Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute.

PubWeight™: 2.54‹?› | Rank: Top 2%

🔗 View Article (PMC 2262800)

Published in Development on August 01, 2004

Authors

Edward R Oliver1, Thomas L Saunders, Susan A Tarlé, Tom Glaser

Author Affiliations

1: Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.

Articles citing this

Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning. Cell (2011) 4.26

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat Genet (2008) 4.02

ER-stress-induced transcriptional regulation increases protein synthesis leading to cell death. Nat Cell Biol (2013) 3.84

Genetic dissection of the oncogenic mTOR pathway reveals druggable addiction to translational control via 4EBP-eIF4E. Cancer Cell (2010) 3.79

Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia. Blood (2008) 3.05

Suppression of Myc oncogenic activity by ribosomal protein haploinsufficiency. Nature (2008) 2.95

Specialized ribosomes: a new frontier in gene regulation and organismal biology. Nat Rev Mol Cell Biol (2012) 2.91

p53-mediated hematopoietic stem and progenitor cell competition. Cell Stem Cell (2010) 2.65

The ribosomal protein genes and Minute loci of Drosophila melanogaster. Genome Biol (2007) 2.40

Competitive interactions between cells: death, growth, and geography. Science (2009) 2.03

An ARF-independent c-MYC-activated tumor suppression pathway mediated by ribosomal protein-Mdm2 Interaction. Cancer Cell (2010) 1.91

Haematopoietic stem cells require a highly regulated protein synthesis rate. Nature (2014) 1.86

An ancient defense system eliminates unfit cells from developing tissues during cell competition. Science (2014) 1.74

Coordination of progenitor specification and growth in mouse and chick spinal cord. Science (2014) 1.74

Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations. Proc Natl Acad Sci U S A (2008) 1.63

Cop1 constitutively regulates c-Jun protein stability and functions as a tumor suppressor in mice. J Clin Invest (2011) 1.59

Gene expression analysis of zebrafish melanocytes, iridophores, and retinal pigmented epithelium reveals indicators of biological function and developmental origin. PLoS One (2013) 1.54

The role of Myc-induced protein synthesis in cancer. Cancer Res (2009) 1.54

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. PLoS Genet (2013) 1.50

A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina. PLoS One (2010) 1.48

The Arabidopsis STV1 protein, responsible for translation reinitiation, is required for auxin-mediated gynoecium patterning. Plant Cell (2005) 1.46

Ribosome biogenesis is sensed at the Start cell cycle checkpoint. Mol Biol Cell (2006) 1.43

Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes. Transgenic Res (2009) 1.43

The p53 tumor suppressor causes congenital malformations in Rpl24-deficient mice and promotes their survival. Mol Cell Biol (2009) 1.40

Loss of ribosomal protein L11 affects zebrafish embryonic development through a p53-dependent apoptotic response. PLoS One (2009) 1.36

Mechanisms of cell competition: themes and variations. J Cell Biol (2013) 1.35

Competition between human cells by entosis. Cell Res (2014) 1.32

Inactivation of ribosomal protein L22 promotes transformation by induction of the stemness factor, Lin28B. Blood (2012) 1.29

Many ribosomal protein mutations are associated with growth impairment and tumor predisposition in zebrafish. Dev Dyn (2009) 1.27

The ribosome filter redux. Cell Cycle (2007) 1.27

Mouse Eri1 interacts with the ribosome and catalyzes 5.8S rRNA processing. Nat Struct Mol Biol (2008) 1.26

Ribosomal protein gene knockdown causes developmental defects in zebrafish. PLoS One (2006) 1.24

A survey of essential gene function in the yeast cell division cycle. Mol Biol Cell (2006) 1.23

Mechanisms and mechanics of cell competition in epithelia. Nat Rev Mol Cell Biol (2013) 1.22

New frontiers in cell competition. Dev Dyn (2012) 1.21

Myc in model organisms: a view from the flyroom. Semin Cancer Biol (2006) 1.21

Balanced production of ribosomal proteins. Gene (2007) 1.17

Cell competition: how to eliminate your neighbours. Development (2014) 1.17

Mechanisms of growth and homeostasis in the Drosophila wing. Annu Rev Cell Dev Biol (2009) 1.12

The other lives of ribosomal proteins. Hum Genomics (2010) 1.10

Stimulation of mTORC1 with L-leucine rescues defects associated with Roberts syndrome. PLoS Genet (2013) 1.07

Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome. Blood (2011) 1.05

The Ribosomal Protein-Mdm2-p53 Pathway and Energy Metabolism: Bridging the Gap between Feast and Famine. Genes Cancer (2011) 1.02

The ribosomal protein Rpl22 controls ribosome composition by directly repressing expression of its own paralog, Rpl22l1. PLoS Genet (2013) 1.02

Feedback regulation of c-Myc by ribosomal protein L11. Cell Cycle (2007) 1.02

Tissue repair through cell competition and compensatory cellular hypertrophy in postmitotic epithelia. Dev Cell (2013) 1.00

Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications. Med Res Rev (2014) 0.98

Ribosomopathies: how a common root can cause a tree of pathologies. Dis Model Mech (2015) 0.95

RACK1 depletion in a mouse model causes lethality, pigmentation deficits and reduction in protein synthesis efficiency. Cell Mol Life Sci (2012) 0.95

Dissecting social cell biology and tumors using Drosophila genetics. Annu Rev Genet (2013) 0.92

Cell wars: regulation of cell survival and proliferation by cell competition. Essays Biochem (2012) 0.91

Chronic rapamycin treatment or lack of S6K1 does not reduce ribosome activity in vivo. Cell Cycle (2013) 0.91

Ribosomal protein L29/HIP deficiency delays osteogenesis and increases fragility of adult bone in mice. J Orthop Res (2009) 0.91

Chemically induced specification of retinal ganglion cells from human embryonic and induced pluripotent stem cells. Stem Cells Transl Med (2014) 0.90

Socializing with MYC: cell competition in development and as a model for premalignant cancer. Cold Spring Harb Perspect Med (2014) 0.89

Myc Function in Drosophila. Genes Cancer (2010) 0.88

Working hard at the nexus between cell signaling and the ribosomal machinery: An insight into the roles of RACK1 in translational regulation. Translation (Austin) (2015) 0.88

Ribosomal protein mutations induce autophagy through S6 kinase inhibition of the insulin pathway. PLoS Genet (2014) 0.88

Animal models of Diamond Blackfan anemia. Semin Hematol (2011) 0.88

A methyltransferase-independent function for Rmt3 in ribosomal subunit homeostasis. J Biol Chem (2009) 0.86

Flower-deficient mice have reduced susceptibility to skin papilloma formation. Dis Model Mech (2012) 0.84

Genetics of ribosomal proteins: "curiouser and curiouser". PLoS Genet (2013) 0.81

Patterns of ribosomal protein expression specify normal and malignant human cells. Genome Biol (2016) 0.80

Genomic characterization of the mouse ribosomal DNA locus. G3 (Bethesda) (2014) 0.80

The global translation profile in a ribosomal protein mutant resembles that of an eIF3 mutant. BMC Biol (2013) 0.80

In Vivo Senescence in the Sbds-Deficient Murine Pancreas: Cell-Type Specific Consequences of Translation Insufficiency. PLoS Genet (2015) 0.80

Effect of HIP/ribosomal protein L29 deficiency on mineral properties of murine bones and teeth. Bone (2010) 0.79

RPLP1, a crucial ribosomal protein for embryonic development of the nervous system. PLoS One (2014) 0.79

Darwin's multicellularity: from neurotrophic theories and cell competition to fitness fingerprints. Curr Opin Cell Biol (2014) 0.79

Ribosomal Protein RPL27a Promotes Female Gametophyte Development in a Dose-Dependent Manner. Plant Physiol (2014) 0.79

Ubiquitin-Mediated Regulation of Cell Death, Inflammation, and Defense of Homeostasis. Curr Top Dev Biol (2015) 0.78

RPL24: a potential therapeutic target whose depletion or acetylation inhibits polysome assembly and cancer cell growth. Oncotarget (2014) 0.78

Drosophila Myc: A master regulator of cellular performance. Biochim Biophys Acta (2014) 0.77

The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling. FASEB J (2011) 0.77

Notchless is required for axial skeleton formation in mice. PLoS One (2014) 0.76

A developmental transcriptomic analysis of Pax1 and Pax9 in embryonic intervertebral disc development. Biol Open (2016) 0.76

Pno1 tissue-specific expression and its functions related to the immune responses and proteasome activities. PLoS One (2012) 0.76

