mouse: cdx2 cre Search Results


86
Jackson Laboratory b6 cg tg
B6 Cg Tg, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory cdx2 cre ert2 mice
Cdx2 Cre Ert2 Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory cdx2 creert2 mice
Cdx2 Creert2 Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse%3A+cdx2+cre/pmc09398964-440-14-52?v=Jackson+Laboratory
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Jackson Laboratory mice
Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory villin cre transgenic mice
Villin Cre Transgenic Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory bmi1 creert transgenic mice
Bmi1 Creert Transgenic Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory cd11c cre
Efficient targeted deletion of Stat2 in mouse tissues. Expression of STAT2 and STAT1 was analyzed in various tissues by Western blot analysis. ( a ) Bone marrow–derived cDCs generated from Stat2 fl/fl mice crossed <t>with</t> <t>CD11c-Cre</t> mice ( Stat2 Δ-cDC ). ( b ) Colons from Stat2 fl/fl mice crossed with Cdx2-Cre mice ( Stat2 Δ-CE ). ( c ) Lungs from Stat2 Δ-cDC and Stat2 Δ-CE mice were included for specificity of targeted deletion. Wild-type (WT) and Stat2KO mice served as positive and negative controls, respectively. ACTIN was used as an internal protein loading control.
Cd11c Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory cmv cre
Generation of conditional Stat2 KO mice. ( a ) Targeting strategy used to construct Stat2 fl/fl mice with exons 5 through 8 flanked with loxP sites. E represents exons with their corresponding number. Brown boxes depict exons in wild type allele and green boxes depict exons after successful integration of targeting vector. ( b ) Confirmation of loxP sites integration in the Stat2 gene by Southern blot analysis (9.8 kb DNA fragment). ( c ) Genotyping of mouse-tail DNA by PCR confirms deletion of Stat2 floxed allele after breeding <t>with</t> <t>CMV-Cre</t> mouse.
Cmv Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory b6 129s2 alox15 tm1fun j homozygous mice
Generation of conditional Stat2 KO mice. ( a ) Targeting strategy used to construct Stat2 fl/fl mice with exons 5 through 8 flanked with loxP sites. E represents exons with their corresponding number. Brown boxes depict exons in wild type allele and green boxes depict exons after successful integration of targeting vector. ( b ) Confirmation of loxP sites integration in the Stat2 gene by Southern blot analysis (9.8 kb DNA fragment). ( c ) Genotyping of mouse-tail DNA by PCR confirms deletion of Stat2 floxed allele after breeding <t>with</t> <t>CMV-Cre</t> mouse.
B6 129s2 Alox15 Tm1fun J Homozygous Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory flpe deleter
Generation of conditional Stat2 KO mice. ( a ) Targeting strategy used to construct Stat2 fl/fl mice with exons 5 through 8 flanked with loxP sites. E represents exons with their corresponding number. Brown boxes depict exons in wild type allele and green boxes depict exons after successful integration of targeting vector. ( b ) Confirmation of loxP sites integration in the Stat2 gene by Southern blot analysis (9.8 kb DNA fragment). ( c ) Genotyping of mouse-tail DNA by PCR confirms deletion of Stat2 floxed allele after breeding <t>with</t> <t>CMV-Cre</t> mouse.
Flpe Deleter, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cyagen Biosciences steap4 f f mice
Fig. 1. Colon Epithelial Cell-Specific <t>Steap4</t> Knockout Suppresses Mouse Colon Tumor
Steap4 F F Mice, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Jackson Laboratory trpc2 knockout mice
a , Distance between mutant and control sample centroids in PCA space (normalized to intra-genotype distance) for excitatory clusters. Control samples included both C57BL/6J and control littermates. Sample numbers, left to right columns, mutant/control: 2/8, 4/10, 2/10, 2/8, 2/8, 2/8, 2/8, 2/7, 2/7, 2/8, 2/8, 2/7, 2/8 and 2/8. cKO, conditional knockout; KO, knockout. b , Mutant–control PCA distance for all clusters in <t>TRPC2</t> P10 experiments, split according to functional role. c , Pseudotime mapping of Trpc2 mutant (−/−) and control (−/+ littermates) across age. Higher pseudotime values correspond to higher maturity (more similar to adult cell types). Pseudotime is averaged within a cluster; boxplot shows distribution across all cluster averages. P value indicates results from two-sided t -test, mutant versus control cell types. n for increasing age: 82, 137, 131 and 128 cell types for controls, and 119, 135, 129 and 108 cell types for mutants, from n for increasing age of 2, 4, 2 and 2 independent experiments per genotype. Boxplots in b and c show median, interquartile range and 1.5× interquartile range. d , Aggregated expression of 243 core neuronal maturation genes in wild-type C57BL/6J cell types at each age (left) or Trpc2 −/+ or Trpc2 −/− cell types at P10 (right). P value indicates results from two-sided t -test, mutant versus control cell types. e , Random-forest classifier approach (Augur) to identify cell types that show differences between Trpc2 −/+ and Trpc2 −/− cell types at P65. Each point represents a single cell type. Cell types with roles in relevant social behaviours affected in Trpc2 −/− adults are shown with coloured dots. AUC, area under the curve.
Trpc2 Knockout Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Efficient targeted deletion of Stat2 in mouse tissues. Expression of STAT2 and STAT1 was analyzed in various tissues by Western blot analysis. ( a ) Bone marrow–derived cDCs generated from Stat2 fl/fl mice crossed with CD11c-Cre mice ( Stat2 Δ-cDC ). ( b ) Colons from Stat2 fl/fl mice crossed with Cdx2-Cre mice ( Stat2 Δ-CE ). ( c ) Lungs from Stat2 Δ-cDC and Stat2 Δ-CE mice were included for specificity of targeted deletion. Wild-type (WT) and Stat2KO mice served as positive and negative controls, respectively. ACTIN was used as an internal protein loading control.

