in SELH/Bc mice due to insertions of early transposons: molecular characterization of null alleles at the nude and albino loci.

T. Boehm, D. Juriloff, M. Hofmann, 1998, Genomics.

Genetic and developmental studies of a new mouse mutation that produces otocephaly.

T. Roderick, K. Sulik, D. Juriloff, 1985, Journal of craniofacial genetics and developmental biology.

Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.

M. J. Harris, D. Juriloff, M. Harris, 1999, Teratology.

Genetic landmarks for defects in mouse neural tube closure.

M. J. Harris, D. Juriloff, M. Harris, 1997, Teratology.

Accelerated embryonic development associated with increased risk of neural tube defects induced by maternal diet in offspring of SELH/Bc mice.

M. J. Harris, D. Juriloff, K. Stoate, 2008, Birth defects research. Part A, Clinical and molecular teratology.

Maternal diet alters exencephaly frequency in SELH/Bc strain mouse embryos.

M. J. Harris, D. Juriloff, M. Harris, 2005, Birth defects research. Part A, Clinical and molecular teratology.

Maternal treatment with cortisone accelerates eyelid closure and other developmental fusion processes in fetal mice.

D. Juriloff, 1987, Development.

Prevention of the eye closure defect in lgMl/lgMl fetal mice by thyroxine.

D. Juriloff, 1985, Teratology.

Thyroxine-induced differential mortality of cleft lip mouse embryos: dose- and time-response studies of the A/WySn strain.

M. J. Harris, D. Juriloff, M. Harris, 1985, Teratology.

Cortisone cure of the lidgap defect in fetal mice: a dose-response and time-response study.

M. J. Harris, D. Juriloff, F. Biddle, 1984, Teratology.

The relationship of cleft palate to riboflavin deficiency and genotype in chickens

D. Juriloff, 1973 .

Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11

M. J. Harris, D. Juriloff, L. Taylor, 2000, Mammalian Genome.

A scanning electron microscope study of fetal eyelid closure accelerated by cortisone in SWV/Bc mice.

M. J. Harris, D. Juriloff, M. Harris, 1989, Teratology.

Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes.

H. McDermid, K. King-Jones, D. Juriloff, 2012, Physiological genomics.

Animal models of neural tube defects

M. J. Harris, D. Juriloff, M. Harris, 1998 .

A classic paper from the early years of teratology, revisited – Trasler 1968

D. Juriloff, 2011 .

The major locus for multifactorial nonsyndromic cleft lip maps to mouse Chromosome 11

D. Juriloff, D. Mah, 1995, Mammalian Genome.

Evidence for multi-site closure of the neural tube in humans.

D. Chitayat, S. Langlois, D. Juriloff, 1993, American journal of medical genetics.

Mouse genetic models of cleft lip with or without cleft palate.

M. J. Harris, D. Juriloff, M. Harris, 2008, Birth defects research. Part A, Clinical and molecular teratology.

A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci.

M. J. Harris, D. Juriloff, S. Dewell, 2004, Birth defects research. Part A, Clinical and molecular teratology.

Genetics of cleft palate in chickens and the relationship between the occurrence of the trait and maternal riboflavin deficiency.

D. Juriloff, C. W. Roberts, 1975, Poultry science.

Selection of a cleft palate line of chickens beginning with the relationship between the trait and the level of riboflavin in the diet.

D. Juriloff, C. W. Roberts, G. Jain, 1974, Poultry science.

Thyroxin-induced differential mortality of mouse embryos with cleft lip.

D. Juriloff, 1981, Developmental pharmacology and therapeutics.

Genetic maternal effects on cleft lip frequency in A/J and CL/Fr mice.

D. Juriloff, F. Fraser, 1980, Teratology.

Test of the hypothesis that embryonic face shape is a causal factor in genetic predisposition to cleft lip in mice.

D. Juriloff, D. Trasler, 1976, Teratology.

A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects.

M. J. Harris, D. Juriloff, M. Harris, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Multifactorial genetics of exencephaly in SELH/Bc mice.

M. J. Harris, D. Juriloff, T. Gunn, 2001, Teratology.

Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.

M. J. Harris, D. Juriloff, M. Harris, 2007, Birth defects research. Part A, Clinical and molecular teratology.

Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies

M. J. Harris, D. Juriloff, M. Harris, 2018, Journal of developmental biology.

of differentially expressed candidate genes identification exencephaly in mice: genetic analysis and -associated Cecr2 Strain-specific modifier genes of

L. Goodrich, H. McDermid, K. Kooistra, 2015 .

Normal mouse strains differ in the site of initiation of closure of the cranial neural tube.

M. J. Harris, D. Juriloff, C. Tom, 1991, Teratology.

An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure.

M. J. Harris, D. Juriloff, M. Harris, 2010, Birth defects research. Part A, Clinical and molecular teratology.

The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene.

M. J. Harris, D. Juriloff, D. Mah, 2005, Genomics.

Test of the isoallele hypothesis at the mouse first arch (far) locus.

