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Healthcare Professionals: Research Fellowships

 

Research Fellowships for nurses, medical students and post-doctoral research are awarded annually. The purpose of these research awards is to attract physicians, PhD scientists and allied heath professionals into conducting research into Myasthenia Gravis or related conditions.

Post-Doctoral Fellowship:
A qualified candidate desiring training in Myasthenia Gravis research first finds a scientist with an established research program who will agree to serve as a mentor and supervise the proposed research plan. The research plan can be basic or clinical research. The Research Committee is appointed by the Chair of the Medical Advisory Board. Scientists are chosen for this committee on the basis of their ability and their special knowledge and experience in Myasthenia Gravis. This twelve-month post-doctoral fellowship is awarded for clinical or basic research related to MG or related neuromuscular disorders. Research may be concerned with the neuromuscular transmission, immunology, molecular or cell biology of the neuromuscular synapse, or the etiology/pathology or diagnosis of mg.

Funding of Post-Doctoral Fellowships is dependent upon available funding. We are currently not accepting applications.

Download the Post-Doctoral Fellowship Application (PDF)

Student Fellowship:
This fellowship is awarded to current medical students or graduate students interested in the scientific basis of myasthenia gravis. Annual deadline for applications is March 15.

Download the Student Fellowship Application (PDF)

Nursing Fellowship:
These fellowships are awarded annually to nurses or nursing students interested in studying problems encountered by patients with MG or related neuromuscular conditions. Annual deadline for applications is October 15.

Download the Nursing Fellowship Application:
Click-and-type Word version | PDF version


Research Fellowships Awarded

Post-Doctoral Fellowships

Student Fellowships

Nursing Fellowships


Post-Doctoral Fellowships

2007

Jianrong Sheng, PhD
University of Illinois, Chicago, Illinois
Project: Immunoregulation of Experimental Autoimmune Myasthenia Gravis using Granulocyte-Macrophange Colony-Stimulating Factor (GM-CSF)
Research conducted under the direction of Dr. Bellur Prabhakar and Dr. Matthew Meriggioli.

This project is investigating the use of a specific growth factor (GM-CSF) to induce a specialized type of immune cell (T regulatory lymphocytes) as a treatment for mice with MG. Previous work in this area has shown this strategy to be effective in preventing mice from acquiring experimentally-induced MG. The desired outcome of this current research is to use the immune system's own regulatory network to establish immune balance, eliminating the need for chronic immunosuppression.

Shalini Muhherjee, PhD
The University of Texas Southwestern Medical Center, Dallas, Texas
Project: Antibody Mediated Modulation of Neuronal Nicotinic Acetylcholine Receptors
Research conducted under the direction Dr. Steven Verino

This project investigates the relationship between two antibody-mediated diseases that involve an attack on acetylcholine receptors (AChRs): autoimmune autonomic neuropathy (AAN) and myasthenia gravis (MG). In MG, the antibodies reduce the amount of AChR available to the muscle and damage muscle membrane, whereas in AAN the antibodies attack AChRs on the nerve cell, impairing communication between nerve cells. This research expects to yield important information about the process that occurs in antibody-mediated diseases such as myasthenia gravis.

Jennifer Anderson, PhD
University of California, Davis, California
Project: "Allele-Specific RNAi Treatment for Slow-Channel Syndrome Caused by M2 Acetylcholine Receptor Mutations"
Research conducted under the direction of Dr. Ricardo Maselli

This project investigates the potential treatment for slow-channel syndrome (SCS), a form of congenital myasthenic syndrome (CMS). This strategy involves developing gene therapy that will silence the abnormal gene, which contributes to the development of slow channel syndrome. The protocol is currently concluded in the in-vitro (test tube) phase and will proceed to in-vivo research in mice.

Amir Sabouri, MD - Second year of funding
The Scripps Research Institute, La Jolla, California
Research: Role of BAFF in the Development of Experimental Autoimmune Myasthenia Gravis
Research conducted under the direction of Nora Sarvetnick, PhD.

