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M Dunlop

Showing results (291-300 of 303) with videos related to

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Journal of the National Comprehensive Cancer Network : JNCCN|February 23, 2024
Disparities in Survival and NCCN Guideline-Concordant Care in Patients With Extremity Soft Tissue SarcomaHayley M Dunlop, Bence Bende, Samantha M Ruff, et al.
Nature Medicine|February 1, 1996
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patientsB Liu, R Parsons, N Papadopoulos, et al.
American Journal of Respiratory Cell and Molecular Biology|July 12, 2008
Endogenous IL-11 signaling is essential in Th2- and IL-13-induced inflammation and mucus productionChun Geun Lee, Dominik Hartl, Hiroshi Matsuura, et al.
Leukemia|January 11, 2008
MicroRNA expression in lymphocyte development and malignancyC H Lawrie, N J Saunders, S Soneji, et al.
Gut|August 14, 1999
Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndromeS Bevan, K Woodford-Richens, P Rozen, et al.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Blood|May 8, 2010
MicroRNA expression in Sezary syndrome: identification, function, and diagnostic potentialErica Ballabio, Tracey Mitchell, Marloes S van Kester, et al.
CNS & Neurological Disorders Drug Targets|December 4, 2014
The putative impact of metabolic health on default mode network activity and functional connectivity in neuropsychiatric disordersDanielle S Cha, Francesco De Michele, Joanna K Soczynska, et al.
Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditionsKelly D Farwell, Layla Shahmirzadi, Dima El-Khechen, et al.
Pageof 31

Showing results (291-300 of 303) with videos related to

Sort By:
Pageof 31
Journal of the National Comprehensive Cancer Network : JNCCN|February 23, 2024
Disparities in Survival and NCCN Guideline-Concordant Care in Patients With Extremity Soft Tissue SarcomaHayley M Dunlop, Bence Bende, Samantha M Ruff, et al.
Nature Medicine|February 1, 1996
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patientsB Liu, R Parsons, N Papadopoulos, et al.
American Journal of Respiratory Cell and Molecular Biology|July 12, 2008
Endogenous IL-11 signaling is essential in Th2- and IL-13-induced inflammation and mucus productionChun Geun Lee, Dominik Hartl, Hiroshi Matsuura, et al.
Leukemia|January 11, 2008
MicroRNA expression in lymphocyte development and malignancyC H Lawrie, N J Saunders, S Soneji, et al.
Gut|August 14, 1999
Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndromeS Bevan, K Woodford-Richens, P Rozen, et al.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Blood|May 8, 2010
MicroRNA expression in Sezary syndrome: identification, function, and diagnostic potentialErica Ballabio, Tracey Mitchell, Marloes S van Kester, et al.
CNS & Neurological Disorders Drug Targets|December 4, 2014
The putative impact of metabolic health on default mode network activity and functional connectivity in neuropsychiatric disordersDanielle S Cha, Francesco De Michele, Joanna K Soczynska, et al.
Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditionsKelly D Farwell, Layla Shahmirzadi, Dima El-Khechen, et al.
Pageof 31