| Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice. Yang M., Bozdagi O., Scattoni M.L., Wohr M., Roullet F.I., Katz A.M., Abrams D.N., Kalikhman D., Simon H., Woldeyohannes L. et al.
J. Neurosci. 32:6525-6541(2012) · Mapped (7) |
| Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Bozdagi O., Sakurai T., Papapetrou D., Wang X., Dickstein D.L., Takahashi N., Kajiwara Y., Yang M., Katz A.M., Scattoni M.L. et al.
Mol Autism 1:15-15(2010) · Mapped (7) |
| Two N-linked glycans are required to maintain the transport activity of the bile salt export pump (ABCB11) in MDCK II cells. Mochizuki K., Kagawa T., Numari A., Harris M.J., Itoh J., Watanabe N., Mine T., Arias I.M.
Am. J. Physiol. 292:G818-G828(2007) · UniProtKB (1) |
| 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. Juriloff D.M., Harris M.J., McMahon A.P., Carroll T.J., Lidral A.C.
Birth Defects Res. Part A Clin. Mol. Teratol. 76:574-579(2006) · Mapped (3) |
| Progressive familial intrahepatic cholestasis: genetic disorders of biliary transporters. Harris M.J., Le Couteur D.G., Arias I.M.
J. Gastroenterol. Hepatol. 20:807-817(2005) · Mapped (1) |
| Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Juriloff D.M., Harris M.J., Dewell S.L., Brown C.J., Mager D.L., Gagnier L., Mah D.G.
Birth Defects Res. Part A Clin. Mol. Teratol. 73:103-113(2005) · Mapped (42) |
| The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Juriloff D.M., Harris M.J., Mah D.G.
Genomics 85:139-142(2005) · Mapped (3) |
| A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci. Juriloff D.M., Harris M.J., Dewell S.L.
Birth Defects Res. Part A Clin. Mol. Teratol. 70:509-518(2004) · Mapped (64) |
| Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse. Baust C., Gagnier L., Baillie G.J., Harris M.J., Juriloff D.M., Mager D.L.
J. Virol. 77:11448-11458(2003) · UniProtKB (8) |
| FIC1, a P-type ATPase linked to cholestatic liver disease, has homologues (ATP8B2 and ATP8B3) expressed throughout the body. Harris M.J., Arias I.M.
Biochim. Biophys. Acta 1633:127-131(2003) · UniProtKB (2) · Mapped (1) |
| Multifactorial genetics of exencephaly in SELH/Bc mice. Juriloff D.M., Gunn T.M., Harris M.J., Mah D.G., Wu M.K., Dewell S.L.
Teratology 64:189-200(2001) · Mapped (44) |
| Unravelling the complex genetics of cleft lip in the mouse model. Juriloff D.M., Harris M.J., Brown C.J.
Mamm. Genome 12:426-435(2001) · Mapped (63) |
| Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Juriloff D.M., Harris M.J., Banks K.G., Mah D.G.
Mamm. Genome 11:440-447(2000) · Mapped (4) |
| Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse chromosome 11. Taylor L.A., Harris M.J., Juriloff D.M.
Mamm. Genome 11:255-259(2000) · Mapped (3) |
| Mini-review: toward understanding mechanisms of genetic neural tube defects in mice. Harris M.J., Juriloff D.M.
Teratology 60:292-305(1999) · Mapped (11) |
| Cloning of mammalian heparanase, an important enzyme in tumor invasion and metastasis. Hulett M.D., Freeman C., Hamdorf B.J., Baker R.T., Harris M.J., Parish C.R.
Nat. Med. 5:803-809(1999) · UniProtKB (3) · Mapped (1) |
| Nonallelic noncomplementation models in mice: the first arch and lidgap-Gates mutations. Harris M.J., Juriloff D.M.
Genome 41:789-796(1998) · Mapped (3) |
| The clf1 gene maps to a 2- to 3-cM region of distal mouse chromosome 11. Juriloff D.M., Harris M.J., Mah D.G.
Mamm. Genome 7:789-789(1996) · Mapped (3) |
| The first arch (Far) mutation in mice recombines with Hoxd and Mdk. Dreger R.T., Harris M.J., Peichel C.L., Vogt T.F., Juriloff D.M.
Mamm. Genome 6:662-663(1995) · Mapped (5) |
| Three spontaneous mutations at the albino locus in SELH/Bc mice. Juriloff D.M., Porter S.D., Harris M.J.
Genome 37:190-197(1994) · Mapped (6) |
| The lidgap defect in mice: update and hypotheses. Juriloff D.M., Harris M.J., Miller J.R.
Can. J. Genet. Cytol. 25:246-254(1983) · Mapped (3) |
| Hemolytic anemia in the mouse. Report of a new mutation and clarification of its genetics. Unger A.E., Harris M.J., Bernstein S.E., Falcone J.C., Lux S.E.
J. Hered. 74:88-92(1983) · Mapped (3) |
| Cortisone cure of the lidgap defect in fetal mice: a dose-response and time-response study. Harris M.J., Juriloff D.M., Biddle F.G.
Teratology 29:287-295(1984) · Mapped (3) |
| Structural studies of hemoglobin alpha-chains from Virginia white-tailed deer. Harris M.J., Wilson J.B., Huisman T.H.J.
Arch. Biochem. Biophys. 151:540-548(1972) · UniProtKB (1) |
| A new mutation at the cmd locus in the mouse. Bell L., Juriloff M., Harris M.J.
J. Hered. 77:205-206(1986) · Mapped (1) |
