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F B Axelrod

Showing results (71-80 of 79) with videos related to

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Genomics|February 10, 1995
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia geneS A Slaugenhaupt, A Blumenfeld, C B Liebert, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Journal of Medical Genetics|January 1, 1993
Exclusion of familial dysautonomia from more than 60% of the genomeA Blumenfeld, F B Axelrod, J A Trofatter, et al.
Autonomic Neuroscience : Basic & Clinical|October 15, 2008
Advanced electrocardiographic predictors of mortality in familial dysautonomiaI Solaimanzadeh, T T Schlegel, A H Feiveson, et al.
Gene|November 24, 1999
Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 geneB P Chadwick, S Gill, M Leyne, et al.
Genomics|June 22, 1999
Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31B P Chadwick, J Mull, L A Helbling, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Cloning, mapping, and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31B P Chadwick, M Leyne, S Gill, et al.
American Journal of Human Genetics|March 26, 1999
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31A Blumenfeld, S A Slaugenhaupt, C B Liebert, et al.
American Journal of Human Genetics|February 17, 2001
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomiaS A Slaugenhaupt, A Blumenfeld, S P Gill, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Genomics|February 10, 1995
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia geneS A Slaugenhaupt, A Blumenfeld, C B Liebert, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Journal of Medical Genetics|January 1, 1993
Exclusion of familial dysautonomia from more than 60% of the genomeA Blumenfeld, F B Axelrod, J A Trofatter, et al.
Autonomic Neuroscience : Basic & Clinical|October 15, 2008
Advanced electrocardiographic predictors of mortality in familial dysautonomiaI Solaimanzadeh, T T Schlegel, A H Feiveson, et al.
Gene|November 24, 1999
Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 geneB P Chadwick, S Gill, M Leyne, et al.
Genomics|June 22, 1999
Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31B P Chadwick, J Mull, L A Helbling, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
Cloning, mapping, and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31B P Chadwick, M Leyne, S Gill, et al.
American Journal of Human Genetics|March 26, 1999
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31A Blumenfeld, S A Slaugenhaupt, C B Liebert, et al.
American Journal of Human Genetics|February 17, 2001
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomiaS A Slaugenhaupt, A Blumenfeld, S P Gill, et al.
Pageof 8