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Home - Intellia Therapeutics
Using CRISPR/Cas9 technology, Intellia Therapeutics is developing revolutionary genome editing therapies to cure genetic diseases with simple, targeted treatments.
Genetic Testing Information from the Genetic Disease Foundation | KnowYourGenes.org
Information about genetic testing and genetic counseling from the Genetic Disease Foundation.
Journal of Translational Genetics and Genomics
Journal of Translational Genetics and Genomics is an open access journal, publishing articles related to single gene disorders, rare genetic disease, specific genetic syndromes, complex disease, etc.
Author: Amaia Hervas; Maria J Arranz
Genomics Enhanced Medicine (CGEM) | Genetic Disease Research | Canada
CGEM in partnership with Dalhousie, IWK & NSHA leading Canadian research in Genetic Disease Diagnosis, Genetic Disease Treatments, Cancer Diagnosis, Microbiome
Epistasis Lab | Identifying the complex genetic architectures of disease
Identifying the complex genetic architectures of disease
3billion | Genetic test for rare disease patients
Patients with rare genetic disease undergo long odyssey to receive a diagnosis. Visit 3billion and find how to order our rare disease genetic testing.
News, Insight, and Clinical Perspective
Rare and genetic disease publisher and learning platform.
Author: Peter Ciszewski
Know Your Disease - Diseases Information, Treatment, Causes, Symptoms
Find information on all diseases and conditions including heart disease, cancer, genetic disorders, allergies, thyroid diseases, anxiety.
GP2 - Understanding the GeneticArchitecture of Parkinson's Disease
Global Parkinson’s Genetics Program is an ambitious five-year program to understand the genetic architecture of Parkinson’s disease.
Author: CARE
GP2 - Understanding the GeneticArchitecture of Parkinson's Disease
Global Parkinson’s Genetics Program is an ambitious five-year program to understand the genetic architecture of Parkinson’s disease.
Author: CARE
GP2 - Understanding the GeneticArchitecture of Parkinson's Disease
Global Parkinson’s Genetics Program is an ambitious five-year program to understand the genetic architecture of Parkinson’s disease.
Home - 2Blades Foundation
Discovering, advancing, and delivering genetic improvements in crop disease resistance for sustainable, environmentally-friendly genetic solutions.
Redcliffe Lifetech Offers Genetic Testings for Health Risks & Effective Disease Management
Our Genetic Testings let's you find out genetic health risks and effectively manage the diseases. We offer Genetic Tests for Mother and child healthcare, Inherited Genetic Disorders & Cancer Genetics.
GENVIP
Genetics, Vaccines, Infectious Diseases and Pediatrics research group
Home - Minded Cofund
Revolutionizing the diagnosis, detection and treatment of complex genetic diseases
Author: Nicholas Dring
Genetics For Trainees - Genetics For Trainees FRACP exam preparation course
A targeted genetics preparation course for physician and paediatric trainees, to demystify genetics for the FRACP exam and clinical practice.
Arrowhead Pharmaceuticals, Inc.
Target the gene, silence the disease
Download PDF The Genetics of Cattle, 2nd Edition
This book reviews major topics from molecular and developmental genetics, disease resistance and immunogenetics to genetic improvement of dairy and beef.
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Other sites like bridgebio com
INSERM U1035 – Bordeaux University, Biotherapy for genetic diseases, inflammation and cancers
INSERM U1035 unit: Biotherapy for genetic diseases, inflammation and cancer
HOPE THROUGH RIGOROUS SCIENCE .
Targeting TTR amyloidosis at its source. Transthyretin (TTR) amyloidosis is a family of rare, devastating diseases with serious unmet medical needs.
Tweesprong (Crossroads), a film by Wouter Bouvijn
A film by Wouter Bouvijn. Maxime is faced with an uncertain future when his father dies from a genetic disease. He must choose: a genetic test or a leap into the unknown.
Metagenomi
Metagenomi is discovering breakthrough gene editing systems for curing genetic disease.
Welcome | The John and Marcia Carver Nonprofit Genetic Testing Laboratory
The Carver Lab is a nonprofit organization which investigates the genetic bases of eye diseases.
Author: Carver Lab
National Gaucher Foundation | Gaucher Disease - Symptoms, Treatment, & Education
Gaucher disease is a genetic disorder and affects the body's organs and tissues. Learn about Gaucher disease symptoms, testing and treatments.
2nd Gene Therapy for Muscular Disorders Summit | April 2022 | Home
The 2nd Gene Therapy for Muscular Disorders Summit will focus on overcoming the challenges of developing genetic therapies targeting muscular disorders, including Duchenne Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Pompe Disease and X-Linked Myotubular Myopathy.
