PubRank

A M Frischauf

Author PubWeight™ 156.92‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Lambda replacement vectors carrying polylinker sequences. J Mol Biol 1983 32.76
2 A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 1990 10.97
3 Nucleotide sequence of cdna coding for Semliki Forest virus membrane glycoproteins. Nature 1980 8.07
4 Rapid restriction mapping of DNA cloned in lambda phage vectors. Gene 1984 6.25
5 The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nat Genet 1996 4.59
6 Selective isolation of cosmid clones by homologous recombination in Escherichia coli. Proc Natl Acad Sci U S A 1984 4.11
7 A subcloning strategy for DNA sequence analysis. Nucleic Acids Res 1980 4.06
8 Construction and characterization of a 2.5-kilobase procollagen clone. Proc Natl Acad Sci U S A 1978 3.26
9 The capsid protein of Semliki Forest virus has clusters of basic amino acids and prolines in its amino-terminal region. Proc Natl Acad Sci U S A 1980 3.26
10 Covalent attachment of DNA to agarose. Improved synthesis and use in affinity chromatography. Eur J Biochem 1975 3.18
11 Isolation of genomic DNA. Methods Enzymol 1987 2.74
12 Skeletal muscle actin mRNA. Characterization of the 3' untranslated region. Nucleic Acids Res 1981 2.67
13 CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli. Proc Natl Acad Sci U S A 1989 2.66
14 Construction and use of human chromosome jumping libraries from NotI-digested DNA. Nature 1987 2.58
15 Molecular clones of the mouse t complex derived from microdissected metaphase chromosomes. Cell 1984 2.55
16 Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster. Hum Mol Genet 2001 2.46
17 Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes. Cell 1986 2.40
18 Procollagen complementary DNA, a probe for messenger RNA purification and the number of type I collagen genes. Biochemistry 1978 2.37
19 Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene. Somat Cell Mol Genet 1991 2.23
20 Construction of recombinant plasmids containing rat muscle actin and myosin light chain DNA sequences. Proc Natl Acad Sci U S A 1980 2.17
21 Construction and characterization of pro alpha 1 collagen complementary deoxyribonucleic acid clones. Biochemistry 1979 2.08
22 Molecular approaches to mammalian genetics. Cold Spring Harb Symp Quant Biol 1986 1.99
23 Molecular probes define different regions of the mouse t complex. Cell 1985 1.65
24 Construction and characterization of a genomic library in lambda. Methods Enzymol 1987 1.60
25 Brain tubulin and actin cDNA sequences: isolation of recombinant plasmids. Nucleic Acids Res 1980 1.35
26 Lambda phage vectors--EMBL series. Methods Enzymol 1987 1.28
27 Molecular evidence for the rapid propagation of mouse t haplotypes from a single, recent, ancestral chromosome. Mol Biol Evol 1987 1.27
28 The CD39-like gene family: identification of three new human members (CD39L2, CD39L3, and CD39L4), their murine homologues, and a member of the gene family from Drosophila melanogaster. Genomics 1998 1.24
29 A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13. Hum Mol Genet 1993 1.23
30 Distribution and developmentally regulated expression of murine polycystin. Am J Physiol 1997 1.23
31 Germline mutations of the CDKN2 gene in UK melanoma families. Hum Mol Genet 1997 1.19
32 Deletion and duplication of DNA sequences is associated with the embryonic lethal phenotype of the t9 complementation group of the mouse t complex. Genes Dev 1987 1.19
33 Isolation and translation of calvaria procollagen messenger ribonucleic acids. Biochemistry 1976 1.17
34 The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome. Nature 1989 1.17
35 A family of cosmid vectors with the multi-copy R6K replication origin. Gene 1987 1.16
36 The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region. Genomics 1992 1.12
37 Nucleotide sequence of cloned cDNA coding for honeybee prepromelittin. Eur J Biochem 1983 1.12
38 Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. Am J Hum Genet 1993 1.12