Research Summary:
These investigators will use a mouse model to determine the role of BAFF as a key factor in the development of MG. This type of research aims to clarify the key steps or ingredients that might explain how and why MG develops. The investigators hypothesize that:
  1. The BAFF molecule is involved in the occurrence of clinical EAMG.
  2. Mice with BAFF deficiency are less susceptible or resistant to EAMG.
  3. Over-expression of BAFF in EAMG-susceptible mice accelerates in incidence and severity of the disease.
  4. BAFF inhibition attenuates the EAMG development.
From the clinician's and patient's standpoint, the importance of this research is in knowing what triggers the immune system to initiate the disease. The work has significant clinical implications, as knowing the trigger for the disease may allow for a new opportunity or strategy for treatment as well as preventative options.

2006

Jing Li, MD
University of Texas Medical Branch
Project: Ocular Myasthenia Gravis in HLA Transgenic mice: Role of DAF. (Second year of funding)

Research Summary:
This research is being conducted under the direction of Permkumar Christadoss, M.D. The basic issues with this research center on gaining a better understanding of the triggers, influences, and factors involved with the initiation of MG and perhaps more importantly those factors involved with a clinical flareup of the disease. We know that complement activation resulting from autoantibody binding to AChR is a key event in the malfunction of the neuromuscular junction. It has been observed that complement activation (the bad stuff) is regulated by a number of factors that serve to prevent complementrelated injury to normal cells. One of these factors is the “decay-accelerating factor,” or DAF. There is evidence that DAF is reduced in extra-ocular muscles (perhaps a reason why extra-ocular muscles are preferentially affected in MG). Dr. Li and colleagues are studying the role of DAF in MG in mice. Mice that lack DAF are markedly more susceptible to anti-AChR-induced MG, and this work may lead to further insight into the development of complement inhibitors as new treatment options for MG. MGFA, its Medical and Scientific Advisory Board (MSAB), our patients, and their families should stay alert to the potential for “complement inhibitors” to become a useful new treatment of MG, especially in acute flares.

Chih-Te Wu, MD
University of California at Davis, CA
Research: Is Glutathione or Another Sulfhydryl-Reducing Agent the Trigger of Autoimmune Myasthenia Gravis?

Research Summary:
The trigger of idiopathic autoimmune MG remains an unsolved riddle. Why is it that only one in 10,000 people develop MG? We need to clarify the fundamental trigger that disrupts our normal immunological tolerance for the acetylcholine receptor and leads to the production of acetylcholine receptor antibodies. Such information will provide new opportunities to treat MG and perhaps prevent it from starting. Certain drugs, such as penicillamine, are known to cause autoimmune MG in occasional patients. Based on prior research of the mechanism for drug-induced MG, Dr. Wu is exploring similar mechanisms that could prove to be the “trigger” or “switch” that turns on the disease. Not only is it essential that we discover the underlying trigger for MG but, from a practical standpoint, such information should be expected to provide us with new strategies to treat MG—and perhaps even prevent it from occurring. It is certainly possible that, if the switch that turns the disease on is located, then a method of turning the switch off will follow.

Amir Sabouri, MD
Research: Role of BAFF in the Development of Experimental Autoimmune Myasthenia Gravis
Research conducted under the direction of Nora Sarvetnick, PhD.

Research Summary:
These investigators will use a mouse model to determine the role of BAFF as a key factor in the development of MG. This type of research aims to clarify the key steps or ingredients that might explain how and why MG develops. The investigators hypothesize that:
  1. The BAFF molecule is involved in the occurrence of clinical EAMG.
  2. Mice with BAFF deficiency are less susceptible or resistant to EAMG.
  3. Over-expression of BAFF in EAMG-susceptible mice accelerates in incidence and severity of the disease.
  4. BAFF inhibition attenuates the EAMG development.
From the clinician’s and patient’s standpoint, the importance of this research is in knowing what triggers the immune system to initiate the disease. The work has significant clinical implications, as knowing the trigger for the disease may allow for a new opportunity or strategy for treatment as well as preventative options.

2005

Jing Li, MD
University of Texas Medical Branch
Project: Ocular Myasthenia Gravis in HLA Transgenic mice: Role of DAF.
Research conducted under the direction of Premkumar Christadoss, M.D.

