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291 results for “C57BL/6J”

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zenodo40/100

Fig. 3 in Peroral Echinococcus multilocularis egg inoculation in Myodes glareolus, Mesocricetus auratus and Mus musculus (CD-1 IGS and C57BL/6j)

Fig. 3. Number of metacestodes of varying sizes in individual species at 6 wpi (M. glareolus at 8 wpi) after receiving 100 viable E. multilocularis eggs. A <1 mm, B 1 - Ý2 mm, C> 2 - Ý3 mm, D> 3 - Ý4 mm, E 4 - Ý5 mm, F> 5 mm. Data from current study and (Woolsey et al., 2015a; Woolsey et al., 2015b).

opencc-by-4.0Aug 2016View details →
zenodo40/100

Fig. 2 in Peroral Echinococcus multilocularis egg inoculation in Myodes glareolus, Mesocricetus auratus and Mus musculus (CD-1 IGS and C57BL/6j)

Fig. 2. Mean establishment of E. multilocularis oncospheres in the different rodent intermediate hosts after receiving 100 viable eggs at 6 wpi (M. glareolus at 8 wpi). Data from current study and (Woolsey et al., 2015a; Woolsey et al., 2015b).

opencc-by-4.0Aug 2016View details →
zenodo36/100

Action potential dependent sIPSCs from juvenile (P21-30) C57BL/6J male mice

<p>species : Mus musculus</p> <p>sex : male</p> <p>strain :&nbsp;C57BL/6J</p> <p>age : post-natal day 21-30</p> <p>Voltage-clamp recordings of GABAA spontaneous inhibitory post-synaptic currents (sIPSCs) were obtained from juvenile (P21-30) C57BL/6J male mice. The dataset contains 267 individual events recorded from 3 different neurons (expA1-A3).&nbsp;</p>

opencc-by-nc-sa-4.0May 2016View details →
zenodo36/100

Action potential dependent sIPSCs from juvenile (P21-30) C57BL/6J male mice from CA1 pyramidal neurons receiving input from PV+ interneurons

<p>species : Mus musculus</p> <p>sex : male</p> <p>strain :&nbsp;C57BL/6J</p> <p>age : post-natal day 21-30</p> <p>Voltage-clamp recordings of GABAA spontaneous inhibitory post-synaptic currents (sIPSCs) were obtained from juvenile (P21-30)&nbsp; C57BL/6J male mice and recorded from hippocampal CA1 pyramidal neurons receiving input from parvalbumin positive (PV+) interneurons. The dataset contains 614 individual events recorded from 3 different neurons (expC1-C3).</p>

opencc-by-nc-sa-4.0Jul 2016View details →
zenodo36/100

Action potential dependent sIPSCs from juvenile (P21-30) C57BL/6J male mice CA1 pyramidal neurons receiving input from PV+ and CCK+ interneurons

<p>species : Mus musculus</p> <p>sex : male</p> <p>strain :&nbsp;C57BL/6J</p> <p>age : post-natal day 21-30</p> <p>Voltage-clamp recordings of GABAA spontaneous inhibitory post-synaptic currents (sIPSCs) were obtained from juvenile (P21-30) C57BL/6J male mice and recorded from hippocampal CA1 pyramidal neurons receiving input from parvalbumin positive and cholecystokinin positive (CCK+) interneurons. The dataset contains 2130 individual events recorded from 3 different neurons (expD1-D3).</p>

opencc-by-nc-sa-4.0Jul 2016View details →
zenodo36/100

Action potential dependent sIPSCs from 3-4 months old C57BL/6J X SJL female mice hippocampus CA1 pyramidal cell

<p>species : Mus musculus</p> <p>sex : female</p> <p>strain :&nbsp;C57BL/6J X SJL</p> <p>age : 3 - 4 months</p> <p>Voltage-clamp recordings of GABAA spontaneous inhibitory post-synaptic currents (sIPSCs) were obtained from 3-4 months old C57BL/6J X SJL female mice . The dataset contains 701 individual events recorded from 7 different neurons (expB1-B7).</p>

opencc-by-nc-sa-4.0Jul 2016View details →
zenodo36/100

IG receptor germline set for species: Mouse subgroup: C57BL/6J set_name: C57BL/6J IGKV

<p>Germline Reference set published on the Open Germline Receptor Database (OGRDB)</p>

openother-openSep 2022View details →
zenodo36/100

IG receptor germline set for species: Mouse subgroup: C57BL/6J set_name: C57BL/6J IGLV

<p>Germline Reference set published on the Open Germline Receptor Database (OGRDB)</p>

openother-openSep 2022View details →
dryad36/100

Data from: Cardiac dysfunction in C57Bl/6J mice with chronic kidney disease shows sex-specific effects: Comparison of dietary adenine and 5/6 nephrectomy models

Open the record for dataset details and reuse information.

publicOct 2025View details →
zenodo32/100

C57BL/6J mouse hippocampus CA1 pyramidal cell morphologies

<p>title : Reconstruction of hippocampus CA1 cell morphologies</p> <p>specimen : Mus musculus</p> <p>sex : male</p> <p>strain : C57BL/6J</p> <p>age : post-natal day 13-16</p> <p>This neuron was recorded and filled with biocytin (3 mg/ml) in a 300 &micro;m thick coronal slice of rat hippocampus, using 2 - 10 MOhm patch pipettes. 3,3&prime;-diaminobenzidine (DAB) was used for revelation. The slice was fixed and the cell reconstructed with Neurolucida using a 100x oil immersion objective.</p>

opencc-by-nc-nd-4.0Jul 2016View details →
zenodo32/100

Female behavior drives the formation of distinct social structures in C57BL/6J versus wild-derived outbred mice in field enclosures

<p>Data files for Vogt et al. 2024</p>

opencc-by-4.0Dec 2023View details →
zenodo32/100

Chronic nicotine exposure alters sperm small RNA content in a C57BL/6J mouse model: Implications for epigenetic inheritance

<p>Raw small RNA sequencing data files to accompany manuscript</p>

opencc-by-4.0Apr 2022View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run3)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 3)</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run1)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 1).</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) Mettl3 Knockout

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ).&nbsp;</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run3-1)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 3-1; the files are splited two two parts because of limitations of file size).</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run2)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 2)</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run2)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 2).&nbsp;</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep1 (run1 and 4)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 1 (run 1 and 4).&nbsp;</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

ONT direct RNA sequencing Fast5 files from mouse embryonic stem cell (C57BL/6J x CAST/EiJ) - Rep2 (run3-2)

<p>We present a novel approach that leverages Oxford Nanopore direct RNA sequencing technology to detect allele-biased patterns of N6-methyladenosine (m6A) modifications in native mRNAs. Our approach utilized human and mouse cells with known genetic variants to ascertain allelic origin of each mRNA molecule. We employed a supervised machine learning model to detect read-level modification ratios, providing a comprehensive understanding of allele-specific m6A modification (ASM) patterns. To analyze the effects of allele specific m6A modification in mouse, we used hybrid mosue embryonic stem cells (C57BL/6J x CAST/EiJ). This page contains replicate 2 (run 3-2; the files are splited two two parts because of limitations of file size).</p>

opencc-by-4.0Sep 2024View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro

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Last verified 2026-04-29Open record