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JOURNAL ARTICLES
Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds
B.A. Parr, M.J. Shea, G. Vassileva, A.P. McMahon
Development 1993 119: 247-261;
B.A. Parr
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M.J. Shea
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G. Vassileva
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A.P. McMahon
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Summary

Mutation and expression studies have implicated the Wnt gene family in early developmental decision making in vertebrates and flies. In a detailed comparative analysis, we have used in situ hybridization of 8.0- to 9.5-day mouse embryos to characterize expression of all ten published Wnt genes in the central nervous system (CNS) and limb buds. Seven of the family members show restricted expression patterns in the brain. At least three genes (Wnt-3, Wnt-3a, and Wnt-7b) exhibit sharp boundaries of expression in the forebrain that may predict subdivisions of the region later in development. In the spinal cord, Wnt-1, Wnt-3, and Wnt-3a are expressed dorsally, Wnt-5a, Wnt-7a, and Wnt-7b more ventrally, and Wnt-4 both dorsally and in the floor plate. In the forelimb primordia, Wnt-3, Wnt-4, Wnt-6 and Wnt-7b are expressed fairly uniformly throughout the limb ectoderm. Wnt-5a RNA is distributed in a proximal to distal gradient through the limb mesenchyme and ectoderm. Along the limb's dorsal-ventral axis, Wnt-5a is expressed in the ventral ectoderm and Wnt-7a in the dorsal ectoderm. We discuss the significance of these patterns of restricted and partially overlapping domains of expression with respect to the putative function of Wnt signalling in early CNS and limb development.

