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Items: 27

1.

A conditional mutant allele for analysis of Mixl1 function in the mouse.

Pulina MV, Sahr KE, Nowotschin S, Baron MH, Hadjantonakis AK.

Genesis. 2014 May;52(5):417-23. doi: 10.1002/dvg.22768. Epub 2014 Mar 13.

2.

Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor.

Siatecka M, Sahr KE, Andersen SG, Mezei M, Bieker JJ, Peters LL.

Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15151-6. doi: 10.1073/pnas.1004996107. Epub 2010 Aug 9.

3.

Targeted deletion of the gamma-adducin gene (Add3) in mice reveals differences in alpha-adducin interactions in erythroid and nonerythroid cells.

Sahr KE, Lambert AJ, Ciciotte SL, Mohandas N, Peters LL.

Am J Hematol. 2009 Jun;84(6):354-61. doi: 10.1002/ajh.21427.

4.

Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice.

Robledo RF, Ciciotte SL, Gwynn B, Sahr KE, Gilligan DM, Mohandas N, Peters LL.

Blood. 2008 Nov 15;112(10):4298-307. doi: 10.1182/blood-2008-05-156000. Epub 2008 Aug 22.

5.

Tg(Afp-GFP) expression marks primitive and definitive endoderm lineages during mouse development.

Kwon GS, Fraser ST, Eakin GS, Mangano M, Isern J, Sahr KE, Hadjantonakis AK, Baron MH.

Dev Dyn. 2006 Sep;235(9):2549-58.

6.

Absence of erythroblast macrophage protein (Emp) leads to failure of erythroblast nuclear extrusion.

Soni S, Bala S, Gwynn B, Sahr KE, Peters LL, Hanspal M.

J Biol Chem. 2006 Jul 21;281(29):20181-9. Epub 2006 May 16.

7.

Acceleration of mesoderm development and expansion of hematopoietic progenitors in differentiating ES cells by the mouse Mix-like homeodomain transcription factor.

Willey S, Ayuso-Sacido A, Zhang H, Fraser ST, Sahr KE, Adlam MJ, Kyba M, Daley GQ, Keller G, Baron MH.

Blood. 2006 Apr 15;107(8):3122-30. Epub 2006 Jan 10.

8.

Using a histone yellow fluorescent protein fusion for tagging and tracking endothelial cells in ES cells and mice.

Fraser ST, Hadjantonakis AK, Sahr KE, Willey S, Kelly OG, Jones EA, Dickinson ME, Baron MH.

Genesis. 2005 Jul;42(3):162-71.

9.

Disruption of the mouse mu-calpain gene reveals an essential role in platelet function.

Azam M, Andrabi SS, Sahr KE, Kamath L, Kuliopulos A, Chishti AH.

Mol Cell Biol. 2001 Mar;21(6):2213-20.

10.

Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene.

Hassoun H, Hanada T, Lutchman M, Sahr KE, Palek J, Hanspal M, Chishti AH.

Blood. 1998 Mar 15;91(6):2146-51.

11.

Identification of the mouse homologue of human discs large and rat SAP97 genes.

Lin L, Sahr KE, Chishti AH.

Biochim Biophys Acta. 1997 Nov 28;1362(1):1-5.

12.
13.

Complete genomic organization of the human erythroid p55 gene (MPP1), a membrane-associated guanylate kinase homologue.

Kim AC, Metzenberg AB, Sahr KE, Marfatia SM, Chishti AH.

Genomics. 1996 Jan 15;31(2):223-9.

PMID:
8824805
14.

The structure and organization of the human erythroid anion exchanger (AE1) gene.

Sahr KE, Taylor WM, Daniels BP, Rubin HL, Jarolim P.

Genomics. 1994 Dec;24(3):491-501.

PMID:
7713501
15.

A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis.

Hassoun H, Coetzer TL, Vassiliadis JN, Sahr KE, Maalouf GJ, Saad ST, Catanzariti L, Palek J.

J Clin Invest. 1994 Aug;94(2):643-8.

16.

Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer.

Sahr KE, Coetzer TL, Moy LS, Derick LH, Chishti AH, Jarolim P, Lorenzo F, Miraglia del Giudice E, Iolascon A, Gallanello R, et al.

J Biol Chem. 1993 Oct 25;268(30):22656-62.

17.

Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis.

Hanspal M, Hanspal JS, Sahr KE, Fibach E, Nachman J, Palek J.

Blood. 1993 Sep 1;82(5):1652-60.

18.
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20.

Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts.

Hanspal M, Hanspal JS, Kalraiya R, Liu SC, Sahr KE, Howard D, Palek J.

Blood. 1992 Jul 15;80(2):530-9.

21.

Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis.

Jarolim P, Palek J, Amato D, Hassan K, Sapak P, Nurse GT, Rubin HL, Zhai S, Sahr KE, Liu SC.

Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11022-6.

22.
23.

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene.

Tse WT, Menninger JC, Yang-Feng TL, Francke U, Sahr KE, Lux SE, Ward DC, Forget BG.

Genomics. 1991 Aug;10(4):858-66.

PMID:
1833308
24.

The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin.

Sahr KE, Laurila P, Kotula L, Scarpa AL, Coupal E, Leto TL, Linnenbach AJ, Winkelmann JC, Speicher DW, Marchesi VT, et al.

J Biol Chem. 1990 Mar 15;265(8):4434-43.

25.

Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.

Sahr KE, Tobe T, Scarpa A, Laughinghouse K, Marchesi SL, Agre P, Linnenbach AJ, Marchesi VT, Forget BG.

J Clin Invest. 1989 Oct;84(4):1243-52.

26.

[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant].

Garbarz M, Devaux I, Grandchamp B, Picat C, Dhermy D, Lecomte MC, Boivin P, Sahr KE, Forget B.

C R Acad Sci III. 1989;308(2):43-8. French.

PMID:
2493313
27.

Molecular cloning of the cDNA for human erythrocyte beta-spectrin.

Winkelmann JC, Leto TL, Watkins PC, Eddy R, Shows TB, Linnenbach AJ, Sahr KE, Kathuria N, Marchesi VT, Forget BG.

Blood. 1988 Jul;72(1):328-34.

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