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Development (Cambridge, England)
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August 18, 2012
Centrosome movements in vivo correlate with specific neurite formation downstream of LIM homeodomain transcription factor activity
Erica F Andersen, Mary C Halloran
Neural Development
|
May 31, 2011
In vivo imaging of cell behaviors and F-actin reveals LIM-HD transcription factor regulation of peripheral versus central sensory axon development
Erica F Andersen, Namrata S Asuri, Mary C Halloran
American Journal of Clinical Pathology
|
June 24, 2021
Flow Cytometry Is More Sensitive Than Fluorescence In Situ Hybridization for Detecting Minimal Residual Disease
David P Ng, Rodney R Miles, Erica F Andersen, et al.
American Journal of Medical Genetics. Part A
|
April 5, 2014
Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability
Erica F Andersen, Erin E Baldwin, Sara Ellingwood, et al.
Molecular and Cellular Biology
|
August 2, 2005
Subunit contributions to histone methyltransferase activities of fly and worm polycomb group complexes
Carrie S Ketel, Erica F Andersen, Marcus L Vargas, et al.
Cytogenetic and Genome Research
|
September 6, 2019
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay
Prabakaran Paulraj, Michelle Bosworth, Maria Longhurst, et al.
Molecular and Cellular Biology
|
October 9, 2013
Elements of the polycomb repressor SU(Z)12 needed for histone H3-K27 methylation, the interface with E(Z), and in vivo function
Aswathy N Rai, Marcus L Vargas, Liangjun Wang, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2013
Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome
Erica F Andersen, John C Carey, Dawn L Earl, et al.
Genes, Chromosomes & Cancer
|
February 2, 2019
Pediatric acute myeloid leukemia with t(7;21)(p22;q22)
Prabakaran Paulraj, Steven Diamond, Faisal Razzaqi, et al.
European Journal of Human Genetics : EJHG
|
July 8, 2025
Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family
Ting Wen, Gulsen Akay, Janice Palumbos, et al.
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of 3
Search research articles
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Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Development (Cambridge, England)
|
August 18, 2012
Centrosome movements in vivo correlate with specific neurite formation downstream of LIM homeodomain transcription factor activity
Erica F Andersen, Mary C Halloran
Neural Development
|
May 31, 2011
In vivo imaging of cell behaviors and F-actin reveals LIM-HD transcription factor regulation of peripheral versus central sensory axon development
Erica F Andersen, Namrata S Asuri, Mary C Halloran
American Journal of Clinical Pathology
|
June 24, 2021
Flow Cytometry Is More Sensitive Than Fluorescence In Situ Hybridization for Detecting Minimal Residual Disease
David P Ng, Rodney R Miles, Erica F Andersen, et al.
American Journal of Medical Genetics. Part A
|
April 5, 2014
Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability
Erica F Andersen, Erin E Baldwin, Sara Ellingwood, et al.
Molecular and Cellular Biology
|
August 2, 2005
Subunit contributions to histone methyltransferase activities of fly and worm polycomb group complexes
Carrie S Ketel, Erica F Andersen, Marcus L Vargas, et al.
Cytogenetic and Genome Research
|
September 6, 2019
A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay
Prabakaran Paulraj, Michelle Bosworth, Maria Longhurst, et al.
Molecular and Cellular Biology
|
October 9, 2013
Elements of the polycomb repressor SU(Z)12 needed for histone H3-K27 methylation, the interface with E(Z), and in vivo function
Aswathy N Rai, Marcus L Vargas, Liangjun Wang, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2013
Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome
Erica F Andersen, John C Carey, Dawn L Earl, et al.
Genes, Chromosomes & Cancer
|
February 2, 2019
Pediatric acute myeloid leukemia with t(7;21)(p22;q22)
Prabakaran Paulraj, Steven Diamond, Faisal Razzaqi, et al.
European Journal of Human Genetics : EJHG
|
July 8, 2025
Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family
Ting Wen, Gulsen Akay, Janice Palumbos, et al.
Page
of 3