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Edmund Cheesman

Showing results (11-20 of 25) with videos related to

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Cancer Cell|September 17, 2015
Frequent Derepression of the Mesenchymal Transcription Factor Gene FOXC1 in Acute Myeloid LeukemiaTim D D Somerville, Daniel H Wiseman, Gary J Spencer, et al.
The Journal of Pathology. Clinical Research|October 3, 2019
Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinismJayne Al Houghton, Indraneel Banerjee, Guftar Shaikh, et al.
Journal of Leukocyte Biology|September 15, 2020
Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiencyAnu Goenka, John A Doherty, Tariq Al-Farsi, et al.
Clinical Genetics|February 4, 2025
Whole Genome Sequencing to Identify Novel Germline Fumarate Hydratase Mutation in Child With Bilateral Renal Cell CarcinomaChristopher Kershaw, Leigh Demain, Eleanor Baker, et al.
The Journal of Clinical Endocrinology and Metabolism|June 13, 2017
Atypical Forms of Congenital Hyperinsulinism in Infancy Are Associated With Mosaic Patterns of Immature Islet CellsBing Han, Zainab Mohamed, Maria Salomon Estebanez, et al.
Cancer Letters|May 30, 2026
Integrated clinical, genomic and functional characterization of a novel ALK variant in neuroblastomaAna Cañadas García, Ketan Thombare, Leila Jahangiri, et al.
American Journal of Clinical Pathology|June 24, 2016
Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the DiseaseBing Han, Melanie Newbould, Gauri Batra, et al.
Frontiers in Endocrinology|November 3, 2018
Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell LesionsRoss J Craigie, Maria Salomon-Estebanez, Daphne Yau, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
Pediatric Blood & Cancer|November 8, 2024
Clinicopathological Analysis of a European Cohort of MYOD1 Mutant Rhabdomyosarcomas in Children and Young AdultsJulia C Chisholm, Joanna L Selfe, Rita Alaggio, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Cancer Cell|September 17, 2015
Frequent Derepression of the Mesenchymal Transcription Factor Gene FOXC1 in Acute Myeloid LeukemiaTim D D Somerville, Daniel H Wiseman, Gary J Spencer, et al.
The Journal of Pathology. Clinical Research|October 3, 2019
Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinismJayne Al Houghton, Indraneel Banerjee, Guftar Shaikh, et al.
Journal of Leukocyte Biology|September 15, 2020
Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiencyAnu Goenka, John A Doherty, Tariq Al-Farsi, et al.
Clinical Genetics|February 4, 2025
Whole Genome Sequencing to Identify Novel Germline Fumarate Hydratase Mutation in Child With Bilateral Renal Cell CarcinomaChristopher Kershaw, Leigh Demain, Eleanor Baker, et al.
The Journal of Clinical Endocrinology and Metabolism|June 13, 2017
Atypical Forms of Congenital Hyperinsulinism in Infancy Are Associated With Mosaic Patterns of Immature Islet CellsBing Han, Zainab Mohamed, Maria Salomon Estebanez, et al.
Cancer Letters|May 30, 2026
Integrated clinical, genomic and functional characterization of a novel ALK variant in neuroblastomaAna Cañadas García, Ketan Thombare, Leila Jahangiri, et al.
American Journal of Clinical Pathology|June 24, 2016
Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the DiseaseBing Han, Melanie Newbould, Gauri Batra, et al.
Frontiers in Endocrinology|November 3, 2018
Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell LesionsRoss J Craigie, Maria Salomon-Estebanez, Daphne Yau, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
Pediatric Blood & Cancer|November 8, 2024
Clinicopathological Analysis of a European Cohort of MYOD1 Mutant Rhabdomyosarcomas in Children and Young AdultsJulia C Chisholm, Joanna L Selfe, Rita Alaggio, et al.
Pageof 3