M. Harris

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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.

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.

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.

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.

Mouse models for neural tube closure defects.

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

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.

Multifactorial genetics of exencephaly in SELH/Bc mice.

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

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.

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

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

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.

Aneuploidy in the embryonic progeny of females heterozygous for the Robertsonian chromosome (9.12) in genetically wild Peru-Coppock mice (Mus musculus).

M. J. Harris, E. P. Evans, M. E. Wallace, 1986, Journal of reproduction and fertility.

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.

Why are the genes that cause risk of human neural tube defects so hard to find?

M. Harris, 2001, Teratology.

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.

Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants.

M. J. Harris, M. Harris, 2009, Birth defects research. Part A, Clinical and molecular teratology.

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

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

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.

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 .

Unravelling the complex genetics of cleft lip in the mouse model

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

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.

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.

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.

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.

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.

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.

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.

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.

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

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

Genetic landmarks for defects in mouse neural tube closure.

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

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

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

Eyelid growth and fusion in fetal mice

M. J. Harris, M. McLeod, M. Harris, 1982, Anatomy and Embryology.

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.

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

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

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.

Kidney agenesis, hypoplastic left heart, and rib and vertebral anomalies in the fetus of a diabetic mother

M. J. Harris, M. Yasuda, B. J. Poland, 1976 .

Animal models of neural tube defects

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

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.

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.

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

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

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.

Disruption of pattern formation in palatal rugae in fetal mice heterozygous for First arch (Far).

D. Juriloff, C. Peters, M. Harris, 1990, Journal of craniofacial genetics and developmental biology.