Published in Mol Biol Evol on March 01, 1987
Identification of a new, abundant superfamily of mammalian LTR-transposons. Nucleic Acids Res (1993) 2.04
Distinct subfamilies of primate L1Gg retroposons, with some elements carrying tandem repeats in the 5' region. Nucleic Acids Res (1988) 0.80
Specific cleavage analysis of mammalian mitochondrial DNA. Proc Natl Acad Sci U S A (1975) 9.65
A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis. Cell (1991) 6.14
Transposition of elements of the 412, copia and 297 dispersed repeated gene families in Drosophila. Cell (1979) 5.61
Maternal inheritance of mammalian mitochondrial DNA. Nature (1974) 4.46
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. J Med Genet (2005) 3.11
Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice. Nature (1997) 2.73
Unusual structure of the FB family of transposable elements in Drosophila. Cell (1981) 2.64
Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11. Nature (1995) 2.40
Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature (1996) 2.35
DNA sequence of a foldback transposable element in Drosophila. Nature (1982) 2.15
Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2. Development (2000) 2.09
Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility. Development (1995) 2.03
Distinct characteristics of loop sequences of two Drosophila foldback transposable elements. Nucleic Acids Res (1985) 1.92
Autosomal XX sex reversal caused by duplication of SOX9. Am J Med Genet (1999) 1.87
Multistep control of pituitary organogenesis. Science (1997) 1.82
Homeotic transformations and limb defects in Hox A11 mutant mice. Genes Dev (1993) 1.74
Sp4, a member of the Sp1-family of zinc finger transcription factors, is required for normal murine growth, viability, and male fertility. Dev Biol (1996) 1.71
Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries. Development (1999) 1.67
Cis-acting sequences from a human surfactant protein gene confer pulmonary-specific gene expression in transgenic mice. Proc Natl Acad Sci U S A (1990) 1.54
Rearranged sequences of a human Kpn I element. Proc Natl Acad Sci U S A (1984) 1.52
The Evi1 proto-oncogene is required at midgestation for neural, heart, and paraxial mesenchyme development. Mech Dev (1997) 1.49
Gsh-1, an orphan Hox gene, is required for normal pituitary development. EMBO J (1996) 1.49
Characterization of cloned human alphoid satellite with an unusual monomeric construction: evidence for enrichment in HeLa small polydisperse circular DNA. Nucleic Acids Res (1985) 1.38
Gsh-1: a novel murine homeobox gene expressed in the central nervous system. Dev Dyn (1995) 1.37
Abnormal uterine stromal and glandular function associated with maternal reproductive defects in Hoxa-11 null mice. Biol Reprod (1997) 1.37
Cyp1a2(-/-) null mutant mice develop normally but show deficient drug metabolism. Proc Natl Acad Sci U S A (1996) 1.35
Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney. Development (2001) 1.31
Two-dimensional restriction analysis of the Bacillus subtilis genome: gene purification and ribosomal ribonucleic acid gene organization. J Bacteriol (1977) 1.29
Functional analysis of the human adenosine deaminase gene thymic regulatory region and its ability to generate position-independent transgene expression. Mol Cell Biol (1992) 1.26
L1 sequences in HeLa extrachromosomal circular DNA: evidence for circularization by homologous recombination. Proc Natl Acad Sci U S A (1985) 1.24
Characterization of npas3, a novel basic helix-loop-helix PAS gene expressed in the developing mouse nervous system. Mech Dev (1999) 1.22
Gsh-2, a murine homeobox gene expressed in the developing brain. Mech Dev (1995) 1.18
Altered forebrain and hindbrain development in mice mutant for the Gsh-2 homeobox gene. Dev Biol (1997) 1.17
DNA sequence analysis of a Drosophila foldback transposable element rearrangement. Mol Gen Genet (1982) 1.15
Mys, a family of mammalian transposable elements isolated by phylogenetic screening. Nature (1985) 1.14
legless insertional mutation: morphological, molecular, and genetic characterization. Genes Dev (1991) 1.13
Unusual domains of human alphoid satellite DNA with contiguous non-satellite sequences: sequence analysis of a junction region. Nucleic Acids Res (1983) 1.09
Dissecting a locus control region: facilitation of enhancer function by extended enhancer-flanking sequences. Mol Cell Biol (1995) 1.08
Identification of 10 murine homeobox genes. Proc Natl Acad Sci U S A (1991) 1.07
prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme. Development (1999) 1.07
Familial 5p- syndrome. Clin Genet (1984) 1.06
A novel murine homeobox gene isolated by a tissue specific PCR cloning strategy. Nucleic Acids Res (1992) 1.05
