John KM - Search Results

1

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.

Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V, et al. Lux SE, et al. Among authors: john km. Nature. 1990 Jun 21;345(6277):736-9. doi: 10.1038/345736a0. Nature. 1990. PMID: 2141669

2

Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins.

Lux SE, John KM, Bennett V. Lux SE, et al. Among authors: john km. Nature. 1990 Mar 1;344(6261):36-42. doi: 10.1038/344036a0. Nature. 1990. PMID: 2137557

3

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis.

Savvides P, Shalev O, John KM, Lux SE. Savvides P, et al. Among authors: john km. Blood. 1993 Nov 15;82(10):2953-60. Blood. 1993. PMID: 8219186 Free article.

4

Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.

Costa FF, Agre P, Watkins PC, Winkelmann JC, Tang TK, John KM, Lux SE, Forget BG. Costa FF, et al. Among authors: john km. N Engl J Med. 1990 Oct 11;323(15):1046-50. doi: 10.1056/NEJM199010113231507. N Engl J Med. 1990. PMID: 1977081 Free article. No abstract available.

5

Demonstration of the deletion of a copy of the ankyrin gene in a patient with hereditary spherocytosis by in situ hybridization.

Tse WT, Menninger JC, Ward DC, Chilcote RR, John KM, Lux SE, Forget BG. Tse WT, et al. Among authors: john km. Trans Assoc Am Physicians. 1990;103:242-8. Trans Assoc Am Physicians. 1990. PMID: 2151901 No abstract available.

6

Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).

Lux SE, John KM, Kopito RR, Lodish HF. Lux SE, et al. Among authors: john km. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9089-93. doi: 10.1073/pnas.86.23.9089. Proc Natl Acad Sci U S A. 1989. PMID: 2594752 Free PMC article.

7

Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain.

Peters LL, John KM, Lu FM, Eicher EM, Higgins A, Yialamas M, Turtzo LC, Otsuka AJ, Lux SE. Peters LL, et al. Among authors: john km. J Cell Biol. 1995 Jul;130(2):313-30. doi: 10.1083/jcb.130.2.313. J Cell Biol. 1995. PMID: 7615634 Free PMC article.

8

A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.

Wolfe LC, John KM, Falcone JC, Byrne AM, Lux SE. Wolfe LC, et al. Among authors: john km. N Engl J Med. 1982 Nov 25;307(22):1367-74. doi: 10.1056/NEJM198211253072203. N Engl J Med. 1982. PMID: 6215583

9

Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.

Tomaselli MB, John KM, Lux SE. Tomaselli MB, et al. Among authors: john km. Proc Natl Acad Sci U S A. 1981 Mar;78(3):1911-5. doi: 10.1073/pnas.78.3.1911. Proc Natl Acad Sci U S A. 1981. PMID: 6940197 Free PMC article.

10

Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice.

Peters LL, Jindel HK, Gwynn B, Korsgren C, John KM, Lux SE, Mohandas N, Cohen CM, Cho MR, Golan DE, Brugnara C. Peters LL, et al. Among authors: john km. J Clin Invest. 1999 Jun;103(11):1527-37. doi: 10.1172/JCI5766. J Clin Invest. 1999. PMID: 10359562 Free PMC article.

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