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Elizabeth McNally

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Stoller Douglas; Pytel Peter; Katz Sophie; Earley Judy U; Collins Keith; Metcalfe Jamie; Lang Roberto M; McNally Elizabeth M
Impaired exercise tolerance and skeletal muscle myopathy in sulfonylurea receptor-2 mutant mice.
Heydemann Ahlke; McNally Elizabeth
NO more muscle fatigue.
Puckelwartz Megan J; Kessler Eric; Zhang Yuan; Hodzic Didier; Randles K Natalie; Morris Glenn; Earley Judy U; Hadhazy Michele; Holaska James M; Mewborn Stephanie K; Pytel Peter; McNally Elizabeth M
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.

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All Publications

2009: Stoller Douglas; Pytel Peter; Katz Sophie; Earley Judy U; Collins Keith; Metcalfe Jamie; Lang Roberto M; McNally Elizabeth M
Impaired exercise tolerance and skeletal muscle myopathy in sulfonylurea receptor-2 mutant mice.
American journal of physiology. Regulatory, integrative and comparative physiology 2009;297(4):R1144-53.
2009: Heydemann Ahlke; McNally Elizabeth
NO more muscle fatigue.
The Journal of clinical investigation 2009;119(3):448-50.
2009: Puckelwartz Megan J; Kessler Eric; Zhang Yuan; Hodzic Didier; Randles K Natalie; Morris Glenn; Earley Judy U; Hadhazy Michele; Holaska James M; Mewborn Stephanie K; Pytel Peter; McNally Elizabeth M
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
Human molecular genetics 2009;18(4):607-20.
2009: McNally Elizabeth; Dellefave Lisa
Sarcomere mutations in cardiogenesis and ventricular noncompaction.
Trends in cardiovascular medicine 2009;19(1):17-21.
2008: MacLeod Heather M; McNally Elizabeth M
A pilot study of a family history risk assessment tool for cardiovascular disease.
Journal of genetic counseling 2008;17(5):499-507.
2008: Wallace Gregory Q; Lapidos Karen A; Kenik Jordan S; McNally Elizabeth M
Long-term survival of transplanted stem cells in immunocompetent mice with muscular dystrophy.
The American journal of pathology 2008;173(3):792-802.
2008: Adebiyi Adebowale; McNally Elizabeth M; Jaggar Jonathan H
Sulfonylurea receptor-dependent and -independent pathways mediate vasodilation induced by ATP-sensitive K+ channel openers.
Molecular pharmacology 2008;74(3):736-43.
2008: McNally Elizabeth M
Duchenne muscular dystrophy: how bad is the heart?
Heart (British Cardiac Society) 2008;94(8):976-7.
2008: Doherty Katherine R; Demonbreun Alexis R; Wallace Gregory Q; Cave Andrew; Posey Avery D; Heretis Konstantina; Pytel Peter; McNally Elizabeth M
The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusion.
The Journal of biological chemistry 2008;283(29):20252-60.
2008: Dellefave Lisa; McNally Elizabeth M
Sarcomere mutations in cardiomyopathy, noncompaction, and the developing heart.
Circulation 2008;117(22):2847-9.
2008: Bogdanovich Sasha; McNally Elizabeth M; Khurana Tejvir S
Myostatin blockade improves function but not histopathology in a murine model of limb-girdle muscular dystrophy 2C.
Muscle & nerve 2008;37(3):308-16.
2008: Pu Jie-Lin; Ye Bin; Kroboth Stacie L; McNally Elizabeth M; Makielski Jonathan C; Shi Nian-Qing
Cardiac sulfonylurea receptor short form-based channels confer a glibenclamide-insensitive KATP activity.
Journal of molecular and cellular cardiology 2008;44(1):188-200.
2007: Allikian Michael J; Bhabha Gira; Dospoy Patrick; Heydemann Ahlke; Ryder Pearl; Earley Judy U; Wolf Matthew J; Rockman Howard A; McNally Elizabeth M
Reduced life span with heart and muscle dysfunction in Drosophila sarcoglycan mutants.
