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Carcinoma of the bone-marrow [PDF]
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A. Piney
openalex +4 more sources
Melanoma exosomes educate bone marrow progenitor cells toward a pro-metastatic phenotype through MET
Tumor-derived exosomes are emerging mediators of tumorigenesis. We explored the function of melanoma-derived exosomes in the formation of primary tumors and metastases in mice and human subjects.
Héctor Peinado+2 more
exaly +2 more sources
Deep imaging of bone marrow shows non-dividing stem cells are mainly perisinusoidal
Haematopoietic stem cells (HSCs) reside in a perivascular niche but the specific location of this niche remains controversial. HSCs are rare and few can be found in thin tissue sections or upon live imaging, making it difficult to comprehensively ...
Malea M Murphy+2 more
exaly +2 more sources
Adipocytes were identified in human bone marrow more than a century ago, yet until recently little has been known about their origin, development, function or interactions with other cells in the bone marrow. Little functional significance has been attributed to these cells, a paradigm that still persists today. However, we now know that marrow adipose
Gene P Ables+10 more
openaire +4 more sources
Mesenchymal and haematopoietic stem cells form a unique bone marrow niche
Simón Méndez-ferrer+2 more
exaly +2 more sources
The bone marrow microenvironment at single-cell resolution
Igor Dolgalev, Hai Hu, Kishor K Sivaraj
exaly +2 more sources
A Cellular Taxonomy of the Bone Marrow Stroma in Homeostasis and Leukemia
Ninib Baryawno+2 more
exaly +2 more sources
Clinical implications of bone marrow adiposity
A G Veldhuis-vlug
exaly +2 more sources
Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma
Getting around the blood–brain barrier The meninges comprise three membranes that surround and protect the central nervous system (CNS). Recent studies have noted the existence of myeloid cells resident there, but little is known about their ontogeny and
A. Cugurra+16 more
semanticscholar +1 more source
Case report: A novel mutation in RTEL1 gene in dyskeratosis congenita
Dyskeratosis congenita (DKC), also known as Zinsser–Cole–Engman syndrome, is a telomeropathy typically presenting as a triad of leukoplakia, nail dystrophy, and reticular hyperpigmentation.
Haider Nisar+5 more
doaj +1 more source