STV1, a ribosomal protein, binds primary microRNA transcripts to promote their interaction with the processing complex in Arabidopsis. Proc Natl Acad Sci U S A (2017) 0.75

MYC, Cell Competition, and Cell Death in Cancer: The Inseparable Triad. Genes (Basel) (2017) 0.75

Spontaneous Cell Competition in Immortalized Mammalian Cell Lines. PLoS One (2015) 0.75

Genetic chimeras reveal the autonomy requirements for Vsx2 in embryonic retinal progenitor cells. Neural Dev (2015) 0.75

Hypertranscription in Development, Stem Cells, and Regeneration. Dev Cell (2016) 0.75

Reduced insulin/insulin-like growth factor signaling decreases translation in Drosophila and mice. Sci Rep (2016) 0.75

p53 pathway is involved in cell competition during mouse embryogenesis. Proc Natl Acad Sci U S A (2017) 0.75

Morphological Characters and Transcriptome Profiles Associated with Black Skin and Red Skin in Crimson Snapper (Lutjanus erythropterus). Int J Mol Sci (2015) 0.75

Phenotypic and functional characterization of Bst+/- mouse retina. Dis Model Mech (2015) 0.75

Chronic activation of JNK JAK/STAT and oxidative stress signalling causes the loser cell status. Nat Commun (2017) 0.75

Articles cited by this

The complete atomic structure of the large ribosomal subunit at 2.4 A resolution. Science (2000) 28.25

Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc Natl Acad Sci U S A (1993) 20.33

The economics of ribosome biosynthesis in yeast. Trends Biochem Sci (1999) 15.22

Coordinated transcription of key pathways in the mouse by the circadian clock. Cell (2002) 14.07

The Minute Reaction in the Development of DROSOPHILA MELANOGASTER. Genetics (1929) 8.56

A genetic map of the mouse suitable for typing intraspecific crosses. Genetics (1992) 8.53

Disruption of overlapping transcripts in the ROSA beta geo 26 gene trap strain leads to widespread expression of beta-galactosidase in mouse embryos and hematopoietic cells. Proc Natl Acad Sci U S A (1997) 8.35

Drosophila S6 kinase: a regulator of cell size. Science (1999) 6.76

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet (1999) 6.23

Gene-specific regulation by general translation factors. Cell (2002) 6.05

Minutes: mutants of drosophila autonomously affecting cell division rate. Dev Biol (1975) 5.76

ABSENCE OF RIBOSOMAL RNA SYNTHESIS IN THE ANUCLEOLATE MUTANT OF XENOPUS LAEVIS. Proc Natl Acad Sci U S A (1964) 5.67

Drosophila myc regulates cellular growth during development. Cell (1999) 5.66

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology (1980) 5.59

Rapamycin suppresses 5'TOP mRNA translation through inhibition of p70s6k. EMBO J (1997) 5.57

Translational regulation of yeast GCN4. A window on factors that control initiator-trna binding to the ribosome. J Biol Chem (1997) 5.37

Vertebrate neural cell-fate determination: lessons from the retina. Nat Rev Neurosci (2001) 5.26

Making ribosomes. Curr Opin Cell Biol (2002) 5.20

Structure of the 80S ribosome from Saccharomyces cerevisiae--tRNA-ribosome and subunit-subunit interactions. Cell (2001) 5.01

Upstream open reading frames as regulators of mRNA translation. Mol Cell Biol (2000) 4.99

c-Myc regulates mammalian body size by controlling cell number but not cell size. Nature (2001) 4.46

Developmental compartmentalisation of the wing disk of Drosophila. Nat New Biol (1973) 4.36

Extraribosomal functions of ribosomal proteins. Trends Biochem Sci (1996) 4.25

Identification of eukaryotic mRNAs that are translated at reduced cap binding complex eIF4F concentrations using a cDNA microarray. Proc Natl Acad Sci U S A (1999) 4.12

Targeted deletion of 5'HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus. Genes Dev (1995) 4.11

Death before birth: clues from gene knockouts and mutations. Trends Genet (1995) 4.07

Many ribosomal protein genes are cancer genes in zebrafish. PLoS Biol (2004) 3.99

Oscillatory expression of the bHLH factor Hes1 regulated by a negative feedback loop. Science (2002) 3.93

Avian hairy gene expression identifies a molecular clock linked to vertebrate segmentation and somitogenesis. Cell (1997) 3.88

