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Janine Altmüller

Showing results (81-90 of 326) with videos related to

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Journal of Hepatology|October 9, 2012
Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cellsAndrea Noetel, Natalia Elfimova, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|March 11, 2021
Clinical and genetic characterization of PYROXD1-related myopathy patients from TurkeyHülya-Sevcan Daimagüler, Ugur Akpulat, Özkan Özdemir, et al.
The Plant Cell|January 27, 2018
The Biotrophic Development of <i>Ustilago maydis</i> Studied by RNA-Seq AnalysisDaniel Lanver, André N Müller, Petra Happel, et al.
Human Mutation|January 3, 2022
Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex developmentHannah L Marko, Nadine C Hornig, Regina C Betz, et al.
Human Molecular Genetics|April 4, 2015
Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instabilityNadine Rosin, Nursel H Elcioglu, Filippo Beleggia, et al.
American Journal of Medical Genetics. Part A|July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromesBenjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Nucleic Acids Research|December 30, 2022
Npl3 functions in mRNP assembly by recruitment of mRNP components to the transcription site and their transfer onto the mRNAPhilipp Keil, Alexander Wulf, Nitin Kachariya, et al.
Plos One|September 17, 2013
SOX9 duplication linked to intersex in deerRegina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Scientific Reports|August 31, 2016
Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18Caroline Flegel, Felix Vogel, Adrian Hofreuter, et al.
Pageof 33

Showing results (81-90 of 326) with videos related to

Sort By:
Pageof 33
Journal of Hepatology|October 9, 2012
Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cellsAndrea Noetel, Natalia Elfimova, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|March 11, 2021
Clinical and genetic characterization of PYROXD1-related myopathy patients from TurkeyHülya-Sevcan Daimagüler, Ugur Akpulat, Özkan Özdemir, et al.
The Plant Cell|January 27, 2018
The Biotrophic Development of <i>Ustilago maydis</i> Studied by RNA-Seq AnalysisDaniel Lanver, André N Müller, Petra Happel, et al.
Human Mutation|January 3, 2022
Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex developmentHannah L Marko, Nadine C Hornig, Regina C Betz, et al.
Human Molecular Genetics|April 4, 2015
Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instabilityNadine Rosin, Nursel H Elcioglu, Filippo Beleggia, et al.
American Journal of Medical Genetics. Part A|July 2, 2015
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromesBenjamin Gollasch, Fitnat Buket Basmanav, Arti Nanda, et al.
Nucleic Acids Research|December 30, 2022
Npl3 functions in mRNP assembly by recruitment of mRNP components to the transcription site and their transfer onto the mRNAPhilipp Keil, Alexander Wulf, Nitin Kachariya, et al.
Plos One|September 17, 2013
SOX9 duplication linked to intersex in deerRegina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Scientific Reports|August 31, 2016
Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18Caroline Flegel, Felix Vogel, Adrian Hofreuter, et al.
Pageof 33