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A Fernald

Showing results (41-50 of 52) with videos related to

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Frontiers in Immunology|March 22, 2024
Dysregulated FGFR3 signaling alters the immune landscape in bladder cancer and presents therapeutic possibilities in an agent-based modelDaniel R Bergman, Yixuan Wang, Erica Trujillo, et al.
Human Molecular Genetics|January 1, 1997
Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domainsD Broccoli, L Chong, S Oelmann, et al.
Genes, Chromosomes & Cancer|August 1, 1993
Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridizationH Kobayashi, R Espinosa, M J Thirman, et al.
Blood|July 15, 1993
Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridizationH Kobayashi, R Espinosa, M J Thirman, et al.
Leukemia|April 17, 2009
Enhanced expression of FHL2 leads to abnormal myelopoiesis in vivoZ Qian, L Mao, A A Fernald, et al.
Blood Cancer Discovery|September 14, 2020
Cytotoxic Therapy-Induced Effects on Both Hematopoietic and Marrow Stromal Cells Promotes Therapy-Related Myeloid NeoplasmsAngela Stoddart, Jianghong Wang, Anthony A Fernald, et al.
Blood|April 11, 2007
Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disordersJohn M Joslin, Anthony A Fernald, Thelma R Tennant, et al.
Genomics|June 10, 1995
Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiencyM R el-Maghrabi, A J Lange, W Jiang, et al.
Blood|June 15, 1992
Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimensR B Jenkins, M M Le Beau, W J Kraker, et al.
Genomics|February 13, 2001
Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q)F Lai, L A Godley, J Joslin, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Immunology|March 22, 2024
Dysregulated FGFR3 signaling alters the immune landscape in bladder cancer and presents therapeutic possibilities in an agent-based modelDaniel R Bergman, Yixuan Wang, Erica Trujillo, et al.
Human Molecular Genetics|January 1, 1997
Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domainsD Broccoli, L Chong, S Oelmann, et al.
Genes, Chromosomes & Cancer|August 1, 1993
Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridizationH Kobayashi, R Espinosa, M J Thirman, et al.
Blood|July 15, 1993
Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridizationH Kobayashi, R Espinosa, M J Thirman, et al.
Leukemia|April 17, 2009
Enhanced expression of FHL2 leads to abnormal myelopoiesis in vivoZ Qian, L Mao, A A Fernald, et al.
Blood Cancer Discovery|September 14, 2020
Cytotoxic Therapy-Induced Effects on Both Hematopoietic and Marrow Stromal Cells Promotes Therapy-Related Myeloid NeoplasmsAngela Stoddart, Jianghong Wang, Anthony A Fernald, et al.
Blood|April 11, 2007
Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disordersJohn M Joslin, Anthony A Fernald, Thelma R Tennant, et al.
Genomics|June 10, 1995
Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiencyM R el-Maghrabi, A J Lange, W Jiang, et al.
Blood|June 15, 1992
Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimensR B Jenkins, M M Le Beau, W J Kraker, et al.
Genomics|February 13, 2001
Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q)F Lai, L A Godley, J Joslin, et al.
Pageof 6