Kathy King - Search Results

Year	Number of Results
2002	2
2003	1
2005	1
2006	3
2007	1
2018	1
2019	1
2024	0

1

All of Us Research Program Investigators; Denny JC, Rutter JL, Goldstein DB, Philippakis A, Smoller JW, Jenkins G, Dishman E. All of Us Research Program Investigators, et al. N Engl J Med. 2019 Aug 15;381(7):668-676. doi: 10.1056/NEJMsr1809937. N Engl J Med. 2019. PMID: 31412182 Free PMC article.

2

Development of MGD007, a gpA33 x CD3-Bispecific DART Protein for T-Cell Immunotherapy of Metastatic Colorectal Cancer.

Moore PA, Shah K, Yang Y, Alderson R, Roberts P, Long V, Liu D, Li JC, Burke S, Ciccarone V, Li H, Fieger CB, Hooley J, Easton A, Licea M, Gorlatov S, King KL, Young P, Adami A, Loo D, Chichili GR, Liu L, Smith DH, Brown JG, Chen FZ, Koenig S, Mather J, Bonvini E, Johnson S. Moore PA, et al. Among authors: king kl. Mol Cancer Ther. 2018 Aug;17(8):1761-1772. doi: 10.1158/1535-7163.MCT-17-1086. Epub 2018 Jun 4. Mol Cancer Ther. 2018. PMID: 29866746

3

Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's disease.

van Heel DA, Hunt KA, King K, Ghosh S, Gabe SM, Mathew CG, Forbes A, Playford RJ. van Heel DA, et al. Among authors: king k. Inflamm Bowel Dis. 2006 Jul;12(7):598-605. doi: 10.1097/01.ibd.0000225344.21979.89. Inflamm Bowel Dis. 2006. PMID: 16804397

4

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

King K, Sheikh MF, Cuthbert AP, Fisher SA, Onnie CM, Mirza MM, Pattni RC, Sanderson J, Forbes A, Mansfield J, Lewis CM, Roberts RG, Mathew CG. King K, et al. Hum Mutat. 2006 Jan;27(1):44-54. doi: 10.1002/humu.20264. Hum Mutat. 2006. PMID: 16278823

5

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

King K, Bagnall R, Fisher SA, Sheikh F, Cuthbert A, Tan S, Mundy NI, Rosenstiel P, Schreiber S, Mathew CG, Roberts RG. King K, et al. Genomics. 2007 Oct;90(4):493-501. doi: 10.1016/j.ygeno.2007.07.009. Epub 2007 Aug 24. Genomics. 2007. PMID: 17719742 Free article.

6

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

Mirza MM, Fisher SA, King K, Cuthbert AP, Hampe J, Sanderson J, Mansfield J, Donaldson P, Macpherson AJ, Forbes A, Schreiber S, Lewis CM, Mathew CG. Mirza MM, et al. Among authors: king k. Am J Hum Genet. 2003 Apr;72(4):1018-22. doi: 10.1086/373880. Epub 2003 Mar 3. Am J Hum Genet. 2003. PMID: 12618963 Free PMC article.

7

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, Mascheretti S, Sanderson J, Forbes A, Mansfield J, Schreiber S, Lewis CM, Mathew CG. Cuthbert AP, et al. Among authors: king k. Gastroenterology. 2002 Apr;122(4):867-74. doi: 10.1053/gast.2002.32415. Gastroenterology. 2002. PMID: 11910337

8

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome.

King K, Flinter FA, Nihalani V, Green PM. King K, et al. Hum Genet. 2002 Dec;111(6):548-54. doi: 10.1007/s00439-002-0830-3. Epub 2002 Sep 14. Hum Genet. 2002. PMID: 12436246

9

A two-tier approach to mutation detection in the COL4A5 gene for Alport syndrome.

King K, Flinter FA, Green PM. King K, et al. Hum Mutat. 2006 Oct;27(10):1061. doi: 10.1002/humu.9453. Hum Mutat. 2006. PMID: 16941480

10

Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates.

d'Amati G, Bagattin A, Bauce B, Rampazzo A, Autore C, Basso C, King K, Romeo MD, Gallo P, Thiene G, Danieli GA, Nava A. d'Amati G, et al. Among authors: king k. Hum Pathol. 2005 Jul;36(7):761-7. doi: 10.1016/j.humpath.2005.04.019. Hum Pathol. 2005. PMID: 16084945

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