Orchestration of primary hemostasis by platelet and endothelial lysosome-related organelles

E Karampini, R Bierings, J Voorberg - … , Thrombosis, and Vascular …, 2020 - ahajournals.org
Megakaryocyte-derived platelets and endothelial cells store their hemostatic cargo in α-and
δ-granules and Weibel-Palade bodies, respectively. These storage granules belong to the …

Roles of G proteins and their GTPase-activating proteins in platelets

L O'Donoghue, A Smolenski - Bioscience Reports, 2024 - portlandpress.com
Platelets are small anucleate blood cells supporting vascular function. They circulate in a
quiescent state monitoring the vasculature for injuries. Platelets adhere to injury sites and …

In Vivo Prenylomic Profiling in the Brain of a Transgenic Mouse Model of Alzheimer's Disease Reveals Increased Prenylation of a Key Set of Proteins

A Jeong, SA Auger, S Maity, K Fredriksen… - ACS chemical …, 2022 - ACS Publications
Dysregulation of protein prenylation has been implicated in many diseases, including
Alzheimer's disease (AD). Prenylomic analysis, the combination of metabolic incorporation …

RAB31 targeted by MiR-30c-2-3p regulates the GLI1 signaling pathway, affecting gastric cancer cell proliferation and apoptosis

CT Tang, Q Liang, L Yang, XL Lin, S Wu, Y Chen… - Frontiers in …, 2018 - frontiersin.org
Background: Gastric cancer (GC), one of the most common cancers worldwide, is highly
malignant and fatal. Ras-related protein in brain 31 (RAB31), a member of the RAB family of …

[HTML][HTML] Platelet transcriptome analysis in patients with germline RUNX1 mutations

V Palma-Barqueros, JM Bastida, MJL Andreo… - Journal of Thrombosis …, 2023 - Elsevier
Background Germline mutations in RUNX1 can cause a familial platelet disorder that may
lead to acute myeloid leukemia, an autosomal dominant disorder characterized by moderate …

RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cells

B Estevez, S Borst, D Jarocha… - Blood, The Journal …, 2021 - ashpublications.org
Patients with familial platelet disorder with a predisposition to myeloid malignancy (FPDMM)
harbor germline monoallelic mutations in a key hematopoietic transcription factor, RUNX-1 …

Altered platelet-megakaryocyte endocytosis and trafficking of albumin and fibrinogen in RUNX1 haplodeficiency

F Del Carpio-Cano, G Mao, LE Goldfinger… - Blood …, 2024 - ashpublications.org
Platelet α-granules have numerous proteins, some synthesized by megakaryocytes (MK)
and others not synthesized but incorporated by endocytosis, an incompletely understood …

RUNX1 isoforms regulate RUNX1 and target genes differentially in platelets-megakaryocytes: association with clinical cardiovascular events

L Guan, D Voora, R Myers, F Del Carpio-Cano… - Journal of Thrombosis …, 2024 - Elsevier
Background Hematopoietic transcription factor RUNX1 is expressed from proximal P2 and
distal P1 promoters to yield isoforms RUNX1 B and C, respectively. The roles of these …

Defective RAB31-mediated megakaryocytic early endosomal trafficking of VWF, EGFR, and M6PR in RUNX1 deficiency

G Jalagadugula, G Mao, LE Goldfinger… - Blood …, 2022 - ashpublications.org
Transcription factor RUNX1 is a master regulator of hematopoiesis and megakaryopoiesis.
RUNX1 haplodeficiency (RHD) is associated with thrombocytopenia and platelet granule …

[HTML][HTML] Comparative analysis of the mitochondrial morphology, energy metabolism, and gene expression signatures in three types of blastocyst-derived stem cells

J Choi, BJ Seo, H La, SH Yoon, YJ Hong, JH Lee… - Redox biology, 2020 - Elsevier
Pre-implantation mouse blastocyst-derived stem cells, namely embryonic stem cells (ESCs),
trophoblast stem cells (TSCs), and extraembryonic endoderm (XEN) cells, have their own …