scholarly article | Q13442814 |
P2093 | author name string | Jose A Cancelas | |
Abhishek K Singh | |||
P2860 | cites work | Dynamic trafficking and delivery of connexons to the plasma membrane and accretion to gap junctions in living cells | Q24533504 |
Intercellular communication in the immune system: differential expression of connexin40 and 43, and perturbation of gap junction channel functions in peripheral blood and tonsil human lymphocyte subpopulations | Q24642743 | ||
Connexin43 gap junctions in normal, regenerating, and cultured mouse bone marrow and in human leukemias: their possible involvement in blood formation | Q24678387 | ||
Differential expression of novel potential regulators in hematopoietic stem cells | Q24811837 | ||
Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche | Q28505006 | ||
Functional role of gap junctions in cytokine-induced leukocyte adhesion to endothelium in vivo | Q28506489 | ||
Osteoblast connexin43 modulates skeletal architecture by regulating both arms of bone remodeling | Q28592164 | ||
Tales of a Dirty Drug: Carbenoxolone, Gap Junctions, and Seizures | Q28972313 | ||
SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells | Q29615006 | ||
Osteoblastic cells regulate the haematopoietic stem cell niche | Q29615007 | ||
Mesenchymal and haematopoietic stem cells form a unique bone marrow niche | Q29616602 | ||
Maintenance of the hematopoietic stem cell pool by CXCL12-CXCR4 chemokine signaling in bone marrow stromal cell niches | Q29617460 | ||
Endothelial cell-specific knockout of connexin 43 causes hypotension and bradycardia in mice | Q30307679 | ||
Mitochondrial transfer between cells can rescue aerobic respiration | Q30476644 | ||
Microtubule plus-end-tracking proteins target gap junctions directly from the cell interior to adherens junctions | Q30479975 | ||
Connexins modulate autophagosome biogenesis | Q30577497 | ||
Gap junction intercellular communication during lymphocyte transendothelial migration | Q30703122 | ||
Angiotensin II Regulation of Proliferation, Differentiation, and Engraftment of Hematopoietic Stem Cells | Q30711427 | ||
Up-regulation of Cx43 expression and GJIC function in acute leukemia bone marrow stromal cells post-chemotherapy | Q30883866 | ||
Adhesion of human hematopoietic progenitor cells to mesenchymal stromal cells involves CD44. | Q33312423 | ||
Bone marrow connexin-43 expression is critical for hematopoietic regeneration after chemotherapy | Q33370523 | ||
Acute myeloid leukemia does not deplete normal hematopoietic stem cells but induces cytopenias by impeding their differentiation | Q33409425 | ||
Endothelial Cells Promote Expansion of Long-Term Engrafting Marrow Hematopoietic Stem and Progenitor Cells in Primates | Q33722264 | ||
p53 regulates hematopoietic stem cell quiescence. | Q33732098 | ||
CD4+ T lymphocyte subsets express connexin 43 and establish gap junction channel communication with macrophages in vitro. | Q33761855 | ||
Endothelial cells are essential for the self-renewal and repopulation of Notch-dependent hematopoietic stem cells | Q33837223 | ||
Connexin43 mediates direct intercellular communication in human osteoblastic cell networks | Q33898016 | ||
Enhanced osteoclastic resorption and responsiveness to mechanical load in gap junction deficient bone | Q34012735 | ||
Human primary endothelial cells stimulate human osteoprogenitor cell differentiation | Q40523937 | ||
Connexin expression and gap-junction-mediated cell interactions in an in vitro model of haemopoietic stroma. | Q40589111 | ||
Fusion of GFP to the carboxyl terminus of connexin43 increases gap junction size in HeLa cells | Q40606454 | ||
Connexin-43 interactions with ZO-1 and alpha- and beta-tubulin | Q40725280 | ||
Gap junction protein connexin-43 interacts directly with microtubules | Q40781090 | ||
The origin of annular junctions: a mechanism of gap junction internalization | Q40828189 | ||
Hepatocyte growth factor is secreted by osteoblasts and cooperatively permits the survival of haematopoietic progenitors. | Q40828878 | ||
Intercellular communication between bone marrow stromal cells and CD34+ haematopoietic progenitor cells is mediated by connexin 43-type gap junctions | Q40836620 | ||
Connexin-43 gap junctions are involved in multiconnexin-expressing stromal support of hemopoietic progenitors and stem cells | Q40869443 | ||
