Published in Mamm Genome on January 01, 1996
Specific expression of long noncoding RNAs in the mouse brain. Proc Natl Acad Sci U S A (2008) 7.19
Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation. Genome Res (2000) 2.73
The Dlk1 and Gtl2 genes are linked and reciprocally imprinted. Genes Dev (2000) 2.68
Maternally expressed gene 3 (MEG3) noncoding ribonucleic acid: isoform structure, expression, and functions. Endocrinology (2009) 1.78
Maternally expressed gene 3, an imprinted noncoding RNA gene, is associated with meningioma pathogenesis and progression. Cancer Res (2010) 1.76
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8. Genome Res (2001) 1.75
At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1. PLoS One (2009) 1.60
Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region. Genome Res (2001) 1.41
Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5' region. BMC Genet (2006) 1.37
Imprinted gene dosage is critical for the transition to independent life. Cell Metab (2012) 1.10
Complex patterns of inheritance of an imprinted murine transgene suggest incomplete germline erasure. Nucleic Acids Res (2000) 1.07
Conditional deletions refine the embryonic requirement for Dlk1. Mech Dev (2012) 0.93
Identification of imprinting regulators at the Meg3 differentially methylated region. Genomics (2012) 0.80
Expression at the imprinted dlk1-gtl2 locus is regulated by proneural genes in the developing telencephalon. PLoS One (2012) 0.79
Perturbations to the IGF1 growth pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting. Acta Physiol (Oxf) (2013) 0.79
Regulation of Mammalian Gene Dosage by Long Noncoding RNAs. Biomolecules (2013) 0.76
The Begain gene marks the centromeric boundary of the imprinted region on mouse chromosome 12. Mamm Genome (2009) 0.76
A human haploid gene trap collection to study lncRNAs with unusual RNA biology. RNA Biol (2016) 0.75
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat Genet (2000) 3.63
Maintenance of somite borders in mice requires the Delta homologue DII1. Nature (1997) 3.44
Transgenesis by means of blastocyst-derived embryonic stem cell lines. Proc Natl Acad Sci U S A (1986) 3.11
Expression and distribution of cell adhesion molecule uvomorulin in mouse preimplantation embryos. Dev Biol (1987) 2.72
Pax: a murine multigene family of paired box-containing genes. Genomics (1991) 2.60
Cell lines derived from teratocarcinomas. Cancer Res (1976) 2.56
Sequence interpretation. Functional annotation of mouse genome sequences. Science (2001) 2.54
Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland. Development (1990) 2.42
Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta. Development (1995) 2.20
A single locus in the mouse encodes both myosin light chains 1 and 3, a second locus corresponds to a related pseudogene. Cell (1984) 2.19
Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7. EMBO J (1986) 2.19
Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development. Mol Cell Neurosci (1996) 2.15
Notch signalling is required for cyclic expression of the hairy-like gene HES1 in the presomitic mesoderm. Development (2000) 2.09
A single base deletion in the Tfm androgen receptor gene creates a short-lived messenger RNA that directs internal translation initiation. Proc Natl Acad Sci U S A (1991) 1.84
Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen. Genet Res (1986) 1.82
The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA. Dev Dyn (1998) 1.74
Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse. Curr Biol (1999) 1.73
A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine. Genes Dev (1988) 1.68
Expression of Delta1 and Serrate1 (Jagged1) in the mouse inner ear. Mech Dev (1999) 1.56
Differentiation of a teratocarcinoma line: preferential development of cholinergic neurons. J Cell Biol (1981) 1.51
Gas lock obstruction of the colon: Ogilvie's syndrome revisited. AJR Am J Roentgenol (1998) 1.41
The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element. Neuron (1994) 1.38
