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Nov 20, 2024 | 
onlinelibrary.wiley.com | Behrooz Khatir |Angela Lin |Thu V. Vuong |Peter Serles
1 Introduction The functional groups and chain confirmations of grafted polymers play a significant role in their surface properties and macroscale behavior.
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Oct 1, 2024 | 
pericles.pericles-prod.literatumonline.com | Angela Lin |Lois J. Starr |Children's Nebraska |Kate Wears
REFERENCES , , , et al. 2012. “A Restrictedspectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhresyndrome.” American Journal of Human Genetics 90: 161–169. , , , et al. 2011. “Mutations at a Single Codon in Madhomology 2 Domain of SMAD4 Cause Myhre Syndrome.” Nature Genetics 44, no. 1: 85–88. https://www.nature.com/articles/ng.1016. , , , et al. 2022. “ Myhre Syndrome.” In GeneReviews®, edited by M. P. Adam, J. Feldman, G. M. Mirzaa, et al., 1993–2024.
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Aug 23, 2024 | 
onlinelibrary.wiley.com | Efpraxia D. Zamani |Mary Beth Watson-Manheim |Pamela A. Abbott |Angela Lin
1 INTRODUCTION The motivation for this special issue lies in the recent resurgence of interest in and the accelerated adoption of hybrid work practices against the backdrop of the COVID-19 pandemic. As a result of enforced lockdown policies, hybrid work emerged as a ‘new form of work’, whereby work arrangements began integrating physical workspace and time with their virtual counterparts to maintain business continuity.
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Jun 6, 2024 | 
nature.com | Dong-Anh Khuong-Quang |Chelsea Mayoh |Marie Wong |Sumanth Nagabushan |Veronica Yeung |Natacha Omer | +15 more
AbstractRecent research showed that precision medicine can identify new treatment strategies for patients with childhood cancers. However, it is unclear which patients will benefit most from precision-guided treatment (PGT).
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Jun 6, 2024 | nature.com | Dong-Anh Khuong-Quang |Chelsea Mayoh |Marie Wong |Sumanth Nagabushan |Veronica Yeung |Natacha Omer | +15 more
AbstractRecent research showed that precision medicine can identify new treatment strategies for patients with childhood cancers. However, it is unclear which patients will benefit most from precision-guided treatment (PGT).
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May 23, 2024 | 
onlinelibrary.wiley.com | Angela Lin |Eleanor Scimone |Robyn P. Thom |Duraisamy Balaguru
1 INTRODUCTION Since the first description in two unrelated male patients (Myhre et al., 1981), Myhre syndrome (MIM #139210, ORPHA #2588) has been increasingly recognized as a distinctive short stature syndrome with a recognizable facial appearance, hearing loss, and progressive abnormalities of the cardiovascular system, upper airway, lungs, skin, bones, and joints.
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Apr 19, 2024 | 
dx.doi.org | Angela Lin |Sumin Lee |Robert R. Knowles
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Sep 27, 2023 | 
dx.doi.org | Angela Lin |Azalea Uva |Helen Tran
Download Hi-Res ImageDownload to MS-PowerPointCite This:Macromolecules 2023, XXXX, XXX Terms & Conditions Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such files may be downloaded by article for research use (if there is a public use license linked to the relevant article, that license may permit other uses).
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Sep 1, 2023 | 
onlinelibrary.wiley.com | Alexandra Lucas |Angela Lin |Andrew Cohen |William Munoz
CONFLICT OF INTEREST STATEMENT The authors declare no conflict of interest. REFERENCES , , , Care4Rare Canada Consortium, , , , , , , , , & (2017). Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1. Journal of Human Genetics, 62(6), 661–663. https://doi.org/10.1038/jhg.2017.18 , , , , , & (2008). A missense mutation in ALDH18A1, encoding Δ1-pyrroline-5-carboxylate synthase (P5CS), causes an autosomal recessive neurocutaneous syndrome.
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Aug 30, 2023 | 
nejm.org | Emily W. Lopes |Angela Lin |Richard C. Cabot |Eric Rosenberg
August 31, 2023N Engl J Med 2023; 389:840-851 DOI: 10.1056/NEJMcpc2300903Richard C. Cabot, Founder, Eric S. Rosenberg, M.D., Editor, David M. Dudzinski, M.D., Associate Editor, Meridale V. Baggett, M.D., Associate Editor, Kathy M. Tran, M.D., Associate Editor, Dennis C. Sgroi, M.D., Associate Editor, Jo-Anne O. Shepard, M.D., Associate Editor, Emily K.