39 Cooperation between GLI and JUN enhances transcription of JUN and selected GLI target genes. Oncogene 2009 1.06
40 PHF2, a novel PHD finger gene located on human chromosome 9q22. Mamm Genome 1999 1.04
41 Construction and characterization of type II collagen complementary deoxyribonucleic acid clones. Nucleic Acids Res 1983 1.03
42 Digestion of DNA: size fractionation. Methods Enzymol 1987 1.03
43 Affinity labeling of E. coli RNA polymerase with substrate and template analogues. Biochem Biophys Res Commun 1973 0.96
44 A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene. Genomics 1989 0.94
45 Expression and characterization of soluble and membrane-bound human nucleoside triphosphate diphosphohydrolase 6 (CD39L2). J Biol Chem 2000 0.93
46 Genetic heterogeneity in familial malignant melanoma. Hum Mol Genet 1994 0.92
47 Isolation and characterization of cDNA clones from mouse skeletal muscle actin mRNA. DNA 1986 0.91
48 FKHL15, a new human member of the forkhead gene family located on chromosome 9q22. Genomics 1997 0.90
49 Construction of a map of chromosome 16 by using radiation hybrids. Proc Natl Acad Sci U S A 1992 0.89
50 Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domain. Genomics 2001 0.88
51 Analysis of gene expression using high-density and IFN-gamma-specific low-density cDNA arrays. Genomics 2001 0.87
52 Expression and differential splicing of the mouse TSC2 homolog. Mamm Genome 1996 0.86
53 Molecular tools for the mapping of the human genome. Prog Clin Biol Res 1985 0.83
54 Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1). Genomics 1992 0.83
55 The mouse homolog of PKD1: sequence analysis and alternative splicing. Mamm Genome 1997 0.83
56 Cloning and mapping of a human and mouse gene with homology to ecto-ATPase genes. Mamm Genome 1997 0.83
57 Saturating the region of the polycystic kidney disease gene with NotI linking clones. Am J Hum Genet 1991 0.82
58 Mapping around the Fused locus on mouse chromosome 17. Mamm Genome 1995 0.82
59 The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI). Genomics 1998 0.81
60 Radiation hybrid map spanning the Huntington disease gene region of chromosome 4. Genomics 1992 0.81
61 cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases. Mamm Genome 1998 0.80
62 Construction and regional localization of clones from a NotI linking library from human chromosome 17q. Genomics 1991 0.80
63 Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4. Mol Cell Probes 1992 0.80
64 Cloning, mapping and expression of UBL3, a novel ubiquitin-like gene. Gene 1999 0.79
65 The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3. Genomics 1995 0.78
66 Yeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region. Proc Natl Acad Sci U S A 1992 0.78
67 Purification of a phosphodiesterase from Bothrops atrox venom by affinity chromatography. Eur J Biochem 1973 0.78
68 Genetic analysis of colorectal cancer. Princess Takamatsu Symp 1989 0.78
69 Mouse cyclin F maps to a conserved linkage group on mouse chromosome 17. Mamm Genome 1995 0.78
70 A novel cyclin gene (CCNF) in the region of the polycystic kidney disease gene (PKD1). Genomics 1994 0.77
71 Structural motifs of the PKD1 protein. Nephrol Dial Transplant 1996 0.76
72 Haplotype analysis in autosomal dominant polycystic kidney disease. J Med Genet 1995 0.75
73 The molecular genetics of autosomal-dominant polycystic kidney disease of the PKD1 type. Contrib Nephrol 1992 0.75
74 A high-resolution radiation hybrid map of the region surrounding the Gorlin syndrome gene. Eur J Hum Genet 1996 0.75
75 Nuclear cap binding protein maps close to the xeroderma pigmentosum complementation group A (XPA) locus in human and mouse. Genomics 1996 0.75
76 Affinity chromatography of phosphodiesterase from snake venom. Methods Enzymol 1974 0.75
77 Gorlin syndrome: identification of 4 novel germ-line mutations of the human patched (PTCH) gene. Mutations in brief no. 137. Online. Hum Mutat 1998 0.75