Research Summary:
This research is being conducted under the direction of Permkumar Christadoss, M.D. The basic issues with this research center on gaining a better understanding of the triggers, influences, and factors involved with the initiation of MG and perhaps more importantly those factors involved with a clinical flareup of the disease. We know that complement activation resulting from autoantibody binding to AChR is a key event in the malfunction of the neuromuscular junction. It has been observed that complement activation (the bad stuff) is regulated by a number of factors that serve to prevent complementrelated injury to normal cells. One of these factors is the “decay-accelerating factor,” or DAF. There is evidence that DAF is reduced in extra-ocular muscles (perhaps a reason why extra-ocular muscles are preferentially affected in MG). Dr. Li and colleagues are studying the role of DAF in MG in mice. Mice that lack DAF are markedly more susceptible to anti-AChR-induced MG, and this work may lead to further insight into the development of complement inhibitors as new treatment options for MG. MGFA, its Medical and Scientific Advisory Board (MSAB), our patients, and their families should stay alert to the potential for “complement inhibitors” to become a useful new treatment of MG, especially in acute flares.

2004
Nicole E. Pardo, MD
Michigan State University
Research: Nerve Terminal Targets in Lambert-Eaton Myasthenic Syndrome.
Research conducted under the direction of William D. Atchison, PhD.

2003
Deepak Yadav, PhD
Scripps Research Institute in La Jolla, CA
Research: Role of inducible costimulatory molecule (ICOS) in the regulation of Myasthenia Gravis
Research conducted under the direction of Nora Sarvetnick, PhD.

Renewed from 2002
Erdem Tuzun, MD
University of Texas Medical Branch at Galveston
Research: Role of the classical complement pathway in experimental myasthenia gravis"
Research conducted under the direction of Premkumar Christadoss, M.D.

Ji-jun Wan, PhD
University of California at Los Angeles
Research: Congenital myasthenic syndrome due to calcium channel mutations
Research conducted under the direction of Joanna Jen, MD, PhD.

2002
Linda L. Kusner
Case Western Reserve University School of Medicine
Research: Susceptibility of Ocular Muscle to Myasthenia Gravis.
Research conducted under the direction of Henry J. Kaminski, MD.

Erdem Tuzun, MD
University of Texas Medical Branch at Galveston
Research: Role of the classical complement pathway in experimental myasthenia gravis"
Research conducted under the direction of Premkumar Christadoss, M.D.

Ji-jun Wan, PhD
University of California at Los Angeles
Research: Congenital myasthenic syndrome due to calcium channel mutations
Research conducted under the direction of Joanna Jen, MD, PhD.

2001
Soon-Ha Kim, PhD
The Scripps Research Institute
Research: Role of Chemokines and Chemokine Receptors in the Pathogenesis of Myasthenia Gravis.
Research conducted under the direction of Nora Sarvetnick, PhD.

Abdelkrim Hmadcha, Ph.D.
Wayne State University
Research: Regulation of Neuregulin Expression at the Neuromuscular Junction
Research conducted under the direction of Jeffrey A. Loeb, M.D., Ph.D.

2000
Albert Fliss, Ph.D.
University of Maryland School of Medicine
Research: Characterization of the MuSK Signaling Pathway Research conducted under the direction of Robert Bloch, Ph.D. Professor of Physiology

Yang Huan, M.D., Ph.D.
University of Texas Medical Branch in Galveston
Research: Human acetylcholine receptor T cell epitope tolerance in HLA transgenic mice
Research conducted under the direction of Premkumar Christadoss, M.D.

Sue Stacy, M.S.
University of Texas Health Science Center at San Antonio
Research: Age-associated changes in immune regulation in relation to late onset MG.
Research conducted under the direction of Dr. Ellen Kraig, Professor, Department of Cellular and Structural Biology,

1999
Mathilde Poussin, M.D., Ph.D.
Mayo Clinic in Rochester, Minnesota
Research: Mechanisms of Resistance of MHC Class II Mutant and HLA Transgenic Mice to Experimental Autoimmune Myasthenia Gravis."
Research conducted under the direction of Premkumar Christadoss, M.D.