Widespread expression of inositol 1,4,5-trisphosphate receptor type 1 gene (Insp3r1) in the mouse central nervous system. Receptors Channels (1993) 1.38
Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines. J Exp Med (1978) 1.38
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice. Nature (1986) 1.36
Maternal IL-11Ralpha function is required for normal decidua and fetoplacental development in mice. Genes Dev (1998) 1.33
Role of H-2 and non-H-2 genes in control of bacterial clearance from the spleen in Salmonella typhimurium-infected mice. Infect Immun (1988) 1.28
Distinct regulatory elements direct delta1 expression in the nervous system and paraxial mesoderm of transgenic mice. Mech Dev (2000) 1.23
Use of coisogenic host blastocysts for efficient establishment of germline chimeras with C57BL/6J ES cell lines. Biotechniques (2001) 1.21
Chromosomal mapping of the structural gene coding for the mouse cell adhesion molecule uvomorulin. Proc Natl Acad Sci U S A (1988) 1.19
Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2. Dev Biol (1995) 1.18
Mapping of the mouse X chromosome using random genomic probes and an interspecific mouse cross. EMBO J (1985) 1.17
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis. Genetics (1988) 1.10
The mouse Enhancer trap locus 1 (Etl-1): a novel mammalian gene related to Drosophila and yeast transcriptional regulator genes. Mech Dev (1992) 1.10
Fragilitas ossium: a new autosomal recessive mutation in the mouse. J Hered (1982) 1.08
Polymorphisms revealed by PCR with single, short-sized, arbitrary primers are reliable markers for mouse and rat gene mapping. Mamm Genome (1992) 1.07
Repeated epilation: a genetic epidermal syndrome in mice. J Hered (1979) 1.07
Developmental expression of an early embryonic antigen common to mouse spermatozoa and cleavage embryos, and to human spermatozoa: its expression during spermatogenesis. Dev Biol (1976) 1.06
Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development. Dev Biol (1999) 1.05
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus. Hum Genet (1990) 1.04
The murine M-CSF gene is localized on chromosome 3. Blood (1989) 1.03
Aberrant regulation of imprinted gene expression in Gtl2lacZ mice. Cytogenet Genome Res (2006) 1.03
Hst-3: an X-linked hybrid sterility gene. Genet Res (1991) 1.02
Mediation of interleukin-11-dependent biological responses by a soluble form of the interleukin-11 receptor. Biochem J (1996) 0.99
Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouse. Genomics (1990) 0.98
Enhancer trap integrations in mouse embryonic stem cells give rise to staining patterns in chimaeric embryos with a high frequency and detect endogenous genes. Mech Dev (1992) 0.98
Comparison of two cell-adhesion molecules, uvomorulin and cell-CAM 105. Exp Cell Res (1985) 0.98
Fertile dominant spotting in the house mouse. J Hered (1979) 0.98
Embryonal carcinoma antigen and the T/t locus of the mouse. Proc Natl Acad Sci U S A (1976) 0.98
Expression of the mouse Delta1 gene during organogenesis and fetal development. Mech Dev (1999) 0.97
Flow cytometry isolation and improved visualization of sorted mouse chromosomes. Purification of chromosomes X and ISO-1 from cell lines with Robertsonian translocations. Exp Cell Res (1984) 0.97
Pathologic changes in the CNS of dystonia musculorum mutant mouse: an animal model for human spinocerebellar ataxia. Neuroscience (1988) 0.97
Phenotypic reversions at the W/Kit locus mediated by mitotic recombination in mice. Mol Cell Biol (1995) 0.96
Etl2, a novel putative type-I cytokine receptor expressed during mouse embryogenesis at high levels in skin and cells with skeletogenic potential. Dev Biol (1994) 0.95
Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1. Hum Genet (1988) 0.94
Genetic interactions suggest that Danforth's short tail (Sd) is a gain-of-function mutation. Dev Genet (1998) 0.94
Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis). Oncogene (1997) 0.94