Human molecular genetics 2007;16(23):2933-43.
2007: Stoller Douglas; Kakkar Rahul; Smelley Matthew; Chalupsky Karel; Earley Judy U; Shi Nian-Qing; Makielski Jonathan C; McNally Elizabeth M
Mice lacking sulfonylurea receptor 2 (SUR2) ATP-sensitive potassium channels are resistant to acute cardiovascular stress.
Journal of molecular and cellular cardiology 2007;43(4):445-54.
2007: Bernatchez Pascal N; Acevedo Lisette; Fernandez-Hernando Carlos; Murata Takahisa; Chalouni Cecile; Kim Jiae; Erdjument-Bromage Hediye; Shah Vijay; Gratton Jean-Philippe; McNally Elizabeth M; Tempst Paul; Sessa William C
Myoferlin regulates vascular endothelial growth factor receptor-2 stability and function.
The Journal of biological chemistry 2007;282(42):30745-53.
2007: MacLeod Heather; Pytel Peter; Wollmann Robert; Chelmicka-Schorr Ewa; Silver Kenneth; Anderson Rebecca Brown; Waggoner Darrel; McNally Elizabeth M
A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex.
Neuromuscular disorders : NMD 2007;17(4):285-9.
2007: Parsons Stephanie A; Millay Douglas P; Sargent Michelle A; Naya Francisco J; McNally Elizabeth M; Sweeney H Lee; Molkentin Jeffery D
Genetic disruption of calcineurin improves skeletal muscle pathology and cardiac disease in a mouse model of limb-girdle muscular dystrophy.
The Journal of biological chemistry 2007;282(13):10068-78.
2007: Allikian Michael J; McNally Elizabeth M
Processing and assembly of the dystrophin glycoprotein complex.
Traffic (Copenhagen, Denmark) 2007;8(3):177-83.
2007: Heydemann Ahlke; McNally Elizabeth M
Consequences of disrupting the dystrophin-sarcoglycan complex in cardiac and skeletal myopathy.
Trends in cardiovascular medicine 2007;17(2):55-9.
2007: Heydemann Ahlke; Demonbreun Alexis; Hadhazy Michele; Earley Judy U; McNally Elizabeth M
Nuclear sequestration of delta-sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes.
Human molecular genetics 2007;16(4):355-63.
2007: Heydemann Ahlke; Doherty Katherine R; McNally Elizabeth M
Genetic modifiers of muscular dystrophy: implications for therapy.
Biochimica et biophysica acta 2007;1772(2):216-28.
2007: McNally Elizabeth M; Pytel Peter
Muscle diseases: the muscular dystrophies.
Annual review of pathology 2007;2():87-109.
2007: McNally Elizabeth M
New approaches in the therapy of cardiomyopathy in muscular dystrophy.
Annual review of medicine 2007;58():75-88.
2006: DeWitt Megan M; MacLeod Heather M; Soliven Betty; McNally Elizabeth M
Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy.
Journal of the American College of Cardiology 2006;48(7):1396-8.
2006: Parsons Stephanie A; Millay Douglas P; Sargent Michelle A; McNally Elizabeth M; Molkentin Jeffery D
Age-dependent effect of myostatin blockade on disease severity in a murine model of limb-girdle muscular dystrophy.
The American journal of pathology 2006;168(6):1975-85.
2006: McNally Elizabeth M
Hypertrophic cardiomyopathy: exercise and eat right.
Circulation research 2006;98(4):443-5.
2006: Kakkar Rahul; Ye Bin; Stoller Douglas A; Smelley Matthew; Shi Nian-Qing; Galles Kevin; Hadhazy Michele; Makielski Jonathan C; McNally Elizabeth M
Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process.
Circulation research 2006;98(5):682-9.
