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European Journal of Immunology|April 26, 2006
Normal responses to specific NOD1-activating peptidoglycan agonists in the presence of the NOD2 frameshift and other mutations in Crohn's diseaseDavid A van Heel, Karen A Hunt, Subrata Ghosh, et al.
Inflammatory Bowel Diseases|June 29, 2006
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's diseaseDavid A van Heel, Karen A Hunt, Kathy King, et al.
BMC Medical Genomics|January 9, 2009
Complex nature of SNP genotype effects on gene expression in primary human leucocytesGraham A Heap, Gosia Trynka, Ritsert C Jansen, et al.
Nature Genetics|April 21, 2015
Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac diseaseJavier Gutierrez-Achury, Alexandra Zhernakova, Sara L Pulit, et al.
Radiology|October 22, 2008
Suspicious breast lesions: assessment of 3D Doppler US indexes for classification in a test population and fourfold cross-validation schemeGerald L LeCarpentier, Marilyn A Roubidoux, J Brian Fowlkes, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
A common CTLA4 haplotype associated with coeliac diseaseKaren A Hunt, Dermot P B McGovern, Parveen J Kumar, et al.
Plos One|January 31, 2015
Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow upVanisha Mistry, Nicholas A Bockett, Adam P Levine, et al.
Breast Cancer Research and Treatment|September 13, 2005
Clinical and radiologic assessments to predict breast cancer pathologic complete response to neoadjuvant chemotherapyAnne F Schott, Marilyn A Roubidoux, Mark A Helvie, et al.
American Journal of Human Genetics|June 4, 2008
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arraysLude Franke, Carolien G F de Kovel, Yurii S Aulchenko, et al.
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