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Brian Kraemer

@brianckraemer.bsky.social

Father Husband Dementia Neuroscientist, Classical Geneticist Outdoor Enthusiast Opinions are my own. https://kraemerlab.uw.edu/

184 Followers  |  300 Following  |  4 Posts  |  Joined: 06.01.2024  |  1.7698

Latest posts by brianckraemer.bsky.social on Bluesky

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An amazing talk from Dr. Kejia Wu in David Bakers lab at the @uwproteindesign at this yearโ€™s HD therapeutics conference in Palm Springs about her amazing designed proteins that bind intrinsically disordered peptides, including poly glutamine, which sheโ€™s working to tune to be selective for long Qโ€™s!

01.03.2025 17:39 โ€” ๐Ÿ‘ 2    ๐Ÿ” 1    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 0
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Please see a collective response from an esteemed group of leaders in the dementia field to the NYT article and book โ€œdoctoredโ€ by Charles Piller. www.nytimes.com/2025/01/24/o...

08.02.2025 17:55 โ€” ๐Ÿ‘ 32    ๐Ÿ” 16    ๐Ÿ’ฌ 1    ๐Ÿ“Œ 1
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Alternative 3' UTR polyadenylation is disrupted in the rNLS8 mouse model of ALS/FTLD - PubMed Recent research has highlighted widespread dysregulation of alternative polyadenylation in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP). H...

TDP-43 proteinopathy also provokes transcriptomic changes consistent with TDP-43 loss of function. The latest side project from Randall Eck in my group: pubmed.ncbi.nlm.nih.gov/39810199/

18.01.2025 06:26 โ€” ๐Ÿ‘ 3    ๐Ÿ” 2    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0
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Identification of TMEM106B amyloid fibrils provides an updated view of TMEM106B biology in health and disease - PubMed Since the initial identification of TMEM106B as a risk factor for frontotemporal lobar degeneration (FTLD), multiple genetic studies have found TMEM106B variants to modulate disease risk in a variety ...

Here's a nice review from Rosa Rademakers & Co if you want to learn more about human TMEM106b proteinopathies. pubmed.ncbi.nlm.nih.gov/36056242/

02.01.2025 21:01 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0

For those of you that haven't heard about it, TMEM106b is an important risk factor for a variety of neurodegenerative diseases. It was first shown as a risk factor for FTLD-TDP by Viviana VanDeerlin & Co more than a decade ago. More recently, it has been show to form fibrils in these diseases.

02.01.2025 21:00 โ€” ๐Ÿ‘ 0    ๐Ÿ” 0    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 0
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Identification of TMEM106B amyloid fibrils provides an updated view of TMEM106B biology in health and disease - PubMed Since the initial identification of TMEM106B as a risk factor for frontotemporal lobar degeneration (FTLD), multiple genetic studies have found TMEM106B variants to modulate disease risk in a variety ...

Here's the latest work from my group! We built a C. elegans model of human TMEM106b proteinopathy by expressing the human gene in neurons. TMEM106b is a new kid on the block in terms of aggregating proteins. Long story short, it can driven neurodegeneration. pubmed.ncbi.nlm.nih.gov/36056242/

02.01.2025 20:58 โ€” ๐Ÿ‘ 5    ๐Ÿ” 1    ๐Ÿ’ฌ 2    ๐Ÿ“Œ 0
Seattle waterfront in the evening

Seattle waterfront in the evening

Love science and Seattle? Come be my colleague! We are recruiting a physician scientist to join the Seattle VA GRECC with a joint appointment at University of Washington. Apply here: apply.interfolio.com/155179. Please share widely - this is an open rank search at Assistant/ Associate/ Full levels

03.10.2024 02:47 โ€” ๐Ÿ‘ 3    ๐Ÿ” 3    ๐Ÿ’ฌ 0    ๐Ÿ“Œ 1

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