2005: Doherty Katherine R; Cave Andrew; Davis Dawn Belt; Delmonte Anthony J; Posey Avery; Earley Judy U; Hadhazy Michele; McNally Elizabeth M
Normal myoblast fusion requires myoferlin.
Development (Cambridge, England) 2005;132(24):5565-75.
2005: Firoved Aaron M; Miller Georgina F; Moayeri Mahtab; Kakkar Rahul; Shen Yuequan; Wiggins Jason F; McNally Elizabeth M; Tang Wei-Jen; Leppla Stephen H
Bacillus anthracis edema toxin causes extensive tissue lesions and rapid lethality in mice.
The American journal of pathology 2005;167(5):1309-20.
2005: Heydemann Ahlke; Huber Jill M; Demonbreun Alexis; Hadhazy Michele; McNally Elizabeth M
Genetic background influences muscular dystrophy.
Neuromuscular disorders : NMD 2005;15(9-10):601-9.
2005: McNally Elizabeth M; MacLeod Heather
Therapy insight: cardiovascular complications associated with muscular dystrophies.
Nature clinical practice. Cardiovascular medicine 2005;2(6):301-8.
2005: Wheeler Matthew T; McNally Elizabeth M
The interaction of coronary tone and cardiac fibrosis.
Current atherosclerosis reports 2005;7(3):219-26.
2005: Pare Genevieve C; Easlick Juliet L; Mislow John M; McNally Elizabeth M; Kapiloff Michael S
Nesprin-1alpha contributes to the targeting of mAKAP to the cardiac myocyte nuclear envelope.
Experimental cell research 2005;303(2):388-99.
2004: Lapidos Karen A; Chen Yiyin E; Earley Judy U; Heydemann Ahlke; Huber Jill M; Chien Marcia; Ma Averil; McNally Elizabeth M
Transplanted hematopoietic stem cells demonstrate impaired sarcoglycan expression after engraftment into cardiac and skeletal muscle.
The Journal of clinical investigation 2004;114(11):1577-85.
2004: Heydemann Ahlke; McNally Elizabeth M
Regenerating more than muscle in muscular dystrophy.
Circulation 2004;110(21):3290-2.
2004: Boone David L; Turer Emre E; Lee Eric G; Ahmad Regina-Celeste; Wheeler Matthew T; Tsui Colleen; Hurley Paula; Chien Marcia; Chai Sophia; Hitotsumatsu Osamu; McNally Elizabeth; Pickart Cecile; Ma Averil
The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses.
Nature immunology 2004;5(10):1052-60.
2004: Allikian Michael J; Hack Andrew A; Mewborn Stephanie; Mayer Ulrike; McNally Elizabeth M
Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle.
Journal of cell science 2004;117(Pt 17):3821-30.
2004: McNally Elizabeth M; Towbin Jeffrey A
Cardiomyopathy in muscular dystrophy workshop. 28-30 September 2003, Tucson, Arizona.
Neuromuscular disorders : NMD 2004;14(7):442-8.
2004: McNally Elizabeth M
Powerful genes--myostatin regulation of human muscle mass.
The New England journal of medicine 2004;350(26):2642-4.
2004: Lapidos Karen A; Kakkar Rahul; McNally Elizabeth M
The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
Circulation research 2004;94(8):1023-31.
2004: Wheeler Matthew T; Allikian Michael J; Heydemann Ahlke; Hadhazy Michele; Zarnegar Sara; McNally Elizabeth M
Smooth muscle cell-extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy.
The Journal of clinical investigation 2004;113(5):668-75.
2004: Wheeler Matthew T; Korcarz Claudia E; Collins Keith A; Lapidos Karen A; Hack Andrew A; Lyons Matthew R; Zarnegar Sara; Earley Judy U; Lang Roberto M; McNally Elizabeth M
Secondary coronary artery vasospasm promotes cardiomyopathy progression.
The American journal of pathology 2004;164(3):1063-71.
