Works by Lanikova, Lucie

Results: 12

Alternatively spliced NFKB1 transcripts enriched in Andean Aymara modulate inflammation, HIF and hemoglobin.

Published in:

Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-56848-0

By:

Song, Jihyun;
Han, Seonggyun;
Amaru, Ricardo;
Lanikova, Lucie;
Quispe, Teddy;
Kim, Dongwook;
Crawford, Jacob E.;
Kim, Soo Jin;
Lee, Younghee;
Prchal, Josef T.

Publication type:

Article

Novel germline JAK2R715T mutation causing PV‐like erythrocytosis in 3 generations. Amelioration by Ropeg‐Interferon.

Published in:

American Journal of Hematology, 2024, v. 99, n. 7, p. 1220, doi. 10.1002/ajh.27311

By:

Song, Jihyun;
Lanikova, Lucie;
Kim, Soo Jin;
Papadopoulos, Nicolas;
Meznarich, Jessica;
Constantinescu, Stefan N.;
Parsegov, Brynn;
Prchal, Jaroslav F.;
Prchal, Josef T.

Publication type:

Article

Differential Sensitivity to JAK Inhibitory Drugs by Isogenic Human Erythroblasts and Hematopoietic Progenitors Generated from Patient-Specific Induced Pluripotent Stem Cells.

Published in:

Stem Cells, 2014, v. 32, n. 1, p. 269, doi. 10.1002/stem.1545

By:

Ye, Zhaohui;
L iu, Cyndi F.;
Lanikova, Lucie;
Dowey, Sarah N.;
He, Chaoxia;
Huang, Xiaosong;
Brodsky, Robert A.;
Spivak, Jerry L.;
Prchal, Josef T.;
Cheng, Linzhao

Publication type:

Article

The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension.

Published in:

2014

By:

Sarangi, Susmita;
Lanikova, Lucie;
Kapralova, Katarina;
Acharya, Suchitra;
Swierczek, Sabina;
Lipton, Jeffrey M;
Wolfe, Lawrence;
Prchal, Josef T

Publication type:

journal article

The homozygous VHLD126N missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension.

Published in:

Pediatric Blood & Cancer, 2014, v. 61, n. 11, p. 2104, doi. 10.1002/pbc.25056

By:

Sarangi, Susmita;
Lanikova, Lucie;
Kapralova, Katarina;
Acharya, Suchitra;
Swierczek, Sabina;
Lipton, Jeffrey M.;
Wolfe, Lawrence;
Prchal, Josef T.

Publication type:

Article

Experimental Modeling of Myeloproliferative Neoplasms.

Published in:

Genes, 2019, v. 10, n. 10, p. 813, doi. 10.3390/genes10100813

By:

Lanikova, Lucie;
Babosova, Olga;
Prchal, Josef T.

Publication type:

Article

Wnt Effector TCF4 Is Dispensable for Wnt Signaling in Human Cancer Cells.

Published in:

Genes, 2018, v. 9, n. 9, p. 439, doi. 10.3390/genes9090439

By:

Janeckova, Lucie;
Lanikova, Lucie;
Kriz, Vitezslav;
Horazna, Monika;
Babosova, Olga;
Vojtechova, Martina;
Galuskova, Katerina;
Sloncova, Eva;
Korinek, Vladimir;
Hrckulak, Dusan

Publication type:

Article

Iron chelation and 2‐oxoglutarate‐dependent dioxygenase inhibition suppress mantle cell lymphoma's cyclin D1.

Published in:

Journal of Cellular & Molecular Medicine, 2019, v. 23, n. 11, p. 7785, doi. 10.1111/jcmm.14655

By:

Babosova, Olga;
Kapralova, Katarina;
Raskova Kafkova, Leona;
Korinek, Vladimir;
Divoky, Vladimir;
Prchal, Josef T.;
Lanikova, Lucie

Publication type:

Article

Novel compound VHL heterozygosity ( VHL T124A/L188V) associated with congenital polycythaemia.

Published in:

British Journal of Haematology, 2013, v. 162, n. 6, p. 851, doi. 10.1111/bjh.12431

By:

Lorenzo, Felipe R.;
Yang, Chunzhang;
Lanikova, Lucie;
Butros, Linda;
Zhuang, Zhengping;
Prchal, Josef T.

Publication type:

Article

Oxidative DNA Damage, Inflammatory Signature, and Altered Erythrocytes Properties in Diamond-Blackfan Anemia.

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 24, p. 9652, doi. 10.3390/ijms21249652

By:

Kapralova, Katarina;
Jahoda, Ondrej;
Koralkova, Pavla;
Gursky, Jan;
Lanikova, Lucie;
Pospisilova, Dagmar;
Divoky, Vladimir;
Horvathova, Monika

Publication type:

Article

Loss of Major DNase I Hypersensitive Sites in Duplicated β-globin Gene Cluster Incompletely Silences HBB Gene Expression.

Published in:

Human Mutation, 2016, v. 37, n. 11, p. 1153, doi. 10.1002/humu.23061

By:

Reading, N. Scott;
Shooter, Claire;
Song, Jihyun;
Miller, Robin;
Agarwal, Archana;
Lanikova, Lucie;
Clark, Barnaby;
Thein, Swee Lay;
Divoky, Vladimir;
Prchal, Josef T.

Publication type:

Article

β-Thalassemia Due to Intronic LINE-1 Insertion in the β-Globin Gene ( HBB): Molecular Mechanisms Underlying Reduced Transcript Levels of the β-Globin L1 Allele.

Published in:

Human Mutation, 2013, v. 34, n. 10, p. 1361, doi. 10.1002/humu.22383

By:

Lanikova, Lucie;
Kucerova, Jana;
Indrak, Karel;
Divoka, Martina;
Issa, Jean‐Pierre;
Papayannopoulou, Thalia;
Prchal, Josef T.;
Divoky, Vladimir

Publication type:

Article

Works by Lanikova, Lucie

Alternatively spliced NFKB1 transcripts enriched in Andean Aymara modulate inflammation, HIF and hemoglobin.

Novel germline JAK2<sup>R715T</sup> mutation causing PV‐like erythrocytosis in 3 generations. Amelioration by Ropeg‐Interferon.

Differential Sensitivity to JAK Inhibitory Drugs by Isogenic Human Erythroblasts and Hematopoietic Progenitors Generated from Patient-Specific Induced Pluripotent Stem Cells.

The homozygous VHL(D126N) missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension.

The homozygous VHL<sup>D126N</sup> missense mutation is associated with dramatically elevated erythropoietin levels, consequent polycythemia, and early onset severe pulmonary hypertension.

Experimental Modeling of Myeloproliferative Neoplasms.

Wnt Effector TCF4 Is Dispensable for Wnt Signaling in Human Cancer Cells.

Iron chelation and 2‐oxoglutarate‐dependent dioxygenase inhibition suppress mantle cell lymphoma's cyclin D1.

Novel compound VHL heterozygosity ( VHL T124A/L188V) associated with congenital polycythaemia.

Oxidative DNA Damage, Inflammatory Signature, and Altered Erythrocytes Properties in Diamond-Blackfan Anemia.

Loss of Major DNase I Hypersensitive Sites in Duplicated β-globin Gene Cluster Incompletely Silences HBB Gene Expression.

β-Thalassemia Due to Intronic LINE-1 Insertion in the β-Globin Gene ( HBB): Molecular Mechanisms Underlying Reduced Transcript Levels of the β-Globin<sub> L1</sub> Allele.