Journal: Immuno

Article Title: Conditional Stat2 Knockout Mice as a Platform for Modeling Human Diseases

doi: 10.3390/immuno6010007

Figure Lengend Snippet: Efficient targeted deletion of Stat2 in mouse tissues. Expression of STAT2 and STAT1 was analyzed in various tissues by Western blot analysis. ( a ) Bone marrow–derived cDCs generated from Stat2 fl/fl mice crossed with CD11c-Cre mice ( Stat2 Δ-cDC ). ( b ) Colons from Stat2 fl/fl mice crossed with Cdx2-Cre mice ( Stat2 Δ-CE ). ( c ) Lungs from Stat2 Δ-cDC and Stat2 Δ-CE mice were included for specificity of targeted deletion. Wild-type (WT) and Stat2KO mice served as positive and negative controls, respectively. ACTIN was used as an internal protein loading control.

Article Snippet: The following mouse strains on the B6 background were purchased from The Jackson Laboratory: FLPe deleter (Strain#: 009086), CMV-Cre (Strain#: 006054), CD11c-Cre (Strain#: 008068) and Cdx2-Cre (Strain#: 009350).

Techniques: Expressing, Western Blot, Derivative Assay, Generated, Control

Generation of conditional Stat2 KO mice. ( a ) Targeting strategy used to construct Stat2 fl/fl mice with exons 5 through 8 flanked with loxP sites. E represents exons with their corresponding number. Brown boxes depict exons in wild type allele and green boxes depict exons after successful integration of targeting vector. ( b ) Confirmation of loxP sites integration in the Stat2 gene by Southern blot analysis (9.8 kb DNA fragment). ( c ) Genotyping of mouse-tail DNA by PCR confirms deletion of Stat2 floxed allele after breeding with CMV-Cre mouse.

Journal: Immuno

Article Title: Conditional Stat2 Knockout Mice as a Platform for Modeling Human Diseases

doi: 10.3390/immuno6010007

Figure Lengend Snippet: Generation of conditional Stat2 KO mice. ( a ) Targeting strategy used to construct Stat2 fl/fl mice with exons 5 through 8 flanked with loxP sites. E represents exons with their corresponding number. Brown boxes depict exons in wild type allele and green boxes depict exons after successful integration of targeting vector. ( b ) Confirmation of loxP sites integration in the Stat2 gene by Southern blot analysis (9.8 kb DNA fragment). ( c ) Genotyping of mouse-tail DNA by PCR confirms deletion of Stat2 floxed allele after breeding with CMV-Cre mouse.