REFERENCES

    1. Baker N. E.
    (1988). Embryonic and imaginal requirements for wingless, a segment polarity gene in Drosophila. Dev. Biol 125, 96–108
    OpenUrlCrossRefPubMedWeb of Science
    1. Bally-Cuif L.,
    2. Alvardo-Mallart R.-M.,
    3. Darnell D. K.,
    4. Wassef M.
    (1992). Relationship between Wnt −1 and En −2 expression domains during early development of normal and ectopic met-mesencephalon. Development 115, 999–1009
    OpenUrlAbstract
    1. Blasband A.,
    2. Schryver B.,
    3. Papkoff J.
    (1992). The biochemical properties and transforming potential of human Wnt-2 are similar to Wnt-1. Oncogene 7, 153–161
    OpenUrlPubMedWeb of Science
    1. Bradley R. S.,
    2. Brown A. M. C.
    (1990). The proto-oncogene int −1 encodes a secreted protein associated with the extracellular matrix. EMBO J 9, 1569–1575
    OpenUrlPubMedWeb of Science
    1. Brown A. M. C.,
    2. Papkoff J.,
    3. Fung Y.-K. T.,
    4. Shackleford G. M.,
    5. Varmus H. E.
    (1987). Identification of protein products encoded by proto-oncogene int −1. Mol. Cell. Biol 7, 3971–3977
    OpenUrlAbstract/FREE Full Text
    1. Chisaka O.,
    2. Capecchi M. R.
    (1991). Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene Hox −1.5. Nature 350, 473–479
    OpenUrlCrossRefPubMed
    1. Chisaka O.,
    2. Musci T. S.,
    3. Capecchi M. R.
    (1992). Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6. Nature 355, 516–520
    OpenUrlCrossRefPubMedWeb of Science
    1. Christian J. L.,
    2. McMahon J. A.,
    3. McMahon A. P.,
    4. Moon R. T.
    (1991). Xwnt −8, a XenopusWnt −1/ int −1-related gene responsive to mesoderm inducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis. Development 111, 1045–1055
    OpenUrlAbstract/FREE Full Text
    1. Cohen S. M.
    (1990). Specification of limb development in the Drosophila embryo by positional cues from segmentation genes. Nature 343, 173–177
    OpenUrlCrossRefPubMed
    1. Couso J. P.,
    2. Bate M.,
    3. Martinez-Arias A.
    (1993). A wingless -dependent polar coordinate system in Drosophila imaginal discs. Science 259, 484–489
    OpenUrlAbstract/FREE Full Text
    1. Davidson D. R.,
    2. Crawley A.,
    3. Hill R. E.,
    4. Tickle C.
    (1991). Position-dependent expression of two related homeobox genes in developing vertebrate limbs. Nature 352, 429–431
    OpenUrlCrossRefPubMedWeb of Science
    1. Davis C. A.,
    2. Holmyard D. P.,
    3. Millen K. J.,
    4. Joyner A. L.
    (1991). Examining pattern formation in mouse, chicken and frog embryos with an EN-specific antiserum. Development 111, 287–298
    OpenUrlAbstract
    1. Dolle P.,
    2. Izpisua-Belmonte J. C.,
    3. Falkenstein H.,
    4. Renucci A.,
    5. Duboule D.
    (1989). Coordinate expression of the murine Hox −5 complex homeobox-containing genes during limb pattern formation. Nature 342, 767–772
    OpenUrlCrossRefPubMed
    1. Gavin B. J.,
    2. McMahon J. A.,
    3. McMahon A. P.
    (1990). Expression of multiple novel Wnt −1/ int −1-related genes during fetal and adult mouse development. Genes Dev 4, 2319–2332
    OpenUrlAbstract/FREE Full Text
    1. Gonzalez F.,
    2. Swales L.,
    3. Bejsovec A.,
    4. Skaer H.,
    5. Martinez-Arias A.
    (1991). Secretion and movement of wingless protein in the epidermis of the Drosophila embryo. Mech. Dev 35, 43–54
    OpenUrlCrossRefPubMedWeb of Science
    1. Goulding M. D.,
    2. Chalipakis G.,
    3. Deutsch U.,
    4. Erselius J. R.,
    5. Gruss P.
    (1991). Pax-3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J 10, 1135–1147
    OpenUrlPubMedWeb of Science
    1. He X.,
    2. Treacy M. N.,
    3. Simmons D. M.,
    4. Ingraham H. A.,
    5. Swanson L. W.,
    6. Rosenfeld M. G.
    (1989). Expression of a large family of Pou-domain regulatory genes in mammalian brain development. Nature 340, 35–42
    OpenUrlCrossRefPubMedWeb of Science
    1. Hunt P.,
    2. Wilkinson D.,
    3. Krumlauf R.
    (1991). Patterning the vertebrate head: murine Hox 2 genes mark distinct subpopulations of premigratory and migrating cranial neural crest. Development 112, 43–51
    OpenUrlAbstract
    1. Immergluck K.,
    2. Lawrence P. A.,
    3. Bienz M.
    (1990). Induction across germ layers in Drosophila mediated by a genetic cascade. Cell 62, 261–268
    OpenUrlCrossRefPubMedWeb of Science
    1. Izpisua-Belmonte J. C.,
    2. Tickle C.,
    3. Dolle P.,
