Detalhe da pesquisa
1.
Differences in bone microarchitecture between genetic and secondary iron-overload mouse models suggest a role for hepcidin deficiency in iron-related osteoporosis.
FASEB J
; 37(11): e23245, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37874260
2.
Uropathogenic E. coli induces DNA damage in the bladder.
PLoS Pathog
; 17(2): e1009310, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33630958
3.
Co-occurring anomalies in congenital oral clefts.
Am J Med Genet A
; 188(6): 1700-1715, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35179301
4.
Co-occurring non-omphalocele and non-gastroschisis anomalies among cases with congenital omphalocele and gastroschisis.
Am J Med Genet A
; 185(7): 1954-1971, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33881198
5.
Spleen iron, molybdenum, and manganese concentrations are coregulated in hepcidin-deficient and secondary iron overload models in mice.
FASEB J
; 33(10): 11072-11081, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31298936
6.
Associated anomalies in cases with congenital clubfoot.
Am J Med Genet A
; 182(9): 2027-2036, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32592281
7.
Deletion of BMP6 worsens the phenotype of HJV-deficient mice and attenuates hepcidin levels reached after LPS challenge.
Blood
; 130(21): 2339-2343, 2017 11 23.
Artigo
Inglês
| MEDLINE | ID: mdl-29021231
8.
Associated anomalies in cases with agenesis of the corpus callosum.
Am J Med Genet A
; 179(10): 2101-2111, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31444900
9.
Hepatocyte neogenin, another key actor in iron homeostasis.
Blood
; 138(6): 423-425, 2021 08 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34383040
10.
Limiting hepatic Bmp-Smad signaling by matriptase-2 is required for erythropoietin-mediated hepcidin suppression in mice.
Blood
; 127(19): 2327-36, 2016 05 12.
Artigo
Inglês
| MEDLINE | ID: mdl-26755707
11.
Associated anomalies in cases with anorectal anomalies.
Am J Med Genet A
; 176(12): 2646-2660, 2018 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30548801
12.
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
; 63(1): 126-37, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-26406355
13.
Erythroferrone contributes to hepcidin repression in a mouse model of malarial anemia.
Haematologica
; 102(1): 60-68, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27658439
14.
Associated anomalies in cases with esophageal atresia.
Am J Med Genet A
; 173(8): 2139-2157, 2017 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-28577344
15.
Activin inhibition limits early innate immune response in rat kidney allografts-a pilot study.
Transpl Int
; 30(1): 96-107, 2017 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-27732750
16.
Endoplasmic reticulum stress controls iron metabolism through TMPRSS6 repression and hepcidin mRNA stabilization by RNA-binding protein HuR.
Haematologica
; 106(4): 1202-1206, 2021 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32703788
17.
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
J Hepatol
; 62(3): 664-72, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25457201
18.
Testosterone perturbs systemic iron balance through activation of epidermal growth factor receptor signaling in the liver and repression of hepcidin.
Hepatology
; 59(2): 683-94, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-23907767
19.
LJ000328, a novel ALK2/3 kinase inhibitor, represses hepcidin and significantly improves the phenotype of IRIDA.
Haematologica
; 105(8): e385-e388, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31806689
20.
A spontaneous mutation of the rat Themis gene leads to impaired function of regulatory T cells linked to inflammatory bowel disease.
PLoS Genet
; 8(1): e1002461, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22275874