Article Snippet: The following mouse strains on the B6 background were purchased from The Jackson Laboratory: FLPe deleter (Strain#: 009086), CMV-Cre (Strain#: 006054), CD11c-Cre (Strain#: 008068) and Cdx2-Cre (Strain#: 009350).

Techniques: Construct, Plasmid Preparation, Southern Blot

Impaired IFN-I signaling after conditional deletion of Stat2 by CMV-Cre—mediated recombination. ( a ) Loss of Stat2 gene expression validated in four different organs by qRT-PCR analysis. ( b ) Western blot analyses performed on several tissues confirm global Stat2 deletion ( Stat2 Δ / Δ ) by ubiquitous CMV-Cre recombinase. ( c ) Splenocytes of the indicated genotypes were left untreated or treated with IFN-β for 6 h, and ISG expression was determined by qRT-PCR. * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001. Data are presented as SEM of three independent experiments. n.s; not significant.

Journal: Immuno

Article Title: Conditional Stat2 Knockout Mice as a Platform for Modeling Human Diseases

doi: 10.3390/immuno6010007

Figure Lengend Snippet: Impaired IFN-I signaling after conditional deletion of Stat2 by CMV-Cre—mediated recombination. ( a ) Loss of Stat2 gene expression validated in four different organs by qRT-PCR analysis. ( b ) Western blot analyses performed on several tissues confirm global Stat2 deletion ( Stat2 Δ / Δ ) by ubiquitous CMV-Cre recombinase. ( c ) Splenocytes of the indicated genotypes were left untreated or treated with IFN-β for 6 h, and ISG expression was determined by qRT-PCR. * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001. Data are presented as SEM of three independent experiments. n.s; not significant.

Article Snippet: The following mouse strains on the B6 background were purchased from The Jackson Laboratory: FLPe deleter (Strain#: 009086), CMV-Cre (Strain#: 006054), CD11c-Cre (Strain#: 008068) and Cdx2-Cre (Strain#: 009350).

Techniques: Gene Expression, Quantitative RT-PCR, Western Blot, Expressing

Fig. 1. Colon Epithelial Cell-Specific Steap4 Knockout Suppresses Mouse Colon Tumor

Journal: Journal of cell science

Article Title: STEAP4 Target NQO1 Mediates Colon Tumorigenesis.

doi: 10.1242/jcs.263402

Figure Lengend Snippet: Fig. 1. Colon Epithelial Cell-Specific Steap4 Knockout Suppresses Mouse Colon Tumor

Article Snippet: Steap4 F/F mice were produced utilizing exon 2~3 of the mouse Steap4 gene as the conditional knockout region at Cyagen (Santa Clara, CA) and crossed with Cdx2 ERT2-Cre Apc F/+ mice to generate Steap4 F/F Cdx2 ERT2-Cre Apc F/+ mice.

Techniques: Knock-Out

Fig. 2. Steap4 Knockdown Suppresses Mouse Colon Tumor Cell Growth In Vitro and In

Journal: Journal of cell science

Article Title: STEAP4 Target NQO1 Mediates Colon Tumorigenesis.

doi: 10.1242/jcs.263402

Figure Lengend Snippet: Fig. 2. Steap4 Knockdown Suppresses Mouse Colon Tumor Cell Growth In Vitro and In

Article Snippet: Steap4 F/F mice were produced utilizing exon 2~3 of the mouse Steap4 gene as the conditional knockout region at Cyagen (Santa Clara, CA) and crossed with Cdx2 ERT2-Cre Apc F/+ mice to generate Steap4 F/F Cdx2 ERT2-Cre Apc F/+ mice.