    4. Wolpert L.,
    5. Duboule D.
    (1991). Expression of the homeobox Hox −4 genes and the specification of position in chick wing development. Nature 350, 585–589
    OpenUrlCrossRefPubMed
    1. Jessell T. M.,
    2. Melton D. A.
    (1992). Diffusible factors in vertebrate embryonic induction. Cell 68, 257–270
    OpenUrlCrossRefPubMedWeb of Science
    1. Jostes B.,
    2. Walther C.,
    3. Gruss P.
    (1991). The murine paired box gene, Pax 7, is expressed specifically during the development of the nervous and muscular system. Mech. Dev 33, 27–38
    1. Kessel M.,
    2. Gruss P.
    (1991). Homeotic transformations of murinevertebrae and concomitant alteration of Hox codes induced by retinoic acid. Cell 67, 89–104
    OpenUrlCrossRefPubMedWeb of Science
    1. Krauss S.,
    2. Johansen T.,
    3. Korzh V.,
    4. Fjose A.
    (1991). Expression pattern of zebrafish pax genes suggests a role in early brain regionalization. Nature 353, 267–270
    OpenUrlCrossRefPubMed
    1. Krauss S.,
    2. Korzh V.,
    3. Fjose A.,
    4. Johansen T.
    (1992). Expression of four zebrafish Wnt -related genes during embryogenesis. Development 116, 249–259
    OpenUrlAbstract
    1. Lufkin T.,
    2. Dierich A.,
    3. Lemeur M.,
    4. Mark M.,
    5. Chambon P.
    (1991). Disruption of the Hox −1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 66, 1105–1119
    OpenUrlCrossRefPubMedWeb of Science
    1. Lumsden A.
    (1990). The cellular basis of segmentation in the developing hindbrain. Trends Neurosci 13, 329–335
    OpenUrlCrossRefPubMedWeb of Science
    1. MacCabe J. A.,
    2. Errick J.,
    3. Saunders J. W.
    (1974). Ectodermal control of the dorsoventral axis in the leg bud of the chick embryo. Dev. Biol 39, 69–82
    OpenUrlPubMed
    1. Mason J. O.,
    2. Kitajewski J.,
    3. Varmus H. E.
    (1992). Mutational analysis of mouse Wnt-1 identifies two temperature-sensitive alleles and attributes of Wnt-1 protein essential for transformation of a mammary epithelial cell line. Mol. Biol. Cell 3, 521–533
    OpenUrlAbstract/FREE Full Text
    1. McGrew L. L.,
    2. Otte A. P.,
    3. Moon R. T.
    (1992). Analysis of Xwnt −4 in embryos of Xenopus laevis: A Wnt family member expressed in the brain and floor plate. Development 115, 463–473
    OpenUrlAbstract
    1. McMahon A. P.
    (1992). The Wnt family of developmental regulators. Trends Genet 8, 236–242
    1. McMahon A. P.,
    2. Bradley A.
    (1990). The Wnt −1 (int −1) proto-oncogene is required for development of a large region of the mouse brain. Cell 62, 1073–1085
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon A. P.,
    2. Joyner A. L.,
    3. Bradley A.,
    4. McMahon J. A.
    (1992). The midbrain-hindbrain phenotype of Wnt −1/ Wnt −1mice results from stepwise deletion of engrailed -expressing cells by 9.5 days postcoitum. Cell 69, 1–20
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon A. P.,
    2. Moon R. T.
    (1989). Ectopic expression of the proto-oncogene int −1 in Xenopus embryos leads to duplication of the embryonic axis. Cell 58, 1075–1084
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon J. A.,
    2. McMahon A. P.
    (1989). Nucleotide sequence, chromosomal localization and developmental expression of the mouse int −1 related gene. Development 107, 643–650
    OpenUrlAbstract
    1. Molven A.,
    2. Njølstad P. R.,
    3. Fjose A.
    (1991). Genomic structure and restricted neural expression of the zebrafish Wnt −1 (int −1) gene. EMBO J 10, 799–807
    OpenUrlPubMedWeb of Science
    1. Morgan B. A.,
    2. Izpisua-Belmonte J.-C.,
    3. Duboule D.,
    4. Tabin C. J.
    (1992). Targeted misexpression of Hox −4.6 in the avian limb bud causes apparent homeotic transformations. Nature 358, 236–239
    OpenUrlCrossRefPubMed
    1. Murtha M. T.,
    2. Leckman J. F.,
    3. Ruddle F. H.
    (1991). Detection of homeobox genes in development and evolution. Proc. Natn. Acad. Sci. USA 88, 10711–10715
    OpenUrlAbstract/FREE Full Text
    1. Nohno T.,
    2. Noji S.,
    3. Koyama E.,
    4. Ohyama K.,
    5. Myokai F.,
    6. Kuroiwa A.,
    7. Saito T.,
    8. Taniguichi S.
    (1991). Involvement of the Chox −4 chicken homeobox genes in determination of anteroposterior axial polarity during limb development. Cell 64, 1197–1205
    OpenUrlCrossRefPubMedWeb of Science
    1. Noordemeer J.,
    2. Meijlink F.,
    3. Verrijzer P.,
    4. Rijsewijk F.,
