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Grants at a Glance — Summer 2011

  • Don Cleveland (ALS)

    ALS — Cleveland

    MDA has awarded a research grant totaling $429,983 over three years to Don Cleveland, departmental chair of cellular and molecular medicine; professor of medicine, neurosciences, and cellular and molecular medicine; and member of the Ludwig Institute for Cancer Research in La Jolla, Calif. The funds will help support Cleveland’s research into the connection between mitochondria and ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Raymond Grill (ALS)

    ALS — Grill

    MDA has awarded a research grant totaling $202,508 over a period of three years to Raymond Grill, assistant professor in the department of integrative biology and pharmacology at the University of Texas Health Science Center, Houston. The funds will support testing in the SOD1 mouse model of an experimental combination drug treatment in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Vasanthi Jayaraman (ALS): This illustration depicts the structure of the agonist binding domain of the AMPA receptor with attached fluorophores, shown as pink and orange balls.

    ALS — Jayaraman

    MDA awarded $294,183 over three years to Vasanthi Jayaraman, an associate professor in the department of biochemistry and molecular biology at the University of Texas Health Science Center in Houston. The funds will help support Jayaraman’s study of the molecular mechanisms underlying motor neuron death in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Jasna Kriz (ALS): This photo of a living “SOD1 mutant reporter mouse” illustrates a 3-dimensional representation of early neuronal stress. Such assessments can be made over a period of time and in a noninvasive manner.

    ALS — Kriz

    Jasna Kriz, associate professor in the department of psychiatry and neuroscience at Laval University, Quebec City, Canada, was awarded an MDA research grant totaling $445,086 over a period of three years to help refine and describe a new mouse model that will enable scientists to visualize different aspects of the disease process in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Clotilde Lagier-Tourenne (ALS)

    ALS — Lagier-Tourenne

    Clotilde Lagier-Tourenne, a postdoctoral fellow at the University of California, San Diego, in La Jolla, was awarded an MDA development grant totaling $180,000 over a period of three years to study the roles of two proteins, TDP43 and FUS, in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Youngjin Lee (ALS)

    ALS — Lee

    Youngjin Lee, postdoctoral associate in the department of neurology at Johns Hopkins University School of Medicine in Baltimore was awarded an MDA development grant totaling $179,997 over three years. The funds will support Lee's study of the role of a protein called MCT-1 in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Junping Xin (ALS)

    ALS — Xin

    MDA has awarded a development grant totaling $180,000 over a period of three years to Junping Xin, research associate at the Neuroscience Institute, Loyola University Medical Center in Chicago, and Edward Hines Jr. Veterans Administration Hospital in Hines, Ill. The funds will help support Xin’s research into the possible effects of immune system dysfunction in ALS (amyotrophic lateral sclerosis, or Lou Gehrig's disease).

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  • Susan Hamilton (CCD/MH): Researchers in Hamilton's lab, postdoctoral fellow Adan Dagnino-Acosta (left) and graduate student Joshua Oakes.

    CCD/MH — Hamilton

    MDA has awarded a research grant totaling $375,000 over a period of three years to Susan Hamilton, L.F. McCollum Chair in Molecular Physiology, department of molecular physiology and biophysics at Baylor College of Medicine in Houston. The funds will help support Hamilton’s study of the molecular mechanisms underlying a wide spectrum of muscle disorders including central core disease (CCD) and malignant hyperthermia (MH).

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  • Sonja Nowotschin (CMD): Here, Nowotschin looks at images of mouse embryos.

    CMD — Nowotschin

    Sonja Nowotschin, a postdoctoral research fellow in the developmental biology department at the Sloan-Kettering Institute in New York, has been awarded an MDA development grant totaling $163,638 over three years. (Development grants are MDA's mechanism for furthering the career development of promising young researchers.)

