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A Ravenscroft

Showing results (21-30 of 31) with videos related to

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Nature Methods|February 6, 2025
Live imaging of the extracellular matrix with a glycan-binding fluorophoreAntonio Fiore, Guoqiang Yu, Jason J Northey, et al.
Neurobiology of Aging|May 3, 2013
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUSThomas A Ravenscroft, Matt C Baker, Nicola J Rutherford, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Imaging the extracellular matrix in live tissues and organisms with a glycan-binding fluorophoreAntonio Fiore, Guoqiang Yu, Jason J Northey, et al.
American Journal of Neurodegenerative Disease|April 14, 2016
The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in FloridaThomas A Ravenscroft, Cyril Pottier, Melissa E Murray, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|April 7, 1999
The mother-to-child HIV transmission debateN Beyers, M F Cotton, P R Donald, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
American Journal of Human Genetics|October 15, 2019
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short StatureMuhammad Ansar, Hyung-Lok Chung, Ali Al-Otaibi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Neurobiology of Aging|September 24, 2016
TYROBP genetic variants in early-onset Alzheimer's diseaseCyril Pottier, Thomas A Ravenscroft, Patricia H Brown, et al.
Neuron|March 15, 2020
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different MechanismsHyung-Lok Chung, Michael F Wangler, Paul C Marcogliese, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Nature Methods|February 6, 2025
Live imaging of the extracellular matrix with a glycan-binding fluorophoreAntonio Fiore, Guoqiang Yu, Jason J Northey, et al.
Neurobiology of Aging|May 3, 2013
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUSThomas A Ravenscroft, Matt C Baker, Nicola J Rutherford, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Imaging the extracellular matrix in live tissues and organisms with a glycan-binding fluorophoreAntonio Fiore, Guoqiang Yu, Jason J Northey, et al.
American Journal of Neurodegenerative Disease|April 14, 2016
The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in FloridaThomas A Ravenscroft, Cyril Pottier, Melissa E Murray, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|April 7, 1999
The mother-to-child HIV transmission debateN Beyers, M F Cotton, P R Donald, et al.
Science Advances|January 19, 2022
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signalingPaul C Marcogliese, Debdeep Dutta, Shrestha Sinha Ray, et al.
American Journal of Human Genetics|October 15, 2019
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short StatureMuhammad Ansar, Hyung-Lok Chung, Ali Al-Otaibi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Neurobiology of Aging|September 24, 2016
TYROBP genetic variants in early-onset Alzheimer's diseaseCyril Pottier, Thomas A Ravenscroft, Patricia H Brown, et al.
Neuron|March 15, 2020
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different MechanismsHyung-Lok Chung, Michael F Wangler, Paul C Marcogliese, et al.
Pageof 4