M. J. Harris, D. Juriloff, M. Harris, 1989, The Journal of heredity.

Abnormal facial development in the mouse mutant first arch.

M. J. Harris, D. Juriloff, 1983, Journal of craniofacial genetics and developmental biology.

Further genetic studies of the cause of exencephaly in SELH mice.

M. J. Harris, D. Juriloff, T. Gunn, 1992, Teratology.

Daphne Trasler: In memoriam.

B. Hales, D. Juriloff, J. Trasler, 2021, Birth defects research.

Studies of the effect of retinoic acid on anterior neural tube closure in mice genetically liable to exencephaly.

M. J. Harris, D. Juriloff, C. Tom, 1991, Teratology.

Genetic analysis of the cause of exencephaly in the SELH/Bc mouse stock.

M. J. Harris, D. Juriloff, K. B. Macdonald, 1989, Teratology.

Developmental study of neural tube closure in a mouse stock with a high incidence of exencephaly.

M. J. Harris, D. Juriloff, K. B. Macdonald, 1989, Teratology.

Genetically determined absence of an initiation site of cranial neural tube closure is causally related to exencephaly in SELH/Bc mouse embryos.

M. J. Harris, D. Juriloff, T. Gunn, 1995, Teratology.

Abnormal head posture associated with induction of cleft palate by methylmercury in C57BL/6J mice.

D. Juriloff, V. Diewert, 1983, Teratology.

Gaping lids, gp, a mutation on centromeric Chromosome 11 that causes defective eyelid development in mice

M. J. Harris, D. Juriloff, K. G. Banks, 2000, Mammalian Genome.

Eyelid development and fusion induced by cortisone treatment in mutant, lidgap-Miller, foetal mice. A scanning electron microscope study.

M. J. Harris, D. Juriloff, M. Harris, 1986, Journal of embryology and experimental morphology.

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.

M. J. Harris, D. Juriloff, M. Harris, 2012, Birth defects research. Part A, Clinical and molecular teratology.

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.

D. Juriloff, 1995, Journal of craniofacial genetics and developmental biology.

Three spontaneous mutations at the albino locus in SELH/Bc mice.

M. J. Harris, D. Juriloff, S. Porter, 1994, Genome.

Retinoic acid, cortisone, or thyroxine suppresses the mutant phenotype of the eyelid development mutation, lgMl, in mice.

M. J. Harris, D. Juriloff, M. Harris, 1993, The Journal of experimental zoology.

Deficient and delayed primary palatal fusion and mesenchymal bridge formation in cleft lip-liable strains of mice.

D. Juriloff, V. Diewert, K. Y. Wang, 1995, Journal of craniofacial genetics and developmental biology.

Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice.

M. J. Harris, Carolyn J. Brown, D. Mager, 2005, Birth defects research. Part A, Clinical and molecular teratology.

Unravelling the complex genetics of cleft lip in the mouse model

M. J. Harris, Carolyn J. Brown, D. Juriloff, 2001, Mammalian Genome.

The lidgap-Gates (lgGa) mutation for open eyelids at birth maps to mouse Chromosome 13

M. J. Harris, D. Juriloff, D. Mah, 1996, Mammalian Genome.

Histological study of the cranial neural folds of mice genetically liable to exencephaly.

M. J. Harris, D. Juriloff, T. Gunn, 1993, Teratology.

Is Far a Hox mutation?

M. J. Harris, D. Juriloff, P. Martin, 1992, Journal of craniofacial genetics and developmental biology.

Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2.

M. J. Harris, D. Juriloff, 1991, The Journal of heredity.

Structure and Expression of Mobile ETnII Retroelements and Their Coding-Competent MusD Relatives in the Mouse

M. J. Harris, D. Mager, D. Juriloff, 2003, Journal of Virology.

Mouse Coding-Competent MusD Relatives in the Retroelements and Their Structure and Expression of Mobile ETnII

M. J. Harris, D. Mager, D. Juriloff, 2003 .

"Palatal pits"--a new trait in chickens?

D. Juriloff, C. W. Roberts, 1977, Poultry science.

Defective feathers in Japanese quail A two-locus model for a new trait

D. Juriloff, K. Cheng, J. Fulton, 1983 .

Genetics of clefting in the mouse.

D. Juriloff, 1980, Progress in clinical and biological research.

Mapping Far (First arch) in relation to molecular markers on mouse Chromosome 2

D. Juriloff, D. Mah, M. Harris, 1994, Mammalian Genome.

The first arch (Far) mutation in mice recombines with Hoxd and Mdk

T. Vogt, C. Peichel, D. Juriloff, 1995, Mammalian Genome.

A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects.

D. Juriloff, M. Harris, 2012, Birth defects research. Part A, Clinical and molecular teratology.

The clf1 gene maps to a 2- to 3-cM region of distal mouse Chromosome 11

D. Juriloff, D. Mah, M. Harris, 1996, Mammalian Genome.