Babcock D - Search Results

1

Sensitivity to targeted therapy differs between HER2-amplified breast cancer cells harboring kinase and helical domain mutations in PIK3CA.

Garay JP, Smith R, Devlin K, Hollern DP, Liby T, Liu M, Boddapati S, Watson SS, Esch A, Zheng T, Thompson W, Babcock D, Kwon S, Chin K, Heiser L, Gray JW, Korkola JE. Garay JP, et al. Among authors: babcock d. Breast Cancer Res. 2021 Aug 3;23(1):81. doi: 10.1186/s13058-021-01457-0. Breast Cancer Res. 2021. PMID: 34344439 Free PMC article.

2

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects.

Redig JK, Fouad GT, Babcock D, Reshey B, Feingold E, Reeves RH, Maslen CL. Redig JK, et al. Among authors: babcock d. AIMS Genet. 2014;1(1):1-19. doi: 10.3934/genet.2014.1.1#sthash.jksuJTeC.dpuf. AIMS Genet. 2014. PMID: 25328912 Free PMC article.

3

CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.

Maslen CL, Babcock D, Robinson SW, Bean LJ, Dooley KJ, Willour VL, Sherman SL. Maslen CL, et al. Among authors: babcock d. Am J Med Genet A. 2006 Nov 15;140(22):2501-5. doi: 10.1002/ajmg.a.31494. Am J Med Genet A. 2006. PMID: 17036335 No abstract available.

4

CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region.

Maslen CL, Babcock D, Redig JK, Kapeli K, Akkari YM, Olson SB. Maslen CL, et al. Among authors: babcock d. Gene. 2006 Nov 1;382:111-20. doi: 10.1016/j.gene.2006.06.016. Epub 2006 Jul 7. Gene. 2006. PMID: 16919896

5

A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly.

Maslen C, Babcock D, Raghunath M, Steinmann B. Maslen C, et al. Among authors: babcock d. Am J Hum Genet. 1997 Jun;60(6):1389-98. doi: 10.1086/515472. Am J Hum Genet. 1997. PMID: 9199560 Free PMC article.

6

A single mutation that results in an Asp to His substitution and partial exon skipping in a family with congenital contractural arachnodactyly.

Babcock D, Gasner C, Francke U, Maslen C. Babcock D, et al. Hum Genet. 1998 Jul;103(1):22-8. doi: 10.1007/s004390050777. Hum Genet. 1998. PMID: 9737771

7

Mechanical property characterization of electrospun recombinant human tropoelastin for vascular graft biomaterials.

McKenna KA, Hinds MT, Sarao RC, Wu PC, Maslen CL, Glanville RW, Babcock D, Gregory KW. McKenna KA, et al. Among authors: babcock d. Acta Biomater. 2012 Jan;8(1):225-33. doi: 10.1016/j.actbio.2011.08.001. Epub 2011 Aug 6. Acta Biomater. 2012. PMID: 21846510 Free PMC article.

8

Prenatal ultrasound findings in a fetus with congenital contractural arachnodactyly.

Kölble N, Wisser J, Babcock D, Maslen C, Huch R, Steinmann B. Kölble N, et al. Among authors: babcock d. Ultrasound Obstet Gynecol. 2002 Oct;20(4):395-9. doi: 10.1046/j.1469-0705.2002.00819.x. Ultrasound Obstet Gynecol. 2002. PMID: 12383326 Free article.

9

Occurrence of a mutation associated with Wolman disease in a family with cholesteryl ester storage disease.

Maslen CL, Babcock D, Illingworth DR. Maslen CL, et al. Among authors: babcock d. J Inherit Metab Dis. 1995;18(5):620-3. doi: 10.1007/BF02436008. J Inherit Metab Dis. 1995. PMID: 8598644

10

A free-radical design featuring an intramolecular migration for a synthetically versatile alkyl-(hetero)arylation of simple olefins.

Babcock DJ, Wolfram AJ, Barney JL, Servagno SM, Sharma A, Nacsa ED. Babcock DJ, et al. Chem Sci. 2024 Feb 2;15(11):4031-4040. doi: 10.1039/d3sc06476j. eCollection 2024 Mar 13. Chem Sci. 2024. PMID: 38487219 Free PMC article.

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