Miriam Eisenstein applies her multidisciplinary studies on Biochemistry and Chromatography in her research. She performs multidisciplinary study on Chromatography and Biochemistry in her works. Her study ties her expertise on Phosphatidylcholine together with the subject of Genetics. Her Organic chemistry study frequently involves adjacent topics like Bacteriocin. Her Bacteriocin study frequently involves adjacent topics like Antimicrobial. Her research on Antimicrobial frequently links to adjacent areas such as Organic chemistry. Miriam Eisenstein integrates many fields, such as Crystallography and Molecule, in her works. She undertakes multidisciplinary investigations into MHC class II and Antigen in her work. In her research, Miriam Eisenstein undertakes multidisciplinary study on Antigen and Major histocompatibility complex.
When carried out as part of a general Docking (animal) research project, her work on Nursing is frequently linked to work in Biological system, therefore connecting diverse disciplines of study. Her research is interdisciplinary, bridging the disciplines of Docking (animal) and Nursing. Miriam Eisenstein combines Crystallography and Crystal structure in her research. Miriam Eisenstein conducts interdisciplinary study in the fields of Crystal structure and Crystallography through her works. Organic chemistry is closely attributed to Bent molecular geometry in her study. Her Bent molecular geometry study frequently links to adjacent areas such as Organic chemistry. Miriam Eisenstein applies her multidisciplinary studies on Molecule and Chemical physics in her research. Miriam Eisenstein brings together Chemical physics and Molecule to produce work in her papers. While working on this project, Miriam Eisenstein studies both Biochemistry and Chromatography.
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Molecular surface recognition: determination of geometric fit between proteins and their ligands by correlation techniques.
Ephraim Katchalski-Katzir;Isaac Shariv;Miriam Eisenstein;Asher A. Friesem.
Proceedings of the National Academy of Sciences of the United States of America (1992)
DAP‐kinase‐mediated phosphorylation on the BH3 domain of beclin 1 promotes dissociation of beclin 1 from Bcl‐XL and induction of autophagy
Einat Zalckvar;Hanna Berissi;Liat Mizrachy;Yulia Idelchuk.
EMBO Reports (2009)
Structural requirements of six naturally occurring isoforms of the IL-18 binding protein to inhibit IL-18
Soo Hyun Kim;Miriam Eisenstein;Leonid Reznikov;Giamila Fantuzzi.
Proceedings of the National Academy of Sciences of the United States of America (2000)
CTL induction by a tumour-associated antigen octapeptide derived from a murine lung carcinoma
Ofer Mandelboim;Gideon Berke;Mati Fridkin;Michael Feldman.
Bivalence of EGF‐like ligands drives the ErbB signaling network
Eldad Tzahar;Ronit Pinkas‐Kramarski;James D. Moyer;Leah N. Klapper.
The EMBO Journal (1997)
Phosphorylation of Beclin 1 by DAP-kinase promotes autophagy by weakening its interactions with Bcl-2 and Bcl-XL.
Einat Zalckvar;Hanna Berissi;Miriam Eisenstein;Adi Kimchi.
The Autophagy Protein Atg12 Associates with Antiapoptotic Bcl-2 Family Members to Promote Mitochondrial Apoptosis
Assaf D. Rubinstein;Miriam Eisenstein;Yaara Ber;Shani Bialik.
Molecular Cell (2011)
Hsp90 recognizes a common surface on client kinases.
Ami Citri;Daniel Harari;Galit Shohat;Parameswaran Ramakrishnan.
Journal of Biological Chemistry (2006)
Role of galectin-8 as a modulator of cell adhesion and cell growth.
Yehiel Zick;Miriam Eisenstein;Rinat A. Goren;Yaron R. Hadari.
Glycoconjugate Journal (2002)
The fourth immunoglobulin domain of the stem cell factor receptor couples ligand binding to signal transduction
Janna M Blechman;Sima Lev;Jacob Barg;Jacob Barg;Miriam Eisenstein.
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