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Henrike Krenz

Showing results (1-10 of 10) with videos related to

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Frontiers in Endocrinology|January 7, 2022
FSHB Genotype Identified as a Relevant Diagnostic Parameter Revealed by Cluster Analysis of Men With Idiopathic InfertilityHenrike Krenz, Andrea Sansone, Sabine Kliesch, et al.
Human Reproduction (Oxford, England)|August 9, 2020
The Male Fertility Gene Atlas: a web tool for collecting and integrating OMICS data in the context of male infertilityHenrike Krenz, Jörg Gromoll, Thomas Darde, et al.
Andrology|February 26, 2020
Does the FSHB c.-211G>T polymorphism impact Sertoli cell number and the spermatogenic potential in infertile patients?Maria Schubert, Sophie Kaldewey, Lina Pérez Lanuza, et al.
Andrology|December 16, 2021
Machine learning based prediction models in male reproductive health: Development of a proof-of-concept model for Klinefelter Syndrome in azoospermic patientsHenrike Krenz, Andrea Sansone, Michael Fujarski, et al.
The Journal of Biological Chemistry|July 25, 2020
The Ca<sup>2+</sup> channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKATao Wang, Samuel Young, Henrike Krenz, et al.
Geroscience|July 14, 2026
Normal spermatogenesis in older men is associated with compensatory transcriptome changesYihan Wang, Sven Berres, Henrike Krenz, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
Life Science Alliance|November 29, 2022
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patternsLara M Siebert-Kuss, Henrike Krenz, Tobias Tekath, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, et al.
American Journal of Human Genetics|July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityMargot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Frontiers in Endocrinology|January 7, 2022
FSHB Genotype Identified as a Relevant Diagnostic Parameter Revealed by Cluster Analysis of Men With Idiopathic InfertilityHenrike Krenz, Andrea Sansone, Sabine Kliesch, et al.
Human Reproduction (Oxford, England)|August 9, 2020
The Male Fertility Gene Atlas: a web tool for collecting and integrating OMICS data in the context of male infertilityHenrike Krenz, Jörg Gromoll, Thomas Darde, et al.
Andrology|February 26, 2020
Does the FSHB c.-211G>T polymorphism impact Sertoli cell number and the spermatogenic potential in infertile patients?Maria Schubert, Sophie Kaldewey, Lina Pérez Lanuza, et al.
Andrology|December 16, 2021
Machine learning based prediction models in male reproductive health: Development of a proof-of-concept model for Klinefelter Syndrome in azoospermic patientsHenrike Krenz, Andrea Sansone, Michael Fujarski, et al.
The Journal of Biological Chemistry|July 25, 2020
The Ca<sup>2+</sup> channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKATao Wang, Samuel Young, Henrike Krenz, et al.
Geroscience|July 14, 2026
Normal spermatogenesis in older men is associated with compensatory transcriptome changesYihan Wang, Sven Berres, Henrike Krenz, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
Life Science Alliance|November 29, 2022
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patternsLara M Siebert-Kuss, Henrike Krenz, Tobias Tekath, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, et al.
American Journal of Human Genetics|July 17, 2020
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityMargot J Wyrwoll, Şehime G Temel, Liina Nagirnaja, et al.
Pageof 1