CENTOGENE - The Rare Disease Company
CENTOGENE is a world leader in the field of genetic diagnostics for rare diseases dedicated to improve patients' lives every day. Order your genetic test!
Genomic Structural Variation Analysis
Genomic structural variation analysis for CRISPR, cancer and genetic diseases. KromaTiD’s dGH™-the Gold Standard for studying complex genetic rearrangements
Μάθετε για την κληρονομική νόσο Fabry | Fabry Disease Family Tree
Learn about Fabry disease inheritance and genetics. Create your Fabry Family Tree.
Jeans for Genes : Home
Fundraise and give hope to sick kids. Fight for kids facing genetic diseases.
Learn About Fabry Disease Inheritance | Fabry Disease Family Tree
Learn about Fabry disease inheritance and genetics. Create your Fabry Family Tree.
Death By Vaccination
How vaccines trigger DNA genetic mutation and cause failure of Methylation, Transsulfuration, and other cycles in genetically susceptible humans resulting in autism and autoimmune disease
Animal Genetics UK | Genetic Testing Services
Animal Genetics UK provides genetic testing services for animals including Avian DNA sexing and diseases and inherited Canine and Equine characteristics and disorders.
ATHERO-FLUX
Targeting novel lipid pathways for treatment of cardiovascular disease
Precision NanoSystems - Create Transformative Medicines
The NanoAssemblr platform enables research of the genetic basis of disease and scaling of nanoparticle **** formulations
LANKTREE LAB - Home
MISSION STATEMENT FURTHER DEFINE THE GENETIC CONTRIBUTION TO KIDNEY DISEASE, TRANSLATE RESEARCH INTO IMPROVED CARE OF PATIENTS WITH KIDNEY DISEASE, AND EDUCATE FUTURE CLINICIANS AND SCIENTISTS...
Home
Latest news Read FIN’s latest updates, upcoming events and all news relating to Fabry Disease More News & Events What is Fabry Disease? Fabry disease is a rare, genetic condition which is estimated to affect
Author: Reejeel
Dog DNA Testing & Cat DNA Testing - Orivet
Genetic Testing for animals include Canine DNA Testing & Feline DNA Testing (dog dna test , cat dna test) | Canine Diseases & Canine Traits (Dog Diseases & Dog Traits) | Feline Diseases
Orivet Genetics
Genetic Testing for animals include Canine DNA Testing & Feline DNA Testing (dog dna test , cat dna test) | Canine Diseases & Canine Traits (Dog Diseases & Dog Traits) | Feline Diseases
What else bridgebio.com alternative websites
Diamond T Ranch | Jacksonville, TX | Wagyu Beef
We are your premier source for recessive genetic disease free Wagyu Cattle, boasting one of the largest full blood herds in Texas. Contact Diamond T Ranch today to order your Wagyu Beef!
BioMarin Pharmacuetical Inc. | Europe, Middle East, and Africa (EMEA)
BioMarin is a world leader in developing and commercializing innovative biopharmaceuticals for rare diseases driven by genetic causes.
Home - Rhythm Pharmaceuticals
Learn more about how Rhythm is changing how rare genetic diseases of obesity are diagnosed and treated.
BioMarin Pharmaceutical Inc.
BioMarin is a world leader in developing and commercializing innovative biopharmaceuticals for rare diseases driven by genetic causes.
CoSTREAM - Understanding **** and Alzheimer
CoSTREAM is a research project combining genetics, imaging, metabolomics and biotechnology to understand **** and Alzheimer's disease
The Genesis Foundation For Children | More Than Medical Care
The Genesis Foundation for Children diagnoses, treats and provide coordinated care for children with rare diseases and genetic disorders.
SMA Support Inc., Home of Spinal Muscular Atrophy
Dedicated to providing information, support and help for anyone facing the incurable genetic disease Spinal Muscular Atrophy (SMA). Learn about the disease, research, treatments, and life with the disease, speak with others in similar positions.
Home - SimulConsult
Diagnostic decision support for clinicians. Get a differential diagnosis with the epected diseases and the unfamiliar diseases that should also be considered. Avoid diagnostic odysseys. Complete coverage of Mendelian genetics.
Author: GENETICIST Academic Medical Center
Molecular Vision Lab | Genetic Testing for Eye Diseases & COVID-19 Saliva RNA Testing
We are a high-complexity, CAP and CLIA-certified diagnostic laboratory. Established privately in 2016 with roots at Oregon Health & Science University, we specialize in COVID-19 testing, Genetic testing, and Infectious Disease testing. Covid-19 Testing Genetic Testing Infectious Disease
About Us
Celldex is developing targeted therapeutics to address devastating diseases for which available treatments are inadequate.