Translational control of protein synthesis. Annu Rev Biochem (1976) 3.66

Composition and functional characterization of yeast 66S ribosome assembly intermediates. Mol Cell (2001) 3.34

Cryptic branch point activation allows accurate in vitro splicing of human beta-globin intron mutants. Cell (1985) 3.25

Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes. Cell (2001) 3.20

Altered cell cycle kinetics, gene expression, and G1 restriction point regulation in Rb-deficient fibroblasts. Mol Cell Biol (1996) 3.15

Transgenesis by means of blastocyst-derived embryonic stem cell lines. Proc Natl Acad Sci U S A (1986) 3.11

Proliferation, but not growth, blocked by conditional deletion of 40S ribosomal protein S6. Science (2000) 3.07

Math5 is required for retinal ganglion cell and optic nerve formation. Development (2001) 3.07

Cells compete for decapentaplegic survival factor to prevent apoptosis in Drosophila wing development. Nature (2002) 2.98

Identification and analysis of over 2000 ribosomal protein pseudogenes in the human genome. Genome Res (2002) 2.88

Lineage-independent determination of cell type in the embryonic mouse retina. Neuron (1990) 2.83

Continuous protein synthesis is required to maintain the probability of entry into S phase. Cell (1977) 2.63

The yin and yang of the exosome. Trends Cell Biol (2002) 2.59

The minute genes in Drosophila and their molecular functions. Adv Genet (1998) 2.57

Unproductively spliced ribosomal protein mRNAs are natural targets of mRNA surveillance in C. elegans. Genes Dev (2000) 2.52

Degradation of ribosomal RNA precursors by the exosome. Nucleic Acids Res (2000) 2.47

Nog2p, a putative GTPase associated with pre-60S subunits and required for late 60S maturation steps. EMBO J (2001) 2.44

Equipotent mouse ribosomal protein promoters have a similar architecture that includes internal sequence elements. Genes Dev (1989) 2.42

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse. Nat Genet (1998) 2.34

Mammalian hairy and Enhancer of split homolog 1 regulates differentiation of retinal neurons and is essential for eye morphogenesis. Neuron (1996) 2.22

Regulating proliferation during retinal development. Nat Rev Neurosci (2001) 2.06

Quantitative analysis of proliferation and cell cycle length during development of the rat retina. Dev Dyn (1996) 1.88

The making of the somite: molecular events in vertebrate segmentation. Nat Rev Genet (2001) 1.88

A complete map of the human ribosomal protein genes: assignment of 80 genes to the cytogenetic map and implications for human disorders. Genomics (2001) 1.83

In the absence of ribosomal RNA synthesis, the ribosomal proteins of HeLa cells are synthesized normally and degraded rapidly. J Mol Biol (1977) 1.82

Ocular colobomata. Surv Ophthalmol (2001) 1.80

Saccharomyces cerevisiae Nip7p is required for efficient 60S ribosome subunit biogenesis. Mol Cell Biol (1997) 1.76

A plant viral "reinitiation" factor interacts with the host translational machinery. Cell (2001) 1.76

Differential mitotic rates and patterns of growth in compartments in the Drosophila wing. Dev Biol (1981) 1.72

Generation of completely embryonic stem cell-derived mutant mice using tetraploid blastocyst injection. Mech Dev (1997) 1.69

CHARGE syndrome: report of 47 cases and review. Am J Med Genet (1998) 1.68

Neuronal determination without cell division in Xenopus embryos. Neuron (1991) 1.64

Yeast ribosomal protein L24 affects the kinetics of protein synthesis and ribosomal protein L39 improves translational accuracy, while mutants lacking both remain viable. Biochemistry (2000) 1.61

Parameters of cell competition in the compartments of the wing disc of Drosophila. Dev Biol (1979) 1.55

Quantitative changes in total RNA, total poly(A), and ribosomes in early mouse embryos. Dev Biol (1982) 1.51

Autoregulation in the biosynthesis of ribosomes. Mol Cell Biol (2003) 1.47

The 67-kDa laminin receptor originated from a ribosomal protein that acquired a dual function during evolution. Mol Biol Evol (1998) 1.33

Ribosomal protein L30 is dispensable in the yeast Saccharomyces cerevisiae. Mol Cell Biol (1990) 1.27

Large scale ENU screens in the mouse: genetics meets genomics. Mutat Res (1998) 1.24

