Rezultati pretrage - Robert B. Weiss

Detaljiziraj rezultate
  1. 1
    Genetic screen for cloned release factor genes

    Genetic screen for cloned release factor genes od Robert B. Weiss, James P. Murphy, Jonathan Gallant

    Izdano 1984
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  2. 2
    Ribosome gymnastics—Degree of difficulty 9.5, style 10.0

    Ribosome gymnastics—Degree of difficulty 9.5, style 10.0 od John F. Atkins, Robert B. Weiss, Raymond F. Gesteland

    Izdano 1990
    Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  3. 3
    Characterization of Hydrogenase II from the Hyperthermophilic Archaeon <i>Pyrococcus furiosus</i> and Assessment of Its Role in Sulfur Reduction

    Characterization of Hydrogenase II from the Hyperthermophilic Archaeon <i>Pyrococcus furiosus</i> and Assessment of Its Role in Sulfur Reduction od Kesen Ma, Robert B. Weiss, Michael W. W. Adams

    Izdano 2000
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  4. 4
    Template-switching during DNA synthesis by<i>Thermus aquaticus</i>DNA polymerase I

    Template-switching during DNA synthesis by<i>Thermus aquaticus</i>DNA polymerase I od Shannon J. Odelberg, Robert B. Weiss, Akira Hata, R. White

    Izdano 1995
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  5. 5
    Transcriptional slippage occurs during elongation at runs of adenine or thymine in<i>Escherichia coli</i>

    Transcriptional slippage occurs during elongation at runs of adenine or thymine in<i>Escherichia coli</i> od Lori A. Wagner, Robert B. Weiss, Robert Driscoll, Diane S. Dunn, R F Gesteland

    Izdano 1990
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  6. 6
    Long‐range genomic regulators of <i>THBS1</i> and <i>LTBP4</i> modify disease severity in duchenne muscular dystrophy

    Long‐range genomic regulators of <i>THBS1</i> and <i>LTBP4</i> modify disease severity in duchenne muscular dystrophy od Robert B. Weiss, Veronica J. Vieland, Diane M. Dunn, Yuuki Kaminoh, Kevin M. Flanigan

    Izdano 2018
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  7. 7
    <i>DMD</i>exon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6

    <i>DMD</i>exon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6 od Olga L. Gurvich, Baijayanta Maiti, Robert B. Weiss, Gaurav Aggarwal, Michael Howard, Kevin M. Flanigan

    Izdano 2009
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  8. 8
    Characterization of Native and Recombinant Forms of an Unusual Cobalt-Dependent Proline Dipeptidase (Prolidase) from the Hyperthermophilic Archaeon <i>Pyrococcus furiosus</i>

    Characterization of Native and Recombinant Forms of an Unusual Cobalt-Dependent Proline Dipeptidase (Prolidase) from the Hyperthermophilic Archaeon <i>Pyrococcus furiosus</i> od Mousumi Ghosh, Amy M. Grunden, Dianne M. Dunn, Robert B. Weiss, Michael W. W. Adams

    Izdano 1998
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  9. 9
    Reading frame switch caused by base-pair formation between the 3′ end of 16S rRNA and the mRNA during elongation of protein synthesis in Escherichia coli.

    Reading frame switch caused by base-pair formation between the 3′ end of 16S rRNA and the mRNA during elongation of protein synthesis in Escherichia coli. od Robert B. Weiss, Diane M. Dunn, Albert E. Dahĺberg, John F. Atkins, R.F. Gesteland

    Izdano 1988
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  10. 10
    DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection

    DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection od Stephen Wooding, W. Scott Watkins, Michael J. Bamshad, Diane M. Dunn, Robert B. Weiss, Lynn B. Jorde

    Izdano 2002
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  11. 11
    Rapid Direct Sequence Analysis of the Dystrophin Gene

    Rapid Direct Sequence Analysis of the Dystrophin Gene od Kevin M. Flanigan, Andrew von Niederhausern, Diane M. Dunn, Jonathan K. Alder, Jerry R. Mendell, Robert B. Weiss