Techniques: Knockdown, In Vitro

Fig. 3. STEAP4 Overexpression in Human HCT116 Cells Activates NRF2 Signaling

Journal: Journal of cell science

Article Title: STEAP4 Target NQO1 Mediates Colon Tumorigenesis.

doi: 10.1242/jcs.263402

Figure Lengend Snippet: Fig. 3. STEAP4 Overexpression in Human HCT116 Cells Activates NRF2 Signaling

Article Snippet: Steap4 F/F mice were produced utilizing exon 2~3 of the mouse Steap4 gene as the conditional knockout region at Cyagen (Santa Clara, CA) and crossed with Cdx2 ERT2-Cre Apc F/+ mice to generate Steap4 F/F Cdx2 ERT2-Cre Apc F/+ mice.

Techniques: Over Expression

Fig. 4. Oxidative Stress Response during STEAP4-Catalyzed Ferric Iron Reduction In

Journal: Journal of cell science

Article Title: STEAP4 Target NQO1 Mediates Colon Tumorigenesis.

doi: 10.1242/jcs.263402

Figure Lengend Snippet: Fig. 4. Oxidative Stress Response during STEAP4-Catalyzed Ferric Iron Reduction In

Article Snippet: Steap4 F/F mice were produced utilizing exon 2~3 of the mouse Steap4 gene as the conditional knockout region at Cyagen (Santa Clara, CA) and crossed with Cdx2 ERT2-Cre Apc F/+ mice to generate Steap4 F/F Cdx2 ERT2-Cre Apc F/+ mice.

Techniques:

Fig. 5. STEAP4 Overexpression Increases Oxidative Stress and Susceptibility to NQO1

Journal: Journal of cell science

Article Title: STEAP4 Target NQO1 Mediates Colon Tumorigenesis.

doi: 10.1242/jcs.263402

Figure Lengend Snippet: Fig. 5. STEAP4 Overexpression Increases Oxidative Stress and Susceptibility to NQO1

Article Snippet: Steap4 F/F mice were produced utilizing exon 2~3 of the mouse Steap4 gene as the conditional knockout region at Cyagen (Santa Clara, CA) and crossed with Cdx2 ERT2-Cre Apc F/+ mice to generate Steap4 F/F Cdx2 ERT2-Cre Apc F/+ mice.

Techniques: Over Expression

a , Distance between mutant and control sample centroids in PCA space (normalized to intra-genotype distance) for excitatory clusters. Control samples included both C57BL/6J and control littermates. Sample numbers, left to right columns, mutant/control: 2/8, 4/10, 2/10, 2/8, 2/8, 2/8, 2/8, 2/7, 2/7, 2/8, 2/8, 2/7, 2/8 and 2/8. cKO, conditional knockout; KO, knockout. b , Mutant–control PCA distance for all clusters in TRPC2 P10 experiments, split according to functional role. c , Pseudotime mapping of Trpc2 mutant (−/−) and control (−/+ littermates) across age. Higher pseudotime values correspond to higher maturity (more similar to adult cell types). Pseudotime is averaged within a cluster; boxplot shows distribution across all cluster averages. P value indicates results from two-sided t -test, mutant versus control cell types. n for increasing age: 82, 137, 131 and 128 cell types for controls, and 119, 135, 129 and 108 cell types for mutants, from n for increasing age of 2, 4, 2 and 2 independent experiments per genotype. Boxplots in b and c show median, interquartile range and 1.5× interquartile range. d , Aggregated expression of 243 core neuronal maturation genes in wild-type C57BL/6J cell types at each age (left) or Trpc2 −/+ or Trpc2 −/− cell types at P10 (right). P value indicates results from two-sided t -test, mutant versus control cell types. e , Random-forest classifier approach (Augur) to identify cell types that show differences between Trpc2 −/+ and Trpc2 −/− cell types at P65. Each point represents a single cell type. Cell types with roles in relevant social behaviours affected in Trpc2 −/− adults are shown with coloured dots. AUC, area under the curve.

Journal: Nature

Article Title: Sensory input, sex and function shape hypothalamic cell type development

doi: 10.1038/s41586-025-08603-0

Figure Lengend Snippet: a , Distance between mutant and control sample centroids in PCA space (normalized to intra-genotype distance) for excitatory clusters. Control samples included both C57BL/6J and control littermates. Sample numbers, left to right columns, mutant/control: 2/8, 4/10, 2/10, 2/8, 2/8, 2/8, 2/8, 2/7, 2/7, 2/8, 2/8, 2/7, 2/8 and 2/8. cKO, conditional knockout; KO, knockout. b , Mutant–control PCA distance for all clusters in TRPC2 P10 experiments, split according to functional role. c , Pseudotime mapping of Trpc2 mutant (−/−) and control (−/+ littermates) across age. Higher pseudotime values correspond to higher maturity (more similar to adult cell types). Pseudotime is averaged within a cluster; boxplot shows distribution across all cluster averages. P value indicates results from two-sided t -test, mutant versus control cell types. n for increasing age: 82, 137, 131 and 128 cell types for controls, and 119, 135, 129 and 108 cell types for mutants, from n for increasing age of 2, 4, 2 and 2 independent experiments per genotype. Boxplots in b and c show median, interquartile range and 1.5× interquartile range. d , Aggregated expression of 243 core neuronal maturation genes in wild-type C57BL/6J cell types at each age (left) or Trpc2 −/+ or Trpc2 −/− cell types at P10 (right). P value indicates results from two-sided t -test, mutant versus control cell types. e , Random-forest classifier approach (Augur) to identify cell types that show differences between Trpc2 −/+ and Trpc2 −/− cell types at P65. Each point represents a single cell type. Cell types with roles in relevant social behaviours affected in Trpc2 −/− adults are shown with coloured dots. AUC, area under the curve.

Article Snippet: Mutant and transgenic strains used in this study were previously published and include (with Jackson Laboratories (RRID:SCR_004633) numbers where applicable): Trpc2 knockout mice (021208; RRID:IMSR_JAX:021208); Cnga2 knockout mice ; Trpm8 knockout mice (008198; RRID :IMSR_JAX:008198); Piezo2 fl (ref. ) (027720; RRID:IMSR_JAX:027720); Piezo2 − (ref. ); Cdx2 - c re ) (009350; RRID:IMSR_JAX:009350); Avil-cre , Gabrb3 fl (ref. ), and Opn5-cre .

Techniques: Mutagenesis, Control, Knock-Out, Functional Assay, Expressing

( a ) Distance between mutant and control sample centroids in PCA space (normalized to intra-genotype distance) for inhibitory clusters. Control samples included both C57BL6/J and control littermates. Sample numbers, left to right columns, mutant/control: 2/8, 4/10, 2/10, 2/8, 2/8, 2/6, 2/7, 2/7, 2/8, 2/8, 2/7. ( b ) Random forest classifier approach (Augur) to identify cell types that show differences between mutant and control samples. Each point represents a single cell type. Number of biological replicates as described in ( a ). ( c ) Mutant-control PCA distance for all clusters in Trpc2 P10 experiments, split according to sub-region, and ordered from most to least affected. Data from n = 4 biological replicates per genotype. ( d ) UMAP showing identification of visual cortex neuronal subtypes in Trpc2 mutants and controls (pooled) at P10. ( e ) Random forest classifier (Augur) for replication of Trpc2 P10 POA (left) and visual cortex (right) from the same brains. Cells pooled from n = 2 biological replicates per genotype. ( f ) Weight of Trpc2−/− pups and Trpc2−/+ littermates at P7 to P14. n = 41 (Trpc2−/+) and 30 (Trpc2−/−). Error bars show standard error of the mean. ( g ) Latency for mothers to retrieve Trpc2−/+ or Trpc2−/− P9-10 pups when given a choice between the two. n = 48 (Trpc2−/+) and 48 (Trpc2−/−). ( h ) Latency for Trpc2−/+ or Trpc2−/− P13-14 pups to first contact their anesthetized mother. n = 26 (Trpc2−/+) and 22 (Trpc2−/−). ( i ) Latency for Trpc2−/+ or Trpc2−/− P11-12 pups to first contact with littermates. n = 36 (Trpc2−/+) and 20 (Trpc2−/−). ( j ) Latency for Trpc2−/+ or Trpc2−/− P11-12 pups to enter behavioral quiescence. n = 48 (Trpc2−/+) and 30 (Trpc2−/−). ( k ) Ultrasonic vocalizations emitted by isolated Trpc2−/+ or Trpc2−/− P13-14 pups, placed in a clean cage for 30 min at room temperature or with a heating pad underneath. Boxed portion quantified in ( l ). n = 22 (Trpc−/+), 21 (Trpc2−/−). Error bars show standard error of the mean. ( l ) Difference in the number of vocalizations between room temperature and heating pad conditions for each pup, at 20-30 min post-isolation (boxed portion in ( k )). In all panels, boxplots show median, interquartile range, and 1.5 * interquartile range. For panels ( g-l ), p-value indicates results from two-sided t-test.

