Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
J.R Lupski

Veröffentlichungen von J.R Lupski zu Lupski, J. R. ->
weitere Veröffentlichungen von J.R Lupski:
The Haemophilus influenzae dnaG sequence and conserved bacterial primase motifs (1993)
The use of transposon Tn5 mutagenesis in the rapid generation of correlated physical and genetic maps of DNA segments cloned into multicopy plasmids - a review (1984)
Charcot-Marie-tooth disease: a new paradigm for the mechanism of inherited disease (1994)
Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13 (2000)
Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance (2000)
Possible new genes as revealed by molecular analysis of a 5-kb Escherichia coli chromosomal region 5' to the rpsU-dnaG-rpoD macromolecular-synthesis operon (1987)
Comparison of left-end DNA sequences of bacteriophages Mu and D108 (1985)
In vitro stimulation of Escherichia coli RNA polymerase sigma subunit synthesis by NusA protein (1985)
Specificity of Tn5 insertions into a 36-bp DNA sequence repeated in tandem seven times (1984)
Characterization of the macromolecular synthesis (MMS) operon from Listeria monocytogenes (1994)
Isolation of region-specific and polymorphic markers from chromosome 17 by restricted Alu polymerase chain reaction (1991)
Epidemiology of infections due to multiresistantEnterobacter aerogenes in a University Hospital (1996)
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1A neuropathy (1996)
A novel locus for Leber congenital amaurosis on chromosome 14q24 (1998)
In vitro and in vivo manipulations of bacteriophage Mu DNA: Cloning of Mu ends and construction of mini-Mu's carrying selectable markers (1981)
Veröffentlichungen zu Lupski, J. R.
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Versalovic, J., Lupski, J.R. The Haemophilus influenzae dnaG sequence and conserved bacterial primase motifs
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 136, No. 1-2 (1993), p. 281-286
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
2
de Bruijn, F.J., Lupski, J.R. The use of transposon Tn5 mutagenesis in the rapid generation of correlated physical and genetic maps of DNA segments cloned into multicopy plasmids - a review
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 27, No. 2 (1984), p. 131-149
Zugang: zum Volltext
ähnliche Vorschläge
1984
zeige Details
3
Patel, P.I., Lupski, J.R. Charcot-Marie-tooth disease: a new paradigm for the mechanism of inherited disease
in: Trends in Genetics, in: Trends in Genetics . - Amsterdam : Elsevier, ISSN 0168-9525, ZDB-ID 2010993-3 Vol. 10, No. 4 (1994), p. 128-133
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
4
Katsanis, N., Venable, S., ... Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13
in: Human genetics , ISSN 1432-1203, Vol. 106 (1. 2000), p. 66-72
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
5
Shroyer, N.F., Lewis, R.A., ... Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance
in: Human genetics , ISSN 1432-1203, Vol. 106 (2. 2000), p. 244-248
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
6
Roa, Benjamin B., Dyck, Peter J., ... Dejerine–Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 3 (1993), p. 269-273
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
7
Nesin, M., Lupski, J.R., ... Possible new genes as revealed by molecular analysis of a 5-kb Escherichia coli chromosomal region 5' to the rpsU-dnaG-rpoD macromolecular-synthesis operon
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 51, No. 2-3 (1987), p. 149-161
Zugang: zum Volltext
ähnliche Vorschläge
1987
zeige Details
8
Bukhari, A.I., Lupski, J.R., ... Comparison of left-end DNA sequences of bacteriophages Mu and D108
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 33, No. 2 (1985), p. 235-239
Zugang: zum Volltext
ähnliche Vorschläge
1985
zeige Details
9
Peacock, S., Lupski, J.R., ... In vitro stimulation of Escherichia coli RNA polymerase sigma subunit synthesis by NusA protein
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 33, No. 2 (1985), p. 227-234
Zugang: zum Volltext
ähnliche Vorschläge
1985
zeige Details
10
Lupski, J.R., Gershon, P., ... Specificity of Tn5 insertions into a 36-bp DNA sequence repeated in tandem seven times
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 30, No. 1-3 (1984), p. 99-106
Zugang: zum Volltext
ähnliche Vorschläge
1984
zeige Details
11
Metzger, R., Brown, D.P., ... Characterization of the macromolecular synthesis (MMS) operon from Listeria monocytogenes
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 151, No. 1-2 (1994), p. 161-166
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
12
Guzzetta, V., de Oca-Luna, R.M., ... Isolation of region-specific and polymorphic markers from chromosome 17 by restricted Alu polymerase chain reaction
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 9, No. 1 (1991), p. 31-36
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
13
Roa, Benjamin B., Greenberg, Frank, ... Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1A neuropathy
in: Human genetics , ISSN 1432-1203, Vol. 97 (5. 1996), p. 642-649
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
14
Warner, Laura E., Mancias, Pedro, ... Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 18, No. 4 (1998), p. 382-384
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
15
Katsanis, Nicholas, Beales, Philip L., ... Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 26, No. 1 (2000), p. 67-70
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
16
Inoue, Ken, Khajavi, Mehrdad, ... Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 36, No. 4 (2004), p. 361-369
Zugang: zum Volltext
ähnliche Vorschläge
2004
zeige Details
17
Franco, Brunella, Lai, Li-Wen, ... Molecular characterization of a patient with del(1)(q23–q25)
in: Human genetics , ISSN 1432-1203, Vol. 87 (3. 1991), p. 269-277
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
18
Allerberger, F., Koeuth, T., ... Epidemiology of infections due to multiresistantEnterobacter aerogenes in a University Hospital
in: European journal of clinical microbiology & infectious diseases , ISSN 1435-4373, Vol. 15 (6. 1996), p. 517-521
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
19
Stockton, David W., Lewis, Richard Alan, ... A novel locus for Leber congenital amaurosis on chromosome 14q24
in: Human genetics , ISSN 1432-1203, Vol. 103 (3. 1998), p. 328-333
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
20
Chaconas, G., de Bruijn, F.J., ... In vitro and in vivo manipulations of bacteriophage Mu DNA: Cloning of Mu ends and construction of mini-Mu's carrying selectable markers
in: Gene, in: Gene . - Amsterdam : Elsevier, ISSN 0378-1119, ZDB-ID 1491012-3 Vol. 13, No. 1 (1981), p. 37-46
Zugang: zum Volltext
ähnliche Vorschläge
1981