SRX7115390 GSM4151169 SRP229108 SRS5626163 GSM4151169 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151169 GSM4151169 GEO Accession GSM4151169 SRX7115391 GSM4151170 SRP229108 SRS5626164 GSM4151170 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151170 GSM4151170 GEO Accession GSM4151170 SRX7115392 GSM4151171 SRP229108 SRS5626165 GSM4151171 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151171 GSM4151171 GEO Accession GSM4151171 SRX7115393 GSM4151172 SRP229108 SRS5626166 GSM4151172 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151172 GSM4151172 GEO Accession GSM4151172 SRX7115394 GSM4151173 SRP229108 SRS5626167 GSM4151173 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151173 GSM4151173 GEO Accession GSM4151173 SRX7115395 GSM4151174 SRP229108 SRS5626168 GSM4151174 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151174 GSM4151174 GEO Accession GSM4151174 SRX7115396 GSM4151175 SRP229108 SRS5626169 GSM4151175 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151175 GSM4151175 GEO Accession GSM4151175 SRX7115397 GSM4151176 SRP229108 SRS5626170 GSM4151176 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151176 GSM4151176 GEO Accession GSM4151176 SRX7115398 GSM4151177 SRP229108 SRS5626171 GSM4151177 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was extracted from the renal cortex of each mouse (n = 3 for each group) using TRIzol reagent (Invitrogen, Carlsbad, CA, USA).A total amount of 3 μg RNA per sample was used as input material for the RNA sample preparations. Ribosomal RNA was removed with an Epicentre Ribo-zero™ rRNA removal kit (Epicenter, USA) according to manufacturer's instructions. Sequencing libraries were generated using the rRNA-depleted RNA by NEBNext® Ultra™ Directional RNA Library prep kit from Illumina® (NEB, USA). HiSeq X Ten gds 304151177 GSM4151177 GEO Accession GSM4151177