2004: Heydemann Ahlke; Huber Jill M; Kakkar Rahul; Wheeler Matthew T; McNally Elizabeth M
Functional nitric oxide synthase mislocalization in cardiomyopathy.
Journal of molecular and cellular cardiology 2004;36(2):213-23.
2003: Muchir Antoine; van Engelen Baziel G; Lammens Martin; Mislow John M; McNally Elizabeth; Schwartz Ketty; Bonne Gisèle
Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene.
Experimental cell research 2003;291(2):352-62.
2003: Doherty Katherine R; McNally Elizabeth M
Repairing the tears: dysferlin in muscle membrane repair.
Trends in molecular medicine 2003;9(8):327-30.
2003: Wheeler Matthew T; McNally Elizabeth M
Sarcoglycans in vascular smooth and striated muscle.
Trends in cardiovascular medicine 2003;13(6):238-43.
2003: MacLeod Heather M; Culley Mary R; Huber Jill M; McNally Elizabeth M
Lamin A/C truncation in dilated cardiomyopathy with conduction disease.
BMC medical genetics 2003;4():4.
2003: McNally Elizabeth; Allikian Michael; Wheeler Matthew T; Mislow John M; Heydemann Ahlke
Cytoskeletal defects in cardiomyopathy.
Journal of molecular and cellular cardiology 2003;35(3):231-41.
2002: Wheeler Matthew T; Zarnegar Sara; McNally Elizabeth M
Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy.
Human molecular genetics 2002;11(18):2147-54.
2002: Mislow John M K; Holaska James M; Kim Marian S; Lee Kenneth K; Segura-Totten Miriam; Wilson Katherine L; McNally Elizabeth M
Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro.
FEBS letters 2002;525(1-3):135-40.
2002: Chutkow William A; Pu Jielin; Wheeler Matthew T; Wada Tomoyuki; Makielski Jonathan C; Burant Charles F; McNally Elizabeth M
Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 K(ATP) channels.
The Journal of clinical investigation 2002;110(2):203-8.
2002: Zhu Xiaolei; Wheeler Matthew T; Hadhazy Michele; Lam Man-Yee J; McNally Elizabeth M
Cardiomyopathy is independent of skeletal muscle disease in muscular dystrophy.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2002;16(9):1096-8.
2002: Davis Dawn Belt; Doherty Katherine R; Delmonte Anthony J; McNally Elizabeth M
Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains.
The Journal of biological chemistry 2002;277(25):22883-8.
2002: McNally Elizabeth M
Beta-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy: the usual suspect?
Circulation research 2002;90(3):246-7.
2002: Mislow John M K; Kim Marian S; Davis Dawn Belt; McNally Elizabeth M
Myne-1, a spectrin repeat transmembrane protein of the myocyte inner nuclear membrane, interacts with lamin A/C.
Journal of cell science 2002;115(Pt 1):61-70.
2002: Wheeler M T; Allikian M J; Heydemann A; McNally E M
The sarcoglycan complex in striated and vascular smooth muscle.
Cold Spring Harbor symposia on quantitative biology 2002;67():389-97.
2001: Vainzof M; Anderson L V; McNally E M; Davis D B; Faulkner G; Valle G; Moreira E S; Pavanello R C; Passos-Bueno M R; Zatz M
Dysferlin protein analysis in limb-girdle muscular dystrophies.
Journal of molecular neuroscience : MN 2001;17(1):71-80.
2001: Zhu X; Hadhazy M; Groh M E; Wheeler M T; Wollmann R; McNally E M
Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly.
The Journal of biological chemistry 2001;276(24):21785-90.
2001: Heydemann A; Wheeler M T; McNally E M
Cardiomyopathy in animal models of muscular dystrophy.
Current opinion in cardiology 2001;16(3):211-7.
2001: Porter J D; Merriam A P; Hack A A; Andrade F H; McNally E M
Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice.
Neuromuscular disorders : NMD 2001;11(2):197-207.
2001: Cordier L; Gao G P; Hack A A; McNally E M; Wilson J M; Chirmule N; Sweeney H L
Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies.
