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Mark R Morris

Showing results (31-40 of 37) with videos related to

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Cancer Discovery|April 16, 2015
Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell CarcinomaMariam Jafri, Naomi C Wake, David B Ascher, et al.
Genes, Chromosomes & Cancer|January 6, 2007
Characterization of a 3;6 translocation associated with renal cell carcinomaRebecca E Foster, Mahera Abdulrahman, Mark R Morris, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Plos Genetics|February 9, 2010
Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman diseaseNeil V Morgan, Mark R Morris, Hakan Cangul, et al.
Nature Genetics|February 7, 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibilityDewi Astuti, Mark R Morris, Wendy N Cooper, et al.
Clinical Epigenetics|June 9, 2015
The GALNT9, BNC1 and CCDC8 genes are frequently epigenetically dysregulated in breast tumours that metastasise to the brainRajendra P Pangeni, Prasanna Channathodiyil, David S Huen, et al.
Science (New York, N.Y.)|July 27, 2019
Relativistic redshift of the star S0-2 orbiting the Galactic Center supermassive black holeTuan Do, Aurelien Hees, Andrea Ghez, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Cancer Discovery|April 16, 2015
Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell CarcinomaMariam Jafri, Naomi C Wake, David B Ascher, et al.
Genes, Chromosomes & Cancer|January 6, 2007
Characterization of a 3;6 translocation associated with renal cell carcinomaRebecca E Foster, Mahera Abdulrahman, Mark R Morris, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
Plos Genetics|February 9, 2010
Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman diseaseNeil V Morgan, Mark R Morris, Hakan Cangul, et al.
Nature Genetics|February 7, 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibilityDewi Astuti, Mark R Morris, Wendy N Cooper, et al.
Clinical Epigenetics|June 9, 2015
The GALNT9, BNC1 and CCDC8 genes are frequently epigenetically dysregulated in breast tumours that metastasise to the brainRajendra P Pangeni, Prasanna Channathodiyil, David S Huen, et al.
Science (New York, N.Y.)|July 27, 2019
Relativistic redshift of the star S0-2 orbiting the Galactic Center supermassive black holeTuan Do, Aurelien Hees, Andrea Ghez, et al.
Pageof 4