    5. Destree O.
    (1989). Isolation of the Xenopus homologue of int −1/ wingless and expression during neurula stages of development. Nucl. Acids Res 17, 11–18
    OpenUrlAbstract/FREE Full Text
    1. Nornes H. O.,
    2. Carry M.
    (1978). Neurogenesis in spinal cord of mice: an autoradiographic analysis. Brain Research 159, 1–16
    OpenUrlCrossRefPubMedWeb of Science
    1. Nusse R.,
    2. Varmus H. E.
    (1982). Many tumors induced by mouse mammary tumor virus contain a provirus integrated in the same region of the host chromosome. Cell 31, 99–109
    OpenUrlCrossRefPubMedWeb of Science
    1. Nusse R.,
    2. Varmus H.
    (1992). Wnt genes. Cell 69, 1073–1087
    OpenUrlCrossRefPubMedWeb of Science
    1. Nusslein-Volhard C.,
    2. Wieschaus E.
    (1980). Mutations affecting segment number and polarity in Drosophila. Nature 287, 795–801
    OpenUrlCrossRefPubMedWeb of Science
    1. Olson D. J.,
    2. Christian J. L.,
    3. Moon R. T.
    (1991). Effect of Wnt-1 and related proteins on gap junctional communication in Xenopus embryos. Science 252, 1173–1176
    OpenUrlFREE Full Text
    1. Papkoff J.,
    2. Brown A. M. C.,
    3. Varmus H. E.
    (1987). The int-1 proto-oncogene products are glycoproteins that appear to enter the secretory pathway. Mol. Cell. Biol 7, 3978–3984
    OpenUrlAbstract/FREE Full Text
    1. Papkoff J.,
    2. Schryver B.
    (1990). Secreted int-1 protein is associated with the cell surface. Mol. Cell. Biol 10, 2723–2730
    OpenUrlAbstract/FREE Full Text
    1. Price M.,
    2. Lemaistre M.,
    3. Pischetola M.,
    4. Di Lauro R.,
    5. Duboule D.B.A.
    (1991). A mouse gene related to Distal-less shows a restricted expression in the developing forebrain. Nature 351, 748–751Parr and others261Wntin embryonic CNS and limb buds
    OpenUrlCrossRefPubMed
    1. Puelles L.,
    2. Amat J. A.,
    3. Martinez-de-la-Torre M.
    (1987). Segment-related, mosaic neurogenetic pattern in the forebrain and mesencephalon of early chick embryos: I. Topography of AChE-positive neuroblasts up to stage HH18. J. Comp. Neurol 266, 247–268
    OpenUrlCrossRefPubMedWeb of Science
    1. Reuter R.,
    2. Panganiban G. E. F.,
    3. Hoffmann F. M.,
    4. Scott M. P.
    (1990). Homeotic genes regulate the spatial expression of putative growth factors in the visceral mesoderm of Drosophila embryos. Development 110, 1031–1040
    OpenUrlAbstract/FREE Full Text
    1. Rijsewijk F.,
    2. Schuermann M.,
    3. Wagenaar E.,
    4. Parren P.,
    5. Weigel D.,
    6. Nusse R.
    (1987). The Drosophila homologue of the mouse mammary oncogene int −1 is identical to the segment polarity gene wingless. Cell 50, 649–657
    OpenUrlCrossRefPubMedWeb of Science
    1. Roelink H.,
    2. Nusse R.
    (1991). Expression of two members of the Wnt family during mouse development- restricted temporal and spatial patterns in the developing neural tube. Genes Dev 5, 381–388
    OpenUrlAbstract/FREE Full Text
    1. Salinas P. C.,
    2. Nusse R.
    (1992). Regional expression of the Wnt −3 gene in the developing mouse forebrain in relationship to diencephalic neuromeres. Mech. Dev 39, 151–160
    OpenUrlCrossRefPubMedWeb of Science
    1. Shackleford G. M.,
    2. Varmus H. E.
    (1987). Expression of the proto-oncogene, int −1, is restricted to postmeiotic male sperm cells and the neural tube of mid-gestational embryos. Cell 50, 89–95
    OpenUrlCrossRefPubMedWeb of Science
    1. Sharma R. P.,
    2. Chopra V. L.
    (1976). Effect of wingless (wg) mutation on wing and haltere development in Drosophilamelanogaster. Dev. Biol 48, 461–465
    OpenUrlCrossRefPubMedWeb of Science
    1. Simeone A.,
    2. Acampora D.,
    3. Gulisano M.,
    4. Stornaiuolo A.,
    5. Boncinelli E.
    (1992). Nested expression domains of four homeobox genes in developing rostral brain. Nature 358, 687–690
    OpenUrlCrossRefPubMed
    1. Simeone A.,
    2. Gulisano M.,
    3. Acampora D.,
    4. Stornaiuolo A.,
    5. Rambaldi M.,
    6. Boncinelli E.
    (1992). Two vertebrate homeobox genes related to the Drosophila empty spiracles gene are expressed in the embryonic cerebral cortex. EMBO J 11, 2541–2550
    OpenUrlPubMedWeb of Science
    1. Singh G.,
    2. Kaur S.,
    3. Stock J. L.,
    4. Jenkins N. A.,
    5. Gilbert D. J.,
    6. Copeland N. G.,
    7. Potter S. S.
    (1991). Identification of 10 murine homeobox genes. Proc. Natn. Acad. Sci. USA 88, 10706–10710
