Craig McIntosh, PhD

[Craig McIntosh, PhD @CraigMcIntosh21]

DYRK1A Day is a special one to me for many reasons. But the main one is to bring awareness to this ultr-rare disease. I look forward to working with the DYRK1A Foundation toward a personalized ASO therapy.

[n-Lorem Foundation @n_lorem]

Sarah Glass, Ph.D., our COO at n-Lorem, is not only a dedicated leader but also a mother to Ethan, a nano-rare child who lives with DYRK1A Syndrome. On #DYRK1AAwarenessDay, we honor the strength of Ethan, Sarah, and the entire DYRK1A community. For us, this mission is personal.

[n-Lorem Foundation @n_lorem]

Sarah Glass, Ph.D., our COO at n-Lorem, is not only a dedicated leader but also a mother to Ethan, a nano-rare child who lives with DYRK1A Syndrome. On #DYRK1AAwarenessDay, we honor the strength of Ethan, Sarah, and the entire DYRK1A community. For us, this mission is personal.

[n-Lorem Foundation @n_lorem]

The ideology of n-Lorem just means more for n-Lorem's Chief Operating Officer, Dr. Sarah Glass. Her son Ethan was diagnosed with a nano-rare mutation.

https://t.co/b9MqYHKwjk

[Sulev Koks @SulevKoks]

ICNMD2024 is open for registration.

[Craig McIntosh, PhD @CraigMcIntosh21]

We are delighted to continue our work on a potential ASO Therapeutic for Malan Syndrome. Thank you to @MalanSyndrome for their continued support.

[Malan Syndrome Foundation @MalanSyndrome]

📣We are thrilled to announce our first research grant award for 2024!
Congratulations, Dr. Jessica Cale, Dr. Craig McIntosh and Isabella Trew at Murdoch University (Perth, Australia).

Grant Title: Antisense Oligonucleotide-Mediated Therapeutic Intervention for Malan Syndrome

[n-Lorem Foundation @n_lorem]

n-Lorem marked a momentous milestone with the #GrandOpening of a new laboratory in San Diego’s biotech hub, Sorrento Valley. A ribbon-cutting ceremony commemorated the facility, which offers expanded lab and office space to meet the needs of our growing patient program pipeline.

[Murdoch University @MurdochUni]

Did you know that two people are diagnosed with motor neurone disease in Australia every day?

Now, scientists are testing a new strategy to repair and protect dying neurons and wasting muscles in hopes of buying precious time for people with the disease.

https://t.co/nrb6EBCbzy

[Craig McIntosh, PhD @CraigMcIntosh21]

The latest work from our group.

[Dr Jessica Cale @Jessica__Cale]

Read my latest #research, published with @SpringerNature in @SciReports

https://t.co/RjANdeI3lR

[n-Lorem Foundation @n_lorem]

What's the rationale behind discovering and developing a treatment for a single patient? The advantage lies in the knowledge we can gain and apply for the betterment of the global population.

Colloquium recap: https://t.co/n6wOQHrnoy

[Malan Syndrome Foundation @MalanSyndrome]

Congratulations to Dr. Manuela Priolo on her new position as Head of Medical and Laboratory Genetics at Antonio Cardarelli Hospital in Naples, Italy.
Dr. Priolo is a champion clinician for the Malan syndrome community. We wish her well in her new position. 👏👏

#medical-genetics

[n-Lorem Foundation @n_lorem]

The beautiful people in this photo are our COO, Sarah Glass, and her son, Ethan. Sarah is not only responsible for implementing n-Lorem’s trailblazing infrastructure for ASO disc. and dev, but also for embracing her greatest role as the Mother to a boy with a nano-rare condition.

[Perron Institute @PerronInstitute]

In exciting news, we are thrilled to announce that Dr David Blacker, Perron Institute Medical Director and Dr Adam Edwards, postdoctoral research fellow in infant stroke, are Western Australian of the Year Finalists. https://t.co/qYLmFpAYuE

[Perron Institute @PerronInstitute]

Today is #RareDiseaseDay. Prof Steve Wilton AO, Dr May Aung-Htut and Dr Craig McIntosh from Perron Institute and @cmmit_mu at @MurdochUni are passionate about rare disease research and the integration of science and community.

[Personalised Medicine Centre @pmc_mu]

Just a few of the #RareDiseases we research into here at @cmmit_mu with the support of @MurdochUni & @PerronInstitute. We believe no one should be left behind, everyone deserves the chance to receive a diagnosis & access potential treatments #RareDiseaseDay #RareDiseaseDay2023

[Global Genes @GlobalGenes]

Rare disease patients often have to face a diagnostic odyssey to get an accurate diagnosis. Our Rare Concierge is here to help you get the resources you need. For more: https://t.co/eE4cjcCMPK

#GlobalGenes #RareDisease #CareAboutRare #RareDiseaseDiagnosis #RareDiseaseDay2023

[Craig McIntosh, PhD @CraigMcIntosh21]

@bisping @bisping you killed it. So happy to have seen you in action. Love the podcast.

[Dan Go @CoachDanGo]

· Drink water
· Get 8-10k steps a day
· Fix your sleeping habits
· Strength train 3-4x a week
· Eat a high protein nutrient dense diet

Do this for 2 years & people will say you have good genetics.

[Craig McIntosh, PhD @CraigMcIntosh21]

@KMartinovichPhD @WCVID @telethonkids Congrats Kelly awesome achievement 👏

[Dr. Rhonda Patrick @foundmyfitness]

Exercise can affect your unborn children's genes by altering the chemistry of DNA in sperm and egg cells.

Aerobic exercise for 3 months altered sperm DNA by silencing genes linked to the risk of autism, OCD, Alzheimer’s, obesity, type 2 diabetes, and atherosclerosis.

[The Australian Society for Medical Research (ASMR) @TheASMR1]

To grow innovation in health & medical research in Australia the sector needs $$$.
Innovation attracts private investment + economic growth.
Neglecting investment into discovery research funded by @NHMRC grants jeopardises future innovation & global competitiveness #ausvotes2022