Hadassah Medical Center: Elkin Michael

1.

Abecassis A, Hermano E, Sheva K, Rubinstein AM, Elkin M, Meirovitz A. Radiation-Induced Nephropathy in the Murine Model Is Ameliorated by Targeting Heparanase. Biomedicines [Internet]. 2023;11(3). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85151544766&doi=10.3390%252fbiomedicines11030710&partnerID=40&md5=d344996f63cf95230603dadcbf50894a

2.

Nahmias Blank D, Hermano E, Sonnenblick A, Maimon O, Rubinstein AM, Drai E, et al. Macrophages Upregulate Estrogen Receptor Expression in the Model of Obesity-Associated Breast Carcinoma. Cells [Internet]. 2022;11(18). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85138336130&doi=10.3390%252fcells11182844&partnerID=40&md5=a6030a3eba87a1c7ff2f67cf449dd938

3.

Zahavi T, Salmon-Divon M, Salgado R, Elkin M, Hermano E, Rubinstein AM, et al. Heparanase: a potential marker of worse prognosis in estrogen receptor-positive breast cancer. npj Breast Cancer [Internet]. 2021;7(1). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85106994943&doi=10.1038%252fs41523-021-00277-x&partnerID=40&md5=907d57ad3d8daaa452e090fc7655f732

4.

Hermano E, Carlotti F, Abecassis A, Meirovitz A, Rubinstein AM, Li JP, et al. Dichotomic role of heparanase in a murine model of metabolic syndrome. Cellular and Molecular Life Sciences [Internet]. 2021;78(6):2771–80. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85092447001&doi=10.1007%252fs00018-020-03660-2&partnerID=40&md5=f5790aa97015a91cdfb59f87a41de729

5.

Gnanasekaran J, Gallimidi AB, Saba E, Pandi K, Berchoer LE, Hermano E, et al. Intracellular Porphyromonas gingivalis promotes the tumorigenic behavior of pancreatic carcinoma cells. Cancers [Internet]. 2020;12(8):1–14. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090534422&doi=10.3390%252fcancers12082331&partnerID=40&md5=901aa31d8f7a3f6ca5fc379a05486101

6.

Visochek L, Castiel A, Mittelman L, Elkin M, Atias D, Golan T, et al. Erratum: Exclusive destruction of mitotic spindles in human cancer cells (Oncotarget (2017) 8 (20813-20824) DOI: 10.18632/oncotarget.15343). Oncotarget [Internet]. 2020;11(14):1290–1. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85085609887&partnerID=40&md5=faa1fc0d9abc7071f6e2adc07a068727

7.

Elkin M. Role of Heparanase in Macrophage Activation. Advances in Experimental Medicine and Biology [Internet]. 2020;1221:445–60. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85083202150&doi=10.1007%252f978-3-030-34521-1_17&partnerID=40&md5=91d7fa6384093dbda254baec01024847

8.

Goldberg R, Meirovitz A, Abecassis A, Hermano E, Rubinstein AM, Nahmias D, et al. Regulation of Heparanase in Diabetes-Associated Pancreatic Carcinoma. Frontiers in Oncology [Internet]. 2019;9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85077268932&doi=10.3389%252ffonc.2019.01405&partnerID=40&md5=fc62d402fd70ea5571f723fe59b1a462

9.

Hermano E, Goldberg R, Rubinstein AM, Sonnenblick A, Maly B, Nahmias D, et al. Heparanase accelerates obesity-associated breast cancer progression. Cancer Research [Internet]. 2019;79(20):5342–54. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85073306052&doi=10.1158%252f0008-5472.CAN-18-4058&partnerID=40&md5=b42fb42f7853355c0c36c08c92ea3b57

10.

Rabelink TJ, Van Den Berg BM, Garsen M, Wang G, Elkin M, Van Der Vlag J. Heparanase: Roles in cell survival, extracellular matrix remodelling and the development of kidney disease. Nature Reviews Nephrology [Internet]. 2017;13(4):201–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85011591327&doi=10.1038%252fnrneph.2017.6&partnerID=40&md5=69dc574edd7f8444ba9866e89ea8d410

11.

Gallimidi AB, Nussbaum G, Hermano E, Weizman B, Meirovitz A, Vlodavsky I, et al. Syndecan-1 deficiency promotes tumor growth in a murine model of colitis-induced colon carcinoma. PLoS ONE [Internet]. 2017;12(3). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016256802&doi=10.1371%252fjournal.pone.0174343&partnerID=40&md5=9cd58cb5dd70c19961c6dc19a749799a

12.

