570 research outputs found
'We lack novelists such as Feuchtwanger, Wassermann, and Döblin':The Dutch Reception of Berlin Alexanderplatz: A Polyphony
Verschrikking en verwondering:Op zoek naar het sublieme in Vallen is als vliegen van Manon Uphoff
Vallen is als vliegen by Manon Uphoff has been widely praised for the author’s courage to face a traumatic past. Critics also admired the novel’s originality, its enchanting style, glowing imagination and rich intertextuality. This article aims to answer the question as to how this novel engages its readers. Which literary techniques are used to seduce and guide the reader in her or his perception of the story? An analysis of the peritexts, some intertexts and the narrator’s point of view reveals the novel’s ambiguous nature. Its fundamental ambivalence can be understood against the background of an aesthetic experience that has come to be known as the sublime
Computational Biology-Driven Genomic and Epigenomic Delineation of Acute Myeloid Leukemia
Hematopoiesis is the deterministic process of blood cell formation taking place in the bone
marrow. Mature blood cells are produced by a tightly controlled mechanism from hematopoietic
stem cells (HSCs) residing in the bone marrow. Upon maturation blood cells are released into the
peripheral blood and from this point onward can be transported to the different locations of the
body. The mature blood cells exert different functions dependent on a strictly controlled path of
maturation. The distinct leukocytes comprising granulocytes, monocytes, macrophages, natural
killer cells and lymphocytes are essential for the defense against pathogens and foreign invaders,
erythrocytes play a pivotal role in the transportation of oxygen to remote organs, and platelets
confer the process of blood clotting.
Mature blood cells are short-lived and require continuous replenishment. The control of
the production and the total number of blood cells is conferred by multipotent progenitors
and a small population of pluripotent HSCs (Figure 1). HSCs reside in the bone marrow of adult
mammals at the apex of a hierarchy of progenitors which become progressively restricted to
several and eventually single lineages of blood cells. Additionally these pluripotent stem cells
have the unique ability to self-renew, generating a source for continuous replenishment of the
complete blood cell system. The hematopoietic stem cell compartment contains stem cells with
progressively decreased self-renewal capacity with the retention of multi-lineage reconstitution.
The rare long term HSC (LT-HSC) is at the pinnacle of the hematopoietic hierarchy and is mainly
quiescent. With the most conserved rate of self-renewal it prevents the depletion of the stem
cell pool. The less rare short term HSC (ST-HSC) still retains a minimal ability for self-renewal
and is the more active effector cell for hematopoietic replenishment in normal situations. The
main constituent of the hematopoietic stem cell compartment is the multipotent progenitor
(MPP) which lost its self-renewal capacity, however, kept the ability to give rise to daughter
cells of different lineages. The daughter cells, common myeloid progenitor (CMP) and common
lymphoid progenitor (CLP), are still oligopotent as they give rise to multiple blood cell types, e.g.,
lymphocytes, granulocytes, platelets and erythrocytes.
The production of mature blood cells is a strictly controlled process that adapts to the needs
of human physiology, e.g., erythrocyte production after blood loss. The control is asserted mainly
by external stimuli, e.g., hematopoietic cytokines or growth factors, which are produced by
constituents of the regulatory microenvironment within the bone marrow niche, other blood
cells or cytokine secreting organs. The microenvironment plays a pivotal role in the formation
of adequate numbers of blood cells of the correct type and the hematopoietic cytokines it
produces allows the hematopoietic system to dynamically adapt to extramedullary events, e.g.,
blood loss, infection or cancer immunoediting
Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3’ MECOM
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