Targeted ablation of alpha-crystallin-synthesizing cells produces lens-deficient eyes in transgenic mice. Development (1989) 1.01
Legless, a novel mutation found in PHT1-1 transgenic mice. Science (1988) 1.00
Functional equivalence and rescue among group 11 Hox gene products in vertebral patterning. Dev Biol (1996) 0.99
Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studies. J Med Genet (2008) 0.97
Evaluating the human engineering of microprocessor-controlled operating room devices. J Clin Monit (1991) 0.95
The two-dimensional fractionation of drosophila DNA. Cold Spring Harb Symp Quant Biol (1978) 0.95
Homeobox genes and heart development. Trends Cardiovasc Med (2011) 0.95
Molecular motors: the driving force behind mammalian left-right development. Trends Cell Biol (2000) 0.94
Functional specificity of the Hoxa13 homeobox. Development (2001) 0.94
Characterization of Hoxa-10/Hoxa-11 transheterozygotes reveals functional redundancy and regulatory interactions. Dev Biol (2000) 0.93
Phenotypic characterization of the transgenic mouse insertional mutation, legless. J Exp Zool (1990) 0.93
Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis. Dev Biol (1999) 0.92
Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2. Clin Genet (2010) 0.92
Complete foldback transposable elements encode a novel protein found in Drosophila melanogaster. EMBO J (1989) 0.91
Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome. J Med Genet (1994) 0.89
Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation. J Med Genet (1999) 0.88
Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis. Hum Reprod (1998) 0.87
Multidimensional restriction enzyme analysis of complex genomes. Anal Biochem (1976) 0.87
Novel cell lines promote the discovery of genes involved in early heart development. Dev Biol (2001) 0.87
A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype. Am J Hum Genet (1992) 0.86
Identification of an unusual marker chromosome by spectral karyotyping. Am J Med Genet (1998) 0.86
Spx1, a novel X-linked homeobox gene expressed during spermatogenesis. Mech Dev (1997) 0.84
Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities. J Exp Zool (1992) 0.84
Analysis of possible repressor elements in the 5'-flanking region of the human beta-globin gene. DNA (1989) 0.83
Ectopic expression of Hox-2.3 induces craniofacial and skeletal malformations in transgenic mice. Mech Dev (1992) 0.81
Distinct subfamilies of primate L1Gg retroposons, with some elements carrying tandem repeats in the 5' region. Nucleic Acids Res (1988) 0.80
Correlation of forelimb malformation asymmetries with visceral organ situs in the transgenic mouse insertional mutation, legless. Dev Biol (1993) 0.80
Genomic organization and chromosome localization of the murine homeobox gene Pmx. Genomics (1994) 0.79
Structural and functional characterization of the mouse Hlx homeobox gene. Mamm Genome (2000) 0.79
Mys retrotransposons in Peromyscus leucopus and transgenic Mus musculus. Nucleic Acids Res (1988) 0.79
Malformations of the heart, kidney, palate, and skeleton in alpha-MHC-Hoxb-7 transgenic mice. Mech Dev (1995) 0.78
Two CCAAT boxes in a novel inverted repeat motif are required for Hlx homeobox gene expression. Biochim Biophys Acta (2001) 0.78
Lens structures exist transiently in development of transgenic mice carrying an alpha-crystallin-diphtheria toxin hybrid gene. Exp Eye Res (1992) 0.78
An enhancer LEF-1/TCF-1 site is essential for insertion site-independent transgene expression in thymus. Nucleic Acids Res (1996) 0.78
Novel strategy yields candidate Gsh-1 homeobox gene targets using hypothalamus progenitor cell lines. Dev Biol (1999) 0.77
Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1. Mol Syndromol (2011) 0.75
pPyLT1 does not always dictate the formation of autonomously replicating elements in transgenic mice. Nucleic Acids Res (1987) 0.75
Enhanced expression of limb malformations and axial skeleton alterations in legless mutants by transplacental exposure to retinoic acid. Dev Biol (1994) 0.75
Overlapping transcriptional units on the same strand within the murine beta-glucuronidase gene complex. J Biol Chem (1988) 0.75
Handed asymmetry in the mouse: understanding how things go right (or left) by studying how they go wrong. Semin Cell Dev Biol (1998) 0.75
Prenatal diagnosis from cystic hygroma fluid: the value of fluorescence in situ hybridization. Am J Obstet Gynecol (2001) 0.75
Exacerbation of limb malformations in legless (lgl) homozygotes by retinoic acid (RA). Prog Clin Biol Res (1993) 0.75
Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results. Prenat Diagn (1999) 0.75