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  • Susan Brown (CMD/LGMD)

    CMD/LGMD — Brown

    Susan Brown, a reader (equivalent to associate professor) in translational medicine at the Royal Veterinary College in London, has been awarded an MDA grant totaling $356,838 over three years. The grant will help support Brown's research on muscular dystrophies related to mutations in the gene for fukutin-related protein (FKRP).

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  • Diego Fraidenraich (DMD)

    DMD — Fraidenraich

    Diego Fraidenraich, an assistant professor in the department of cell biology & molecular medicine at the University of Medicine and Dentistry of New Jersey, was awarded an MDA grant totaling $375,000 over three years. The funds will support his study of the relationship between muscle and fat formation in a mouse model of Duchenne muscular dystrophy (DMD).

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  • Jasprina Noordermeer (DMD): Jasprina with co-investigator Lee Fradkin (left).

    DMD — Noordermeer

    MDA has awarded a research grant totaling $278,570 over three years to Jasprina Noordermeer, a professor in the department of molecular cell biology at Leiden University Medical Center in the Netherlands. The grant will support Noordermeer's studies of the role of dystrophin in the brain. The dystrophin protein is absent or deficient in boys with Duchenne muscular dystrophy (DMD).

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  • Margaret Zacharin (DMD): Photo of Margaret Zacharin (left) and Craig Munns (right).

    DMD — Zacharin

    Margaret Zacharin, an associate professor in the department of endocrinology and diabetes at Royal Children's Hospital in Parkville, Victoria, Australia, has been awarded an MDA research grant totaling $268,021 over two years. The award will help support a clinical trial of the drug zoledronic acid in children and adolescents with Duchenne muscular dystrophy (DMD).

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  • Martin Childers (DMD/BMD)

    DMD/BMD — Childers

    Martin Childers, a professor at the Institute for Regenerative Medicine in Winston-Salem, N.C., has been awarded an MDA grant totaling $480,000 over three years. The Institute is part of Wake Forest University Baptist Medical Center.

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  • Peter Currie (DMD/BMD)

    DMD/BMD — Currie

    Peter Currie, a professor of medicine at Monash University in Clayton, Victoria, Australia, was awarded an MDA research grant totaling $375,000 over three years. The funds will help support Currie's research, which involves screening for possible therapeutic molecules using the zebrafish model of Duchenne muscular dystrophy (DMD).

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  • Emanuela Gussoni (DMD/BMD): Immature muscle fibers called myotubes (green) and their nuclei (blue) developed from MCAM-producing cells extracted from human muscle and cultured in the laboratory. Cells with the MCAM protein on the surface may be good candidates for cell transplantation to treat muscular dystrophies.

    DMD/BMD — Gussoni

    MDA has awarded a grant totaling $384,066 over three years to Emanuela Gussoni, an assistant professor in the division of genetics and program in genomics at Children's Hospital Boston and Harvard University. The grant will support Gussoni's studies to improve the efficacy of stem cell transplantation as a strategy to treat Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD) and possibly other forms of muscular dystrophy.

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  • Tejvir Khurana (DMD/BMD)

    DMD/BMD — Khurana

    MDA has awarded a research grant totaling $379,500 over three years to Tejvir Khurana, a professor of physiology at the University of Pennsylvania. The grant will support Khurana's research to increase the production of utrophin, a protein that may improve muscle strength and function in Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD).

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  • Paul Martin (DMD/BMD)

    DMD/BMD — Martin

    Paul Martin, a professor of pediatrics and of physiology and cell biology at Ohio State University College of Medicine, has been awarded an MDA grant totaling $396,000 over three years. The award will help support Martin's study of the possible therapeutic effects of an enzyme called GALGT2 in Duchenne muscular dystrophy (DMD).

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  • Terence Partridge (DMD/BMD)

    DMD/BMD — Partridge

    MDA has awarded a research grant totaling $474,278 over three years to Terence Partridge, a professor of pediatrics at George Washington University Medical School and Children's National Medical Center in Washington, D.C. The award will help support Partridge's work to improve the usefulness of the standard mouse model of Duchenne muscular dystrophy (DMD), the so-called "mdx" mouse.

