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...

Co‐occurring anomalies in congenital oral clefts

American journal of medical genetics. Part A, 2022-06, Vol.188 (6), p.1700-1715

2022

Volltextzugriff (PDF)

Associated anomalies in cases with agenesis of the corpus callosum

American journal of medical genetics. Part A, 2019-10, Vol.179 (10), p.2101-2111

2019

Volltextzugriff (PDF)

Co‐occurring non‐omphalocele and non‐gastroschisis anomalies among cases with congenital omphalocele and gastroschisis

American journal of medical genetics. Part A, 2021-07, Vol.185 (7), p.1954-1971

2021

Volltextzugriff (PDF)

Evidence for distinct pathways of hepcidin regulation by acute and chronic iron loading in mice

Hepatology (Baltimore, Md.), 2011-04, Vol.53 (4), p.1333-1341

2011

Volltextzugriff (PDF)

Lack of the bone morphogenetic protein BMP6 induces massive iron overload

Nature genetics, 2009-04, Vol.41 (4), p.478-481

2009

Volltextzugriff (PDF)

Associated anomalies in cases with esophageal atresia

American journal of medical genetics. Part A, 2017-08, Vol.173 (8), p.2139-2157

2017

Volltextzugriff (PDF)

Associated anomalies in cases with congenital clubfoot

American journal of medical genetics. Part A, 2020-09, Vol.182 (9), p.2027-2036

2020

Volltextzugriff (PDF)

Associated anomalies in cases with anorectal anomalies

American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2646-2660

2018

Volltextzugriff (PDF)

Differing impact of the deletion of hemochromatosis‐associated molecules HFE and transferrin receptor‐2 on the iron phenotype of mice lacking bone morphogenetic protein 6 or hemojuvelin

Hepatology (Baltimore, Md.), 2016-01, Vol.63 (1), p.126-137

2016

Volltextzugriff (PDF)

Testosterone perturbs systemic iron balance through activation of epidermal growth factor receptor signaling in the liver and repression of hepcidin

Hepatology (Baltimore, Md.), 2014-02, Vol.59 (2), p.683-694

2014

Volltextzugriff (PDF)

Induction of activin B by inflammatory stimuli up-regulates expression of the iron-regulatory peptide hepcidin through Smad1/5/8 signaling

Blood, 2012-07, Vol.120 (2), p.431-439

2012

Volltextzugriff (PDF)

Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver

Blood, 2008-08, Vol.112 (4), p.1503-1509

2008

Volltextzugriff (PDF)

Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of Hemochromatosiss

PloS one, 2016-02, Vol.11 (2), p.e0148292-e0148292

2016

Volltextzugriff (PDF)

Differences in bone microarchitecture between genetic and secondary iron‐overload mouse models suggest a role for hepcidin deficiency in iron‐related osteoporosis

The FASEB journal, 2023-11, Vol.37 (11), p.e23245-n/a

2023

Volltextzugriff (PDF)

Uropathogenic E. coli induces DNA damage in the bladder

PLoS pathogens, 2021-02, Vol.17 (2), p.e1009310

2021

Volltextzugriff (PDF)

Omphalocele and gastroschisis and associated malformations

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1280-1285

2008

Volltextzugriff (PDF)

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

Journal of hepatology, 2015-03, Vol.62 (3), p.664-672

2015

Volltextzugriff (PDF)

Erythroferrone contributes to hepcidin repression in a mouse model of malarial anemia

Haematologica (Roma), 2017-01, Vol.102 (1), p.60-68

2017

Volltextzugriff (PDF)

Hepatocyte neogenin, another key actor in iron homeostasis

Blood, 2021-08, Vol.138 (6), p.423-425

Roth, Marie-Paule

2021

Volltextzugriff (PDF)

Evidence for IL‐6/STAT3‐independent induction of lipocalin‐2 in the liver of mice infected with Escherichia coli

Hepatology (Baltimore, Md.), 2016-02, Vol.63 (2), p.673-674

2016

Volltextzugriff (PDF)

Endoplasmic reticulum stress controls iron metabolism through TMPRSS6 repression and hepcidin mRNA stabilization by RNA-binding protein HuR

Haematologica (Roma), 2021-04, Vol.106 (4), p.1202-1206

2021

Volltextzugriff (PDF)

Further support for the association of GNPAT variant rs11558492 with severe iron overload in hemochromatosis

Hepatology (Baltimore, Md.), 2016-06, Vol.63 (6), p.2054-2055

2016

Volltextzugriff (PDF)

Associated Anomalies in Radial Ray Deficiency

American journal of medical genetics. Part A, 2024-09, p.e63874

2024

Volltextzugriff (PDF)

Associated malformations among infants with neural tube defects

American journal of medical genetics. Part A, 2011-03, Vol.155A (3), p.565-568

2011

Volltextzugriff (PDF)

Associated congenital anomalies among cases with Down syndrome

European journal of medical genetics, 2015-12, Vol.58 (12), p.674-680

2015

Volltextzugriff (PDF)

1 – 25 von 153

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(145)
Mit Volltextzugriff
(141)

Publikationsform

Sprache

Englisch
(149)
Französisch
(4)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Co‐occurring anomalies in congenital oral clefts

Associated anomalies in cases with agenesis of the corpus callosum

Co‐occurring non‐omphalocele and non‐gastroschisis anomalies among cases with congenital omphalocele and gastroschisis

Evidence for distinct pathways of hepcidin regulation by acute and chronic iron loading in mice

Lack of the bone morphogenetic protein BMP6 induces massive iron overload

Associated anomalies in cases with esophageal atresia

Associated anomalies in cases with congenital clubfoot

Associated anomalies in cases with anorectal anomalies

Differing impact of the deletion of hemochromatosis‐associated molecules HFE and transferrin receptor‐2 on the iron phenotype of mice lacking bone morphogenetic protein 6 or hemojuvelin

Testosterone perturbs systemic iron balance through activation of epidermal growth factor receptor signaling in the liver and repression of hepcidin

Induction of activin B by inflammatory stimuli up-regulates expression of the iron-regulatory peptide hepcidin through Smad1/5/8 signaling

Iron regulates phosphorylation of Smad1/5/8 and gene expression of Bmp6, Smad7, Id1, and Atoh8 in the mouse liver

Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of Hemochromatosiss

Differences in bone microarchitecture between genetic and secondary iron‐overload mouse models suggest a role for hepcidin deficiency in iron‐related osteoporosis

Uropathogenic E. coli induces DNA damage in the bladder

Omphalocele and gastroschisis and associated malformations

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

Erythroferrone contributes to hepcidin repression in a mouse model of malarial anemia

Hepatocyte neogenin, another key actor in iron homeostasis

Evidence for IL‐6/STAT3‐independent induction of lipocalin‐2 in the liver of mice infected with Escherichia coli

Endoplasmic reticulum stress controls iron metabolism through TMPRSS6 repression and hepcidin mRNA stabilization by RNA-binding protein HuR

Further support for the association of GNPAT variant rs11558492 with severe iron overload in hemochromatosis

Associated Anomalies in Radial Ray Deficiency

Associated malformations among infants with neural tube defects

Associated congenital anomalies among cases with Down syndrome

Suchergebnisse filtern