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Ann-Marie Patch

Showing results (11-20 of 78) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2018
Correction: Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian diseaseMatthew Neil Wakeling, Thomas William Laver, Caroline Fiona Wright, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 17, 2020
FGFR2c Mesenchymal Isoform Expression Is Associated with Poor Prognosis and Further Refines Risk Stratification within Endometrial Cancer Molecular SubtypesAsmerom T Sengal, Ann-Marie Patch, Cameron E Snell, et al.
The Journal of Endocrinology|September 3, 2010
In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human isletsKaren Piper Hanley, Tom Hearn, Andrew Berry, et al.
Pediatric Diabetes|February 29, 2012
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemiaCharles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, et al.
BMC Cancer|June 5, 2017
Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesotheliomaSophie Sneddon, Ann-Marie Patch, Ian M Dick, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 2007
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetesHeidi de Wet, Mathew G Rees, Kenju Shimomura, et al.
Diabetes|April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthoodSarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
Clinical Endocrinology|November 22, 2008
Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotypeTomasz Klupa, Irina Kowalska, Krystyna Wyka, et al.
Cancers|March 13, 2025
Spatial Transcriptomics Reveals Novel Mechanisms Involved in Perineural Invasion in Pancreatic Ductal AdenocarcinomasVanessa Lakis, Noni L Chan, Ruth Lyons, et al.
JOP : Journal of the Pancreas|January 13, 2010
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiologyEmma L Edghill, Jayne A L Minton, Christopher J Groves, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2018
Correction: Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian diseaseMatthew Neil Wakeling, Thomas William Laver, Caroline Fiona Wright, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 17, 2020
FGFR2c Mesenchymal Isoform Expression Is Associated with Poor Prognosis and Further Refines Risk Stratification within Endometrial Cancer Molecular SubtypesAsmerom T Sengal, Ann-Marie Patch, Cameron E Snell, et al.
The Journal of Endocrinology|September 3, 2010
In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human isletsKaren Piper Hanley, Tom Hearn, Andrew Berry, et al.
Pediatric Diabetes|February 29, 2012
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemiaCharles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, et al.
BMC Cancer|June 5, 2017
Whole exome sequencing of an asbestos-induced wild-type murine model of malignant mesotheliomaSophie Sneddon, Ann-Marie Patch, Ian M Dick, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 2007
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetesHeidi de Wet, Mathew G Rees, Kenju Shimomura, et al.
Diabetes|April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthoodSarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
Clinical Endocrinology|November 22, 2008
Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotypeTomasz Klupa, Irina Kowalska, Krystyna Wyka, et al.
Cancers|March 13, 2025
Spatial Transcriptomics Reveals Novel Mechanisms Involved in Perineural Invasion in Pancreatic Ductal AdenocarcinomasVanessa Lakis, Noni L Chan, Ruth Lyons, et al.
JOP : Journal of the Pancreas|January 13, 2010
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiologyEmma L Edghill, Jayne A L Minton, Christopher J Groves, et al.
Pageof 8