Zhiya Yu, M.D., Ph.D.
Mayo Clinic in Rochester, Minnesota.
Research: Modulation of Human Autoimmune Responses Specific for Acetylcholine Receptor in Chimeric Hu-SCID Mice.
Research conducted under the direction of Dr. Vanda Lennon at Mayo

1998 Marika Falcone, M.D.
University of Arizona
Research: Role of B-lymphocytes as antigen-presenting cells in the induction of the pathogenic T-cell responses against nicotinic acetylcholine receptor

Brian Hare, M.D.
Harvard Medical School
Research: Solution structure determination of a single chain T-cell receptor and design of T-cell ligands with therapeutic potential

Anthony Auerbach, Ph.D. and Claudio Grosman, Ph.D.
State University of New York at Buffalo
Research: Binding, gating and desensitization of the acetylcholine receptor channel

1997
Wade A. Grow, Ph.D.
The Scripps Research Institute
Research: Carbohydrate remodeling in neuromuscular synaptogenesis

Alejandro F. Schinder, PhD
University of California - San Diego
Research: Morphological correlates of activity and neurotropin-induced synaptic modulation

Eleana Smirnova, Ph.D.
University of California - Los Angeles
Research: How dynamin assembles into spirals and then constricts

Hai-Long Wang, Ph.D.
Mayo Clinic
Research: Structural and mechanistic studies of mutations in human AChR underlying congenital myasthenic syndromes

1996
Balaji Balasa, Ph.D.
The Scripps Research Institute
Research: Identification and characterization of the antigen recognized by auto antibodies in myasthenia gravis patients and cytokine transgenic mice: understanding of the pathogenesis of myasthenia gravis

Gabriele Besakova, Ph.D
University of Maryland
Research: The role of 43K and other cytoskeletal proteins in synapse formation

Richard J. Prince, Ph.D.
Mayo Clinic
Research: Structure function studies of nicotinic acetylcholine receptor agonist selectivity

Raghavanpillai Raju, Ph.D.
Mayo Clinic
Research: Role of HLA class II genes in experimental autoimmune myasthenia gravis: studies with HLA-DR3 and HLA-DQ8 transgenic mice

1995
Jacobo Andreose, Pharm.D.
Yale University
Research: Mechanisms of surface delivery of newly synthesized acetylcholine receptors in muscle cells

Caishu Deng, M.D.
University of Texas, Galveston
Research: Interferon-alpha therapy for experimental myasthenia gravis

Medha Gautam, Ph.D.
Washington University, St. Louis
Research: Neuromuscular defects in S-laminin and 43K/RAPSYN mutant mice

Mendell Rimer, Ph.D.
Stanford University
Research: Overexpression of agrin at neuromuscular junctions of rats having experimentally-induced myasthenia gravis

Neelam Wagle, Ph.D.
Northwestern University
Research: The antigen processing pathway in cell-mediated immunity

1994
Eswari Gudipati, Ph.D.
University of California at Davis
Research: Mapping conformationally dependent epitopes of monoclonal antibodies on the acetylcholine receptor

Drake LaFace, Ph.D.
La Jolla Institute for Allergy and Immunology
Research: T-cell receptor utilization in experimental autoimmune myasthenia gravis

Michele A. Sciamanna, Ph.D.
Mayo Clinic
Research: AChR expressed in tumors as a stimulator of myasthenia gravis

1993 Henry Kaminski, M.D.
Case Western Reserve University
Research: Extraocular muscle involvement in myasthenia gravis

Rashimi Kaul, Ph.D.
University of Texas, Galveston
Research: Role of regulator/suppressor cells in experimental autoimmune myasthenia gravis

Lisa Wheatley, M.D.
University of Pennsylvania
Research: Localization of sites of acetylcholine receptor (AChR) expression in the human thymus

1992
William Phillips, Ph.D.
Washington University, St. Louis
Research: Mechanisms controlling AChR density at the neuromuscular junction

Samia Ragheb, PhD.
Wayne State University
Research: T cell receptor in MG

1991
Reneé Anand, Ph.D.
Salk Institute
Research: Structural analysis of muscle and brain AChR subunits by in vitro mutagenesis

Neil Miller, Ph.D.
Yale University
Research: Molecular mechanisms of AChR clustering and modulation

Mary Nastuk, Ph.D.
Worcester Foundation for Experimental Biology
Research: Isolation and characterization of the agrin receptor of muscle


Student Fellowships

2007
Wendy Allman, B.S. Neuroscience, Ph.D. candidate
University of Texas, Galveston
Project: Ocular Experimental MG progresses to Generalized MG by Epitope Spread.
Research conducted under the direction Dr. Premkumar Christadoss
Ms. Allman will investigate the development of B cells, the lymphocytes whose progeny, the plasma cells, produce antibodies, including those autoreactive cells responsible for myasthenia. She will work on the model of MG and investigate how the B cells are initially triggered to become autoreactive.