Human gene therapy 2001;12(2):205-15.
2000: Hack A A; Lam M Y; Cordier L; Shoturma D I; Ly C T; Hadhazy M A; Hadhazy M R; Sweeney H L; McNally E M
Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.
Journal of cell science 2000;113 ( Pt 14)():2535-44.
2000: Zhu X; Hadhazy M; Wehling M; Tidball J G; McNally E M
Dominant negative myostatin produces hypertrophy without hyperplasia in muscle.
FEBS letters 2000;474(1):71-5.
2000: McNally E M; Ly C T; Rosenmann H; Mitrani Rosenbaum S; Jiang W; Anderson L V; Soffer D; Argov Z
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
American journal of medical genetics 2000;91(4):305-12.
2000: Cordier L; Hack A A; Scott M O; Barton-Davis E R; Gao G; Wilson J M; McNally E M; Sweeney H L
Rescue of skeletal muscles of gamma-sarcoglycan-deficient mice with adeno-associated virus-mediated gene transfer.
Molecular therapy : the journal of the American Society of Gene Therapy 2000;1(2):119-29.
2000: Nowak K J; Walsh P; Jacob R L; Johnsen R D; Peverall J; McNally E M; Wilton S D; Kakulas B A; Laing N G
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion.
Neuromuscular disorders : NMD 2000;10(2):100-7.
2000: Hack A A; Groh M E; McNally E M
Sarcoglycans in muscular dystrophy.
Microscopy research and technique 2000;48(3-4):167-80.
2000: Thompson T G; Chan Y M; Hack A A; Brosius M; Rajala M; Lidov H G; McNally E M; Watkins S; Kunkel L M
Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein.
The Journal of cell biology 2000;148(1):115-26.
2000: Davis D B; Delmonte A J; Ly C T; McNally E M
Myoferlin, a candidate gene and potential modifier of muscular dystrophy.
Human molecular genetics 2000;9(2):217-26.
1999: Hack A A; Cordier L; Shoturma D I; Lam M Y; Sweeney H L; McNally E M
Muscle degeneration without mechanical injury in sarcoglycan deficiency.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(19):10723-8.
1998: Hack A A; Ly C T; Jiang F; Clendenin C J; Sigrist K S; Wollmann R L; McNally E M
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin.
The Journal of cell biology 1998;142(5):1279-87.
1998: McNally E M; de Sá Moreira E; Duggan D J; Bönnemann C G; Lisanti M P; Lidov H G; Vainzof M; Passos-Bueno M R; Hoffman E P; Zatz M; Kunkel L M
Caveolin-3 in muscular dystrophy.
Human molecular genetics 1998;7(5):871-7.
1998: McNally E M; Ly C T; Kunkel L M
Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene.
FEBS letters 1998;422(1):27-32.
1997: Messina D N; Speer M C; Pericak-Vance M A; McNally E M
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.
American journal of human genetics 1997;61(4):909-17.
1997: van der Kooi A J; van Meegen M; Ledderhof T M; McNally E M; de Visser M; Bolhuis P A
Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.
American journal of human genetics 1997;60(4):891-5.
1996: Bönnemann C G; McNally E M; Kunkel L M
Beyond dystrophin: current progress in the muscular dystrophies.
Current opinion in pediatrics 1996;8(6):569-82.
1996: Vainzof M; Passos-Bueno M R; Canovas M; Moreira E S; Pavanello R C; Marie S K; Anderson L V; Bonnemann C G; McNally E M; Nigro V; Kunkel L M; Zatz M
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics 1996;5(12):1963-9.
1996: Bönnemann C G; Passos-Bueno M R; McNally E M; Vainzof M; de Sá Moreira E; Marie S K; Pavanello R C; Noguchi S; Ozawa E; Zatz M; Kunkel L M
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
Human molecular genetics 1996;5(12):1953-61.