    OpenUrlAbstract/FREE Full Text
    1. Skaer H.,
    2. Martinez-Arias A.
    (1992). The wingless product is required for cell proliferation in the Malpighian tubule anlage of Drosophila melanogaster. Development 116, 745–754
    OpenUrlAbstract
    1. Smith W. C.,
    2. Harland R. M.
    (1991). Injected Xwnt −8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center. Cell 67, 753–765
    OpenUrlCrossRefPubMedWeb of Science
    1. Sokol S.,
    2. Christian J. L.,
    3. Moon R. T.,
    4. Melton D. A.
    (1991). Injected Wnt RNA induces a complete body axis in Xenopus embryos. Cell 67, 741–752
    OpenUrlCrossRefPubMedWeb of Science
    1. Struhl G.,
    2. Basler K.
    (1993). Organizing activity of wingless protein in Drosophila. Cell 72, 527–540
    OpenUrlCrossRefPubMedWeb of Science
    1. Tabin C. J.
    (1991). Retinoids, homeoboxes, and growth factors: toward molecular models for limb development. Cell 66, 199–217
    OpenUrlCrossRefPubMedWeb of Science
    1. Tessier-Lavigne M.,
    2. Placzek M.,
    3. Lumsden A. G. S.,
    4. Dodd J.,
    5. Jessell T. M.
    (1988). Chemotropic guidance of developing axons in the mammalian central nervous system. Nature 336, 775–778
    OpenUrlCrossRefPubMed
    1. Thomas K. R.,
    2. Capecchi M. R.
    (1990). Targeted disruption of the murine int −1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development. Nature 346, 847–850
    OpenUrlCrossRefPubMedWeb of Science
    1. Tsukamoto A. S.,
    2. Grosschedl R.,
    3. Guzman R. C.,
    4. Parslow T.,
    5. Varmus H. E.
    (1988). Expression of the int −1 gene in transgenic mice is associated with mammary gland hyperplasia and adenocarcinomas in male and female mice. Cell 55, 619–625
    OpenUrlCrossRefPubMedWeb of Science
    1. van den Heuvel M.,
    2. Nusse R.,
    3. Johnston P.,
    4. Lawrence P. A.
    (1989). Distribution of the wingless gene product in Drosophila embryos: a protein involved in cell-cell communication. Cell 59, 739–749
    OpenUrlCrossRefPubMedWeb of Science
    1. Walther C.,
    2. Gruss P.
    (1991). Pax −6, a murine paired box gene, is expressed in the developing CNS. Development 113, 1435–1449
    OpenUrlAbstract
    1. Wilkinson D. G.,
    2. Bailes J. A.,
    3. McMahon A. P.
    (1987). Expression of the proto-oncogene int −1 is restricted to specific neural cells in the developing mouse embryo. Cell 50, 79–88
    OpenUrlCrossRefPubMedWeb of Science
    1. Wilkinson D. G.,
    2. Bhatt S.,
    3. Cook M.,
    4. Boncinelli E.,
    5. Krumlauf R.
    (1989). Segmental expression of Hox −2 homeobox-containing genes in the developing mouse hindbrain. Nature 341, 405–409
    OpenUrlCrossRefPubMed
    1. Wilkinson D. G.,
    2. Krumlauf R.
    (1990). Molecular approaches to the segmentation of the hindbrain. Trends Neurosci 13, 335–339
    OpenUrlCrossRefPubMedWeb of Science
    1. Wolda S. L.,
    2. Moody C. J.,
    3. Moon R. T.
    (1993). Overlapping expression of Xwnt −3A and Xwnt −1 in neural tissue of Xenopus laevis embryos. Dev. Biol 155, 46–57
    OpenUrlCrossRefPubMedWeb of Science
    1. Wolda S. L.,
    2. Moon R. T.
    (1992). Cloning and developmental expression in Xenopus laevis of seven additional members of the Wnt family. Oncogene 7, 1941–1947
    OpenUrlPubMedWeb of Science
    1. Yamada T.,
    2. Placzek M.,
    3. Tanaka H.,
    4. Dodd J.,
    5. Jessell T. M.
    (1991). Control of cell pattern in the developing nervous system: Polarizing activity of the floor plate and notochord. Cell 64, 635–647
    OpenUrlCrossRefPubMedWeb of Science
    1. Yokouchi Y.,
    2. Sasaki H.,
    3. Kuroiwa A.
    (1991). Homeobox gene expression correlated with the bifurcation process of limb cartilage development. Nature 353, 443–445
    OpenUrlCrossRefPubMedWeb of Science
    1. Zakany J.,
    2. Duboule D.
    (1993). Correlation of expression of Wnt −1 in developing limbs with abnormalities in growth and skeletal patterning. Nature 362, 546–549
    OpenUrlCrossRefPubMed
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JOURNAL ARTICLES
Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds
B.A. Parr, M.J. Shea, G. Vassileva, A.P. McMahon
Development 1993 119: 247-261;
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JOURNAL ARTICLES
Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds
B.A. Parr, M.J. Shea, G. Vassileva, A.P. McMahon
Development 1993 119: 247-261;