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  • Thomas Rando (DMD/BMD)

    DMD/BMD — Rando

    MDA has awarded a research grant totaling $602,087 over three years to Thomas Rando, a professor in the department of neurology and neurological sciences at Stanford (Calif.) University School of Medicine. The grant will help support Rando's studies to understand how scar-tissue formation (fibrosis) occurs in muscular dystrophies, especially Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). DMD is caused by an absence of the dystrophin protein, and BMD is caused by dystrophin protein that's only partially functional.

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  • Michael Rudnicki (DMD/BMD)

    DMD/BMD — Rudnicki

    MDA has awarded a grant totaling $375,000 over three years to Michael Rudnicki, director of the Regenerative Medicine Program at Ottawa Hospital Research Institute and a professor in the department of medicine at the University of Ottawa, Canada. This funding will support Rudnicki's continuing studies on the function of muscle satellite cells in mice with a disease resembling human Duchenne muscular dystrophy (DMD).

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  • Alessandra Sacco (DMD/BMD)

    DMD/BMD — Sacco

    MDA has awarded a research grant totaling $447,092 over three years to Alessandra Sacco, an assistant professor in the Muscle Development and Regeneration Program at Sanford-Burnham Medical Research Institute in La Jolla, Calif. The grant will help support Sacco's research on early-stage transplantation of muscle stem cells to treat a mouse model of Duchenne muscular dystrophy (DMD).

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  • Melissa Spencer (DMD/BMD): Pictured is a section (left) of a diaphragm muscle taken from a dystrophin-deficient mouse (top, lower magnification; bottom, higher magnification). Immune system cells are stained red. On the right is a section of a diaphragm muscle taken from a dystrophin-deficient, osteopontin-deficient mouse. There are almost no immune system cells in this sample.

    DMD/BMD — Spencer

    Melissa Spencer, professor of neurology and co-director of the Center for Duchenne Muscular Dystrophy at the University of California, Los Angeles, has been awarded an MDA grant totaling $501,493 over three years. The funds will help support Spencer's continuing studies of the role of a protein called osteopontin and of inflammatory processes in a mouse model of Duchenne muscular dystrophy (DMD).

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  • David Lynch (FA): Lynch's research team will use a process called frataxin dipstick testing in its studies to determine the relationship between abnormal resistance of the hormone insulin and Friedreich's ataxia.

    FA — Lynch

    MDA has awarded a research grant totaling $202,222 over two years to David Lynch, professor of neurology at Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine. The funds will help support Lynch's study of the relationship between diabetes and Friedreich's ataxia (FA).

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  • Des Richardson (FA): Richardson (back, right) and colleagues, aim to obtain new information regarding the function of frataxin protein, a deficiency of which is the cause of Friedreich's ataxia.

    FA — Richardson

    MDA has awarded a research grant totaling $625,959 over a period of three years to Des Richardson, professor and senior principal research fellow at the University of Sydney (Australia) School of Medical Sciences. The funds will help support Richardson's continued research into iron metabolism in Friedreich's ataxia (FA).

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  • Michael Kyba (FSHD): Kyba displays a plate that shows the results of testing on different inhibitors for DUX4. The inhibitors are candidate therapies for facioscapulohumeral muscular dystrophy.

    FSHD — Kyba

    MDA awarded a research grant totaling $375,000 over three years to Michael Kyba, assistant professor in the Lillehei Heart Institute and department of pediatrics at the University of Minnesota in Minneapolis. The funds will help support Kyba's efforts to identify and test experimental therapies in facioscapulohumeral muscular dystrophy (FSH, or FSHD).

