Pacific Northwest Research Institute

Tomorrow! Join Dr. Davut Pehlivan from Baylor College of Medicine at PNRI's Science Matters seminar. Discover insights on MECP2 Duplication Syndrome. Register now! https://ow.ly/bOpV50SyiWQ

Our friends at the HNRNP Family Foundation are hosting their Annual Conference & Family Meeting later this month! 🌟This is a wonderful opportunity to connect with others who are living with HNRNP-Related Neurodevelopmental Disorders and learn about the latest advances in research, therapeutics, and family support systems. See the link below for more details and registration: https://www.hnrnp.org/2024symposium

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Don't miss PNRI's Science Matters seminar with Dr. Davut Pehlivan from Baylor College of Medicine. Learn about clinical and genomic studies of MECP2 Duplication Syndrome and its impact on treatment. Register now! https://ow.ly/79a450Stjir

📢 Attention Rare Disease Advocates! 📢 Join NW Rare Disease Coalition's fantastic opportunity to prepare for upcoming legislative engagements and outreach. Learn from experienced advocates about their successes and how to apply them for the 2025 state legislative session!

On July 31st, we're holding a virtual briefing for advocates to discuss upcoming legislative engagements and outreach.

We'll hear from advocates about their grassroots advocacy experiences!

RSVP today to prepare for the 2025 session: https://secure.everyaction.com/QYjHoiSVNkaXExg9H-sGkA2?nvep=&hmac=&emci=58a0e24a-e137-ef11-86d2-6045bdd9e096&emdi=ea000000-0000-0000-0000-000000000001&ceid=

Join us for PNRI's Science Matters upcoming seminar with Dr. Davut Pehlivan, MD, joining us from Baylor College of Medicine to discuss genomic studies of MECP2 Duplication Syndrome. Register now! https://ow.ly/Q95Y50Squgz

Researchers in PNRI's Carvalho Lab and collaborating scientists from Baylor College of Medicine have just unveiled groundbreaking research in Cell Genomics! 🧬✨ Their study uncovers the role of complex DNA rearrangements in the development of rare genetic diseases, such as MECP2 duplication syndrome. This discovery opens new doors for understanding and treating rare genetic disorders. 🔬💡 Learn more at: https://bit.ly/3REJgPA

Cell Press

Pacific Northwest Research Institute Uncovers Hidden DNA Mechanisms of Rare Genetic Diseases PNRI researchers and collaborators have discovered that DNA rearrangements called inverted triplications play a key role in various genetic diseases.

Our Science Matters seminar is just a day away! Dr. Alkuraya from Alfaisal University will share insights into the genomic research opportunities in Middle Eastern populations during his presentation tomorrow. There will be 15 minutes of Q&A at the end. Click the link to register now 🧬🔬 https://ow.ly/NIMo50SgctK

Don't miss out on our Science Matters seminar just a week away! Join the discussion with Dr. Fowzan Alkuraya from Alfaisal University to gain valuable insights into the genomic research opportunities in Middle Eastern populations. Register today 🧬🔬 https://ow.ly/ztQi50Sa9lY

Last weekend, the Carvalho Lab hosted PNRI's first-ever Rare Disease Hackathon, bringing together a global team of experts from Karolinska Institutet, Baylor College of Medicine, and Seattle Children's to decode genetic puzzles in rare diseases. This collaborative event uncovered vital genetic variants, paving the way for future research and treatments. Learn more about the hackathon and the promising future it holds for rare disease research at https://bit.ly/453Xr6i
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Join us June 12 for a discussion with Dr. Fowzan Alkuraya from exploring the clinical challenges and genomic research opportunities unique to Middle Eastern populations. 🧬🔬 Secure your spot and register today! https://ow.ly/cynG50S4FWL

Attending the NW Rare Disease Coalition's Rare Disease Fair today? Don’t miss the inspiring lineup of speakers, including PNRI’s Dr. Aimée Dudley. It’s a fantastic opportunity to learn about advances in diagnosing rare diseases and connect with the amazing rare disease community!

Join us in cheering on our amazing McLaughlin Lab member, Ricky Padilla Del Valle, as they defend their dissertation! 📚✨Don't miss this chance to learn about Ricky’s innovative genetic research 🧬 and celebrate their hard work and dedication. See details below.

