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Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. LGMD2B/Miyoshi Myopathy (collectively called dysferlinopathy) are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective (recessive inheritance). Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe...

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Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. LGMD2B/Miyoshi Myopathy (collectively called dysferlinopathy) are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective (recessive inheritance). Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe...

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1 patient registration

2 apply for funding

3 search form

4 scientific resources

5 institute overview

6 dysferlin background

7 therapeutic strategies

8 research tools

9 funded projects

10 conferences

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Home | Jain Foundation | jain-foundation.org Reviews

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Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. LGMD2B/Miyoshi Myopathy (collectively called dysferlinopathy) are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective (recessive inheritance). Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe...

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Home | Jain Foundation

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. LGMD2B/Miyoshi Myopathy (collectively called dysferlinopathy) are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective (recessive inheritance). Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe...

sharing.jain-foundation.org

Jain Foundation Resource Sharing Database

Return to jain-foundation.org. Jain Foundation Resource Sharing Network. This is a private community where scientists search for lab resources such as reagents, cell lines, animal models, protocols, facilities/equipment, and expertise developed by other scientists to facilitate research on dysferlin and LGMD2B/MM. As a user, you will be able to search for resources, view the conditions associated with obtaining them, and access contact information for the Principal Investigator (PI) who is offering them.

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jain-foundation.org

1

Clinical Studies and Trials | Jain Foundation

http://www.jain-foundation.org/patient-physician-resources/clinical-studies-and-trials

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. Patient and Physician Resources. Clinical Studies and Trials. Clinical Studies and Trials. There are two types of studies that dysferlinopathy (LGMD2B/Miyoshi) patients can participate in and both types are critical to the development of therapies for dysferlinopathy:. Effective clinical trials cannot be performed without the knowlege we gain from these studies.

2

2016 LGMD Awareness Scholarship | Jain Foundation

http://www.jain-foundation.org/scholarship

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. 2016 LGMD Awareness Scholarship. 2016 LGMD Awareness Scholarship. Category A: Merit-Based Scholarship ($3000, 2 winners). Entrants will be ranked based on their academic achievements, extracurricular activities, and leadership experience as well as their ability to teach their friends, family and acquaintances about LGMDs to help spread awareness. Facebook is a regis...

3

Dysferlin Background | Jain Foundation

http://www.jain-foundation.org/scientific-resources/dysferlin-background

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. A catalog of the vast body of experimental results and resources pertaining to dysferlin research in a comprehensive and easy-to-navigate question-based format. A searchable listing of important publications in the dysferlin field, including those that acknowledge Jain Foundation funding. Dysferlin Gene and Protein Sequence Information.

4

International Clinical Outcome Study for Dysferlinopathy (LGMD2B/Miyoshi) | Jain Foundation

http://www.jain-foundation.org/dysferlinoutcomestudy

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. Patient and Physician Resources. Clinical Studies and Trials. International Clinical Outcome Study for Dysferlinopathy (LGMD2B/Miyoshi). International Clinical Outcome Study for Dysferlinopathy (LGMD2B/Miyoshi). Why is this study so important? The outcome measures identified in this study are needed for the development and success of future clinical trials. The clini...

5

Patient Registration | Jain Foundation

http://www.jain-foundation.org/form1.php

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. Thank you for your interest in registering with the Jain Foundation. The Jain Foundation has partnered with several other LGMD family foundations to offer free genetic testing for individuals suffering from muscular dystrophy to help them obtain a definitive and specific genetic diagnosis. Undiagnosed Patients in the United States. Undiagnosed Patients in India.

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sharing.jain-foundation.org

Jain Foundation Resource Sharing Network

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Return to jain-foundation.org. Please enter the email address you provided when you signed up at this site.

agadabio.com

Important Preclinical Research Information and Links

http://www.agadabio.com/links

INFORMATION ABOUT PRECLINICAL RESEARCH. A call for transparent reporting to optimize the predictive value of preclinical research [LINK]. Standards in pre-clinical efficacy studies [LINK]. Center for Genetic Medicine Research, Washington, DC [LINK]. INFORMATION ABOUT MUSCULAR DYSTROPHY. Centers for Disease Control and Prevention [LINK]. Coalition to cure Calpain 3. Foundation to Eradicate Duchenne (FED). Limb Girdle Muscular Dystrophy 2D Foundation. Limb Girdle Muscular Dystrophy 2I Fund.

proofcentre.ca

PROOF Centre and MRM Proteomics Collaborate with the Jain Foundation to Identify Blood-Based Biomarkers of LGMD2B/Miyoshi Muscular Dystrophy | PROOF Centre

http://www.proofcentre.ca/news-room/media-releases/proof-centre-mrm-proteomics-collaborate-with-jain-foundation