1996: McNally E M; Duggan D; Gorospe J R; Bönnemann C G; Fanin M; Pegoraro E; Lidov H G; Noguchi S; Ozawa E; Finkel R S; Cruse R P; Angelini C; Kunkel L M; Hoffman E P
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.
Human molecular genetics 1996;5(11):1841-7.
1996: McNally E M; Passos-Bueno M R; Bönnemann C G; Vainzof M; de Sá Moreira E; Lidov H G; Othmane K B; Denton P H; Vance J M; Zatz M; Kunkel L M
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
American journal of human genetics 1996;59(5):1040-7.
1996: McNally E M; Bönnemann C G; Kunkel L M; Bhattacharya S K
Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy.
The New England journal of medicine 1996;334(24):1610-1.
1995: Bönnemann C G; Modi R; Noguchi S; Mizuno Y; Yoshida M; Gussoni E; McNally E M; Duggan D J; Angelini C; Hoffman E P
Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex.
Nature genetics 1995;11(3):266-73.
1995: Noguchi S; McNally E M; Ben Othmane K; Hagiwara Y; Mizuno Y; Yoshida M; Yamamoto H; Bönnemann C G; Gussoni E; Denton P H; Kyriakides T; Middleton L; Hentati F; Ben Hamida M; Nonaka I; Vance J M; Kunkel L M; Ozawa E
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.
Science (New York, N.Y.) 1995;270(5237):819-22.
1995: Byers T J; Beggs A H; McNally E M; Kunkel L M
Novel actin crosslinker superfamily member identified by a two step degenerate PCR procedure.
FEBS letters 1995;368(3):500-4.
1994: McNally E M; Yoshida M; Mizuno Y; Ozawa E; Kunkel L M
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(21):9690-4.
1991: Kitsis R N; Buttrick P M; McNally E M; Kaplan M L; Leinwand L A
Hormonal modulation of a gene injected into rat heart in vivo.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(10):4138-42.
1991: McNally E M; Bravo-Zehnder M M; Leinwand L A
Identification of sequences necessary for the association of cardiac myosin subunits.
The Journal of cell biology 1991;113(3):585-90.
1990: Rovner A S; McNally E M; Leinwand L A
Complete cDNA sequence of rat atrial myosin light chain 1: patterns of expression during development and with hypertension.
Nucleic acids research 1990;18(6):1581-6.
1989: McNally E M; Kraft R; Bravo-Zehnder M; Taylor D A; Leinwand L A
Full-length rat alpha and beta cardiac myosin heavy chain sequences. Comparisons suggest a molecular basis for functional differences.
Journal of molecular biology 1989;210(3):665-71.
1989: McNally E M; Gianola K M; Leinwand L A
Complete nucleotide sequence of full length cDNA for rat alpha cardiac myosin heavy chain.
Nucleic acids research 1989;17(18):7527-8.
1989: McNally E M; Buttrick P M; Leinwand L A
Ventricular myosin light chain 1 is developmentally regulated and does not change in hypertension.
Nucleic acids research 1989;17(7):2753-67.
1989: Leinwand L A; Sohn R; Frankel S A; Goodwin E B; McNally E M
Bacterial expression of eukaryotic contractile proteins.
Cell motility and the cytoskeleton 1989;14(1):3-11.
1988: McNally E M; Goodwin E B; Spudich J A; Leinwand L A
Coexpression and assembly of myosin heavy chain and myosin light chain in Escherichia coli.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(19):7270-3.
1987: Toyoshima Y Y; Kron S J; McNally E M; Niebling K R; Toyoshima C; Spudich J A
Myosin subfragment-1 is sufficient to move actin filaments in vitro.
Nature 1987;328(6130):536-9.
1987: Saez L J; Gianola K M; McNally E M; Feghali R; Eddy R; Shows T B; Leinwand L A
Human cardiac myosin heavy chain genes and their linkage in the genome.
Nucleic acids research 1987;15(13):5443-59.

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Elizabeth McNally

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