PubRank

S S Potter

Author PubWeight™ 103.34‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Specific cleavage analysis of mammalian mitochondrial DNA. Proc Natl Acad Sci U S A 1975 9.65
2 A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis. Cell 1991 6.14
3 Transposition of elements of the 412, copia and 297 dispersed repeated gene families in Drosophila. Cell 1979 5.61
4 Maternal inheritance of mammalian mitochondrial DNA. Nature 1974 4.46
5 Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice. Nature 1997 2.73
6 Unusual structure of the FB family of transposable elements in Drosophila. Cell 1981 2.64
7 Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11. Nature 1995 2.40
8 Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature 1996 2.35
9 DNA sequence of a foldback transposable element in Drosophila. Nature 1982 2.15
10 Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2. Development 2000 2.09
11 Hoxa 11 structure, extensive antisense transcription, and function in male and female fertility. Development 1995 2.03
12 Distinct characteristics of loop sequences of two Drosophila foldback transposable elements. Nucleic Acids Res 1985 1.92
13 Multistep control of pituitary organogenesis. Science 1997 1.82
14 Homeotic transformations and limb defects in Hox A11 mutant mice. Genes Dev 1993 1.74
15 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
16 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
17 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
18 Rearranged sequences of a human Kpn I element. Proc Natl Acad Sci U S A 1984 1.52
19 The Evi1 proto-oncogene is required at midgestation for neural, heart, and paraxial mesenchyme development. Mech Dev 1997 1.49
20 Gsh-1, an orphan Hox gene, is required for normal pituitary development. EMBO J 1996 1.49
21 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
22 Gsh-1: a novel murine homeobox gene expressed in the central nervous system. Dev Dyn 1995 1.37
23 Abnormal uterine stromal and glandular function associated with maternal reproductive defects in Hoxa-11 null mice. Biol Reprod 1997 1.37
24 Cyp1a2(-/-) null mutant mice develop normally but show deficient drug metabolism. Proc Natl Acad Sci U S A 1996 1.35
25 Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney. Development 2001 1.31
26 Two-dimensional restriction analysis of the Bacillus subtilis genome: gene purification and ribosomal ribonucleic acid gene organization. J Bacteriol 1977 1.29
27 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
28 L1 sequences in HeLa extrachromosomal circular DNA: evidence for circularization by homologous recombination. Proc Natl Acad Sci U S A 1985 1.24
29 Characterization of npas3, a novel basic helix-loop-helix PAS gene expressed in the developing mouse nervous system. Mech Dev 1999 1.22
30 Gsh-2, a murine homeobox gene expressed in the developing brain. Mech Dev 1995 1.18
31 Altered forebrain and hindbrain development in mice mutant for the Gsh-2 homeobox gene. Dev Biol 1997 1.17
32 DNA sequence analysis of a Drosophila foldback transposable element rearrangement. Mol Gen Genet 1982 1.15
33 Mys, a family of mammalian transposable elements isolated by phylogenetic screening. Nature 1985 1.14
34 legless insertional mutation: morphological, molecular, and genetic characterization. Genes Dev 1991 1.13
35 Unusual domains of human alphoid satellite DNA with contiguous non-satellite sequences: sequence analysis of a junction region. Nucleic Acids Res 1983 1.09
36 Dissecting a locus control region: facilitation of enhancer function by extended enhancer-flanking sequences. Mol Cell Biol 1995 1.08
37 prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme. Development 1999 1.07
38 Identification of 10 murine homeobox genes. Proc Natl Acad Sci U S A 1991 1.07
39 A novel murine homeobox gene isolated by a tissue specific PCR cloning strategy. Nucleic Acids Res 1992 1.05
40 Targeted ablation of alpha-crystallin-synthesizing cells produces lens-deficient eyes in transgenic mice. Development 1989 1.01
41 Legless, a novel mutation found in PHT1-1 transgenic mice. Science 1988 1.00
42 Functional equivalence and rescue among group 11 Hox gene products in vertebral patterning. Dev Biol 1996 0.99
43 Evaluating the human engineering of microprocessor-controlled operating room devices. J Clin Monit 1991 0.95
44 The two-dimensional fractionation of drosophila DNA. Cold Spring Harb Symp Quant Biol 1978 0.95
45 Homeobox genes and heart development. Trends Cardiovasc Med 2011 0.95
46 Molecular motors: the driving force behind mammalian left-right development. Trends Cell Biol 2000 0.94
47 Functional specificity of the Hoxa13 homeobox. Development 2001 0.94
48 Characterization of Hoxa-10/Hoxa-11 transheterozygotes reveals functional redundancy and regulatory interactions. Dev Biol 2000 0.93
49 Phenotypic characterization of the transgenic mouse insertional mutation, legless. J Exp Zool 1990 0.93
50 Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis. Dev Biol 1999 0.92
51 Complete foldback transposable elements encode a novel protein found in Drosophila melanogaster. EMBO J 1989 0.91
52 Novel cell lines promote the discovery of genes involved in early heart development. Dev Biol 2001 0.87
53 Multidimensional restriction enzyme analysis of complex genomes. Anal Biochem 1976 0.87
54 Spx1, a novel X-linked homeobox gene expressed during spermatogenesis. Mech Dev 1997 0.84
55 Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities. J Exp Zool 1992 0.84
56 Analysis of possible repressor elements in the 5'-flanking region of the human beta-globin gene. DNA 1989 0.83
57 Phylogenetic screening of the human genome: identification of differentially hybridizing repetitive sequence families. Mol Biol Evol 1987 0.81
58 Ectopic expression of Hox-2.3 induces craniofacial and skeletal malformations in transgenic mice. Mech Dev 1992 0.81
59 Correlation of forelimb malformation asymmetries with visceral organ situs in the transgenic mouse insertional mutation, legless. Dev Biol 1993 0.80
60 Distinct subfamilies of primate L1Gg retroposons, with some elements carrying tandem repeats in the 5' region. Nucleic Acids Res 1988 0.80
61 Genomic organization and chromosome localization of the murine homeobox gene Pmx. Genomics 1994 0.79
62 Mys retrotransposons in Peromyscus leucopus and transgenic Mus musculus. Nucleic Acids Res 1988 0.79
63 Structural and functional characterization of the mouse Hlx homeobox gene. Mamm Genome 2000 0.79
64 Malformations of the heart, kidney, palate, and skeleton in alpha-MHC-Hoxb-7 transgenic mice. Mech Dev 1995 0.78
65 Lens structures exist transiently in development of transgenic mice carrying an alpha-crystallin-diphtheria toxin hybrid gene. Exp Eye Res 1992 0.78
66 Two CCAAT boxes in a novel inverted repeat motif are required for Hlx homeobox gene expression. Biochim Biophys Acta 2001 0.78
67 An enhancer LEF-1/TCF-1 site is essential for insertion site-independent transgene expression in thymus. Nucleic Acids Res 1996 0.78
68 Novel strategy yields candidate Gsh-1 homeobox gene targets using hypothalamus progenitor cell lines. Dev Biol 1999 0.77
69 pPyLT1 does not always dictate the formation of autonomously replicating elements in transgenic mice. Nucleic Acids Res 1987 0.75
70 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
71 Enhanced expression of limb malformations and axial skeleton alterations in legless mutants by transplacental exposure to retinoic acid. Dev Biol 1994 0.75
72 Exacerbation of limb malformations in legless (lgl) homozygotes by retinoic acid (RA). Prog Clin Biol Res 1993 0.75
73 Overlapping transcriptional units on the same strand within the murine beta-glucuronidase gene complex. J Biol Chem 1988 0.75