Our Vision & Mission. Mr Frank Holler, Chairman of the Board. Dr Bruce McManus, CEO. Dr Bruce McManus, CEO. Dr Raymond Ng, Chief Informatics Officer. Dr Scott Tebbutt, Chief Scientific Officer. Dr Karen Lam, Chief Business Officer. Dr Zsuzsanna Hollander, Chief Data Officer. Ms Jo Lynn Mervyn, Finance Manager. Ms Janet Wilson-McManus, Special Advisor. Dr Robert Balshaw, Special Advisor. Ms Sara Assadian, Director, Clinical Research. Ms Breanne Crouch, Clinical Research Manager. Our Community of Partners.

dysferlinregistry.org

The International Dysferlinopathy Registry

http://www.dysferlinregistry.org//DYSFL2/EN

The International Dysferlinopathy Registry. The Clinical Outcome Study for Dysferlinopathy. Dysferlinopathies are characterized by progressive muscle wasting and are clinically divided into four main types:. Limb-Girdle Muscular Dystrophy type 2B (LGMD2B),. Distal Myopathy with Anterior Tibial onset (DMAT),.

dysferlinregistry.org

The International Dysferlinopathy Registry

http://www.dysferlinregistry.org//DYSFL4/EN

The International Dysferlinopathy Registry. Learn more about the registration process. Participating in the International Dysferlinopathy Registry will provide the following benefits for you:. The more patient information collected, the better equipped researchers will be for finding therapies for this disease. You will receive information relevant to you or your condition for example you will be notified if researchers find better ways of caring for patients with a dysferlinopathy.

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JAIN BOOKS and PERIODICALS. By WOWSlider.com v5.6. FOOD SCIENCE AND TECHNOLOGY. PLANT BREEDING AND GENETICS. VETERINARY AND ANIMAL SCI. Biotechnology and Plant Breeding. Biotechnology in Agriculture and Food Processing: Opportunities and Challenges. Honey in Traditional and Modern Medicine. Gender in Agriculture; Closing the Knowledge Gap. Handbook of Chemical and Biological Plant Analytical Methods. Sustainable Energy Solutions in Agriculture. Seeds; Physiology of Development Germination and Dormancy 3ed.

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Family, Cosmetic, and Implant Dentistry for Patients of All Ages. WELCOME TO JAIN DENTAL. Your Dentist Serving St. Louis Park, St. Paul, Golden Valley and the Surrounding Communities. Each of our office locations. Is equipped with latest in dental technology and offers patients a comprehensive list of general, restorative and cosmetic dental services. Some of the services we provide include:. JAIN DENTAL offers a variety of dental services for our patients at multiple locations. View our services.

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Home | Jain Foundation

Patient and Physician Resources. Clinical Studies and Trials. Automated LGMD Diagnostic Assistant (ALDA). Free Genetic Diagnosis for LGMDs. LGMD2B/Miyoshi Myopathy (collectively called dysferlinopathy) are rare forms of muscular dystrophy caused by mutations in the dysferlin gene. For the disease to occur both copies of the dysferlin gene must be defective (recessive inheritance). Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe...

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Jaina-Religion, Philosophie, Ethik, Gewaltlosigkeit, Vegetarismus. 3 Nicht nehmen was Nicht-. 4 Wille zum Wachsen. Jain Association International, (Germany) e.V. Schweriner Str. 5,. 24558 Henstedt-Ulzburg, Germany. Tel : 04193- 968360, Fax: 04193 - 968362. Diese Homepage: http:/ www.jain-germany.de. Seelen helfen einander, AHIMSA(Gewaltlosigkeit) ist die größte Religion. Der Jain-Kanon beinhaltet 60 Texte, Purvas(Alttexte: 12 Bücher), Angas(Glieder: 12 Bücher) und Angabahya (außerhalb der...Jain Associat...

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Monday, December 18, 2006. Jainism is one of the oldest religions. Jainism traces its roots to a succession of 24 Jinas ("those who overcome", or conqueror) in ancient East India. Shree Vimalnath swami is 13th Jina. He is Son of King Kritvarma and queen Shyanan Devi of Kampilpur. Bhagavan Vimalnath got Nirvana at Sammetshikhar on the seventh day of the dark half of the month of Ashadh. Every jain should once in a life visit Balsana. Subscribe to: Posts (Atom). View my complete profile.

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Jain Science Jain History Jain Tirths Jain Songs Jain Temple Tours Jain Temple in India. Dec 2, 2010. Jain Dharmashala, Jain Tirth, Jain Temples. Jain Tirth In Gujrat. Jain Tirth In Maharastra. Jain Tirth In Rajasthan. Links to this post. Subscribe to: Posts (Atom). Check out the latest video. Watch the latest videos on YouTube.com. Jain Tirth In Gujrat. Jain Tirth In Maharastra. Jain Tirth In Rajasthan. Jain Dharmashala, Jain Tirth, Jain Temples. Jain Tirth In Rajasthan. Jain Tirth In Maharastra.