Page last updated: 2024-10-15

phosphoserine and Acute Disease

phosphoserine has been researched along with Acute Disease in 3 studies

Phosphoserine: The phosphoric acid ester of serine.

Acute Disease: Disease having a short and relatively severe course.

Research Excerpts

ExcerptRelevanceReference
"Bcl-2 and Bcl-XL were both expressed in minimal residual disease cells."1.30Expression of Bcl-2-related genes in normal and AML progenitors: changes induced by chemotherapy and retinoic acid. ( Andreeff, M; Champlin, RC; Dong, J; Estey, EH; Estrov, Z; Jiang, S; Konopleva, M; Kornblau, SM; Okcu, MF; Reed, JC; Sanchez-Williams, G; Snell, VE; Xie, Z; Zhang, X; Zhao, S, 1999)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Li, L1
Thompson, LH1
Zhao, L1
Messina, JL1
Andreeff, M1
Jiang, S1
Zhang, X1
Konopleva, M1
Estrov, Z1
Snell, VE1
Xie, Z1
Okcu, MF1
Sanchez-Williams, G1
Dong, J1
Estey, EH1
Champlin, RC1
Kornblau, SM1
Reed, JC1
Zhao, S1
Schuringa, JJ1
Wierenga, AT1
Kruijer, W1
Vellenga, E1

Other Studies

3 other studies available for phosphoserine and Acute Disease

ArticleYear
Tissue-specific difference in the molecular mechanisms for the development of acute insulin resistance after injury.
    Endocrinology, 2009, Volume: 150, Issue:1

    Topics: Acute Disease; Animals; Corticosterone; Fatty Acids, Nonesterified; Hemorrhage; Hormone Antagonists;

2009
Expression of Bcl-2-related genes in normal and AML progenitors: changes induced by chemotherapy and retinoic acid.
    Leukemia, 1999, Volume: 13, Issue:11

    Topics: Acute Disease; Antigens, CD34; Antineoplastic Agents; Apoptosis; bcl-2-Associated X Protein; bcl-Ass

1999
Constitutive Stat3, Tyr705, and Ser727 phosphorylation in acute myeloid leukemia cells caused by the autocrine secretion of interleukin-6.
    Blood, 2000, Jun-15, Volume: 95, Issue:12

    Topics: Acute Disease; Carrier Proteins; DNA-Binding Proteins; Gene Expression Regulation, Neoplastic; Human

2000