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M F Arlt

Showing results (1-10 of 9) with videos related to

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Cytogenetic and Genome Research|October 4, 2003
Common fragile sitesM F Arlt, A M Casper, T W Glover
Disease Markers|August 1, 1996
Dinucleotide repeat in the third intron of the FABP3/MDGI putative tumor suppressor geneM F Arlt, P J Goodfellow, J N Rottman
Genomics|April 7, 1999
A 1-Mb bacterial clone contig spanning the endometrial cancer deletion region at 1p32-p33M F Arlt, M Li, T J Herzog, et al.
Oncogene|May 30, 2006
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.
Gynecologic Oncology|February 1, 1996
Loss of heterozygosity of chromosome 3p sequences is an infrequent event in endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Gene|March 20, 2001
Cloning, characterization and chromosome mapping of the human SOX6 geneO Cohen-Barak, N Hagiwara, M F Arlt, et al.
Human Molecular Genetics|July 1, 1996
Frequent deletion of chromosome 1p sequences in an aggressive histologic subtype of endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Genes, Chromosomes & Cancer|February 15, 2001
Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinomaJ M Fang, M F Arlt, A C Burgess, et al.
American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Cytogenetic and Genome Research|October 4, 2003
Common fragile sitesM F Arlt, A M Casper, T W Glover
Disease Markers|August 1, 1996
Dinucleotide repeat in the third intron of the FABP3/MDGI putative tumor suppressor geneM F Arlt, P J Goodfellow, J N Rottman
Genomics|April 7, 1999
A 1-Mb bacterial clone contig spanning the endometrial cancer deletion region at 1p32-p33M F Arlt, M Li, T J Herzog, et al.
Oncogene|May 30, 2006
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.
Gynecologic Oncology|February 1, 1996
Loss of heterozygosity of chromosome 3p sequences is an infrequent event in endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Gene|March 20, 2001
Cloning, characterization and chromosome mapping of the human SOX6 geneO Cohen-Barak, N Hagiwara, M F Arlt, et al.
Human Molecular Genetics|July 1, 1996
Frequent deletion of chromosome 1p sequences in an aggressive histologic subtype of endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Genes, Chromosomes & Cancer|February 15, 2001
Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinomaJ M Fang, M F Arlt, A C Burgess, et al.
American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.
Pageof 1