Competition and compensation: coupled to death in development and cancer. Cell (2002) 1.10

The eye in the CHARGE association. Br J Ophthalmol (1990) 1.10

Suppression of cytoplasmic protein uptake by lysosomes as the mechanism of protein regain in livers of starved-refed mice. J Biol Chem (1982) 1.09

Ocular findings in CHARGE syndrome. Six case reports and a review. Ophthalmology (1988) 1.06

Modulation of cell proliferation in the embryonic retina of zebrafish (Danio rerio). Dev Dyn (2000) 1.04

A new tail-short mutation in the mouse whose lethal effects are conditioned by the residual genotypes. J Hered (1950) 1.00

Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions. Am J Med Genet A (2003) 0.92

Program of early development in the mammal: changes in absolute rates of synthesis of ribosomal proteins during oogenesis and early embryogenesis in the mouse. Dev Biol (1979) 0.92

Decreased retinal ganglion cell number and misdirected axon growth associated with fissure defects in Bst/+ mutant mice. Invest Ophthalmol Vis Sci (1997) 0.91

Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy. Mamm Genome (1995) 0.90

The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization. Proc Natl Acad Sci U S A (2000) 0.88

Experimental phenocopy of a minute maternal-effect mutation alters blastoderm determination in embryos of Drosophila melanogaster. Dev Biol (1989) 0.88

Disrupted retinal development in the embryonic belly spot and tail mutant mouse. Dev Biol (1999) 0.86

Posterior segment neovascularization associated with optic nerve aplasia. Am J Ophthalmol (1996) 0.85

Cell allocation in mammalian CNS formation: evidence from murine interspecies aggregation chimeras. Neuron (1989) 0.85

On cell lethals in Drosophila. Proc Natl Acad Sci U S A (1971) 0.77

Articles by these authors

Endothelial and perivascular cells maintain haematopoietic stem cells. Nature (2012) 6.60

Podocyte depletion causes glomerulosclerosis: diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene. J Am Soc Nephrol (2005) 4.79

Sox17 dependence distinguishes the transcriptional regulation of fetal from adult hematopoietic stem cells. Cell (2007) 4.18

Lkb1 regulates cell cycle and energy metabolism in haematopoietic stem cells. Nature (2010) 3.93

Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. Proc Natl Acad Sci U S A (2006) 3.27

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet (2003) 2.36

Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice. Nature (2003) 2.22

Mesenchymal cells reactivate Snail1 expression to drive three-dimensional invasion programs. J Cell Biol (2009) 1.99

Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture. J Neurosci (2004) 1.92

To knockout in 129 or in C57BL/6: that is the question. Trends Genet (2004) 1.76

An inactivating caspase 11 passenger mutation originating from the 129 murine strain in mice targeted for c-IAP1. Biochem J (2012) 1.71

Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line. Mamm Genome (2007) 1.68

RNF8-dependent histone modifications regulate nucleosome removal during spermatogenesis. Dev Cell (2010) 1.57

Distant regulatory elements in a Sox10-beta GEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues. Dev Dyn (2006) 1.54

Reduced sodium channel density, altered voltage dependence of inactivation, and increased susceptibility to seizures in mice lacking sodium channel beta 2-subunits. Proc Natl Acad Sci U S A (2002) 1.52

Pleiotropic phenotype of a genomic knock-in of an RGS-insensitive G184S Gnai2 allele. Mol Cell Biol (2006) 1.51

A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina. PLoS One (2010) 1.48

Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes. Transgenic Res (2009) 1.43

Secreted versus membrane-anchored collagenases: relative roles in fibroblast-dependent collagenolysis and invasion. J Biol Chem (2009) 1.37

Advances in transgenic rat production. Transgenic Res (2006) 1.36

Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nat Neurosci (2011) 1.35

Polo-like kinase 1 is essential for early embryonic development and tumor suppression. Mol Cell Biol (2008) 1.29

Pituitary-specific Gata2 knockout: effects on gonadotrope and thyrotrope function. Mol Endocrinol (2006) 1.27

Pituitary hypoplasia and respiratory distress syndrome in Prop1 knockout mice. Hum Mol Genet (2004) 1.26

Activator of G protein signaling 3 null mice: I. Unexpected alterations in metabolic and cardiovascular function. Endocrinology (2008) 1.17

Aurora A is essential for early embryonic development and tumor suppression. J Biol Chem (2008) 1.17