    Izdano 2003
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  12. 12
    Divergence of the Hyperthermophilic Archaea Pyrococcus furiosus and P. horikoshii Inferred From Complete Genomic Sequences

    Divergence of the Hyperthermophilic Archaea Pyrococcus furiosus and P. horikoshii Inferred From Complete Genomic Sequences od Dennis Maeder, Robert B. Weiss, Diane M. Dunn, Joshua L. Cherry, Juan Miguel González Grau, Jocelyne DiRuggiero, Frank T. Robb

    Izdano 1999
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  13. 13
    Gene Expression Profiling Reveals Unique Pathways Associated with Differential Severity of Lyme Arthritis

    Gene Expression Profiling Reveals Unique Pathways Associated with Differential Severity of Lyme Arthritis od Hillary Crandall, Diane M. Dunn, Ying Ma, R. Mark Wooten, James F. Zachary, John H. Weis, Robert B. Weiss, Janis J. Weis

    Izdano 2006
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  14. 14
    Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program

    Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program od Nicholas E. Johnson, Russell J. Butterfield, Katie Mayne, Tara Newcomb, Carina Imburgia, Diane M. Dunn, Brett Duval, Marcia L. Feldkamp, Robert B. Weiss

    Izdano 2021
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  15. 15
    Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

    Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript od Diane M. Dunn, Tomoaki Ishigami, James S. Pankow, Andrew von Niederhausern, Jonathan K. Alder, Steven C. Hunt, Mark Leppert, J.-M. Lalouel, Robert B. Weiss

    Izdano 2002
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  16. 16
    Identification and characterization of transcripts from the neurofibromatosis 1 region: The sequence and genomic structure of EVI2 and mapping of other transcripts

    Identification and characterization of transcripts from the neurofibromatosis 1 region: The sequence and genomic structure of EVI2 and mapping of other transcripts od Richard Cawthon, P. OʼConnell, Arthur M. Buchberg, David Viskochil, Robert B. Weiss, Melanie Culver, Jeffrey Stevens, Nancy A. Jenkins, Neal G. Copeland, R. White

    Izdano 1990
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  17. 17
    EGO, a novel, noncoding RNA gene, regulates eosinophil granule protein transcript expression

    EGO, a novel, noncoding RNA gene, regulates eosinophil granule protein transcript expression od Lori A. Wagner, Clarissa Christensen, Diane M. Dunn, Gerald J. Spangrude, Ann Georgelas, Linda Kelley, M. Sean Esplin, Robert B. Weiss, Gerald J. Gleich

    Izdano 2007
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  18. 18
    <i>DMD</i> pseudoexon mutations: splicing efficiency, phenotype, and potential therapy

    <i>DMD</i> pseudoexon mutations: splicing efficiency, phenotype, and potential therapy od Olga L. Gurvich, Thérèse M.F. Tuohy, Michael Howard, Richard S. Finkel, Līvija Medne, Christine B. Anderson, Robert B. Weiss, Steve D. Wilton, Kevin M. Flanigan

    Izdano 2007
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  19. 19
    Fine-scaled human genetic structure revealed by SNP microarrays

    Fine-scaled human genetic structure revealed by SNP microarrays od Jinchuan Xing, W. Scott Watkins, David J. Witherspoon, Yuhua Zhang, Stephen L. Guthery, R. Thara, Bryan Mowry, Kazima Bulayeva, Robert B. Weiss, Lynn B. Jorde

    Izdano 2009
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  20. 20
    Analysis of Dystrophin Deletion Mutations Predicts Age of Cardiomyopathy Onset in Becker Muscular Dystrophy

    Analysis of Dystrophin Deletion Mutations Predicts Age of Cardiomyopathy Onset in Becker Muscular Dystrophy od Rita Wen Kaspar, Hugh D. Allen, Will C. Ray, Carlos E. Alvarez, John T. Kissel, Alan Pestronk, Robert B. Weiss, Kevin M. Flanigan, Jerry R. Mendell, Federica Montanaro

    Izdano 2009
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:

Alati za pretragu: