نتایج جستجو برای: dysplastic hematopoiesis

تعداد نتایج: 13958  

Journal: :Pediatric Neurology Briefs 1989

Journal: :In vivo 2006
Anna D Panani

Myelodysplastic syndrome (MDS) is a clonal disorder of the pluripotent hematopoietic stem cells which is characterized by ineffective and dysplastic hematopoiesis. The pathogenesis of MDS is not well defined and it appears that multiple genetic changes are involved. Several studies have shown that certain chromosomal abnormalities may be influenced by environmental factors, while differences in...

Journal: :Haematologica 2014
Haley Ramsey Qi Zhang Diane E Brown David P Steensma Charles P Lin Mei X Wu

Expression of the immediate early response gene X-1 (IEX-1, IER3) is diminished significantly in hematopoietic stem cells in a subgroup of patients with early stage myelodysplastic syndromes, but it is not clear whether the deregulation contributes to the disease. The current study demonstrates increased apoptosis and a concomitant decrease in the number of hematopoietic stem cells lacking this...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2016
Sadia Sultan Syed Mohammed Irfan Syeda Narisa Jawed

BACKGROUND Myelodysplastic syndrome (MDS) is a clonal disorder of hemopoeitic stem cells, characterized by infective hematopoiesis, peripheral cytopenias along with hypercellularity of marrow and marked dysplastic features. Our aim was to study the spectrum of the WHO classification in adult Pakistani patients with MDS at disease presentation. MATERIALS AND METHODS This retrospective descript...

2010
Chiharu Sugimori Alan F. List Pearlie K. Epling-Burnette

Myelodysplastic syndrome (MDS) represents one of the most challenging health-related problems in the elderly. Characterized by dysplastic morphology in the bone marrow in association with ineffective hematopoiesis, pathophysiological causes of this disease are diverse including genetic abnormalities within myeloid progenitors, altered epigenetics, and changes in the bone marrow microenvironment...

Journal: :Archives of dermatology 2005
David Moreno-Ramirez Lara Ferrandiz Juan J Rios-Martin Francisco M Camacho

BACKGROUND Three cases of pointillist nevus, which is a distinctive clinical type of benign melanocytic nevus with variegated pigment, have been described in the literature to date. OBSERVATIONS A 24-year-old man presented with an acquired melanocytic lesion composed of multiple tiny pigmented dots. Dermoscopy revealed multiple brown globules on a reddish skin-colored background, and histolog...

Journal: :The Kobe journal of medical sciences 2006
I Teoman Benli Hakan Ciçek Alper Kaya

BACKGROUND CONTEXT In situ fusion is the gold standard method of treatment of spondylolisthesis. There is no study in the literature evaluating the effect of sagittal contour realignment on clinical outcomes in comparison with the addition of anterior slippage reduction. PURPOSE The correction of sagittal plane vs. reduction with instrumentation in the patients with low or high dysplastic spo...

Journal: :Cold Spring Harbor perspectives in biology 2012
Michael A Rieger Timm Schroeder

Enormous numbers of adult blood cells are constantly regenerated throughout life from hematopoietic stem cells through a series of progenitor stages. Accessibility, robust functional assays, well-established prospective isolation, and successful clinical application made hematopoiesis the classical mammalian stem cell system. Most of the basic concepts of stem cell biology have been defined in ...

2015
Robert M. Hurwitz Morton E. Tavel

The so-called dysplastic nevus first entered medical parlance in 1980 [1], originally known as the B-K mole in 1978, only to evolve over the next 34 years into a variety of names including familiar and atypical sporadic mole, melanocytic nevus with persistent lentiginous melanocytic hyperplasia, junctional or compound nevus with architectural atypia/disorder with or without cytological atypia, ...

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