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Search life-sciences literature (45,105,671 articles, preprints and more)

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Application Factors Associated With Clinical Performance During Pediatric Internship.
Gross C, O'Halloran C, Winn AS, Lux SE, Michelson CD, Sectish T, Sox CM
Acad Pediatr, 20(7):1007-1012, 05 Apr 2020
Cited by: 2 articles | PMID: 32268217
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Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia.
Lacy JN, Ulirsch JC, Grace RF, Towne MC, Hale J, Mohandas N, Lux SE, Agrawal PB, Sankaran VG
Cold Spring Harb Mol Case Stud, 2(4):a000885, 01 Jul 2016
Cited by: 9 articles | PMID: 27551681 | PMCID: PMC4990811
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Anatomy of the red cell membrane skeleton: unanswered questions.
Lux SE
Blood, 127(2):187-199, 04 Nov 2015
Cited by: 148 articles | PMID: 26537302
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Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.
Stewart AK, Shmukler BE, Vandorpe DH, Rivera A, Heneghan JF, Li X, Hsu A, Karpatkin M, O'Neill AF, Bauer DE, Heeney MM, John K, Kuypers FA, Gallagher PG, Lux SE, Brugnara C, Westhoff CM, Alper SL
Am J Physiol Cell Physiol, 301(6):C1325-43, 17 Aug 2011
Cited by: 17 articles | PMID: 21849667 | PMCID: PMC3233792
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Training program in cancer and blood diseases: Pediatric Hematology/Oncology Fellowship Program, Children's Hospital Boston/Dana-Farber Cancer Institute.
Williams DA, Porter ES, Lux SE, Grier HE, Mack JW, Orkin SH
Am J Hematol, 85(10):793-794, 01 Oct 2010
Cited by: 2 articles | PMID: 20730793
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Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes.
Stankewich MC, Gwynn B, Ardito T, Ji L, Kim J, Robledo RF, Lux SE, Peters LL, Morrow JS
Proc Natl Acad Sci U S A, 107(13):6022-6027, 15 Mar 2010
Cited by: 55 articles | PMID: 20231455 | PMCID: PMC2851889
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The carboxyterminal EF domain of erythroid alpha-spectrin is necessary for optimal spectrin-actin binding.
Korsgren C, Lux SE
Blood, 116(14):2600-2607, 28 Jun 2010
Cited by: 7 articles | PMID: 20585040 | PMCID: PMC2953892
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Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.
Robledo RF, Lambert AJ, Birkenmeier CS, Cirlan MV, Cirlan AF, Campagna DR, Lux SE, Peters LL
Blood, 115(9):1804-1814, 07 Jan 2010
Cited by: 7 articles | PMID: 20056793 | PMCID: PMC2832806
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Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner.
Korsgren C, Peters LL, Lux SE
J Biol Chem, 285(7):4757-4770, 11 Dec 2009
Cited by: 13 articles | PMID: 20007969 | PMCID: PMC2836081
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A uniform third-year application and offer date for pediatric fellow applicants: pro and con.
Stapleton FB, Lux SE
J Pediatr, 149(5):587-588, 01 Nov 2006
Cited by: 3 articles | PMID: 17095320
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Identification and functional characterization of protein 4.1R and actin-binding sites in erythrocyte beta spectrin: regulation of the interactions by phosphatidylinositol-4,5-bisphosphate.
An X, Debnath G, Guo X, Liu S, Lux SE, Baines A, Gratzer W, Mohandas N
Biochemistry, 44(31):10681-10688, 01 Aug 2005
Cited by: 44 articles | PMID: 16060676
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Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer.
Eber S, Lux SE
Semin Hematol, 41(2):118-141, 01 Apr 2004
Cited by: 110 articles | PMID: 15071790
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Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency.
Peters LL, Swearingen RA, Andersen SG, Gwynn B, Lambert AJ, Li R, Lux SE, Churchill GA
Blood, 103(8):3233-3240, 30 Dec 2003
Cited by: 19 articles | PMID: 15070709
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Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosis.
Ozcan R, Jarolim P, Lux SE, Ungewickell E, Eber SW
Br J Haematol, 122(4):669-677, 01 Aug 2003
Cited by: 11 articles | PMID: 12899723
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Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.
Paw BH, Davidson AJ, Zhou Y, Li R, Pratt SJ, Lee C, Trede NS, Brownlie A, Donovan A, Liao EC, Ziai JM, Drejer AH, Guo W, Kim CH, Gwynn B, Peters LL, Chernova MN, Alper SL, Zapata A, [...] Zon LI
Nat Genet, 34(1):59-64, 01 May 2003
Cited by: 89 articles | PMID: 12669066
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A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix.
Tse WT, Tang J, Jin O, Korsgren C, John KM, Kung AL, Gwynn B, Peters LL, Lux SE
J Biol Chem, 276(26):23974-23985, 06 Apr 2001
Cited by: 42 articles | PMID: 11294830
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The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.
Gallagher PG, Romana M, Tse WT, Lux SE, Forget BG
Blood, 96(3):1136-1143, 01 Aug 2000
Cited by: 32 articles | PMID: 10910934
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Immunolocalization of AE2 anion exchanger in rat and mouse epididymis.
Jensen LJ, Stuart-Tilley AK, Peters LL, Lux SE, Alper SL, Breton S
Biol Reprod, 61(4):973-980, 01 Oct 1999
Cited by: 34 articles | PMID: 10491632
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Dependence of nodal sodium channel clustering on paranodal axoglial contact in the developing CNS.
Rasband MN, Peles E, Trimmer JS, Levinson SR, Lux SE, Shrager P
J Neurosci, 19(17):7516-7528, 01 Sep 1999
Cited by: 240 articles | PMID: 10460258 | PMCID: PMC6782503
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Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter.
Donovan A, Brownlie A, Zhou Y, Shepard J, Pratt SJ, Moynihan J, Paw BH, Drejer A, Barut B, Zapata A, Law TC, Brugnara C, Lux SE, Pinkus GS, Pinkus JL, Kingsley PD, Palis J, Fleming MD, Andrews NC, Zon LI
Nature, 403(6771):776-781, 01 Feb 2000
Cited by: 938 articles | PMID: 10693807
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The Alzheimer-related gene presenilin 1 facilitates notch 1 in primary mammalian neurons.
Berezovska O, Frosch M, McLean P, Knowles R, Koo E, Kang D, Shen J, Lu FM, Lux SE, Tonegawa S, Hyman BT
Brain Res Mol Brain Res, 69(2):273-280, 01 Jun 1999
Cited by: 41 articles | PMID: 10366748
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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
J Clin Invest, 103(11):1527-1537, 01 Jun 1999
Cited by: 52 articles | PMID: 10359562 | PMCID: PMC408368
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Red blood cell membrane disorders.
Tse WT, Lux SE
Br J Haematol, 104(1):2-13, 01 Jan 1999
Cited by: 131 articles | PMID: 10027705
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Distribution of epithelial ankyrin (Ank3) spliceoforms in renal proximal and distal tubules.
Doctor RB, Chen J, Peters LL, Lux SE, Mandel LJ
Am J Physiol, 274(1):F129-38, 01 Jan 1998
Cited by: 25 articles | PMID: 9458832
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Notch1 inhibits neurite outgrowth in postmitotic primary neurons.
Berezovska O, McLean P, Knowles R, Frosh M, Lu FM, Lux SE, Hyman BT
Neuroscience, 93(2):433-439, 01 Jan 1999
Cited by: 154 articles | PMID: 10465425
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