Sagar Pathak, Undergraduate Biology Major
Northeastern University, Boston, MA
Project: Analysis of a Newly Identified Splicing Variant of Muscle-Specific Kinase
Research conducted under the direction of Dr. David Richman at University of California, Davis.
Mr. Pathak will investigate Muscle-specific kinase (MuSK) recently identified to be another antigen at the neuromuscular junction which initiates auto-antibodies producing MG. He will work with Dr. Richman to obtain the isoforms of human MuSK from human skeletal muscle using molecular biological techniques to clone and express these isoforms.

2005
Iris Wingrove
University of Texas Medical Branch
Research: Ocular Experimental MG progresses to Generalized MG by Epitope Spread.
Research conducted under the direction of Premkumar Christadoss, M.D.

Gina Eom
University of British Columbia
Research: Review the clinical characteristics as well as the results of patients who had "a false positive" acetylcholine receptor antibody level.
Research conducted under the direction of Joel Oger D en M, FRCPC

Lindsey Knudsen
University of Wisconsin - Milwaukee
Research: The effects of psychological counseling of people with myasthenia gravis.
Research conducted under the direction of Deborah E. Renard PhD:

2004
Dan Chao
Stanford University
Research: Elucidating Molecular Mechanisms of Synapse Specificity
Research conducted under the direction of Kang Shen, MD, PhD

Sidharth Ghosh
University of Texas Medical Branch at Galveston
Research: Role of NK Cells in Secondary Immune Response to Acetylcholine Receptor in Experimental Autoimmune Myasthenia Gravis
Research conducted under the direction of Premkumar Christadoss, M.D.

Joshua Mozes
University of California at Davis
Research: Efficient Production of Recombinant Anti-Acetylcholine Receptor Monoclonal Antibodies"
Research conducted under the direction of David Richman, MD

2003
Suzanne E. Biehn
University of North Carolina School of Medicine
Research: The Incidence of Depression in Myasthenia Gravis.
Sponsoring Preceptor: James F. Howard, Jr., MD. T

Sara Rask
London Health Science Centre, London, Ontario
Research: Sleep Apnea in Patients with MG.
Sponsoring Preceptor: Michael W. Nicolle, MD, FRCPC, D.Phil.

2002
Alexander L. Friend
University of California at Davis
Research: Epitope Mapping the mAb 132A Binding Site on the Torpedo AchR
Sponsoring Preceptor: Robert H. Fairclough, Ph.D.

Evangelos Karras
University of Texas Medical Branch, Galveston
Research: Induction of myasthenia gravis and thyroiditis in HLA transgenic mice
Sponsoring Preceptor: Premkumar Christadoss, MD

Julie Lefebvre
University of Pennsylvania Medical Center, Philadelphia
Research: The Effects of Unregulated Neuromuscular Activity on Innervation and Synaptic Maintenance: A model for SCCMS
Sponsoring Preceptor: Michael Granato, PhD

Stuart W. Morell
University of California at Davis
Research: Production of Recombinant Anti-Acetylcholine Receptor Monoclonal Antibodies
Sponsoring Preceptor: David P. Richman, MD

2001
M. Dominik Fischer
University of Pennsylvania School of Medicine
Research: Cloning of eom 4: A novel gene differentially expressed in extraocular muscle
Research conducted under the direction of Tejvir A. Khurana, M.D. Ph.D.

Richard J. Pearson
University of Alabama at Birmingham
Research: Analysis of the effects of neuregulin overexpression on motor neuron survival and neuromuscular junction formation in transgenic mice
Research conducted under the direction of Steven L. Carroll, M.D., Ph.D.

