M W Krause

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc A widespread distribution of genomic CeMyoD binding sites revealed and cross validated by ChIP-Chip and ChIP-Seq techniques
    Haiyan Lei
    National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America
    PLoS ONE 5:e15898. 2010
  2. pmc Somatic muscle specification during embryonic and post-embryonic development in the nematode C. elegans
    Michael Krause
    Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA
    Wiley Interdiscip Rev Dev Biol 1:203-14. 2012
  3. ncbi request reprint A C. elegans E/Daughterless bHLH protein marks neuronal but not striated muscle development
    M Krause
    Laboratory of Molecular Biology, NIDDK, NIH, Bethesda, MD 20892 0510, USA
    Development 124:2179-89. 1997
  4. ncbi request reprint Regulation of postembryonic G(1) cell cycle progression in Caenorhabditis elegans by a cyclin D/CDK-like complex
    M Park
    Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Building 5, Room B1 04, Bethesda, Maryland 20892 0510, USA
    Development 126:4849-60. 1999
  5. ncbi request reprint The IA-2 gene family: homologs in Caenorhabditis elegans, Drosophila and zebrafish
    T Cai
    Experimental Medicine Section, Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892 4322, USA
    Diabetologia 44:81-8. 2001
  6. ncbi request reprint Supplementary nuclear receptor NHR-60 is required for normal embryonic and early larval development of Caenorhabditis elegans
    K Simeckova
    Laboratory of Molecular Biology and Genetics, Institute of Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University, Prague, Czech Republic
    Folia Biol (Praha) 53:85-96. 2007

Collaborators

  • Jun Liu
  • J Yuan
  • I Greenwald
  • A Fire
  • Haiyan Lei
  • K Simeckova
  • T Cai
  • Valerie Reinke
  • Mihail Sarov
  • Tetsunari Fukushige
  • Wei Niu
  • M Park
  • M Pohludka
  • M Kostrouchova
  • Z Kostrouch
  • E Brozova
  • J E Rall
  • J Vohanka
  • A L Notkins
  • R Toyama
  • W F Odenwald

Detail Information

Publications6

  1. pmc A widespread distribution of genomic CeMyoD binding sites revealed and cross validated by ChIP-Chip and ChIP-Seq techniques
    Haiyan Lei
    National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America
    PLoS ONE 5:e15898. 2010
    ..Our results also provide a comparison of ChIP methodologies that can overcome limitations commonly encountered in these types of studies while highlighting the complications of assigning in vivo functions to identified target sites...
  2. pmc Somatic muscle specification during embryonic and post-embryonic development in the nematode C. elegans
    Michael Krause
    Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA
    Wiley Interdiscip Rev Dev Biol 1:203-14. 2012
    ..Comparisons of myogenesis between C. elegans and other model systems provide insights into the evolution of contractile cell types, demonstrating the conservation of regulatory schemes for muscles throughout the animal kingdom...
  3. ncbi request reprint A C. elegans E/Daughterless bHLH protein marks neuronal but not striated muscle development
    M Krause
    Laboratory of Molecular Biology, NIDDK, NIH, Bethesda, MD 20892 0510, USA
    Development 124:2179-89. 1997
    ..These studies suggest multiple roles for CeE/DA in C. elegans development and provide evidence that both common and alternative strategies have evolved for the use of related HLH proteins in controlling cell fates in different species...
  4. ncbi request reprint Regulation of postembryonic G(1) cell cycle progression in Caenorhabditis elegans by a cyclin D/CDK-like complex
    M Park
    Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Building 5, Room B1 04, Bethesda, Maryland 20892 0510, USA
    Development 126:4849-60. 1999
    ..We propose that the cyd-1 and cdk-4 gene products are an integral part of the developmental control of larval cell proliferation through the regulation of G(1) progression...
  5. ncbi request reprint The IA-2 gene family: homologs in Caenorhabditis elegans, Drosophila and zebrafish
    T Cai
    Experimental Medicine Section, Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland 20892 4322, USA
    Diabetologia 44:81-8. 2001
    ..We studied the evolutionary conservation of IA-2 and IA-2beta genes and searched for homologs in non-mammalian vertebrates and invertebrates...
  6. ncbi request reprint Supplementary nuclear receptor NHR-60 is required for normal embryonic and early larval development of Caenorhabditis elegans
    K Simeckova
    Laboratory of Molecular Biology and Genetics, Institute of Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University, Prague, Czech Republic
    Folia Biol (Praha) 53:85-96. 2007
    ..This adds NHR-60 to the list of C. elegans NHRs playing important roles in development...