Visochek L, Castiel A, Mittelman L, Elkin M, Atias D, Golan T, et al. Exclusive destruction of mitotic spindles in human cancer cells. Oncotarget [Internet]. 2017;8(13):20813–24. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016445778&doi=10.18632%252foncotarget.15343&partnerID=40&md5=08faab8a076c6bce2d72bf74796bdb4b

13.

Goldberg R, Sonnenblick A, Hermano E, Hamburger T, Meirovitz A, Peretz T, et al. Heparanase augments insulin receptor signaling in breast carcinoma. Oncotarget [Internet]. 2017;8(12):19403–12. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015790975&doi=10.18632%252foncotarget.14292&partnerID=40&md5=3e6c018de38d1123739a6841b3b2eeca

14.

Sanderson RD, Elkin M, Rapraeger AC, Ilan N, Vlodavsky I. Heparanase regulation of cancer, autophagy and inflammation: new mechanisms and targets for therapy. FEBS Journal [Internet]. 2017;284(1):42–55. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85003881572&doi=10.1111%252ffebs.13932&partnerID=40&md5=8d9f05c6ed58668023ccd300c3da0472

15.

Vlodavsky I, Singh P, Boyango I, Gutter-Kapon L, Elkin M, Sanderson RD, et al. Heparanase: From basic research to therapeutic applications in cancer and inflammation. Drug Resistance Updates [Internet]. 2016;29:54–75. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84991768946&doi=10.1016%252fj.drup.2016.10.001&partnerID=40&md5=f21d64ba662734438cc45867ddf21367

16.

Garsen M, Benner M, Dijkman HB, Van Kuppevelt TH, Li JP, Rabelink TJ, et al. Heparanase is essential for the development of acute experimental glomerulonephritis. American Journal of Pathology [Internet]. 2016;186(4):805–15. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962613993&doi=10.1016%252fj.ajpath.2015.12.008&partnerID=40&md5=8223c50267d6e7d6400a4d8079ec1fdb

17.

Gallimidi AB, Fischman S, Revach B, Bulvik R, Maliutina A, Rubinstein AM, et al. Periodontal pathogens Porphyromonas gingivalis and Fusobacterium nucleatum promote tumor progression in an oral-specific chemical carcinogenesis model. Oncotarget [Internet]. 2015;6(26):22613–23. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941242708&doi=10.18632%252foncotarget.4209&partnerID=40&md5=e13faae6409e3a3226f4f05e483bc0a6

18.

Hermano E, Meirovitz A, Meir K, Nussbaum G, Appelbaum L, Peretz T, et al. Macrophage polarization in pancreatic carcinoma: Role of heparanase enzyme. Journal of the National Cancer Institute [Internet]. 2014;106(12). Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84922395352&doi=10.1093%252fjnci%252fdju332&partnerID=40&md5=8090359c75714911f3c0b7adf2ab0ffc

19.

Goldberg R, Rubinstein AM, Gil N, Hermano E, Li JP, Van Der Vlag J, et al. Role of heparanase-driven inflammatory cascade in pathogenesis of diabetic nephropathy. Diabetes [Internet]. 2014;63(12):4302–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84911938045&doi=10.2337%252fdb14-0001&partnerID=40&md5=eef0086520b0c69c90e3ce9334a7b2c9

20.

Lerner I, Zcharia E, Neuman T, Hermano E, Rubinstein AM, Vlodavsky I, et al. Heparanase is preferentially expressed in human psoriatic lesions and induces development of psoriasiform skin inflammation in mice. Cellular and Molecular Life Sciences [Internet]. 2014;71(12):2347–57. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84901690129&doi=10.1007%252fs00018-013-1496-9&partnerID=40&md5=ca1c899292d5bda18446a751b189539e

21.

Hirshoren N, Bulvik R, Neuman T, Rubinstein AM, Meirovitz A, Elkin M. Induction of heparanase by HPV E6 oncogene in head and neck squamous cell carcinoma. Journal of Cellular and Molecular Medicine [Internet]. 2014;18(1):181–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84891371170&doi=10.1111%252fjcmm.12179&partnerID=40&md5=2e94b3928106a2b5d6e8be8c40dae044

22.

Goldberg R, Meirovitz A, Hirshoren N, Bulvik R, Binder A, Rubinstein AM, et al. Versatile role of heparanase in inflammation. Matrix Biology [Internet]. 2013;32(5):234–40. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84879602314&doi=10.1016%252fj.matbio.2013.02.008&partnerID=40&md5=97e668acef1a4542ae7d5389ce38834e

23.

