نتایج جستجو برای: dba

تعداد نتایج: 3851  

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2004
Lianhui Tao Wei Wang Long Li Paula M Kramer Michael A Pereira

Dibromoacetic acid (DBA) is a drinking water disinfection by-product. Its analogs, dichloroacetic acid (DCA) and trichloroacetic acid (TCA), are liver carcinogens in rodents. We evaluated the ability of DBA to cause DNA hypomethylation, glycogen accumulation, and peroxisome proliferation that are activities previously reported for the two other haloacetic acids. Female B6C3F1 mice and male Fisc...

2001
Hanna Gazda Jeffrey M. Lipton Thiébaut-Noël Willig Sarah Ball Charlotte M. Niemeyer Gil Tchernia Narla Mohandas Mark J. Daly Anna Ploszynska Karen A. Orfali Adrianna Vlachos Bertil E. Glader Roma Rokicka-Milewska Akira Ohara David Baker Dagmar Pospisilova Allison Webber David H. Viskochil David G. Nathan Alan H. Beggs Colin A. Sieff

Diamond-Blackfan anemia (DBA) is a rare congenital hypoplastic anemia that usually presents early in infancy and is inherited in 10% to 20% of cases. Linkage analysis has shown that DBA in many of both dominant and recessive DBA families mapped to chromosome 19q13.2 leading to the cloning of a gene on chromosome 19q13.2 that encodes a ribosomal protein, RPS19. However, subsequently, mutations o...

Journal: :Journal of molecular endocrinology 2005
Suwattanee Kooptiwut Melkam Kebede Sakeneh Zraika Sherley Visinoni Kathryn Aston-Mourney Jenny Favaloro Chris Tikellis Merlin C Thomas Josephine M Forbes Mark E Cooper Marjorie Dunlop Joseph Proietto Sofianos Andrikopoulos

Type 2 diabetes is characterized by islet dysfunction resulting in hyperglycemia, which can then lead to further deterioration in islet function. A possible mechanism for hyperglycemia-induced islet dysfunction is the accumulation of advanced glycation end products (AGE). The DBA/2 mouse develops pancreatic islet dysfunction when exposed to a high glucose environment and/or obesity-induced insu...

Journal: :Journal of virology 1995
T Bartman D M Murasko K J Blank

We previously described an endogenous murine retrovirus, rv-DBA/2aged, isolated from an aged DBA/2 mouse. The previous report showed that a recombination which resulted in the replacement of Emv-3 gag sequences with gag sequences homologous to those found in the AKT-8 virus had taken place. This recombination allowed production of a competent virus from the defective Emv-3 locus. However, the e...

Journal: :Blood 2001
H Gazda J M Lipton T N Willig S Ball C M Niemeyer G Tchernia N Mohandas M J Daly A Ploszynska K A Orfali A Vlachos B E Glader R Rokicka-Milewska A Ohara D Baker D Pospisilova A Webber D H Viskochil D G Nathan A H Beggs C A Sieff

Diamond-Blackfan anemia (DBA) is a rare congenital hypoplastic anemia that usually presents early in infancy and is inherited in 10% to 20% of cases. Linkage analysis has shown that DBA in many of both dominant and recessive DBA families mapped to chromosome 19q13.2 leading to the cloning of a gene on chromosome 19q13.2 that encodes a ribosomal protein, RPS19. However, subsequently, mutations o...

Journal: :Blood 2005
Yaw Ohene-Abuakwa Karen A Orfali Carine Marius Sarah E Ball

The erythroid defect in Diamond Blackfan anemia (DBA) is known to be intrinsic to the stem cell, but its molecular pathophysiology remains obscure. Using a 2-phase liquid erythroid culture system, we have demonstrated a consistent defect in DBA, regardless of clinical severity, including 3 first-degree relatives with normal hemoglobin levels but increased erythrocyte adenosine deaminase activit...

Journal: :Arthritis Research & Therapy 2005
Kristin Bauer Annika Knipper Hoang Tu-Rapp Dirk Koczan Hans-Jürgen Kreutzer Horst Nizze Eilhard Mix Hans-Juergen Thiesen Rikard Holmdahl Saleh M Ibrahim

Collagen-induced arthritis (CIA), an approved animal model for rheumatoid arthritis, is thought to be a T cell-dependent disease. There is evidence that CD8+ T cells are a major subset controlling the pathogenesis of CIA. They probably contribute to certain features of disease, namely tissue destruction and synovial hyperplasia. In this study we examined the role of perforin (pfp), a key molecu...

2004
Yaw Ohene-Abuakwa Karen A. Orfali

The erythroid defect in Diamond Blackfan anemia (DBA) is known to be intrinsic to the stem cell, but its molecular pathophysiology remains obscure. Using a 2-phase liquid erythroid culture system, we have demonstrated a consistent defect in DBA, regardless of clinical severity, including 3 first-degree relatives with normal hemoglobin levels but increased erythrocyte adenosine deaminase activit...

Journal: :Haematologica 2006
Jana Cmejlova Ludmila Dolezalova Dagmar Pospisilova Kvetoslava Petrtylova Jiri Petrak Radek Cmejla

BACKGROUND AND OBJECTIVES Diamond-Blackfan anemia (DBA) is a rare congenital pure red cell aplasia characterized by normochromic macrocytic anemia, reticulocytopenia, and normocellular bone marrow with a selective deficiency of erythroid precursors. Ribosomal protein S19 (RPS19), currently the only gene associated with DBA, is mutated in 25% of DBA patients, but its role in erythropoiesis is un...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2017
Yukako Kayashima Natalia Makhanova Nobuyo Maeda

OBJECTIVE Arch atherosclerosis 4 (Aath4) is a quantitative trait locus for atherosclerotic plaque formation in the inner curve of the aortic arch previously identified in an F2 cross of Apoe-/- mice on DBA/2J and 129S6 backgrounds. C-mer proto-oncogene tyrosine kinase (Mertk), coding for a ligand-activated transmembrane tyrosine kinase, is a candidate gene within the same chromosomal region. Ou...

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