Cardiac intercellular communication: consequences of connexin distribution and diversity | Q40922017 | ||
Gap junctions in blood forming tissues | Q40930969 | ||
Mesenchymal stem cells sense mitochondria released from damaged cells as danger signals to activate their rescue properties | Q41078616 | ||
Connexins, connexons, and intercellular communication | Q41114815 | ||
Multiple connexin proteins in single intercellular channels: connexin compatibility and functional consequences | Q41141420 | ||
Bone Marrow Macrophages Contribute to Diabetic Stem Cell Mobilopathy by Producing Oncostatin M. | Q41169174 | ||
Are there functional gap junctions or junctional hemichannels in macrophages? | Q41189158 | ||
Connexin-43-type gap junctions mediate communication between bone marrow stromal cells. | Q41543729 | ||
Formation of B type gap junctions between PHA-stimulated rabbit lymphocytes | Q41555211 | ||
Mitochondrial transfer from bone-marrow-derived stromal cells to pulmonary alveoli protects against acute lung injury | Q42128038 | ||
Autophagy maintains the metabolism and function of young and old stem cells. | Q42317229 | ||
Control of the proliferation of activated CD4+ T cells by connexins | Q43127224 | ||
CXCL12 in early mesenchymal progenitors is required for haematopoietic stem-cell maintenance | Q43226905 | ||
Connexon integrity is maintained by non-covalent bonds: intramolecular disulfide bonds link the extracellular domains in rat connexin-43. | Q43517108 | ||
Immunoglobulin and cytokine expression in mixed lymphocyte cultures is reduced by disruption of gap junction intercellular communication | Q43548115 | ||
Direct cell-cell communication in the blood-forming system | Q43867901 | ||
Sl/Sld mice have an increased number of gap junctions in their bone marrow stromal cells | Q43904595 | ||
Stromal cells prevent apoptosis of AML cells by up-regulation of anti-apoptotic proteins | Q44117862 | ||
Hematopoietic capacity of connexin43 wild-type and knock-out fetal liver cells not different on wild-type stroma | Q44240273 | ||
TNF-alpha plus IFN-gamma induce connexin43 expression and formation of gap junctions between human monocytes/macrophages that enhance physiological responses | Q44285411 | ||
Enhancement of repopulation haemopoiesis by heterozygous connexin 43 stem cells seeded on wild-type connexin 43 stroma | Q44498865 | ||
Ultrastructural morphometric study of efferent nerve terminals on murine bone marrow stromal cells, and the recognition of a novel anatomical unit: the "neuro-reticular complex". | Q44772551 | ||
Extracellular nucleotides are potent stimulators of human hematopoietic stem cells in vitro and in vivo | Q44909366 | ||
Osteoblasts promote engraftment of allogeneic hematopoietic stem cells | Q46292035 | ||
Identification of regulatory networks in HSCs and their immediate progeny via integrated proteome, transcriptome, and DNA methylome analysis. | Q46456469 | ||
Distinct bone marrow blood vessels differentially regulate haematopoiesis. | Q46564265 | ||
Endothelial jagged-2 sustains hematopoietic stem and progenitor reconstitution after myelosuppression | Q47421531 | ||
Cx30 exhibits unique characteristics including a long half-life when assembled into gap junctions | Q50351931 | ||
Cx25 contributes to leukemia cell communication and chemosensitivity. | Q34044927 | ||
Adenovirus vector E4 gene regulates connexin 40 and 43 expression in endothelial cells via PKA and PI3K signal pathways | Q34109505 | ||
Multicolor and electron microscopic imaging of connexin trafficking | Q34124663 | ||
Regulatory pathways in blood-forming tissue with particular reference to gap junctional communication | Q34138184 | ||
Hematopoiesis is severely altered in mice with an induced osteoblast deficiency | Q34290169 | ||
Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER | Q34306752 | ||
NADPH oxidase-2 derived superoxide drives mitochondrial transfer from bone marrow stromal cells to leukemic blasts. | Q34558873 | ||
Bone marrow CD169+ macrophages promote the retention of hematopoietic stem and progenitor cells in the mesenchymal stem cell niche | Q34577717 | ||
p62 is required for stem cell/progenitor retention through inhibition of IKK/NF-κB/Ccl4 signaling at the bone marrow macrophage-osteoblast niche. | Q34777301 | ||
