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Limor Minai

Showing results (11-20 of 17) with videos related to

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Nano Letters|June 9, 2016
Experimental Proof for the Role of Nonlinear Photoionization in Plasmonic PhototherapyLimor Minai, Adel Zeidan, Daniella Yeheskely-Hayon, et al.
Small (Weinheim an Der Bergstrasse, Germany)|March 21, 2012
Optical nanomanipulations of malignant cells: controlled cell damage and fusionLimor Minai, Daniella Yeheskely-Hayon, Lior Golan, et al.
Molecular Genetics and Metabolism|February 6, 2008
Mitochondrial respiratory chain complex assembly and function during human fetal developmentLimor Minai, Jelena Martinovic, Dominique Chretien, et al.
Scientific Reports|October 14, 2017
In vivo noninvasive microscopy of human leucocytesMatan M Winer, Adel Zeidan, Daniella Yeheskely-Hayon, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Molecular Genetics and Metabolism|July 3, 2007
A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndromeSophie Lebon, Limor Minai, Dominique Chretien, et al.
Nature Genetics|May 9, 2007
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletionAlice Bourdon, Limor Minai, Valérie Serre, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Nano Letters|June 9, 2016
Experimental Proof for the Role of Nonlinear Photoionization in Plasmonic PhototherapyLimor Minai, Adel Zeidan, Daniella Yeheskely-Hayon, et al.
Small (Weinheim an Der Bergstrasse, Germany)|March 21, 2012
Optical nanomanipulations of malignant cells: controlled cell damage and fusionLimor Minai, Daniella Yeheskely-Hayon, Lior Golan, et al.
Molecular Genetics and Metabolism|February 6, 2008
Mitochondrial respiratory chain complex assembly and function during human fetal developmentLimor Minai, Jelena Martinovic, Dominique Chretien, et al.
Scientific Reports|October 14, 2017
In vivo noninvasive microscopy of human leucocytesMatan M Winer, Adel Zeidan, Daniella Yeheskely-Hayon, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Molecular Genetics and Metabolism|July 3, 2007
A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndromeSophie Lebon, Limor Minai, Dominique Chretien, et al.
Nature Genetics|May 9, 2007
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletionAlice Bourdon, Limor Minai, Valérie Serre, et al.
Pageof 2