The Danforth's short tail mutation acts cell autonomously in notochord cells and ventral hindgut endoderm. Development (1997) 0.94
Structure, expression and chromosomal localization of Zfp-1, a murine zinc finger protein gene. Nucleic Acids Res (1989) 0.93
The Etl-1 gene encodes a nuclear protein differentially expressed during early mouse development. Dev Dyn (1993) 0.93
Isolation of Vgr-2, a novel member of the transforming growth factor-beta-related gene family. Mol Endocrinol (1992) 0.93
Monoclonal antibody to neural cell surface protein: identification of a glycoprotein family of restricted cellular localization. Neuroscience (1983) 0.92
A mouse model for Fraser syndrome? Clin Dysmorphol (1994) 0.91
Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively. J Virol (1988) 0.90
Skeletal dysplasias, growth retardation, reduced postnatal survival, and impaired fertility in mice lacking the SNF2/SWI2 family member ETL1. Mech Dev (1999) 0.90
Wobbler, a mutation affecting motoneuron survival and gonadal functions in the mouse, maps to proximal chromosome 11. Genomics (1992) 0.90
Ferrochelatase structural mutant (Fechm1Pas) in the house mouse. Genomics (1993) 0.89
Encyclopedia of the mouse genome V. Mouse chromosome 19. Mamm Genome (1996) 0.89
Genetic control of Salmonella typhimurium-induced depression of delayed-type hypersensitivity to sheep erythrocytes in mice. Infect Immun (1988) 0.88
DNA segments mapped by reciprocal use of microsatellite primers between mouse and rat. Mamm Genome (1993) 0.88
Genetic analysis of diabetes and insulitis in an interspecific cross of the nonobese diabetic mouse with Mus spretus. Proc Natl Acad Sci U S A (1993) 0.88
The murine vik gene (chromosome 9) encodes a putative receptor with unique protein kinase motifs. Oncogene (1993) 0.88
The mouse rib-vertebrae mutation disrupts anterior-posterior somite patterning and genetically interacts with a Delta1 null allele. Mech Dev (2000) 0.86
Male sterility caused by sperm cell-specific structural abnormalities in ebouriffé, a new mutation of the house mouse. Biol Reprod (1996) 0.85
Lambda light chain constant and variable gene complements in wild-derived inbred mouse strains. Eur J Immunol (1985) 0.85
Efficient isolation of novel mouse genes differentially expressed in early postimplantation embryos. Genomics (1995) 0.85
Cardiac and skeletal muscle troponin I isoforms are encoded by a dispersed gene family on mouse chromosomes 1 and 7. Mamm Genome (1996) 0.84
Immunogenetic studies of spontaneous abortion in mice. Preimmunization of females with allogeneic cells. J Immunol (1985) 0.84
Ascorbic acid and alkaptonuria. Eur J Pediatr (1992) 0.83
Recent evolutionary origin of the expression of the glial fibrillary acidic protein (GFAP) in lens epithelial cells. A molecular and genetic analysis of various mouse species. Brain Res Mol Brain Res (1991) 0.83
The use of interspecific mouse crosses for gene localization: present status and future perspectives. Curr Top Microbiol Immunol (1988) 0.83
Multiple cutaneous papillomas and carcinomas that develop spontaneously in a mouse mutant, the repeated epilation heterozygote Er/+. J Natl Cancer Inst (1985) 0.83
Myogenin is in an evolutionarily conserved linkage group on human chromosome 1q31-q41 and unlinked to other mapped muscle regulatory factor genes. Genomics (1990) 0.82
Electromyographical and motor performance studies in the pmn mouse model of neurodegenerative disease. Neurobiol Dis (1996) 0.82
Hyperspiny Purkinje cell, a new neurological mutation in the mouse. J Hered (1983) 0.82
A new spontaneous deletion on chromosome 17 including brachyury. Mamm Genome (1997) 0.82
A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus. Mamm Genome (1995) 0.82
[Action of total microflora of the rat on mitotic activity of Lieberkuhn's crypts]. C R Acad Sci Hebd Seances Acad Sci D (1970) 0.82
Studies on "repeated epilation" mouse mutant embryos: I. Development of facial malformations. J Craniofac Genet Dev Biol (1983) 0.80