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  • Fedik Rahimov (FSHD)

    FSHD — Rahimov

    MDA has awarded a development grant totaling $180,000 over a period of three years to Fedik Rahimov, a postdoctoral research fellow at the program in genomics at Harvard Medical School and Children's Hospital Boston. The funds will help further elucidate the molecular mechanisms underlying facioscapulohumeral muscular dystrophy (FSH, or FSHD).

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  • Eric Wagner (FSHD): The top panels show the amount of green fluorescence in cells when DUX4 is expressed normally, and the bottom panels demonstrate how the reporter will express green fluorescence when DUX4 expression is inhibited.

    FSHD — Wagner

    MDA awarded a research grant totaling $284,778 over a period of three years to Eric Wagner, an assistant professor in the department of biochemistry and molecular biology at the University of Texas Health Science Center in Houston. The funds will help support Wagner’s investigations into the role of the DUX4 gene in facioscapulohumeral muscular dystrophy (FSH, or FSHD).

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  • Jennifer Levy (LGMD/DD)

    LGMD/DD — Levy

    Jennifer Levy, a postdoctoral research fellow in the department of molecular physiology & biophysics at the University of Iowa Carver College of Medicine, has been awarded an MDA development grant totaling $180,000 over three years. (This type of grant reflects MDA's commitment to the career development of promising young researchers.) The funds will support Levy's research on repair of the muscle-fiber membrane.

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  • Alfred Goldberg (LGMD/IBM)

    LGMD/IBM — Goldberg

    Alfred Goldberg, professor or cell biology at Harvard Medical School in Boston, has received an MDA research grant totaling $410,777 over three years to continue research into the mechanisms underlying muscle atrophy, with particular relevance for limb-girdle muscular dystrophy (LGMD) and possibly inclusion-body myositis (IBM).

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  • Kathryn Wagner (MD)

    MD — Wagner

    MDA has awarded a research grant totaling $362,760 over three years to Kathryn Wagner, an associate professor of neurology and neuroscience at the Johns Hopkins School of Medicine and director of the Center for Genetic Muscle Disorders at the Kennedy Krieger Institute, both in Baltimore.

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  • Carlos Morales (Mito. Myopathy)

    Mito. Myopathy - Morales

    MDA awarded a grant totaling $363,672 to Carlos Moraes, professor of neurology at the University of Miami School of Medicine, to study the effects generated by an increase in functional mitochondria (the "energy factories" in cells) in mitochondrial myopathy.

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  • Edward Owusu-Ansah (Mito. Myopathy)

    Mito. Myopathy — Owusu-Ansah

    MDA has awarded a development grant totaling $180,000 over three years to Edward Owusu-Ansah, a postdoctoral fellow in the department of genetics at Harvard Medical School in Boston. The funds will help support Owusu-Ansah's research into the molecular mechanisms underlying mitochondrial myopathies.

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  • Pere Puigserver (Mito. Myopathy)

    Mito. Myopathy — Puigserver

    MDA has awarded a research grant totaling $313,551 over three years to Pere Puigserver, associate professor in the department of cancer biology at the Dana-Farber Cancer Institute, and department of cell biology at Harvard Medical School in Boston. The funds will help support Puigserver’s research into the study of two newly identified genes that may increase muscle performance in mitochondrial myopathies.

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  • Samantha Harris (Muscle Physiology): Shown in green is myosin binding protein C. The red bands indicate another protein, called myomesin. Each green and red unit is a sarcomere, the basic contractile unit of muscle tissue.

    Muscle Physiology — Harris

    Samantha Harris, an associate professor in the department of neurobiology, physiology and behavior at the University of California, Davis, has been awarded an MDA grant totaling $244,024 over two years. The funding will help Harris in her quest to determine the properties of a skeletal-muscle protein called myosin binding protein C.