Benjamin G. Scott
University of Texas Medical Branch at Galveston
Research: Elucidating the mechanisms of EAMG immunipathogenesis.
Research conducted under the direction of Premkumar Christadoss, M.D.

2000
Mr. Bryan Chang
University of Connecticut and University of California at Davis
Research: Hypothesis that antibodies to synapse-localized proteins in the neuromuscular junction other than the AChR, contribute to pathogenicity in MG.

Carole J. Smith
University of Massachusetts
Research: Examining an important quality of life issue for myasthenics: does the variable course of MG contribute to diagnosis delays?
Research conducted under the direction of Dr. David Chad

Thomas Watkins
Youngstown State University, Ohio
Research: Determine the relationship between observed immunoreactivity patterns in patients with rippling muscles associated with MG and stretch activated Ca2+ in the triad of skeletal muscles.
Research conducted under the direction of Dr Gary Walker

1999
Anna Rostedt
Duke University
Research: Improve the predictive value of the EMG tests for Ocular MG.
Research conducted under the direction of Dr. Donald Sanders

Jennifer Ward
Washington State University
Research: The dog model of MG.
Research conducted under the direction of Dr. Joseph Harding

Thomas Watkins
Kent State University School of Biomedical Sciences
Research: The Characterization of Skeletal Muscle Antibodies in Patients with Autoimmune Rippling Muscles and Myasthenia Gravis.
Research conducted under the direction of Dr. Gary Walker at Youngstown State University.

1998
Edward Kim
Case Western Reserve University
Research: Preferential involvement of ocular muscles in myasthenia gravis

Regina Cho
Case Western Reserve University
Research: Sleep disturbances in myasthenia gravis

Sara Richman
University of California at Davis
Research: Methods of identifying components of the acetylcholine receptor recognized by anti-AChR antibodies that resist epitope mapping by Western blots

1996
Vinesh Dedhia
University of Texas, Galveston
Research: Role of CD8+ T cells in the pathogenesis of experimental autoimmune myasthenia gravis

Geoffrey T. Lamke
Mayo Clinic
Research: Basis of Lambert-Eaton Syndrome and its relation to parneoplastic autoimmunity

One R. Pagan-Ojeda
Universidad Central del Caribe Medical School, Bayamon, PR
Study of the inhibition of the nicotinic acetylcholine receptor

Anne Shafer
University of California, Davis
The pathogenic role of antibodies directed against synaptic organizing proteins in MG 1995
Alison Eertmoed
University of Chicago
Research: Regions of the nicotinic acetylcholine receptor involved in assembly

Pamela Jacobs
University of Rochester, New York
Research: Serial quantitative myometric evaluation in patients with neuromuscular junction transmission defects

Christine Kirvan
University of California at Davis
Research: Pathogenesis of MG in the laboratory

Sue Stacy
University of Texas at San Antonio
Research: Work in the development of a transgenic mouse model which would help clarify the molecular basis for loss of peripheral tolerance in experimental autoimmune MG

1994
Karen Deffenbacher
Mayo Clinic
Research: Anti-striational autoantibody isotypes in graft vs host disease following bone marrow transplantation

Jessica Glassman
California Pacific Medical Center
Research: Inactivation of specific T-cells responsible for modulating the antibody mediated response against the AChR in MG

Yamac Gungo
Columbia University
Research: The impact of modern neurological intensive care on the outcome in MG crisis

Tanaz Moazami
Columbia University
Research: Immunostaining of thymus sections in both normal and myasthenic, using positive sera to evaluate the presence of thin filament proteins in 'myoid' cells

1993
Jefrey Jacques
Columbia University
Research: Isolation and determination of dendritic and macrophage populations from the myasthenic thymus

Joe McCormick
Mayo Clinic
Research: Definition of the nature of the tumor-associated ionic channel antigen that appears to be responsible for breaking self tolerance to motor neurons in Eaton Lambert Myasthenic Syndrome

Phillip Ondocin
State University of New York
Research: Pre-synaptic effects of specific pharmacological agents at the neuromuscular junction


Nursing Research Fellowships

1993
Mary Ellen Grohar-Murray, RN, PhD
St. Louis University
Research: Testing of a fatigue scale for myasthenia gravis


 
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