Meirovitz A, Goldberg R, Binder A, Rubinstein AM, Hermano E, Elkin M. Heparanase in inflammation and inflammation-associated cancer. FEBS Journal [Internet]. 2013;280(10):2307–19. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84877691115&doi=10.1111%252ffebs.12184&partnerID=40&md5=2b5d60aa91e5554e5a1dc28df8bf80c1

24.

Vlodavsky I, Elkin M, Casu B, Li JP, Sanderson RD, Ilan N. Heparanase, a multifaceted protein involved in cancer, chronic inflammation, and kidney dysfunction [Internet]. Extracellular Matrix: Pathobiology and Signaling. 2012. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981693151&partnerID=40&md5=194d384a574d74dfc4364087ce7e3e57

25.

Vlodavsky I, Beckhove P, Lerner I, Pisano C, Meirovitz A, Ilan N, et al. Significance of heparanase in cancer and inflammation. Cancer Microenvironment [Internet]. 2012;5(2):115–32. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84866351573&doi=10.1007%252fs12307-011-0082-7&partnerID=40&md5=08dccb6e79632de7bab24691bbbece99

26.

Hermano E, Lerner I, Elkin M. Heparanase enzyme in chronic inflammatory bowel disease and colon cancer. Cellular and Molecular Life Sciences [Internet]. 2012;69(15):2501–13. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84864340290&doi=10.1007%252fs00018-012-0930-8&partnerID=40&md5=a2bd0105909af4cad1db2e3d8efd2df1

27.

Gil N, Goldberg R, Neuman T, Garsen M, Zcharia E, Rubinstein AM, et al. Heparanase is essential for the development of diabetic nephropathy in mice. Diabetes [Internet]. 2012;61(1):208–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84555188487&doi=10.2337%252fdb11-1024&partnerID=40&md5=6086d5113a262b7fdc0a8628c745d93a

28.

Lerner I, Hermano E, Zcharia E, Rodkin D, Bulvik R, Doviner V, et al. Heparanase powers a chronic inflammatory circuit that promotes colitis-associated tumorigenesis in mice. Journal of Clinical Investigation [Internet]. 2011;121(5):1709–21. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79955509614&doi=10.1172%252fJCI43792&partnerID=40&md5=890a830cede1da386b3eb8bfcb9f8f5b

29.

Meirovitz A, Hermano E, Lerner I, Zcharia E, Pisano C, Peretz T, et al. Role of heparanase in radiation-enhanced invasiveness of pancreatic carcinoma. Cancer Research [Internet]. 2011;71(7):2772–80. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-79953293124&doi=10.1158%252f0008-5472.CAN-10-3402&partnerID=40&md5=8e82e41f1053e045c7a7414ab0ac870d

30.

Ilan N, Fux L, Elkin M, Vlodavsky I. Molecular and cellular aspects of heparanase [Internet]. Tumor Angiogenesis: Basic Mechanisms and Cancer Therapy. 2008. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84892109911&doi=10.1007%252f978-3-540-33177-3_14&partnerID=40&md5=c59904e0b3e1743251761cdc62b84bbf

31.

Vlodavsky I, Elkin M, Abboud-Jarrous G, Levi-Adam F, Fuks L, Shafat I, et al. Heparanase: One molecule with multiple functions in cancer progression. Connective Tissue Research [Internet]. 2008;49(3–4):207–10. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-48549085133&doi=10.1080%252f03008200802143281&partnerID=40&md5=74ea5fc76a97ac13075041a4b3dbafcb

32.

Lerner I, Baraz L, Pikarsky E, Meirovitz A, Edovitsky E, Peretz T, et al. Function of heparanase in prostate tumorigenesis: Potential for therapy. Clinical Cancer Research [Internet]. 2008;14(3):668–76. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-38949137097&doi=10.1158%252f1078-0432.CCR-07-1866&partnerID=40&md5=792173cc3ff5c14f627574528cc2f92a

33.

Patel VN, Knox SM, Likar KM, Lathrop CA, Hossain R, Eftekhari S, et al. Heparanase cleavage of perlecan heparan sulfate modulates FGF10 activity during ex vivo submandibular gland branching morphogenesis. Development [Internet]. 2007;134(23):4177–86. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-38349091953&doi=10.1242%252fdev.011171&partnerID=40&md5=08f1a92744c6f334faf8b671c80d37e1

34.