Vasculopathy-associated hyperangiotensinemia mobilizes haematopoietic stem cells/progenitors through endothelial AT₂R and cytoskeletal dysregulation. | Q34940868 | ||
Engraftment and reconstitution of hematopoiesis is dependent on VEGFR2-mediated regeneration of sinusoidal endothelial cells | Q34957840 | ||
Gap junctions and connexins: potential contributors to the immunological synapse | Q34961018 | ||
Connexin expression in human acute myeloid leukemia cells: identification of patient subsets based on protein and global gene expression profiles | Q35040043 | ||
Inhibition of GSK-3β rescues the impairments in bone formation and mechanical properties associated with fracture healing in osteoblast selective connexin 43 deficient mice | Q35049558 | ||
Gap junctions between human T-colony cells | Q35174667 | ||
Inhibition of mitochondrial translation as a therapeutic strategy for human acute myeloid leukemia | Q35564841 | ||
Gap junctions and connexin-mediated communication in the immune system | Q35700140 | ||
Endothelial and perivascular cells maintain haematopoietic stem cells | Q35724815 | ||
Cell autonomous requirement of connexin 43 for osteocyte survival: consequences for endocortical resorption and periosteal bone formation. | Q35729489 | ||
Gap junctions and the connexin protein family | Q35749952 | ||
Pathways for degradation of connexins and gap junctions. | Q35749961 | ||
Transplantation of vascular endothelial cells mediates the hematopoietic recovery and survival of lethally irradiated mice | Q35750865 | ||
VCAM-1 expression in adult hematopoietic and nonhematopoietic cells is controlled by tissue-inductive signals and reflects their developmental origin. | Q35847871 | ||
Connexin-43 in the osteogenic BM niche regulates its cellular composition and the bidirectional traffic of hematopoietic stem cells and progenitors. | Q36014990 | ||
Connexin-43 prevents hematopoietic stem cell senescence through transfer of reactive oxygen species to bone marrow stromal cells | Q36061498 | ||
All-trans retinoic acid arrests cell cycle in leukemic bone marrow stromal cells by increasing intercellular communication through connexin 43-mediated gap junction | Q36134845 | ||
Connexin phosphorylation as a regulatory event linked to gap junction internalization and degradation | Q36162592 | ||
Detection of gap junctions between the progeny of a canine macrophage colony-forming cell in vitro | Q36200866 | ||
Pathways and control of connexin oligomerization. | Q36401843 | ||
Expression of connexin 32 and connexin 43 in acute myeloid leukemia and their roles in proliferation | Q36403429 | ||
Osteopontin is a hematopoietic stem cell niche component that negatively regulates stem cell pool size | Q36403763 | ||
Gap‐Junction Communication Pathways in Germinal Center Reactions | Q36511307 | ||
Immunohistological detection of gap junctions in human lymphoid tissue: connexin43 in follicular dendritic and lymphoendothelial cells | Q36681938 | ||
Increased expression of CX43 on stromal cells promotes leukemia apoptosis | Q36688963 | ||
Connexin 43 Modulates Osteogenic Differentiation of Bone Marrow Stromal Cells Through GSK-3beta/Beta-Catenin Signaling Pathways | Q88680551 | ||
Myelopoiesis in the Context of Innate Immunity | Q89011465 | ||
Activated stromal cells transfer mitochondria to rescue acute lymphoblastic leukemia cells from oxidative stress | Q90000799 | ||
PGC-1α driven mitochondrial biogenesis in stromal cells underpins mitochondrial trafficking to leukemic blasts | Q90376250 | ||
CD38-Driven Mitochondrial Trafficking Promotes Bioenergetic Plasticity in Multiple Myeloma | Q90949081 | ||
Identification of Miro1 and Miro2 as mitochondrial receptors for myosin XIX | Q90965346 | ||
Connexin43 regulates osteoprotegerin expression via ERK1/2 -dependent recruitment of Sp1 | Q90968649 | ||
Correction: Disruption of gap junctions attenuates acute myeloid leukemia chemoresistance induced by bone marrow mesenchymal stromal cells | Q91174407 | ||
The Yin and Yang of the Bone Marrow Microenvironment: Pros and Cons of Mesenchymal Stromal Cells in Acute Myeloid Leukemia | Q91219461 | ||
ROS-mediated PI3K activation drives mitochondrial transfer from stromal cells to hematopoietic stem cells in response to infection | Q91286420 | ||
Apelin+ Endothelial Niche Cells Control Hematopoiesis and Mediate Vascular Regeneration after Myeloablative Injury | Q91422158 | ||
