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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

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Co‐occurring anomalies in congenital oral clefts

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

2022

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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

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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

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Associated anomalies in cases with esophageal atresia

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

2017

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Lack of the bone morphogenetic protein BMP6 induces massive iron overload

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

2009

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Associated anomalies in cases with congenital clubfoot

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

2020

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Associated anomalies in cases with anorectal anomalies

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

2018

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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

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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

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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

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

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

2016

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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

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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

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Uropathogenic E. coli induces DNA damage in the bladder

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

2021

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Hepatocyte neogenin, another key actor in iron homeostasis

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

Roth, Marie-Paule

2021

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Omphalocele and gastroschisis and associated malformations

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

2008

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

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

2017

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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

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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

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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

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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

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Associated congenital anomalies among cases with Down syndrome

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

2015

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Associated malformations among infants with neural tube defects

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

2011

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Associated malformations among infants with anophthalmia and microphthalmia

Birth defects research. A Clinical and molecular teratology, 2012-03, Vol.94 (3), p.147-152

2012

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Associated anomalies in cases with agenesis of the corpus callosum

Co‐occurring anomalies in congenital oral clefts

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

Associated anomalies in cases with esophageal atresia

Lack of the bone morphogenetic protein BMP6 induces massive iron overload

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

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

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

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

Hepatocyte neogenin, another key actor in iron homeostasis

Omphalocele and gastroschisis and associated malformations

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

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

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

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

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

Associated congenital anomalies among cases with Down syndrome

Associated malformations among infants with neural tube defects

Associated malformations among infants with anophthalmia and microphthalmia

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