Cohen I, Maly B, Simon I, Meirovitz A, Pikarsky E, Zcharia E, et al. Tamoxifen induces heparanase expression in estrogen receptor - Positive breast cancer. Clinical Cancer Research [Internet]. 2007;13(14):4069–77. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-34547121192&doi=10.1158%252f1078-0432.CCR-06-2546&partnerID=40&md5=d6b0e4a291a3c5b68aa5185848e5f7ca

35.

Philp D, St-Surin S, Cha HJ, Moon HS, Kleinman HK, Elkin M. Thymosin beta 4 induces hair growth via stem cell migration and differentiation. Annals of the New York Academy of Sciences [Internet]. 2007;1112:95–103. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-35348973918&doi=10.1196%252fannals.1415.009&partnerID=40&md5=6e5ba6886adee9cc6c67f933956c96c6

36.

Cid MC, Hoffman MP, Hernández-Rodríguez J, Segarra M, Elkin M, Sánchez M, et al. Association between increased CCL2 (MCP-1) expression in lesions and persistence of disease activity in giant-cell arteritis. Rheumatology [Internet]. 2006;45(11):1356–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33750202397&doi=10.1093%252frheumatology%252fkel128&partnerID=40&md5=ffe4b1ce6c4ddd902d76e1c5ab247020

37.

Ilan N, Elkin M, Vlodavsky I. Regulation, function and clinical significance of heparanase in cancer metastasis and angiogenesis. International Journal of Biochemistry and Cell Biology [Internet]. 2006;38(12):2018–39. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33748683743&doi=10.1016%252fj.biocel.2006.06.004&partnerID=40&md5=8abbdb80f5f3de6b14c0bf381578d492

38.

Baraz L, Haupt Y, Elkin M, Peretz T, Vlodavsky I. Tumor suppressor p53 regulates heparanase gene expression. Oncogene [Internet]. 2006;25(28):3939–47. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33745606964&doi=10.1038%252fsj.onc.1209425&partnerID=40&md5=80315b327e03887478000c7d0e6f0f50

39.

Vlodavsky I, Abboud-Jarrous G, Elkin M, Naggi A, Casu B, Sasisekharan R, et al. The impact of heparanase and heparin on cancer metastasis and angiogenesis. Pathophysiology of Haemostasis and Thrombosis [Internet]. 2006;35(1–2):P116–27. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33748458505&partnerID=40&md5=fd927a6c52d995575aa8b51915c30169

40.

Edovitsky E, Lerner I, Zcharia E, Peretz T, Vlodavsky I, Elkin M. Role of endothelial heparanase in delayed-type hypersensitivity. Blood [Internet]. 2006;107(9):3609–16. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33646430296&doi=10.1182%252fblood-2005-08-3301&partnerID=40&md5=c93f14002f7e20e911849c5f947d02f5

41.

Cohen I, Pappo O, Elkin M, San T, Bar-Shavit R, Hazan R, et al. Heparanase promotes growth, angiogenesis and survival of primary breast tumors. International Journal of Cancer [Internet]. 2006;118(7):1609–17. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-33644863802&doi=10.1002%252fijc.21552&partnerID=40&md5=8579c06442a7ad33ac0431525d1b5d5e

42.

Zcharia E, Philp D, Edovitsky E, Aingorn H, Metzger S, Kleinman HK, et al. Heparanase regulates murine hair growth. American Journal of Pathology [Internet]. 2005;166(4):999–1008. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-17144396758&doi=10.1016%2fS0002-9440%2810%2962321-8&partnerID=40&md5=9566f1d9c41b7df4c26f65c3f1f65a52

43.

Edovitsky E, Elkin M, Zcharia E, Peretz T, Vlodavsky I. Heparanase gene silencing, tumor invasiveness, angiogenesis, and metastasis. Journal of the National Cancer Institute [Internet]. 2004;96(16):1219–30. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-4344598247&doi=10.1093%252fjnci%252fdjh230&partnerID=40&md5=ddbeb7de03baefbaf086e678a3d9a4bc

44.

Elkin M, Orgel A, Kleinman HK. An angiogenic switch in breast cancer involves estrogen and soluble vascular endothelial growth factor receptor 1. Journal of the National Cancer Institute [Internet]. 2004;96(11):875–8. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-2942511783&doi=10.1093%252fjnci%252fdjh140&partnerID=40&md5=ae86bfe9850c3c7a1d26ae6f70582fc0

45.