RBX1/ROC1 disruption results in early embryonic lethality due to proliferation failure, partially rescued by simultaneous loss of p27. Proc Natl Acad Sci U S A (2009) 1.16

Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle. Dev Biol (2012) 1.15

SAG/RBX2/ROC2 E3 ubiquitin ligase is essential for vascular and neural development by targeting NF1 for degradation. Dev Cell (2011) 1.13

Math5 expression and function in the central auditory system. Mol Cell Neurosci (2007) 1.11

Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice. Invest Ophthalmol Vis Sci (2005) 1.08

Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition. J Clin Invest (2011) 1.07

Targeted disruption of the meprin beta gene in mice leads to underrepresentation of knockout mice and changes in renal gene expression profiles. Mol Cell Biol (2003) 1.03

Generation of mice with a conditional allele of the p120 Ras GTPase-activating protein. Genesis (2007) 1.03

Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. Mamm Genome (2002) 1.03

Mouse eye gene microarrays for investigating ocular development and disease. Vision Res (2002) 1.00

A simple qPCR-based method to detect correct insertion of homologous targeting vectors in murine ES cells. Transgenic Res (2007) 1.00

Targeted disruption of Adamts16 gene in a rat genetic model of hypertension. Proc Natl Acad Sci U S A (2012) 1.00

Rederivation of transgenic and gene-targeted mice by embryo transfer. Transgenic Res (2004) 0.98

Further support of the role of CYP1B1 in patients with Peters anomaly. Mol Vis (2006) 0.94

Production of the butyrylcholinesterase knockout mouse. J Mol Neurosci (2006) 0.93

Lgi4 promotes the proliferation and differentiation of glial lineage cells throughout the developing peripheral nervous system. J Neurosci (2010) 0.91

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Hum Mol Genet (2012) 0.90

Beta-mannosidosis mice: a model for the human lysosomal storage disease. Hum Mol Genet (2005) 0.89

Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Hum Mol Genet (2012) 0.89

Tissue-specific expression of ferritin H regulates cellular iron homoeostasis in vivo. Biochem J (2006) 0.89

SRA gene knockout protects against diet-induced obesity and improves glucose tolerance. J Biol Chem (2014) 0.87

Pushing the envelope of retinal ganglion cell genesis: context dependent function of Math5 (Atoh7). Dev Biol (2012) 0.87

Specific inhibition of mouse oocyte nuclear protein phosphatase-1 stimulates germinal vesicle breakdown. Mol Reprod Dev (2003) 0.86

A rat 8 kb dentin sialoprotein-phosphophoryn (DSP-PP) promoter directs spatial and temporal LacZ activity in mouse tissues. Dev Biol (2005) 0.85

Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle. Mol Cell Neurosci (2012) 0.85

Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis. Neuroreport (2012) 0.83

Two pathways for cyclooxygenase-2 protein degradation in vivo. J Biol Chem (2009) 0.83

Resistance to organophosphorus agent toxicity in transgenic mice expressing the G117H mutant of human butyrylcholinesterase. Toxicol Appl Pharmacol (2004) 0.83

A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development. PLoS One (2010) 0.83

Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes. Genesis (2013) 0.82

Genetic analysis of SH2D4A, a novel adapter protein related to T cell-specific adapter and adapter protein in lymphocytes of unknown function, reveals a redundant function in T cells. J Immunol (2008) 0.81

Conserved and divergent functions of Drosophila atonal, amphibian, and mammalian Ath5 genes. Evol Dev (2003) 0.81

Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2. J Assoc Res Otolaryngol (2015) 0.79

Normal TCR signal transduction in mice that lack catalytically active PTPN3 protein tyrosine phosphatase. J Immunol (2007) 0.79

Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response. Mamm Genome (2009) 0.78

Heterochronic misexpression of Ascl1 in the Atoh7 retinal cell lineage blocks cell cycle exit. Mol Cell Neurosci (2013) 0.78

Dentin sialophosphoprotein: a regulatory protein for dental pulp stem cell identity and fate. Stem Cells Dev (2014) 0.77

Analysis of FOXD3 sequence variation in human ocular disease. Mol Vis (2012) 0.76

Fidelity of a BAC-EGFP transgene in reporting dynamic expression of IL-7Rα in T cells. Transgenic Res (2011) 0.75

A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice. PLoS Genet (2013) 0.75