ATHERO-B-CELL
ATHERO-B-CELL: Targeting and exploiting B cell functions for treatment in cardiovascular diseases
Targeted Lymphatic and Microvessel Treatments in metabolic-DISease HFpEF - Inserm U1096
Targeted Lymphatic and Microvessel Treatments in metabolic-DISease HFpEF - Inserm U1096
Author: Eric Mennier
Atlas of Genetics and Cytogenetics in Oncology and Haematology
The Atlas of Genetics and Cytogenetics in Oncology and Haematology gives reviews on genes involved in cancer, leukemias, solid tumors, and cancer-prone diseases. It also provides lectures in Genetics for students in medicine/sciences.
Samsara Therapeutics - Restoring Autophagy, Reversing Disease
We are restoring autophagy to boost cell rejuvenation and treat currently incurable neurodegenerative and rare genetic diseases.
The French Muscular Dystrophy Association (AFM-Téléthon)
AFM-Téléthon is an association composed of patients and their families who are affected by a genetic, rare, progressive and severely disabling disease
Alinity mCMV and EBV assaysNow CE Marked
Providing molecular intelligence for personalized healthcare. Offerings include assays and automation for infectious disease, oncology, and genetics.
COST ACTION (CA 15214) An Integrative Action for Multidisciplinary Studies on Cellular Structural Networks | EuroCellNet
The Action targets researchers from molecular and cell biology, genetics, biophysics, structural biology, mechanobiology, neurobiology, developmental …
Modelis - Simple Models. Complex Diseases. Revolutionizing **** Discovery
Modelis is a world leader in **** discovery for rare and genetic diseases, and is revolutionizing how new therapies are being developed.
Anavex Life Sciences
Anavex utilizes precision genetic medicine to treat severe and devastating neurological disorders and is focusing on rare diseases with no available therapy
We don’t follow footsteps. We create the path.
Spark Therapeutics is challenging the inevitability of genetic disease by discovering, developing and delivering treatments in ways unimaginable – until now.
Other websites similar as bridgebio.com
unknown.
Passage Bio, a genetic medicines company, is changing the future of monogenic CNS disease and transforming the lives of patients and their families.
Home Page - IBX : IBX
Infinity BiologiX aims to understand the genetic causes of common, complex diseases and to discover diagnoses, treatments and, eventually, cures for these
Author: Johndaltrey
Jesse's Journey | Duchenne Muscular Dystrophy | Canada
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5,000 boys.
Neurogene | Developing life-changing Genetic Medicines
Neurogene is focused on developing life-changing genetic medicines for patients & families affected by rare, devastating neurological diseases.
CE-IVD, Easy & Fast Mutations & Alleles Detection Without DNA Extraction - LaCAR MDx
LaCAR MDx's innovative alternative to qPCR through LAMP based CE-IVD diagnostic kits for molecular genetics. Newborn Screening, Genetic Thrombosis, Hemochromatosis, Pharmacogenetics, Food Intolerances, Autoimmune Diseases and many others.
Micropathology: Rapid Diagnosis for Clinical Microbiology & Virology, DNA Paternity Testing, Forensic Genetics Work
Micropathology Ltd provides a clinically supported service for the rapid diagnosis and management of infectious and genetic disease, DNA paternity testing, a forensic genetics service and undertakes biomedical research on human and veterinary pathology.
Goldendoodle | Niagara, ON, Canada | Goldendoodles of Niagara
Goldendoodles of Niagara is a top breeder specializing in home raised chocolate and red goldendoodles in minature, medium and standard sizes. A responsible breeder that genetically tests for disease, trait, coat and colour through Paw Print Genetics.
Rdzeniowy zanik mięśni | Razem w SMA – pracownik ochrony zdrowia
Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
Spinal muskelatrofi | Together in SMA Hälso- och sjukvårdspersonal
Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
Rady Children's Institute for Genomic Medicine
We are transforming pediatric healthcare through the power of Rapid Precision Medicine™ and expediting personalized treatment of rare genetic disease.
Spinal Muscular Atrophy | Together in SMA HCP
Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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Mit modernster Technik für Ton, Licht, IT und Video sind wir Ihr spezialisierter Partner im AV und Medienbereich.
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Mit modernster Technik für Ton, Licht, IT und Video sind wir Ihr spezialisierter Partner im AV und Medienbereich.
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