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P Laissue

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

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Cytoskeleton (Hoboken, N.J.)|April 10, 2025
Conserved Phosphorylation of the Myosin1e TH1 Domain Impacts Membrane Association and Function in Yeast and WormsHolly R Brooker, Karen Baker, Marina Ezcurra, et al.
Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, et al.
The British Journal of Dermatology|July 28, 2012
A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 geneD J Fonseca, R F Rojas, J I Vergara, et al.
Clinical and Experimental Dermatology|March 11, 2015
A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosisO Ortega-Recalde, M B Moreno, J I Vergara, et al.
Biofilm|March 23, 2026
A quantitative framework for multiscale analysis of <i>Candida albicans</i> biofilm developmentKai Li, Samantha Skivens, J Edward F Green, et al.
Endocrine Oncology (Bristol, England)|July 11, 2025
Thieno[2,3-<i>b</i>]pyridine compounds potently inhibit prostate cancer growth and motilityM A Alkheilewi, D A Leach, A Mohr, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|April 26, 2012
Key cellular components and interactive histocompatibility molecules regulating tolerance to the fetal allograftPatrick S Spencer, Soukaina M Hakam, Phillipe P Laissue, 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.
Cytoskeleton (Hoboken, N.J.)|April 10, 2025
Conserved Phosphorylation of the Myosin1e TH1 Domain Impacts Membrane Association and Function in Yeast and WormsHolly R Brooker, Karen Baker, Marina Ezcurra, et al.
Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, et al.
The British Journal of Dermatology|July 28, 2012
A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 geneD J Fonseca, R F Rojas, J I Vergara, et al.
Clinical and Experimental Dermatology|March 11, 2015
A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosisO Ortega-Recalde, M B Moreno, J I Vergara, et al.
Biofilm|March 23, 2026
A quantitative framework for multiscale analysis of <i>Candida albicans</i> biofilm developmentKai Li, Samantha Skivens, J Edward F Green, et al.
Endocrine Oncology (Bristol, England)|July 11, 2025
Thieno[2,3-<i>b</i>]pyridine compounds potently inhibit prostate cancer growth and motilityM A Alkheilewi, D A Leach, A Mohr, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|April 26, 2012
Key cellular components and interactive histocompatibility molecules regulating tolerance to the fetal allograftPatrick S Spencer, Soukaina M Hakam, Phillipe P Laissue, et al.
Pageof 2