Journal: Nature

Article Title: Sensory input, sex and function shape hypothalamic cell type development

doi: 10.1038/s41586-025-08603-0

Figure Lengend Snippet: ( a ) Distance between mutant and control sample centroids in PCA space (normalized to intra-genotype distance) for inhibitory clusters. Control samples included both C57BL6/J and control littermates. Sample numbers, left to right columns, mutant/control: 2/8, 4/10, 2/10, 2/8, 2/8, 2/6, 2/7, 2/7, 2/8, 2/8, 2/7. ( b ) Random forest classifier approach (Augur) to identify cell types that show differences between mutant and control samples. Each point represents a single cell type. Number of biological replicates as described in ( a ). ( c ) Mutant-control PCA distance for all clusters in Trpc2 P10 experiments, split according to sub-region, and ordered from most to least affected. Data from n = 4 biological replicates per genotype. ( d ) UMAP showing identification of visual cortex neuronal subtypes in Trpc2 mutants and controls (pooled) at P10. ( e ) Random forest classifier (Augur) for replication of Trpc2 P10 POA (left) and visual cortex (right) from the same brains. Cells pooled from n = 2 biological replicates per genotype. ( f ) Weight of Trpc2−/− pups and Trpc2−/+ littermates at P7 to P14. n = 41 (Trpc2−/+) and 30 (Trpc2−/−). Error bars show standard error of the mean. ( g ) Latency for mothers to retrieve Trpc2−/+ or Trpc2−/− P9-10 pups when given a choice between the two. n = 48 (Trpc2−/+) and 48 (Trpc2−/−). ( h ) Latency for Trpc2−/+ or Trpc2−/− P13-14 pups to first contact their anesthetized mother. n = 26 (Trpc2−/+) and 22 (Trpc2−/−). ( i ) Latency for Trpc2−/+ or Trpc2−/− P11-12 pups to first contact with littermates. n = 36 (Trpc2−/+) and 20 (Trpc2−/−). ( j ) Latency for Trpc2−/+ or Trpc2−/− P11-12 pups to enter behavioral quiescence. n = 48 (Trpc2−/+) and 30 (Trpc2−/−). ( k ) Ultrasonic vocalizations emitted by isolated Trpc2−/+ or Trpc2−/− P13-14 pups, placed in a clean cage for 30 min at room temperature or with a heating pad underneath. Boxed portion quantified in ( l ). n = 22 (Trpc−/+), 21 (Trpc2−/−). Error bars show standard error of the mean. ( l ) Difference in the number of vocalizations between room temperature and heating pad conditions for each pup, at 20-30 min post-isolation (boxed portion in ( k )). In all panels, boxplots show median, interquartile range, and 1.5 * interquartile range. For panels ( g-l ), p-value indicates results from two-sided t-test.

Article Snippet: Mutant and transgenic strains used in this study were previously published and include (with Jackson Laboratories (RRID:SCR_004633) numbers where applicable): Trpc2 knockout mice (021208; RRID:IMSR_JAX:021208); Cnga2 knockout mice ; Trpm8 knockout mice (008198; RRID :IMSR_JAX:008198); Piezo2 fl (ref. ) (027720; RRID:IMSR_JAX:027720); Piezo2 − (ref. ); Cdx2 - c re ) (009350; RRID:IMSR_JAX:009350); Avil-cre , Gabrb3 fl (ref. ), and Opn5-cre .

Techniques: Mutagenesis, Control, Isolation