Pesquisa | Biblioteca Virtual em Saúde

1.

Hepatocellular Adenoma: Report of 2 Cases That Highlight the Relevance of Phenotype-Genotype Correlation in the Pediatric Population.

Jiao, Jingjing; Finberg, Karin E; Jain, Dhanpat; Morotti, Raffaella.

Pediatr Dev Pathol ; 26(4): 394-403, 2023.

Artigo em Inglês | MEDLINE | ID: mdl-37334553

2.

NCOA4 is regulated by HIF and mediates mobilization of murine hepatic iron stores after blood loss.

Li, Xiuqi; Lozovatsky, Larisa; Sukumaran, Abitha; Gonzalez, Luis; Jain, Anisha; Liu, Dong; Ayala-Lopez, Nadia; Finberg, Karin E.

Blood ; 136(23): 2691-2702, 2020 12 03.

Artigo em Inglês | MEDLINE | ID: mdl-32659785

3.

Endometrial Carcinoma as the Presenting Malignancy in a Teenager With a Pathogenic TP53 Germline Mutation: A Case Report and Literature Review.

Irshaid, Lina; Clark, Mitchell; Fadare, Oluwole; Finberg, Karin E; Parkash, Vinita.

Int J Gynecol Pathol ; 41(3): 258-267, 2022 May 01.

Artigo em Inglês | MEDLINE | ID: mdl-33990091

4.

Low iron promotes megakaryocytic commitment of megakaryocytic-erythroid progenitors in humans and mice.

Xavier-Ferrucio, Juliana; Scanlon, Vanessa; Li, Xiuqi; Zhang, Ping-Xia; Lozovatsky, Larisa; Ayala-Lopez, Nadia; Tebaldi, Toma; Halene, Stephanie; Cao, Chang; Fleming, Mark D; Finberg, Karin E; Krause, Diane S.

Blood ; 134(18): 1547-1557, 2019 10 31.

Artigo em Inglês | MEDLINE | ID: mdl-31439541

5.

Blocking (iron) traffic in the gut.

Finberg, Karin E.

Blood ; 139(16): 2424-2425, 2022 04 21.

Artigo em Inglês | MEDLINE | ID: mdl-35446376

6.

Yale Precision Medicine Tumor Board: reawakening the guardian of the genome.

Grant, Michael J; Finberg, Karin E; Walther, Zenta; Stein, Stacey M; Lacy, Jill; Eder, Joseph P; Goldberg, Sarah B.

Lancet Oncol ; 23(3): 337-338, 2022 03.

Artigo em Inglês | MEDLINE | ID: mdl-35240081

7.

Pathogenic BRCA2 germline variants in combined hepatocellular-cholangiocarcinoma.

Li, Hongjie; Zhang, Xuchen; Finberg, Karin E; Walther, Zenta; Jain, Dhanpat; Gibson, Joanna.

Pathol Int ; 72(2): 138-140, 2022 Feb.

Artigo em Inglês | MEDLINE | ID: mdl-34808016

8.

Yale Cancer Center Precision Medicine Tumor Board: molecular findings alter a diagnosis and treatment plan.

Gibson, Joanna A; Finberg, Karin E; Nalbantoglu, ILKe; Cecchini, Michael; Ganzak, Amanda; Walther, Zenta; Sklar, Jeffrey L; Eder, Joseph P; Goldberg, Sarah B.

Lancet Oncol ; 22(3): 306-307, 2021 03.

Artigo em Inglês | MEDLINE | ID: mdl-33662283

9.

Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomy.

Womack, Jihad; Sukumaran, Abitha; Li, Xiuqi; Lozovatsky, Larisa; Gallagher, Patrick G; Seid, Jerome E; Finberg, Karin E.

Blood Cells Mol Dis ; 87: 102532, 2021 03.

Artigo em Inglês | MEDLINE | ID: mdl-33385755

10.

Going solo in iron transport.

Finberg, Karin E.

Blood ; 134(17): 1363-1364, 2019 10 24.

Artigo em Inglês | MEDLINE | ID: mdl-31698431

11.

Ironing out an approach to alleviate the hypoferremia of acute inflammation.

Finberg, Karin E.

Haematologica ; 106(2): 326-328, 2021 02 01.

Artigo em Inglês | MEDLINE | ID: mdl-33522782

12.

Yale Cancer Center Precision Medicine Tumor Board: new technology, new drugs, and the value of repeat testing.

Hafez, Navid; Walther, Zenta; Eder, Joseph P; Sklar, Jeffrey L; Gettinger, Scott N; Finberg, Karin E; Goldberg, Sarah B.

Lancet Oncol ; 21(3): 343-344, 2020 03.

Artigo em Inglês | MEDLINE | ID: mdl-32950226

13.

Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency.

