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Naomi L Bowers

Showing results (1-10 of 24) with videos related to

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Cancer Genetics|June 17, 2014
SMARCB1 mutations in schwannomatosis and genotype correlations with rhabdoid tumorsMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
Human Molecular Genetics|May 16, 2006
Frequent genetic and epigenetic abnormalities contribute to the deregulation of cytoglobin in non-small cell lung cancerGeorge Xinarianos, Fiona E McRonald, Janet M Risk, et al.
Oral Oncology|January 30, 2007
CpG island methylation phenotype (CIMP) in oral cancer: associated with a marked inflammatory response and less aggressive tumour biologyRichard J Shaw, Gillian L Hall, Derek Lowe, et al.
Lung Cancer (Amsterdam, Netherlands)|January 13, 2006
Cyclin D1 (CCND1) A870G gene polymorphism modulates smoking-induced lung cancer risk and response to platinum-based chemotherapy in non-small cell lung cancer (NSCLC) patientsOliver Gautschi, Barbara Hugli, Annemarie Ziegler, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosisMiriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
Neurogenetics|March 22, 2012
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
BMJ Case Reports|November 20, 2014
A patient with mosaic neurofibromatosis type 2 presenting with early onset meningiomaYoyo Wing-Yiu Chu, Daniel Ka Leung Cheuk, Brian Hon Yin Chung, et al.
Human Mutation|June 20, 2022
Screening of potential novel candidate genes in schwannomatosis patientsCristina Perez-Becerril, Andrew J Wallace, Helene Schlecht, et al.
Human Mutation|December 1, 2015
The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing SyndromesMiriam J Smith, Jill E Urquhart, Elaine F Harkness, et al.
Cancers|February 13, 2020
Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in <i>BRCA1, BRCA2</i>, and <i>TP53</i> Genes in Women with Very Early-Onset (<36 Years) Breast CancerZerin Hyder, Elaine F Harkness, Emma R Woodward, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Cancer Genetics|June 17, 2014
SMARCB1 mutations in schwannomatosis and genotype correlations with rhabdoid tumorsMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
Human Molecular Genetics|May 16, 2006
Frequent genetic and epigenetic abnormalities contribute to the deregulation of cytoglobin in non-small cell lung cancerGeorge Xinarianos, Fiona E McRonald, Janet M Risk, et al.
Oral Oncology|January 30, 2007
CpG island methylation phenotype (CIMP) in oral cancer: associated with a marked inflammatory response and less aggressive tumour biologyRichard J Shaw, Gillian L Hall, Derek Lowe, et al.
Lung Cancer (Amsterdam, Netherlands)|January 13, 2006
Cyclin D1 (CCND1) A870G gene polymorphism modulates smoking-induced lung cancer risk and response to platinum-based chemotherapy in non-small cell lung cancer (NSCLC) patientsOliver Gautschi, Barbara Hugli, Annemarie Ziegler, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosisMiriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
Neurogenetics|March 22, 2012
Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisMiriam J Smith, Andrew J Wallace, Naomi L Bowers, et al.
BMJ Case Reports|November 20, 2014
A patient with mosaic neurofibromatosis type 2 presenting with early onset meningiomaYoyo Wing-Yiu Chu, Daniel Ka Leung Cheuk, Brian Hon Yin Chung, et al.
Human Mutation|June 20, 2022
Screening of potential novel candidate genes in schwannomatosis patientsCristina Perez-Becerril, Andrew J Wallace, Helene Schlecht, et al.
Human Mutation|December 1, 2015
The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing SyndromesMiriam J Smith, Jill E Urquhart, Elaine F Harkness, et al.
Cancers|February 13, 2020
Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in <i>BRCA1, BRCA2</i>, and <i>TP53</i> Genes in Women with Very Early-Onset (<36 Years) Breast CancerZerin Hyder, Elaine F Harkness, Emma R Woodward, et al.
Pageof 3