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Limb development in a “nonmodel” vertebrate, the direct‐developing frog Eleutherodactylus coqui
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Outgoing claims: the papers this work cites, builds on, or argues with.
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The molecular ZPA
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Modularity in animal development and evolution: Elements of a conceptual framework for EvoDevo
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Hedgehog family member is expressed throughout regenerating and developing limbs
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199607)229:1<105::aid-jmor7>3.0.co;2-2openalex-snapshot
Cranial neural-crest migration and chondrogenic fate in the oriental fire-bellied toadBombina orientalis: Defining the ancestral pattern of head development in anuran amphibians
inferredcites →https://doi.org/10.1002/(sici)1097-4687(199607)229:1<1::aid-jmor1>3.0.co;2-7openalex-snapshot
Ontogenesis and functional metamorphosis of the head-kidney in bottomspawner and mouthbrooder cichlid fishes (Cichlidae, Teleostei)
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Genetics and limb development
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Vertebrate evolution: The developmental origins of adult variation
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Plasticity, evolvability, and modularity in RNA
inferredcites →https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1026>3.0.co;2-bopenalex-snapshot
Regulation and function of Dlx3 in vertebrate development
inferredcites →https://doi.org/10.1002/1097-0177(200008)218:4<554::aid-dvdy1023>3.0.co;2-#openalex-snapshot
Distal‐less function during Drosophila appendage and sense organ development
inferredcites →https://doi.org/10.1002/1521-1878(200011)22:11<1043::aid-bies11>3.0.co;2-copenalex-snapshot
Modularity in development and evolution
inferredcites →https://doi.org/10.1002/1521-1878(200103)23:3<233::aid-bies1033>3.0.co;2-qopenalex-snapshot
Frogs without polliwogs: Evolution of anuran direct development
inferredcites →https://doi.org/10.1002/1526-968x(200102)29:2<91::aid-gene1009>3.0.co;2-6openalex-snapshot
Direct development: an alternative way to make a frog
inferredcites →https://doi.org/10.1002/jez.1104openalex-snapshot
Using heterochrony plots to detect the dissociated coevolution of characters
inferredcites →https://doi.org/10.1002/jez.1401080304openalex-snapshot
The proximo‐distal sequence of origin of the parts of the chick wing and the role of the ectoderm
inferredcites →https://doi.org/10.1002/jez.1402700209openalex-snapshot
Leg development in a frog without a tadpole (Eleutherodactylus coqui)
inferredcites →https://doi.org/10.1002/jmor.1051290404openalex-snapshot
Sequence of ossification in the skeleton of growing and metamorphosing tadpoles of Rana pipiens
inferredcites →https://doi.org/10.1002/jmor.1052110111openalex-snapshot
Cranial ontogeny in the direct‐developing frog, Eleutherodactylus coqui (anura: Leptodactylidae), analyzed using whole‐mount immunohistochemistry
inferredcites →https://doi.org/10.1002/jmor.1052140102openalex-snapshot
Skeletal development in Xenopus laevis (Anura: Pipidae)
inferredcites →https://doi.org/10.1006/dbio.1995.1211openalex-snapshot
Anterior Duplication of the Sonic hedgehog Expression Pattern in the Pectoral Fin Buds of Zebrafish Treated with Retinoic Acid
inferredcites →https://doi.org/10.1006/dbio.1995.8041openalex-snapshot
Heterochrony and the Phylotypic Period
inferredcites →https://doi.org/10.1006/dbio.1996.0248openalex-snapshot
Patterns of Distal-less Gene Expression and Inductive Interactions in the Head of the Direct Developing FrogEleutherodactylus coqui
inferredcites →https://doi.org/10.1006/dbio.1996.0282openalex-snapshot
Surgical Removal of Limb BudSonic hedgehogResults in Posterior Skeletal Defects
inferredcites →https://doi.org/10.1006/dbio.1997.8732openalex-snapshot
FGF-8Is Associated with Anteroposterior Patterning and Limb Regeneration inXenopus
inferredcites →https://doi.org/10.1006/dbio.1998.8856openalex-snapshot
Multiple Digit Formation inXenopusLimb Bud Recombinants
inferredcites →https://doi.org/10.1006/dbio.1998.8956openalex-snapshot
Expression ofHoxDGenes in Developing and Regenerating Axolotl Limbs
inferredcites →https://doi.org/10.1007/978-1-4615-6983-1_6openalex-snapshot
A Morphogenetic Approach to the Origin and Basic Organization of the Tetrapod Limb
inferredcites →https://doi.org/10.1007/978-1-4615-6983-1_7openalex-snapshot
Developmental Evidence for Amphibian Origins
inferredcites →https://doi.org/10.1007/bf01002716openalex-snapshot
The role of the zone of polarizing activity in controlling the differentiation of the apical mesenchyme of the chick wing-bud: histochemical thechniques in the analysis of a developmental problem
inferredcites →https://doi.org/10.1007/s004270000070openalex-snapshot