Haematopoietic stem cell activity and interactions with the niche | Q91468445 | ||
The NAD-Booster Nicotinamide Riboside Potently Stimulates Hematopoiesis through Increased Mitochondrial Clearance | Q92229587 | ||
Signaling Pathways Regulating Hematopoietic Stem Cell and Progenitor Aging | Q92892162 | ||
Bone marrow adherent layers inhibit apoptosis of acute myeloid leukemia cells. | Q36726478 | ||
Cell-cell communication in the osteoblast/osteocyte lineage. | Q36740282 | ||
Osteoblast and osteocyte‐specific loss of Connexin43 results in delayed bone formation and healing during murine fracture healing | Q36807175 | ||
The warburg effect in leukemia-stroma cocultures is mediated by mitochondrial uncoupling associated with uncoupling protein 2 activation | Q36925362 | ||
SLAM family markers resolve functionally distinct subpopulations of hematopoietic stem cells and multipotent progenitors | Q37078786 | ||
Osteal macrophages: a new twist on coupling during bone dynamics | Q37286721 | ||
Self-renewal of a purified Tie2+ hematopoietic stem cell population relies on mitochondrial clearance. | Q37511781 | ||
Cx43 expressed on bone marrow stromal cells plays an essential role in multiple myeloma cell survival and drug resistance | Q37549419 | ||
High bone mass in mice lacking Cx37 because of defective osteoclast differentiation | Q37653316 | ||
A niche-like culture system allowing the maintenance of primary human acute myeloid leukemia-initiating cells: a new tool to decipher their chemoresistance and self-renewal mechanisms | Q37681007 | ||
Horizontal transfer of whole mitochondria restores tumorigenic potential in mitochondrial DNA-deficient cancer cells | Q37723101 | ||
Evolutionary analyses of gap junction protein families | Q37988232 | ||
The sixth sense: hematopoietic stem cells detect danger through purinergic signaling | Q38025606 | ||
Mix and match: investigating heteromeric and heterotypic gap junction channels in model systems and native tissues | Q38190331 | ||
Emergency granulopoiesis | Q38206076 | ||
Leukemogenic AML1-ETO fusion protein upregulates expression of connexin 43: the role in AML 1-ETO-induced growth arrest in leukemic cells | Q38312651 | ||
Connexins: Intercellular Signal Transmitters in Lymphohematopoietic Tissues. | Q38575569 | ||
Connexin 43 is required for the maintenance of mitochondrial integrity in brown adipose tissue. | Q38645888 | ||
Communication of Ca(2+) signals via tunneling membrane nanotubes is mediated by transmission of inositol trisphosphate through gap junctions | Q38759284 | ||
B-cell precursor acute lymphoblastic leukemia cells use tunneling nanotubes to orchestrate their microenvironment | Q38841779 | ||
Protective mitochondrial transfer from bone marrow stromal cells to acute myeloid leukemic cells during chemotherapy | Q38858729 | ||
Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA. | Q38922496 | ||
Up-regulation of connexin-43 expression in bone marrow mesenchymal stem cells plays a crucial role in adhesion and migration of multiple myeloma cells | Q39005146 | ||
Adult haematopoietic stem cell niches | Q39366652 | ||
Effect of Cx43 gene-modified leukemic bone marrow stromal cells on the regulation of Jurkat cell line in vitro | Q39452161 | ||
Energy metabolism of leukemia cells: glycolysis versus oxidative phosphorylation. | Q39652880 | ||
Leukemic cells create bone marrow niches that disrupt the behavior of normal hematopoietic progenitor cells | Q39903574 | ||
Activated macrophages inhibit enterocyte gap junctions via the release of nitric oxide | Q40059029 | ||
Establishing long-term cultures with self-renewing acute myeloid leukemia stem/progenitor cells. | Q40077330 | ||
Connexin37 protects against atherosclerosis by regulating monocyte adhesion | Q40252212 | ||
Reactive oxygen species act through p38 MAPK to limit the lifespan of hematopoietic stem cells | Q40299682 | ||
Hematopoietic Stem Cell Niches Produce Lineage-Instructive Signals to Control Multipotent Progenitor Differentiation | Q40444284 | ||
Gap junctions in hematopoietic stroma control proliferation and differentiation of blood cell precursors | Q40488934 | ||
Alteration Analysis of Bone Marrow Mesenchymal Stromal Cells from De Novo Acute Myeloid Leukemia Patients at Diagnosis | Q50445214 | ||
