Accès ouvert
2026
preprint
OpenAlex
Mitsutoshi Nakamura, Justin Hui, Jeffrey M. Verboon, Susan M. Parkhurst
Abstract Injuries to individual cells happen frequently as a result of physiological and environmental stresses during their normal daily functions that can lead to a ruptured cell cortex (plasma membrane and underlying cortical cytoskeleton). The capacity of cells to rapidly repair general …
us
(code pays fourni par la source)
2025
conference-abstract
OpenAlex
Burcu Yigit, Prasuna Paluru, Eglė Jurgaitytė, Kevin A. Nuno et autres
T cell engagers (TCEs) are proving to be a potent therapeutic strategy for the treatment of solid tumors. Clinical data have shown that TCEs can drive T cell activity in "cold" tumors, including colorectal cancer. However, identifying highly specific tumor antigen targets …
us
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Accès ouvert
2024
article
OpenAlex
Matthew A. Nix, Caleb A. Lareau, Jeffrey M. Verboon, David Kugler
Targeted antibody-based therapy for oncology represents a highly efficacious approach that has demonstrated robust responses against single tumor-associated antigen (TAA) targets. However, tumor heterogeneity presents a major obstacle for targeting most solid tumors due to a lack of single targets that possess …
us
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Accès ouvert
2024
conference-abstract
OpenAlex
Burcu Yigit, Prasuna Paluru, Eglė Jurgaitytė, Kevin A. Nuno et autres
Background Colorectal cancer (CRC) remains of high unmet medical need. T cell engagers as a modality have gained attraction in solid tumors, but despite the early data that T cells can infiltrate cold CRC tumors with therapies such as Cibisatamab, treatment remains …
Accès ouvert
2024
article
OpenAlex
Monica H. Wojcik, Gabrielle Lemire, Eva Berger, Maha S. Zaki et autres
BACKGROUND: Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative evaluation, remains poorly defined. METHODS: We sequenced and analyzed the genomes of families with …
us
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Accès ouvert
2023
article
OpenAlex
Caleb A. Lareau, Yajie Yin, Katie Maurer, Katalin Sándor et autres
us, nl, de
(code pays fourni par la source)
Accès ouvert
2023
erratum
OpenAlex
Caleb A. Lareau, Leif S. Ludwig, Christoph Muus, Satyen H. Gohil et autres
us, gb
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Parsa Akbari, Dragana Vuckovic, Luca Stefanucci, Tao Jiang et autres
Blood cells contain functionally important intracellular structures, such as granules, critical to immunity and thrombosis. Quantitative variation in these structures has not been subjected previously to large-scale genetic analysis. We perform genome-wide association studies of 63 flow-cytometry derived cellular phenotypes-including cell-type specific …
gb, us, de, it, nl
(code pays fourni par la source)
Accès ouvert
2023
preprint
OpenAlex
Monica H. Wojcik, Gabrielle Lemire, Maha S. Zaki, Mariel Wissman et autres
Background: Causal variants underlying rare disorders may remain elusive even after expansive gene panels or exome sequencing (ES). Clinicians and researchers may then turn to genome sequencing (GS), though the added value of this technique and its optimal use remain poorly defined. …
us, Égypte, au, gb, ca, ee
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Caleb A. Lareau, Sonia M. Dubois, Frank A. Buquicchio, Yu-Hsin Hsieh et autres
us, de, ch
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Accès ouvert
2023
article
OpenAlex
Kerri Davidson, Mitsutoshi Nakamura, Jeffrey M. Verboon, Susan M. Parkhurst
Nuclear envelope (NE) budding is a nuclear pore-independent nuclear export pathway, analogous to the egress of herpesviruses, and required for protein quality control, synapse development, and mitochondrial integrity. The physical formation of NE buds is dependent on the Wiskott-Aldrich Syndrome protein, Wash, …
Afrique du Sud, us
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Accès ouvert
2022
preprint
OpenAlex
Caleb A. Lareau, Sonia M. Dubois, Frank A. Buquicchio, Yu-Hsin Hsieh et autres
Abstract Cells experience intrinsic and extrinsic pressures that affect their proclivity to expand and persist in vivo . In congenital disorders caused by loss-of-function mutations in mitochondrial DNA (mtDNA), metabolic vulnerabilities may result in cell-type specific phenotypes and depletion of pathogenic alleles, …
us, de
(code pays fourni par la source)