受强制性开放获取政策约束的文章 - sarah king-smith了解详情
可在其他位置公开访问的文章：25 篇
Characterizing the O-glycosylation landscape of human plasma, platelets, and endothelial cells
SL King, HJ Joshi, KT Schjoldager, A Halim, TD Madsen, MH Dziegiel, ...
Blood advances 1 (7), 429-442, 2017
强制性开放获取政策： Danish Council for Independent Research, Danish National Research Foundation …
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
AL Brown, P Arts, CL Carmichael, M Babic, J Dobbins, CE Chong, ...
Blood advances 4 (6), 1131-1144, 2020
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Global functions of O‐glycosylation: promises and challenges in O‐glycobiology
HH Wandall, MAI Nielsen, S King‐Smith, N de Haan, I Bagdonaite
The FEBS journal 288 (24), 7183-7212, 2021
强制性开放获取政策： Danish Council for Independent Research, Danish National Research Foundation …
Deconstruction of O‐glycosylation—Gal NA c‐T isoforms direct distinct subsets of the O‐glycoproteome
KT Schjoldager, HJ Joshi, Y Kong, CK Goth, SL King, HH Wandall, ...
EMBO reports 16 (12), 1713-1722, 2015
强制性开放获取政策： Danish Council for Independent Research, Danish National Research Foundation
Global mapping of O-glycosylation of varicella zoster virus, human cytomegalovirus, and Epstein-Barr virus
I Bagdonaite, R Norden, HJ Joshi, SL King, SY Vakhrushev, S Olofsson, ...
Journal of Biological Chemistry 291 (23), 12014-12028, 2016
强制性开放获取政策： Danish Council for Independent Research, Danish National Research Foundation
GATA2 deficiency syndrome: a decade of discovery
CC Homan, P Venugopal, P Arts, NH Shahrin, S Feurstein, L Rawlings, ...
Human Mutation 42 (11), 1399-1421, 2021
强制性开放获取政策： National Health and Medical Research Council, Australia
Parental experiences of ultrarapid genomic testing for their critically unwell infants and children
GR Brett, M Martyn, F Lynch, MG de Silva, S Ayres, L Gallacher, K Boggs, ...
Genetics in Medicine 22 (12), 1976-1985, 2020
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
CC Homan, SL King-Smith, DM Lawrence, P Arts, J Feng, J Andrews, ...
Haematologica 106 (11), 3004, 2021
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
TAILS N-terminomics and proteomics reveal complex regulation of proteolytic cleavage by O-glycosylation
SL King, CK Goth, U Eckhard, HJ Joshi, AD Haue, SY Vakhrushev, ...
Journal of Biological Chemistry 293 (20), 7629-7644, 2018
强制性开放获取政策： Canadian Institutes of Health Research, Danish Council for Independent …
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death
AB Byrne, P Arts, TT Ha, KS Kassahn, LS Pais, A O’Donnell-Luria, ...
Nature Medicine 29 (1), 180-189, 2023
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema
AB Byrne, P Brouillard, DL Sutton, J Kazenwadel, S Montazaribarforoushi, ...
Science translational medicine 14 (634), eabm4869, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia, National Fund for …
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
CC Homan, MW Drazer, K Yu, DM Lawrence, J Feng, L Arriola-Martinez, ...
Blood Advances 7 (20), 6092-6107, 2023
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
A validated collection of mouse monoclonal antibodies to human glycosyltransferases functioning in mucin-type O-glycosylation
C Steentoft, Z Yang, S Wang, T Ju, MB Vester-Christensen, MF Festari, ...
Glycobiology 29 (9), 645-656, 2019
强制性开放获取政策： US National Institutes of Health, Danish Council for Independent Research …
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation
E Tudini, J Andrews, DM Lawrence, SL King-Smith, N Baker, L Baxter, ...
The American Journal of Human Genetics 109 (11), 1960-1973, 2022
强制性开放获取政策： National Health and Medical Research Council, Australia
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
MW Drazer, CC Homan, K Yu, M Cavalcante de Andrade Silva, ...
Blood advances 6 (15), 4357-4359, 2022
强制性开放获取政策： US National Institutes of Health, Damon Runyon Cancer Research Foundation
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome
P Arts, J Garland, AB Byrne, TSE Hardy, M Babic, J Feng, P Wang, T Ha, ...
American Journal of Medical Genetics Part A 182 (5), 1273-1277, 2020
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
AB Byrne, S Mizumoto, P Arts, P Yap, J Feng, AW Schreiber, M Babic, ...
Journal of Medical Genetics 57 (7), 454-460, 2020
强制性开放获取政策： National Health and Medical Research Council, Australia
Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia
C De Angelis, AB Byrne, R Morrow, J Feng, T Ha, P Wang, AW Schreiber, ...
BMC Medical Genomics 14, 1-7, 2021
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Glycoengineered keratinocyte library reveals essential functions of specific glycans for all stages of HSV-1 infection
I Bagdonaite, IN Marinova, AM Rudjord-Levann, EMH Pallesen, ...
Nature Communications 14 (1), 7000, 2023
强制性开放获取政策： Danish National Research Foundation, European Commission
The Australian Genomics Mitochondrial Flagship: A National Program Delivering Mitochondrial Diagnoses.
R Rius, AG Compton, NL Baker, S Balasubramaniam, S Best, ...
Genetics in Medicine, 101271, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia
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