Bella Banjanin

2024

Endothelial LATS2 is a suppressor of bone marrow fibrosis

Sivaraj, K. K., Majev, P.-G., Dharmalingam, B., Schroeder, S., Banjanin, B., Stehling, M., Zeuschner, D., Nordheim, A., Schneider, R. K. & Adams, R. H., Aug 2024, In: Nature Cardiovascular Research. 3, 8, p. 951–969 19 p.

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Collaborative effect of Csnk1a1 haploinsufficiency and mutant p53 in Myc induction can promote leukemic transformation

Fuchs, S. N. R., Stalmann, U. S. A., Snoeren, I. A. M., Bindels, E., Schmitz, S., Banjanin, B., Hoogenboezem, R. M., van Herk, S., Saad, M., Walter, W., Haferlach, T., Seillier, L., Saez-Rodriguez, J., Dugourd, A. J. F., Lehmann, K. V., Ben-Neriah, Y., Gleitz, H. F. E. & Schneider, R. K., 1 Feb 2024, In: Blood Advances. 8, 3, p. 766-779 14 p.

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Non-canonical Hedgehog signaling mediates profibrotic hematopoiesis-stroma crosstalk in myeloproliferative neoplasms

Pritchard, J. E., Pearce, J. E., Snoeren, I. A. M., Fuchs, S. N. R., Götz, K., Peisker, F., Wagner, S., Benabid, A., Lutterbach, N., Klöker, V., Nagai, J. S., Hannani, M. T., Galyga, A. K., Sistemich, E., Banjanin, B., Flosdorf, N., Bindels, E., Olschok, K., Biaesch, K. & Chatain, N. & 11 others, Bhagwat, N., Dunbar, A., Sarkis, R., Naveiras, O., Berres, M. L., Koschmieder, S., Levine, R. L., Costa, I. G., Gleitz, H. F. E., Kramann, R. & Schneider, R. K., 23 Jan 2024, In: Cell Reports. 43, 1, 113608.

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2023

Expansion-enhanced super-resolution radial fluctuations enable nanoscale molecular profiling of pathology specimens

Kylies, D., Zimmermann, M., Haas, F., Schwerk, M., Kuehl, M., Brehler, M., Czogalla, J., Hernandez, L. C., Konczalla, L., Okabayashi, Y., Menzel, J., Edenhofer, I., Mezher, S., Aypek, H., Dumoulin, B., Wu, H., Hofmann, S., Kretz, O., Wanner, N. & Tomas, N. M. & 17 others, Krasemann, S., Glatzel, M., Kuppe, C., Kramann, R., Banjanin, B., Schneider, R. K., Urbschat, C., Arck, P., Gagliani, N., van Zandvoort, M., Wiech, T., Grahammer, F., Sáez, P. J., Wong, M. N., Bonn, S., Huber, T. B. & Puelles, V. G., 10 Apr 2023, In: Nature Nanotechnology. 18, 4, p. 336-342 7 p.

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13 Citations (Scopus)

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2022

Single-cell analysis of cultured bone marrow stromal cells reveals high similarity to fibroblasts in situ

Stalmann, U. S. A., Banjanin, B., Snoeren, I. A. M., Nagai, J. S., Leimkühler, N. B., Li, R., Benabid, A., Pritchard, J. E., Malyaran, H., Neuss, S., Bindels, E. M., Costa, I. G. & Schneider, R. K., 1 Jun 2022, In: Experimental Hematology. 110, p. 28-33 6 p.

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Genetic barcoding systematically compares genes in del(5q) MDS and reveals a central role for CSNK1A1 in clonal expansion

Stalmann, U. S. A., Ticconi, F., Snoeren, I. A. M., Li, R., Gleitz, H. F. E., Cowley, G. S., McConkey, M. E., Wong, A. B., Schmitz, S., Fuchs, S. N. R., Sood, S., Leimkuhler, N. B., Martinez-Høyer, S., Banjanin, B., Root, D., Brummendorf, T. H., Pearce, J. E., Schuppert, A., Bindels, E. M. J. & Essers, M. A. & 5 others, Heckl, D., Stiehl, T., Costa, I. G., Ebert, B. L. & Schneider, R. K., 22 Mar 2022, In: Blood advances. 6, 6, p. 1780-1796 17 p.

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2021

Heterogeneous bone-marrow stromal progenitors drive myelofibrosis via a druggable alarmin axis

Leimkühler, N. B., Gleitz, H. F. E., Ronghui, L., Snoeren, I. A. M., Fuchs, S. N. R., Nagai, J. S., Banjanin, B., Lam, K. H., Vogl, T., Kuppe, C., Stalmann, U. S. A., Büsche, G., Kreipe, H., Gütgemann, I., Krebs, P., Banz, Y., Boor, P., Tai, E. W. Y., Brümmendorf, T. H. & Koschmieder, S. & 5 others, Crysandt, M., Bindels, E., Kramann, R., Costa, I. G. & Schneider, R. K., 1 Apr 2021, In: Cell Stem Cell. 28, 4, p. 637-652.e8

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94 Citations (Scopus)

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2020

Increased CXCL4 expression in hematopoietic cells links inflammation and progression of bone marrow fibrosis in MPN

Gleitz - Broeders, H., Dugourd, A., Bayer, N., Snoeren, I., Fuchs, S., Menzel, S., Ziegler, S., Kroger, N., Triviai, I., Busche, G., Kreipe, H., Banjanin, B., Pritchard, J., Hoogenboezem, R., Bindels, E., Schumacher, N., Rose-John, S., Elf, S., Saez-Rodriguez, J. & Kramann, R. & 1 others, Schneider, R., 2020, In: Blood. 136, 18, p. 2051-2064 14 p.

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64 Citations (Scopus)

2017

Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion

Natiq, A., Lysy, P., Gillemans, N., Schaap, R., Sefiani, A., Amzazi, S., El-Alaoui, S., Cantu, I., Banjanin, B., van Lom, K., Harteveld, C. & Philipsen, S., 2017, In: American Journal of Hematology. 92, 1, p. E2-E3

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5 Citations (Scopus)

Bella Banjanin

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