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  • Kristen Nowak (Muscle Physiology)

    Muscle Physiology — Nowak

    MDA awarded a research grant totaling $329,091 over two years to Kristen Nowak, an associate professor at the University of Western Australia in Perth, and the Western Australian Institute for Medical Research. The funds will support Nowak's study of diseases caused by defects in the skeletal muscle actin gene, which include "essentially any genetic neuromuscular disease that tends to be severe in some patients and mild in others." 

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  • Alan Beggs (Myopathies)

    Myopathies — Beggs

    Alan Beggs, a professor of pediatrics at Harvard Medical School and director of the Manton Center for Orphan Disease Research at Children's Hospital Boston, has been awarded an MDA grant totaling $396,990 over three years. The funds will help support Beggs' research on the molecular genetics of congenital myopathies.

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  • Stephen Cannon (Periodic Paralysis)

    Periodic Paralysis — Cannon

    MDA has awarded a research grant totaling $404,274 over three years to Stephen Cannon, professor of neurology and associate dean for undergraduate medical education at the University of Texas Southwestern Medical Center in Dallas. The funds will help support Cannon’s research into attacks of paralysis in people with periodic paralysis (PP).

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  • Maria Pennuto (SBMA)

    SBMA — Pennuto

    MDA has awarded a research grant totaling $330,000 over three years to Maria Pennuto at the Italian Institute of Technology in Genova, Italy. The funds will help support Pennuto's continued studies of the molecular mechanisms underlying spinal-bulbar muscular atrophy (SBMA).

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  • Lisa Baumbach (SMA): Baumbach (front, right) with the other members of the lab team.

    SMA — Baumbach

    MDA has awarded a research grant totaling $387,228 over three years to Lisa Baumbach, associate professor in the departments of neurology, pediatrics and biochemistry at the Miller School of Medicine at the University of Miami. The funds will help Baumbach continue to search for disease-causing genes responsible for infantile (either X-linked or type 1) spinal muscular atrophy (SMA).

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In July 2011, the MDA Board of Directors approved funding for 40 research projects, targeting nearly two dozen neuromuscular diseases. These projects are in addition to some 300 grants currently funded by MDA.

For an overview of grants awarded by MDA in July 2011, see:

  • MDA Awards $13.7 Million in Research Grants
  • MDA Awards More Than $2.5 Million in Grants to Stop ALS

For a list of some 300 grants currently being funded by MDA, view this PDF.

ALS — Cleveland ›

Grants at a Glance

Summer 2012
Winter 2012
Summer 2011
Winter 2011
Summer 2010

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    • Volume 1, Issue 1, October 2011
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Grants at a Glance — Summer 2011

  • ALS — Cleveland
  • ALS — Grill
  • ALS — Jayaraman
  • ALS — Kriz
  • ALS — Lagier-Tourenne
  • ALS — Lee
  • ALS — Xin
  • CCD/MH — Hamilton
  • CMD — Nowotschin
  • CMD/LGMD — Brown
  • DMD — Fraidenraich
  • DMD — Noordermeer
  • DMD — Zacharin
  • DMD/BMD — Childers
  • DMD/BMD — Currie
  • DMD/BMD — Gussoni
  • DMD/BMD — Khurana
  • DMD/BMD — Martin
  • DMD/BMD — Partridge
  • DMD/BMD — Rando
  • DMD/BMD — Rudnicki
  • DMD/BMD — Sacco
  • DMD/BMD — Spencer
  • FA — Lynch
  • FA — Richardson
  • FSHD — Kyba
  • FSHD — Rahimov
  • FSHD — Wagner
  • LGMD/DD — Levy
  • LGMD/IBM — Goldberg
  • MD — Wagner
  • Mito. Myopathy - Morales
  • Mito. Myopathy — Owusu-Ansah
  • Mito. Myopathy — Puigserver
  • Muscle Physiology — Harris
  • Muscle Physiology — Nowak
  • Myopathies — Beggs
  • Periodic Paralysis — Cannon
  • SBMA — Pennuto
  • SMA — Baumbach
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