Ensing GJ - Search Results

1

Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis.

Li DY, Toland AE, Boak BB, Atkinson DL, Ensing GJ, Morris CA, Keating MT. Li DY, et al. Among authors: ensing gj. Hum Mol Genet. 1997 Jul;6(7):1021-8. doi: 10.1093/hmg/6.7.1021. Hum Mol Genet. 1997. PMID: 9215670

2

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

Ewart AK, Morris CA, Ensing GJ, Loker J, Moore C, Leppert M, Keating M. Ewart AK, et al. Among authors: ensing gj. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3226-30. doi: 10.1073/pnas.90.8.3226. Proc Natl Acad Sci U S A. 1993. PMID: 8475063 Free PMC article.

3

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition.

Frangiskakis JM, Ewart AK, Morris CA, Mervis CB, Bertrand J, Robinson BF, Klein BP, Ensing GJ, Everett LA, Green ED, Pröschel C, Gutowski NJ, Noble M, Atkinson DL, Odelberg SJ, Keating MT. Frangiskakis JM, et al. Among authors: ensing gj. Cell. 1996 Jul 12;86(1):59-69. doi: 10.1016/s0092-8674(00)80077-x. Cell. 1996. PMID: 8689688 Free article.

4

Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene.

Morris CA, Loker J, Ensing G, Stock AD. Morris CA, et al. Am J Med Genet. 1993 Jul 1;46(6):737-44. doi: 10.1002/ajmg.1320460634. Am J Med Genet. 1993. PMID: 8362925

5

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

Morris CA, Mervis CB, Hobart HH, Gregg RG, Bertrand J, Ensing GJ, Sommer A, Moore CA, Hopkin RJ, Spallone PA, Keating MT, Osborne L, Kimberley KW, Stock AD. Morris CA, et al. Among authors: ensing gj. Am J Med Genet A. 2003 Nov 15;123A(1):45-59. doi: 10.1002/ajmg.a.20496. Am J Med Genet A. 2003. PMID: 14556246

6

Autosomal dominant supravalvular aortic stenosis: large three-generation family.

Schmidt MA, Ensing GJ, Michels VV, Carter GA, Hagler DJ, Feldt RH. Schmidt MA, et al. Among authors: ensing gj. Am J Med Genet. 1989 Mar;32(3):384-9. doi: 10.1002/ajmg.1320320324. Am J Med Genet. 1989. PMID: 2658589 Review.

7

Spectrum of findings in a family with nonsyndromic autosomal dominant supravalvular aortic stenosis: a Doppler echocardiographic study.

Ensing GJ, Schmidt MA, Hagler DJ, Michels VV, Carter GA, Feldt RH. Ensing GJ, et al. J Am Coll Cardiol. 1989 Feb;13(2):413-9. doi: 10.1016/0735-1097(89)90520-2. J Am Coll Cardiol. 1989. PMID: 2913119 Free article.

8

Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.

Stefanelli CB, Rosenthal A, Borisov AB, Ensing GJ, Russell MW. Stefanelli CB, et al. Among authors: ensing gj. Mol Genet Metab. 2004 Sep-Oct;83(1-2):188-96. doi: 10.1016/j.ymgme.2004.04.013. Mol Genet Metab. 2004. PMID: 15464434

9

Caveats of balloon dilation of conduits and conduit valves.

Ensing GJ, Hagler DJ, Seward JB, Julsrud PR, Mair DD. Ensing GJ, et al. J Am Coll Cardiol. 1989 Aug;14(2):397-400. doi: 10.1016/0735-1097(89)90192-7. J Am Coll Cardiol. 1989. PMID: 2526832 Free article.

10

Echocardiographic analysis of rejection in the infant heart transplant recipient.

Loker J, Darragh R, Ensing G, Caldwell R. Loker J, et al. J Heart Lung Transplant. 1994 Nov-Dec;13(6):1014-8. J Heart Lung Transplant. 1994. PMID: 7865507

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