Does transmembrane communication through gap junctions enable stem cells to overcome stromal inhibition? | Q52193295 | ||
Up-regulation of the connexin43+ gap junction network in haemopoietic tissue before the growth of stem cells. | Q52219664 | ||
Gap junctions between cells of bone marrow: an ultrastructural study using tannic acid | Q52299852 | ||
Niches for Hematopoietic Stem Cells and Their Progeny | Q52317346 | ||
Protective role of connexin 32 in steady-state hematopoiesis, regeneration state, and leukemogenesis | Q53556975 | ||
Regulation of osteoclastogenesis by gap junction communication | Q53625746 | ||
Vascular endothelial cells produce soluble factors that mediate the recovery of human hematopoietic stem cells after radiation injury | Q53625988 | ||
Bone marrow macrophages maintain hematopoietic stem cell (HSC) niches and their depletion mobilizes HSCs | Q54415335 | ||
Gap junctional communication is involved in differentiation of osteoclasts from bone marrow and peripheral blood monocytes. | Q55019516 | ||
Therapeutic strategies targeting connexins | Q57471977 | ||
Connexin 43-Mediated Mitochondrial Transfer of iPSC-MSCs Alleviates Asthma Inflammation | Q57814615 | ||
Human osteoblasts support human hematopoietic progenitor cells in vitro bone marrow cultures | Q60504433 | ||
Amplification of mitochondrial DNA in acute myeloid leukaemia | Q63248800 | ||
Haematopoiesis in the era of advanced single-cell technologies | Q64008432 | ||
CXCL12 secretion by bone marrow stromal cells is dependent on cell contact and mediated by connexin-43 and connexin-45 gap junctions. | Q64883908 | ||
Distinct Bone Marrow Sources of Pleiotrophin Control Hematopoietic Stem Cell Maintenance and Regeneration. | Q64922350 | ||
Ultrastructural and morphometric alterations in bone marrow stromal tissue after 7 Gy irradiation | Q67801685 | ||
Possible communication between murine macrophages oriented in linear chains in tissue culture | Q68210387 | ||
A comparative morphometric study on the ultrastructure of adherent cells in long-term bone marrow culture from normal and congenitally anemic mice | Q69693099 | ||
A study of intercellular relationships between trabecular bone and marrow stromal cells in the murine femoral metaphysis | Q71554517 | ||
Bone marrow stromal cell blockade of human leukemic cell differentiation | Q71619532 | ||
Functional gap junctions in thymic epithelial cells are formed by connexin 43 | Q72589366 | ||
Posttranslational phosphorylation of lens fiber connexin46: a slow occurrence | Q72650857 | ||
Direct cell/cell communication in the lymphoid germinal center: connexin43 gap junctions functionally couple follicular dendritic cells to each other and to B lymphocytes | Q73481235 | ||
Detection and characterization of primitive malignant and normal progenitors in patients with acute myelogenous leukemia using long-term coculture with supportive feeder layers and cytokines | Q73774745 | ||
Connexin45 interacts with zonula occludens-1 and connexin43 in osteoblastic cells | Q73785250 | ||
Bone marrow stroma inhibits proliferation and apoptosis in leukemic cells through gap junction-mediated cell communication | Q73839468 | ||
Hematopoiesis: Gap Junction Intercellular Communication is Likely to be Involved in Regulation of Stroma-dependent Proliferation of Hemopoietic Stem Cells | Q74000673 | ||
Expression of connexin 43 (Cx43) is critical for normal hematopoiesis | Q74055050 | ||
Membrane channel connexin 32 maintains Lin(-)/c-kit(+) hematopoietic progenitor cell compartment: analysis of the cell cycle | Q80608548 | ||
Osteopontin, a key component of the hematopoietic stem cell niche and regulator of primitive hematopoietic progenitor cells | Q81676385 | ||
Vascular niche E-selectin regulates hematopoietic stem cell dormancy, self renewal and chemoresistance | Q85243285 | ||
Connexin 43 expressed in endothelial cells modulates monocyte‑endothelial adhesion by regulating cell adhesion proteins | Q86042232 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P921 | main subject | stem cell niche | Q16729831 |
P577 | publication date | 2020-01-25 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
P1476 | title | Gap Junctions in the Bone Marrow Lympho-Hematopoietic Stem Cell Niche, Leukemia Progression, and Chemoresistance | |
P478 | volume | 21 |
Search more.