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Farida Latif

Showing results (61-70 of 84) with videos related to

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Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Cancer Research|June 3, 2005
Tumor suppressor activity and epigenetic inactivation of hepatocyte growth factor activator inhibitor type 2/SPINT2 in papillary and clear cell renal cell carcinomaMark R Morris, Dean Gentle, Mahera Abdulrahman, et al.
Molecular Cancer|June 5, 2009
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinomaFiona E McRonald, Mark R Morris, Dean Gentle, et al.
Human Mutation|May 4, 2011
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stabilityMichael S Nahorski, Anne Reiman, Derek H K Lim, et al.
Genes, Chromosomes & Cancer|February 25, 2017
ETV transcriptional upregulation is more reliable than RNA sequencing algorithms and FISH in diagnosing round cell sarcomas with CIC gene rearrangementsYu-Chien Kao, Yun-Shao Sung, Chun-Liang Chen, et al.
Oncogene|March 12, 2003
Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancersAngelo Agathanggelou, Ashraf Dallol, Sabine Zöchbauer-Müller, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 17, 2008
Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCNEmma R Woodward, Christopher Ricketts, Pip Killick, et al.
Clinical Endocrinology|February 21, 2004
Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibilityDewi Astuti, Niki Hart-Holden, Farida Latif, et al.
The Journal of Pathology|March 14, 2018
Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1-SS18 gene fusionAbdullah Alholle, Marie Karanian, Anna T Brini, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Cancer Research|June 3, 2005
Tumor suppressor activity and epigenetic inactivation of hepatocyte growth factor activator inhibitor type 2/SPINT2 in papillary and clear cell renal cell carcinomaMark R Morris, Dean Gentle, Mahera Abdulrahman, et al.
Molecular Cancer|June 5, 2009
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinomaFiona E McRonald, Mark R Morris, Dean Gentle, et al.
Human Mutation|May 4, 2011
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stabilityMichael S Nahorski, Anne Reiman, Derek H K Lim, et al.
Genes, Chromosomes & Cancer|February 25, 2017
ETV transcriptional upregulation is more reliable than RNA sequencing algorithms and FISH in diagnosing round cell sarcomas with CIC gene rearrangementsYu-Chien Kao, Yun-Shao Sung, Chun-Liang Chen, et al.
Oncogene|March 12, 2003
Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancersAngelo Agathanggelou, Ashraf Dallol, Sabine Zöchbauer-Müller, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 17, 2008
Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCNEmma R Woodward, Christopher Ricketts, Pip Killick, et al.
Clinical Endocrinology|February 21, 2004
Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibilityDewi Astuti, Niki Hart-Holden, Farida Latif, et al.
The Journal of Pathology|March 14, 2018
Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1-SS18 gene fusionAbdullah Alholle, Marie Karanian, Anna T Brini, et al.
Pageof 9