Tomorrow's the day! Join us at 12:00pm PT for our Science Matters seminar with Dr. Anna Lindstrand from Karolinska Institutet. Learn about the latest advancements in rare diseases diagnostics and participate in the Q&A session.
Register now to save your seat! https://ow.ly/ggUy50RQ6Pe

Join our Science Matters seminar next week with Dr. Anna Lindstrand from Karolinska Institutet. Mark your calendars for May 22 at 12:00pm PT to gain insights into how multiomics approaches are improving rare disease diagnosis. 🧬Register now!
https://ow.ly/7w6r50RIXHY

Join us for "From Sweden to Seattle" on Thurs. May 23rd, 4-5pm at PNRI! Discover the impact of global collaborations on local rare disease research. 🌍 🧬🔬 Appetizers, wine, and parking provided. For more details and to RSVP, visit:
https://pnri.org/events/from-sweden-to-seattle/

Last Saturday, we opened our doors for an exclusive peek behind the scenes of our groundbreaking genetics research! 🔬✨ 🧬 From tracing cancer evolution to unraveling the mysteries of jumping genes, guests were treated to a whirlwind tour of innovation. Read all about it here: https://bit.ly/3UJSjzA

Don't miss out on our upcoming Science Matters seminar! Join us on May 22 at 12:00pm PT for an insightful conversation with Dr. Anna Lindstrand from Karolinska Institutet. 🧬Register today to learn about cutting-edge research in rare disease diagnostics. https://ow.ly/N5Sk50RzXuw

We're excited to share some dates you won't want to miss!

Payer Forum: May 30
Seattle Rare Disease Fair: May 31 to June 1

RSVP today for FREE. These events will have a lots of great speakers, discussions and advocacy opportunities!

https://secure.everyaction.com/zJjdmbR7F0S75A1CavSC7g2

We're thrilled to see our Science Matters seminars inspiring the next generation of scientists worldwide! Huge thanks to Prof. Juliana Mazzeu and her students at the UnB - Universidade de Brasília in Brazil for joining us this week! 🌍🧬 For details about upcoming Science Matters seminars, visit: https://pnri.org/events/science-matters/

A team of researchers from Baylor College of Medicine, including PNRI’s own Dr. Cláudia Carvalho, conducted a decade-long exploration into Turkish genetics, uncovering a vital piece of the puzzle behind why some rare diseases emerge. Read more at: https://bit.ly/4aYg9hb

Don't miss out at Life Science Innovation Northwest 2024! PNRI's CEO Jack Faris presents our latest advances in genetics research during the Biotechnology Session TODAY from 1-3:30pm.🧬✨ Get ready to be inspired! See you there! For more conference details, visit: https://bit.ly/4db8Chc

🔬 Tomorrow's agenda: mark your calendars for our Science Matters seminar on Wednesday, April 17th! 📆 Dr. Alysson Muotri from will be leading a discussion on cutting-edge research into stem cell-derived "brain organoids". Dive into disease modeling, brain evolution, and bioengineering applications. Dr. Muotri will tackle the technology's limitations and implications in this live-only session.
Reserve your spot now for free! https://ow.ly/YzyP50RhJmu

🔬 Mark your calendars for our upcoming Science Matters seminar! 🗓️ Join us on Wednesday, April 17th, as we delve into research examining stem cell-derived "brain organoids" with Dr. Alysson Muotri from UC San Diego. Discover the latest in disease modeling, brain evolution, and bioengineering applications. Dr. Muotri will speak on the technology's limitations and implications in this live-only session. Don't miss out - register now for free! https://ow.ly/Kks950RcMAa

Attending the National Urea Cycle Disorders Foundation's Legacy of Hope Family Conference? Don’t miss Saturday’s panel discussion on family planning with PNRI’s Dr. Aimée Dudley and other experts. It's a fantastic opportunity to gain valuable insights and connect with fellow attendees.

Calling all National Urea Cycle Disorders Foundation Legacy of Hope attendees! Join us for Dr. Aimée Dudley's talk and discover how the Dudley Lab's groundbreaking genetic screening tool helps clinicians interpret genetic testing results quickly and accurately and dramatically improves the diagnosis of UCDs. 🧬

Join us Wed., April 17th for our next Science Matters seminar. Dr. Alysson Muotri from UC San Diego Dept. of Pediatrics and Cellular & Molecular Medicine will discuss applications of disease modeling, brain evolution, and the interplay with bioengineering. He will also address the limitations and implications of this technology. 🧬Register today for free at: https://bit.ly/4cCiGiY

Missed PNRI's March Science Matters seminar with Dr. John Ray from the Benaroya Research Institute? 🧬 Don't worry! 🎥 Catch the recording on PNRI's YouTube channel! Watch, learn, and share the excitement: https://youtu.be/ZDE8VYiRh1U

Dissecting the Many Causal Roots Driving Autoimmune Disease Genetic Risk In this PNRI Science Matters seminar recorded on 3/20/24, John Ray, PhD, Principal Investigator at Benaroya Research Institute discusses how genetic risk for...