Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B H Paw

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Blood Cells, Molecules & Diseases|May 19, 2001
Cloning of the zebrafish retsina blood mutation: a genetic model for dyserythropoiesis and erythroid cytokinesisB H Paw
Current Opinion in Hematology|March 4, 2000
Zebrafish: a genetic approach in studying hematopoiesisB H Paw, L I Zon
Methods in Cell Biology|January 19, 1999
Primary fibroblast cell cultureB H Paw, L I Zon
The Journal of Biological Chemistry|February 25, 1988
Normal transcription of the beta-hexosaminidase alpha-chain gene in the Ashkenazi Tay-Sachs mutationB H Paw, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1989
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidaseB H Paw, M M Kaback, E F Neufeld
American Journal of Human Genetics|June 1, 1991
A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A geneB H Paw, L C Wood, E F Neufeld
Biochemistry|May 6, 1986
Isolation and properties of N epsilon-hydroxylysine:acetyl coenzyme A N epsilon-transacetylase from Escherichia coli pABN11M Coy, B H Paw, A Bindereif, et al.
Journal of Bacteriology|February 1, 1986
Aerobactin biosynthesis and transport genes of plasmid ColV-K30 in Escherichia coli K-12V de Lorenzo, A Bindereif, B H Paw, et al.
American Journal of Human Genetics|October 1, 1990
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening programB H Paw, P T Tieu, M M Kaback, et al.
The Journal of Biological Chemistry|June 5, 1990
Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidaseB H Paw, S M Moskowitz, N Uhrhammer, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Blood Cells, Molecules & Diseases|May 19, 2001
Cloning of the zebrafish retsina blood mutation: a genetic model for dyserythropoiesis and erythroid cytokinesisB H Paw
Current Opinion in Hematology|March 4, 2000
Zebrafish: a genetic approach in studying hematopoiesisB H Paw, L I Zon
Methods in Cell Biology|January 19, 1999
Primary fibroblast cell cultureB H Paw, L I Zon
The Journal of Biological Chemistry|February 25, 1988
Normal transcription of the beta-hexosaminidase alpha-chain gene in the Ashkenazi Tay-Sachs mutationB H Paw, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1989
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidaseB H Paw, M M Kaback, E F Neufeld
American Journal of Human Genetics|June 1, 1991
A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A geneB H Paw, L C Wood, E F Neufeld
Biochemistry|May 6, 1986
Isolation and properties of N epsilon-hydroxylysine:acetyl coenzyme A N epsilon-transacetylase from Escherichia coli pABN11M Coy, B H Paw, A Bindereif, et al.
Journal of Bacteriology|February 1, 1986
Aerobactin biosynthesis and transport genes of plasmid ColV-K30 in Escherichia coli K-12V de Lorenzo, A Bindereif, B H Paw, et al.
American Journal of Human Genetics|October 1, 1990
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening programB H Paw, P T Tieu, M M Kaback, et al.
The Journal of Biological Chemistry|June 5, 1990
Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidaseB H Paw, S M Moskowitz, N Uhrhammer, et al.
Pageof 2