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New funding scheme supports sustainable events

As part of our Sustainable Conferencing Initiative, we are pleased to announce funding for organisers that seek to reduce the environmental footprint of their event. The next deadline to apply for a Scientific Meeting grant is 26 March 2021.


Read & Publish participation continues to grow

“I’d heard of Read & Publish deals and knew that many universities, including mine, had signed up to them but I had not previously understood the benefits that these deals bring to authors who work at those universities.”

Professor Sally Lowell (University of Edinburgh) shares her experience of publishing Open Access as part of our growing Read & Publish initiative. We now have over 150 institutions in 15 countries and four library consortia taking part – find out more and view our full list of participating institutions.


Upcoming special issues

Imaging Development, Stem Cells and Regeneration
Submission deadline: 30 March 2021
Publication: mid-2021

The Immune System in Development and Regeneration
Guest editors: Florent Ginhoux and Paul Martin
Submission deadline: 1 September 2021
Publication: Spring 2022

Both special issues welcome Review articles as well as Research articles, and will be widely promoted online and at key global conferences.


Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Here, Michèle Romanos talks about her new preprint, which mixes experimentation in quail embryos and computational modelling to understand how heterogeneity in a tissue influences cell rate.

Save your spot at our next session:

10 March
Time: 9:00 (GMT)
Chaired by: Thomas Lecuit

Join our mailing list to receive news and updates on the series.

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