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pro vyhledávání: '"V. T. Chang"'
Autor:
M. Fritzsche, D. Li, H. Colin-York, V. T. Chang, E. Moeendarbary, J. H. Felce, E. Sezgin, G. Charras, E. Betzig, C. Eggeling
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
In vitro models of actin organization show the formation of vortices, asters and stars. Here Fritzsche et al. show that such actin structures form in living cells in a manner dependent on the Arp2/3 complex but not myosin, and such structures influen
Externí odkaz:
https://doaj.org/article/3a96443ee39545ee85e6aa27308be298
Publikováno v:
Journal of Clinical Pathology. 60:431-433
Infection-associated haemophagocytic syndrome (IAHS) is an uncommon disorder usually occurring in immunocompromised patients. IAHS is a systemic reactive proliferation of phagocytic histiocytes induced by an infection usually of viral origin.1 We rep
Publikováno v:
Cancer. 89(5)
The Memorial Symptom Assessment Scale Short Form (MSAS-SF), an abbreviated version of the Memorial Symptom Assessment Scale, measures each of 32 symptoms with respect to distress or frequency alone. A physical symptom subscale (PHYS), psychologic sym
Publikováno v:
Cancer. 88(9)
The Edmonton Symptom Assessment Scale (ESAS) is a nine-item patient-rated symptom visual analogue scale developed for use in assessing the symptoms of patients receiving palliative care. The purpose of this study was to validate the ESAS in a differe
Publikováno v:
Cancer. 88(5)
The current study was conducted to assess symptom prevalence and symptom intensity and their relation to quality of life in medical oncology patients at a Veterans Affairs medical center.Consecutive inpatients and outpatients were asked to complete t
Publikováno v:
American journal of hematology. 59(2)
Idiopathic myelofibrosis (IMF) and secondary myelofibrosis (MF) are characterized by bone marrow (BM) fibrosis, neoangiogenesis, and increased extracellular matrix (ECM) proteins. These characteristics may be partially attributed to transforming grow
Publikováno v:
Cancer. 83(1)
Recent data from clinical trials suggest that quality-of-life (QOL) measurements may independently predict survival. The relation between survival and QOL measurements was tested among 122 inpatients and 96 outpatients with malignancies at one of fou
Autor:
M. Fisch, J. Lee, M. Weiss, L. I. Wagner, V. T. Chang, D. Cella, J. Manola, L. M. Minasian, W. J. McCaskill-Stevens, T. R. Mendoza, C. S. Cleeland
Publikováno v:
Journal of Clinical Oncology. 29:6008-6008
Publikováno v:
Blood. 69:341-344
Fetal hemoglobin (HbF) levels vary widely among individuals with sickle cell anemia (SS). Previous studies have suggested that HbF levels in SS individuals with alpha-thalassemia (two or three functional alpha- globin genes) are lower than HbF levels
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