Zcharia E, Metzger S, Chajek-Shaul T, Aingorn H, Elkin M, Friedmann Y, et al. Transgenic expression of mammalian heparanase uncovers physiological functions of heparan sulfate in tissue morphogenesis, vascularization, and feeding behavior. FASEB Journal [Internet]. 2004;18(2):252–63. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-10744232455&doi=10.1096%252ffj.03-0572com&partnerID=40&md5=fb4627838be12f068108793ef2a92116

46.

Philp D, Nguyen M, Scheremeta B, St-Surin S, Villa AM, Orgel A, et al. Thymosin beta4 increases hair growth by activation of hair follicle stem cells. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology [Internet]. 2004;18(2):385–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-1442290141&partnerID=40&md5=15d5c23a2b5d08ac40eecf7d4ef6fd11

47.

Elkin M, Cohen I, Zcharia E, Orgel A, Guatta-Rangini Z, Peretz T, et al. Regulation of Heparanase Gene Expression by Estrogen in Breast Cancer. Cancer Research [Internet]. 2003;63(24):8821–6. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0347320783&partnerID=40&md5=f85789d322519e963a65901785d21734

48.

Vlodavsky I, Goldshmidt O, Zcharia E, Atzmon R, Rangini-Guatta Z, Elkin M, et al. Mammalian heparanase: Involvement in cancer metastasis, angiogenesis and normal development. Seminars in Cancer Biology [Internet]. 2002;12(2):121–9. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035999158&doi=10.1006%252fscbi.2001.0420&partnerID=40&md5=967a6656d42de13e9425f02d504e6c08

49.

Zcharia E, Metzger S, Chajek-Shaul T, Friedmann Y, Pappo O, Aviv A, et al. Molecular properties and involvement of heparanase in cancer progression and mammary gland morphogenesis. Journal of Mammary Gland Biology and Neoplasia [Internet]. 2001;6(3):311–22. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-10044294056&doi=10.1023%252fA%253a1011375624902&partnerID=40&md5=200d3985de88425094c99cf5795633b5

50.

Song Gho Y, Kim PN, Li HC, Elkin M, Kleinman HK. Stimulation of tumor growth by human soluble intercellular adhesion molecule-1. Cancer Research [Internet]. 2001;61(10):4253–7. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035872451&partnerID=40&md5=02e631da76952c94713e0447ae622c7b

51.

Elkin M, Vlodavsky I. Tail vein assay of cancer metastasis. Current protocols in cell biology / editorial board, Juan S Bonifacino . [et al] [Internet]. 2001;Chapter 19:Unit 19.2. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-40349108482&doi=10.1002%252f0471143030.cb1902s12&partnerID=40&md5=dc3af91ff90c2ba3767a30602d55f27c

52.

Elkin M, Ilan N, Ishai-Michaeli R, Friedmann Y, Papo O, Pecker I, et al. Heparanase as mediator of angiogenesis: mode of action. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology [Internet]. 2001;15(9):1661–3. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035405778&doi=10.1096%252ffj.00-0895fje&partnerID=40&md5=df1903fd30df1e66305b599f9e964db5

53.

Vlodavsky I, Elkin M, Pappo O, Aingorn H, Atzmon R, Ishai-Michaeli R, et al. Mammalian heparanase as mediator of tumor metastasis and angiogenesis. Israel Medical Association Journal [Internet]. 2000;2(SUPPL. JULY):37–45. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033861341&partnerID=40&md5=570d0b9d647e823b8addf3fd2c5ed105

54.

Elkin M, Miao HQ, Nagler A, Aingorn E, Reich R, Hemo I, et al. Halofuginone: A potent inhibitor of critical steps in angiogenesis progression. FASEB Journal [Internet]. 2000;14(15):2477–85. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033664318&doi=10.1096%252ffj.00-0292com&partnerID=40&md5=871f11a4fbf862de236f6ed8b8e428e5

55.

Miao HQ, Elkin M, Aingorn E, Ishai-Michaeli R, Stein CA, Vlodavsky I. Inhibition of heparanase activity and tumor metastasis by laminarin sulfate and synthetic phosphorothioate oligodeoxynucleotides. International Journal of Cancer [Internet]. 1999;83(3):424–31. Available from: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032879625&doi=10.1002%2f%28SICI%291097-0215%2819991029%2983%3a3%3c424%3a%3aAID-IJC20%3e3.0.CO%3b2-L&partnerID=40&md5=83e048abb48bce4f8b3d5b3c51b7718f

56.

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