Cargando…

Novel function of GATA-3, revealed by conditional deficient mice

Detalles Bibliográficos
Autores principales:	Ho, IC, Pai, SY, Truitt, ML
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2003
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833871/ http://dx.doi.org/10.1186/ar881

Ejemplares similares

GATA-3 in human T helper cell type 2 development
por: Skapenko, A, et al.
Publicado: (2004)

A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
por: Wong, SMY, et al.
Publicado: (2013)

P718: EPIGENOME PROFILING REVEALS ABERRANT DNA METHYLATION SIGNATURE IN GATA2 DEFICIENCY
por: Marin-Bejar, Oskar, et al.
Publicado: (2023)

Elucidating the mechanisms underlying GATA-1 activity
por: Gamsjaeger, Roland, et al.
Publicado: (2013)

Lethal influenza virus A H1N1 infection in two relatives with autosomal dominant GATA-2 deficiency
por: Sole-Violan, J, et al.
Publicado: (2013)

P054: Prevalence and risk factor analysis for methicillin-resistant Staphylococcus aureus colonization in an acute care hospital
por: Oh, ML, et al.
Publicado: (2013)

Identification of NKX2-5 and GATA4 sequence variations in patients with cardiac septation defects
por: Borkar, Yashvanthi, et al.
Publicado: (2014)

Cardiovascular response to NO donors in mice deficient in NO-GC
por: Groneberg, Dieter, et al.
Publicado: (2013)

sGCα(1)-deficient mice: a novel murine model of spontaneous primary open angle glaucoma
por: Buys, Emmanuel S, et al.
Publicado: (2011)

Pyruvate dehydrogenase activity is required for optimal growth under lipid deficient conditions
por: Rajagopalan, Kartik, et al.
Publicado: (2014)

Caspase-1-deficient mice are more resistant to severe sepsis
por: Sônego, F, et al.
Publicado: (2009)

P-14 Multiple acyl-coa dehydrogenase deficiency: a possibly treatable condition
por: Todeschini, A., et al.
Publicado: (2011)

Inhibition of myostatin signaling increases glucose in insulin-deficient diabetic mice
por: Wang, Qian, et al.
Publicado: (2012)

Leukemia/lymphoma development in IL-15-deficient TCR-transgenic mice
por: Dubois, Sigrid, et al.
Publicado: (2015)

PReS-FINAL-2256: Panniculitis revealing quantitative alpha 1 antitrypsine deficiency
por: Gagro, A, et al.
Publicado: (2013)

Fas deficiency attenuates bone loss during antigen induced arthritis in mice
por: Mosler, Elvira Lazic, et al.
Publicado: (2012)

Intrinsic hippocampal network activity is altered in MeCP2-deficient mice
por: Zhang, Liang, et al.
Publicado: (2007)

Generation of mice harbouring a conditional loss-of-function allele of Gata6
por: Sodhi, Chhinder P, et al.
Publicado: (2006)

Evaluation of ODQ as specific inhibitor of NO-sensitive guanylyl cyclase using mice deficient for the enzyme
por: Groneberg, Dieter, et al.
Publicado: (2009)

Identification of three ADA2 deficiency families with novel CECR1 mutations
por: Sarrabay, G, et al.
Publicado: (2015)

In vivo cardiac diffusion tensor imaging in free-breathing conditions
por: Wei, Hongjiang, et al.
Publicado: (2013)

Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
por: Vasanwala, Rashida, et al.
Publicado: (2013)

P698: CRISPR/CAS9 GENE EDITING IN HEMATOPOIETIC STEM CELLS TO MODEL CLONAL COMPETITION IN VIVO AND IN VITRO FOR GATA2 DEFICIENCY
por: Romero-Moya, Damia, et al.
Publicado: (2023)

GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS1
por: Singh, Preeti, et al.
Publicado: (2021)

P12-14. Design of hydrophilic, helical peptides that mimic the 4E10 epitope of HIV-1 gp41
por: Lorenz, IC, et al.
Publicado: (2009)

Genetic mapping of a modifier locus affecting hypertension in soluble guanylate cyclase α(1) deficient mice
por: Buys, Emmanuel S, et al.
Publicado: (2011)

Cryopyrin associated periodic syndromes (CAPS): immunological characterization of knock-in mouse model to exploit novel approaches for the modulation of the NLRP3 inflammasome.
por: Bertoni, A, et al.
Publicado: (2015)

Clinical and molecular characterization of patients with classic 3β-hydroxysteroid dehydrogenase deficiency
por: Wiromrat, Pattara, et al.
Publicado: (2015)

Multiple pituitary hormone deficiency: beware of combined hormones deficiency
por: Rochmah, Nur, et al.
Publicado: (2013)

Propofol is the induction agent of choice for urgent intubations with UK physicians
por: Rooney, KD, et al.
Publicado: (2011)

Comparative genomics reveals novel genes associated with sensory cilia
por: Piasecki, B, et al.
Publicado: (2015)

Survival of retinal ganglion cells in transgenic mice with deficiencies in sialyltransferases or neural cell adhesion molecule (NCAM) or after the administration of neuraminidase
por: Lobanovskaya, Natalia, et al.
Publicado: (2015)

Validation of a novel surveillance paradigm for ventilator-associated events
por: Klein Klouwenberg, Peter MC, et al.
Publicado: (2013)

Early use of immunoglobulin in septic shock
por: Cavazzuti, IC, et al.
Publicado: (2010)

Development of small-molecule transforming growth factor beta antagonists
por: Warner, DJ, et al.
Publicado: (2006)

The confounding effect of hyperchloraemia on the base deficit in diabetic ketoacidosis
por: Taylor, D, et al.
Publicado: (2004)

Cine interleaved sequences enabled imaging of mice on clinical 3T MRI and analysis of their cardiac function after myocardial infarction
por: Belin, Alexandre, et al.
Publicado: (2012)

MHC class I/II deficient NOG mice are useful for analysis of human T/B cell responses for human tumor immunology research
por: Yaguchi, Tomonori, et al.
Publicado: (2013)

Microarray analysis reveals age-related differences in gene expression during the development of osteoarthritis in mice
por: Olex, Amy, et al.
Publicado: (2010)

Inhalation injury and clinical course in major burned patients
por: Henrich, S, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_n1hgpjpup2h9ep5he8ujcuf3lv