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Christian Becker

Showing results (271-280 of 296) with videos related to

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Nature Immunology|November 7, 2018
Tumor immunoevasion via acidosis-dependent induction of regulatory tumor-associated macrophagesToszka Bohn, Steffen Rapp, Natascha Luther, et al.
Aging Cell|January 29, 2008
Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegansMichael Morcos, Xueliang Du, Friederike Pfisterer, et al.
Journal of Medicinal Chemistry|August 15, 2015
Targeting Drug Resistance in EGFR with Covalent Inhibitors: A Structure-Based Design ApproachJulian Engel, André Richters, Matthäus Getlik, et al.
Plos Genetics|January 24, 2009
A systematic approach to mapping recessive disease genes in individuals from outbred populationsFriedhelm Hildebrandt, Saskia F Heeringa, Franz Rüschendorf, et al.
Clinical Genetics|July 16, 2021
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndromeEmrah Kaygusuz, Arwa Ishaq A Khayyat, Uzma Abdullah, et al.
Human Mutation|June 6, 2006
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing lossErsan Kalay, Yun Li, Abdullah Uzumcu, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European populationTimothy Tehua Lu, Oscar Lao, Michael Nothnagel, et al.
Current Biology : CB|August 12, 2008
Correlation between genetic and geographic structure in EuropeOscar Lao, Timothy T Lu, Michael Nothnagel, et al.
American Journal of Human Genetics|September 2, 2008
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment traitJeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, et al.
Communications Biology|August 16, 2023
Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial functionSally Mortlock, Sahar Houshdaran, Idit Kosti, et al.
Pageof 30

Showing results (271-280 of 296) with videos related to

Sort By:
Pageof 30
Nature Immunology|November 7, 2018
Tumor immunoevasion via acidosis-dependent induction of regulatory tumor-associated macrophagesToszka Bohn, Steffen Rapp, Natascha Luther, et al.
Aging Cell|January 29, 2008
Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegansMichael Morcos, Xueliang Du, Friederike Pfisterer, et al.
Journal of Medicinal Chemistry|August 15, 2015
Targeting Drug Resistance in EGFR with Covalent Inhibitors: A Structure-Based Design ApproachJulian Engel, André Richters, Matthäus Getlik, et al.
Plos Genetics|January 24, 2009
A systematic approach to mapping recessive disease genes in individuals from outbred populationsFriedhelm Hildebrandt, Saskia F Heeringa, Franz Rüschendorf, et al.
Clinical Genetics|July 16, 2021
A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndromeEmrah Kaygusuz, Arwa Ishaq A Khayyat, Uzma Abdullah, et al.
Human Mutation|June 6, 2006
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing lossErsan Kalay, Yun Li, Abdullah Uzumcu, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European populationTimothy Tehua Lu, Oscar Lao, Michael Nothnagel, et al.
Current Biology : CB|August 12, 2008
Correlation between genetic and geographic structure in EuropeOscar Lao, Timothy T Lu, Michael Nothnagel, et al.
American Journal of Human Genetics|September 2, 2008
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment traitJeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, et al.
Communications Biology|August 16, 2023
Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial functionSally Mortlock, Sahar Houshdaran, Idit Kosti, et al.
Pageof 30