Heeney, Matthew M; Guo, Dongjing; De Falco, Luigia; Campagna, Dean R; Olbina, Gordana; Kao, Paige P-C; Schmitz-Abe, Klaus; Rahimov, Fedik; Gutschow, Patrick; Westerman, Keith; Ostland, Vaughn; Jackson, Tracy; Klaassen, Robert J; Markianos, Kyriacos; Finberg, Karin E; Iolascon, Achille; Westerman, Mark; London, Wendy B; Fleming, Mark D.

Blood ; 132(4): 448-452, 2018 07 26.

Artigo em Inglês | MEDLINE | ID: mdl-29895660

14.

Genetic loss of Tmprss6 alters terminal erythroid differentiation in a mouse model of ß-thalassemia intermedia.

Stagg, David B; Whittlesey, Rebecca L; Li, Xiuqi; Lozovatsky, Larisa; Gardenghi, Sara; Rivella, Stefano; Finberg, Karin E.

Haematologica ; 104(10): e442-e446, 2019 10.

Artigo em Inglês | MEDLINE | ID: mdl-30819909

15.

Regulation of systemic iron homeostasis.

Finberg, Karin E.

Curr Opin Hematol ; 20(3): 208-14, 2013 May.

Artigo em Inglês | MEDLINE | ID: mdl-23426198

16.

Altered V-ATPase expression in renal intercalated cells isolated from B1 subunit-deficient mice by fluorescence-activated cell sorting.

Vedovelli, Luca; Rothermel, John T; Finberg, Karin E; Wagner, Carsten A; Azroyan, Anie; Hill, Eric; Breton, Sylvie; Brown, Dennis; Paunescu, Teodor G.

Am J Physiol Renal Physiol ; 304(5): F522-32, 2013 Mar 01.

Artigo em Inglês | MEDLINE | ID: mdl-23269648

17.

Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice.

Finberg, Karin E; Whittlesey, Rebecca L; Andrews, Nancy C.

Blood ; 117(17): 4590-9, 2011 Apr 28.

Artigo em Inglês | MEDLINE | ID: mdl-21355094

18.

Fibrosis-associated single-nucleotide polymorphisms in TGFB1 and CAV1 are not associated with the development of nephrogenic systemic fibrosis.

Le, Long P; Garibyan, Lilit; Lara, Daniel; Finberg, Karin E; Iafrate, A John; Duncan, Lyn M; Kay, Jonathan; Nazarian, Rosalynn M.

Am J Dermatopathol ; 35(3): 351-6, 2013 May.

Artigo em Inglês | MEDLINE | ID: mdl-23051628

19.

Bone marrow sinusoidal endothelial cells are a site of Fgf23 upregulation in a mouse model of iron deficiency anemia.

Li, Xiuqi; Lozovatsky, Larisa; Tommasini, Steven M; Fretz, Jackie; Finberg, Karin E.

Blood Adv ; 7(17): 5156-5171, 2023 09 12.

Artigo em Inglês | MEDLINE | ID: mdl-37417950

20.

Ironing out the role of Toll-like receptors.

Finberg, Karin E.

Blood ; 125(14): 2183-4, 2015 Apr 02.

Artigo em Inglês | MEDLINE | ID: mdl-25838278

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Hepatocellular Adenoma: Report of 2 Cases That Highlight the Relevance of Phenotype-Genotype Correlation in the Pediatric Population.

NCOA4 is regulated by HIF and mediates mobilization of murine hepatic iron stores after blood loss.

Endometrial Carcinoma as the Presenting Malignancy in a Teenager With a Pathogenic TP53 Germline Mutation: A Case Report and Literature Review.

Low iron promotes megakaryocytic commitment of megakaryocytic-erythroid progenitors in humans and mice.

Blocking (iron) traffic in the gut.

Yale Precision Medicine Tumor Board: reawakening the guardian of the genome.

Pathogenic BRCA2 germline variants in combined hepatocellular-cholangiocarcinoma.

Yale Cancer Center Precision Medicine Tumor Board: molecular findings alter a diagnosis and treatment plan.

Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomy.

Going solo in iron transport.

Ironing out an approach to alleviate the hypoferremia of acute inflammation.

Yale Cancer Center Precision Medicine Tumor Board: new technology, new drugs, and the value of repeat testing.

Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency.

Genetic loss of Tmprss6 alters terminal erythroid differentiation in a mouse model of ß-thalassemia intermedia.

Regulation of systemic iron homeostasis.

Altered V-ATPase expression in renal intercalated cells isolated from B1 subunit-deficient mice by fluorescence-activated cell sorting.

Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice.

Fibrosis-associated single-nucleotide polymorphisms in TGFB1 and CAV1 are not associated with the development of nephrogenic systemic fibrosis.

Bone marrow sinusoidal endothelial cells are a site of Fgf23 upregulation in a mouse model of iron deficiency anemia.

Ironing out the role of Toll-like receptors.