UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

B cell lymphoma and myeloma in murine Gaucher's disease

The Journal of pathology, 2013-09, Vol.231 (1), p.88-97

2013

Volltextzugriff (PDF)

Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta

Kidney international, 2004-10, Vol.66 (4), p.1589-1595

2004

Volltextzugriff (PDF)

Vasculopathy in patients with Fabry disease: Current controversies and research directions

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.99-108

2010

Volltextzugriff (PDF)

Characterization of human phagocyte-derived chitotriosidase, a component of innate immunity

International immunology, 2005-11, Vol.17 (11), p.1505-1512

2005

Volltextzugriff (PDF)

Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention

Blood, 2004-01, Vol.103 (1), p.33-39

2004

Volltextzugriff (PDF)

Identification of a Novel Acidic Mammalian Chitinase Distinct from Chitotriosidase

The Journal of biological chemistry, 2001-03, Vol.276 (9), p.6770-6778

2001

Volltextzugriff (PDF)

Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: Disease spectrum and natural course in attenuated patients

Molecular genetics and metabolism, 2012-11, Vol.107 (3), p.526-533

2012

Volltextzugriff (PDF)

Markers of Bone Turnover in Gaucher Disease: Modeling the Evolution of Bone Disease

The journal of clinical endocrinology and metabolism, 2011-07, Vol.96 (7), p.2194-2205

2011

Volltextzugriff (PDF)

Chemical Proteomic Analysis of Serine Hydrolase Activity in Niemann-Pick Type C Mouse Brain

Frontiers in neuroscience, 2018-07, Vol.12, p.440-440

2018

Volltextzugriff (PDF)

Sustained therapeutic effects of oral miglustat (Zavesca, N‐butyldeoxynojirimycin, OGT 918) in type I Gaucher disease

Journal of inherited metabolic disease, 2004-11, Vol.27 (6), p.757-766

2004

Volltextzugriff (PDF)

Marked Differences in Tissue-specific Expression of Chitinases in Mouse and Man

The journal of histochemistry and cytochemistry, 2005-10, Vol.53 (10), p.1283-1292

2005

Volltextzugriff (PDF)

Structure of human chitotriosidase. Implications for specific inhibitor design and function of mammalian chitinase-like lectins

The Journal of biological chemistry, 2002-07, Vol.277 (28), p.25537-25544

2002

Volltextzugriff (PDF)

Impaired trafficking of mutants of lysosomal glucocerebrosidase in Gaucher's disease

The international journal of biochemistry & cell biology, 2005-11, Vol.37 (11), p.2310-2320

2005

Volltextzugriff (PDF)

The human chitotriosidase gene. Nature of inherited enzyme deficiency

The Journal of biological chemistry, 1998-10, Vol.273 (40), p.25680-25685

1998

Volltextzugriff (PDF)

Pharmacological small molecules for the treatment of lysosomal storage disorders

Expert opinion on investigational drugs, 2010-11, Vol.19 (11), p.1367-1379

2010

Volltextzugriff (PDF)

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease

Blood cells, molecules, & diseases, 2005-09, Vol.35 (2), p.259-267

2005

Volltextzugriff (PDF)

Screening for Fabry disease using whole blood spots fails to identify one-third of female carriers

Clinica chimica acta, 2005-03, Vol.353 (1), p.201-203

2005

Volltextzugriff (PDF)

Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase

The Journal of biological chemistry, 2003-10, Vol.278 (42), p.40911-40916

2003

Volltextzugriff (PDF)

Cytokine-mediated modulation of leptin and adiponectin secretion during in vitro adipogenesis: Evidence that tumor necrosis factor-α- and interleukin-1β-treated human preadipocytes are potent leptin producers

Cytokine (Philadelphia, Pa.), 2005-10, Vol.32 (2), p.94-103

2005

Volltextzugriff (PDF)

Strong induction of members of the chitinase family of proteins in atherosclerosis: chitotriosidase and human cartilage gp-39 expressed in lesion macrophages

Arteriosclerosis, thrombosis, and vascular biology, 1999-03, Vol.19 (3), p.687-694

1999

Volltextzugriff (PDF)

Increased chitotriosidase activity in serum of leprosy patients: Association with bacillary leprosy

Clinical immunology (Orlando, Fla.), 2009-06, Vol.131 (3), p.501-509

2009

Volltextzugriff (PDF)

Manifestations of Fabry disease in placental tissue

Journal of inherited metabolic disease, 2006-02, Vol.29 (1), p.106-111

2006

Volltextzugriff (PDF)

Marked elevation of plasma chitotriosidase activity : a novel hallmark of gaucher disease

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1288-1292

1994

Volltextzugriff (PDF)

TLR- and NOD2-dependent regulation of human phagocyte-specific chitotriosidase

FEBS letters, 2007-11, Vol.581 (28), p.5389-5395

2007

Volltextzugriff (PDF)

Quantification of skeletal involvement in adults with type I Gaucher's disease: fat fraction measured by Dixon quantitative chemical shift imaging as a valid parameter

American journal of roentgenology (1976), 2002-10, Vol.179 (4), p.961-965

2002

Volltextzugriff (PDF)

1 – 25 von 92

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(86)
Mit Volltextzugriff
(83)

Publikationsform

Artikel
(91)
Tagungsberichte
(1)

Sprache

Englisch
(91)
Japanisch
(25)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

B cell lymphoma and myeloma in murine Gaucher's disease

Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta

Vasculopathy in patients with Fabry disease: Current controversies and research directions

Characterization of human phagocyte-derived chitotriosidase, a component of innate immunity

Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention

Identification of a Novel Acidic Mammalian Chitinase Distinct from Chitotriosidase

Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: Disease spectrum and natural course in attenuated patients

Markers of Bone Turnover in Gaucher Disease: Modeling the Evolution of Bone Disease

Chemical Proteomic Analysis of Serine Hydrolase Activity in Niemann-Pick Type C Mouse Brain

Sustained therapeutic effects of oral miglustat (Zavesca, N‐butyldeoxynojirimycin, OGT 918) in type I Gaucher disease

Marked Differences in Tissue-specific Expression of Chitinases in Mouse and Man

Structure of human chitotriosidase. Implications for specific inhibitor design and function of mammalian chitinase-like lectins

Impaired trafficking of mutants of lysosomal glucocerebrosidase in Gaucher's disease

The human chitotriosidase gene. Nature of inherited enzyme deficiency

Pharmacological small molecules for the treatment of lysosomal storage disorders

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease

Screening for Fabry disease using whole blood spots fails to identify one-third of female carriers

Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase

Cytokine-mediated modulation of leptin and adiponectin secretion during in vitro adipogenesis: Evidence that tumor necrosis factor-α- and interleukin-1β-treated human preadipocytes are potent leptin producers

Strong induction of members of the chitinase family of proteins in atherosclerosis: chitotriosidase and human cartilage gp-39 expressed in lesion macrophages

Increased chitotriosidase activity in serum of leprosy patients: Association with bacillary leprosy

Manifestations of Fabry disease in placental tissue

Marked elevation of plasma chitotriosidase activity : a novel hallmark of gaucher disease

TLR- and NOD2-dependent regulation of human phagocyte-specific chitotriosidase

Quantification of skeletal involvement in adults with type I Gaucher's disease: fat fraction measured by Dixon quantitative chemical shift imaging as a valid parameter

Suchergebnisse filtern