SRX10404564 GSM5194612 SRP311584 SRS8527033 GSM5194612 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194612 GSM5194612 GEO Accession GSM5194612 SRX10404565 GSM5194613 SRP311584 SRS8527034 GSM5194613 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194613 GSM5194613 GEO Accession GSM5194613 SRX10404566 GSM5194614 SRP311584 SRS8527035 GSM5194614 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194614 GSM5194614 GEO Accession GSM5194614 SRX10404567 GSM5194615 SRP311584 SRS8527036 GSM5194615 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194615 GSM5194615 GEO Accession GSM5194615 SRX10404568 GSM5194616 SRP311584 SRS8527037 GSM5194616 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194616 GSM5194616 GEO Accession GSM5194616 SRX10404569 GSM5194617 SRP311584 SRS8527038 GSM5194617 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194617 GSM5194617 GEO Accession GSM5194617 SRX10404570 GSM5194618 SRP311584 SRS8527039 GSM5194618 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194618 GSM5194618 GEO Accession GSM5194618 SRX10404571 GSM5194619 SRP311584 SRS8527040 GSM5194619 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194619 GSM5194619 GEO Accession GSM5194619 SRX10404572 GSM5194620 SRP311584 SRS8527041 GSM5194620 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194620 GSM5194620 GEO Accession GSM5194620 SRX10404573 GSM5194621 SRP311584 SRS8527042 GSM5194621 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194621 GSM5194621 GEO Accession GSM5194621 SRX10404574 GSM5194622 SRP311584 SRS8527043 GSM5194622 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194622 GSM5194622 GEO Accession GSM5194622 SRX10404575 GSM5194623 SRP311584 SRS8527044 GSM5194623 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194623 GSM5194623 GEO Accession GSM5194623 SRX10404576 GSM5194626 SRP311584 SRS8527045 GSM5194626 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194626 GSM5194626 GEO Accession GSM5194626 SRX10404577 GSM5194629 SRP311584 SRS8527046 GSM5194629 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194629 GSM5194629 GEO Accession GSM5194629 SRX10404578 GSM5194632 SRP311584 SRS8527047 GSM5194632 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194632 GSM5194632 GEO Accession GSM5194632 SRX10404579 GSM5194635 SRP311584 SRS8527048 GSM5194635 RNA-Seq TRANSCRIPTOMIC cDNA After cutting the ends of bones and flushing marrow with PBS, the cortical bone was placed in an Eppendorf tube and immediately snap-frozen in liquid nitrogen. Subsequently, Trizol was added while the bone is maintained frozen in an eppendorf tube placed in a liquid nitrogen bath, homogenized in the same eppendorf tube with the Fastprep24 machine (MP Biomdicals), and subsequently total RNA was isolated and purified using manufacture recommendations for the PureLink RNA kit (Life Technologies). RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 305194635 GSM5194635 GEO Accession GSM5194635