Opercular development and ontogenetic re-organization in a direct-developing frog
inferredcites →https://doi.org/10.1007/s004270050172openalex-snapshot
Heterochronic differences of Hoxa-11 expression in Xenopus fore- and hind limb development: Evidence for lower limb identity of the anuran ankle bones
inferredcites →https://doi.org/10.1016/0012-1606(77)90175-0openalex-snapshot
Evidence for polarizing zone in the limb buds of Xenopus laevis
inferredcites →https://doi.org/10.1016/0047-2484(87)90007-8openalex-snapshot
Development as an evolutionary process
inferredcites →https://doi.org/10.1016/0092-8674(93)90391-3openalex-snapshot
FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb
inferredcites →https://doi.org/10.1016/0092-8674(93)90626-2openalex-snapshot
Sonic hedgehog mediates the polarizing activity of the ZPA
inferredcites →https://doi.org/10.1016/0925-4773(93)90071-5openalex-snapshot
The mouse Dlx-2 (Tes-1) gene is expressed in spatially restricted domains of the forebrain, face and limbs in midgestation mouse embryos
inferredcites →https://doi.org/10.1016/0925-4773(95)98113-oopenalex-snapshot
The expression pattern of the Distal-less homeo☐-containing gene Dlx-5 in the developing chick limb bud suggests its involvement in apical ectodermal ridge activity, pattern formation, and cartilage differentiation
inferredcites →https://doi.org/10.1016/0959-437x(95)90052-iopenalex-snapshot
Vertebrate limb development
inferredcites →https://doi.org/10.1016/b978-012730935-4/50004-3openalex-snapshot
Larvae in Amphibian Development and Evolution
inferredcites →https://doi.org/10.1016/s0091-679x(08)60290-3openalex-snapshot
Chapter 22 Whole-Mount Staining of Xenopus and Other Vertebrates
inferredcites →https://doi.org/10.1016/s0091-679x(08)60307-6openalex-snapshot
Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos
inferredcites →https://doi.org/10.1016/s0092-8674(00)80364-5openalex-snapshot
Molecular Models for Vertebrate Limb Development
inferredcites →https://doi.org/10.1016/s0960-9822(00)00151-2openalex-snapshot
The role of the Distal-less gene in the development and evolution of insect limbs
inferredcites →https://doi.org/10.1016/s0960-9822(95)00157-6openalex-snapshot
A role for FGF-8 in the initiation and maintenance of vertebrate limb bud outgrowth
inferredcites →https://doi.org/10.1016/s0968-0004(97)89823-4openalex-snapshot
Cells, embryos and evolution
inferredcites →https://doi.org/10.1038/254199a0openalex-snapshot
Positional signalling and specification of digits in chick limb morphogenesis
inferredcites →https://doi.org/10.1038/35011540openalex-snapshot
From molecular to modular cell biology
inferredcites →https://doi.org/10.1038/35059227openalex-snapshot
Chance and necessity: the evolution of morphological complexity and diversity
inferredcites →https://doi.org/10.1038/371609a0openalex-snapshot
A positive feedback loop coordinates growth and patterning in the vertebrate limb
inferredcites →https://doi.org/10.1038/41710openalex-snapshot
Fossils, genes and the evolution of animal limbs
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Heterochrony: Developmental mechanisms and evolutionary results
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Life history and morphological evolution
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Limb development and evolution: a frog embryo with no apical ectodermal ridge (AER)
inferredcites →https://doi.org/10.1073/pnas.94.10.5162openalex-snapshot
The origin and evolution of animal appendages
inferredcites →https://doi.org/10.1093/aesa/36.3.364openalex-snapshot
A Manual of Experimental Embryology
inferredcites →https://doi.org/10.1093/icb/40.5.711openalex-snapshot
General Introduction to the Symposium on Evolutionary Developmental Biology: Paradigms, Problems, and Prospects
inferredcites →https://doi.org/10.1101/gad.12.11.1571openalex-snapshot
The roles of FGFs in the early development of vertebrate limbs
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00560.xopenalex-snapshot
MORPHOLOGICAL INTEGRATION BETWEEN DEVELOPMENTAL COMPARTMENTS IN THE DROSOPHILA WING
inferredcites →https://doi.org/10.1111/j.1432-0436.1992.tb00773.xopenalex-snapshot
Expression of the murine Dlx-1 homeobox gene during facial, ocular and limb development
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb02339.xopenalex-snapshot
PERSPECTIVE: COMPLEX ADAPTATIONS AND THE EVOLUTION OF EVOLVABILITY
inferredcites →https://doi.org/10.1111/j.1749-6632.1996.tb56239.xopenalex-snapshot
Growth Factor Interactions in Limb Development
inferredcites →https://doi.org/10.1126/science.157.3795.1472openalex-snapshot
Epithelial-Mesenchymal Interactions
inferredcites →https://doi.org/10.1139/bcb-78-5-593openalex-snapshot
Distal-less-related homeobox genes of vertebrates: Evolution, function, and regulation
inferredcites →https://doi.org/10.1159/000113325openalex-snapshot
Evolution of Nerve Development in Frogs; pp. 94–112
inferredcites →https://doi.org/10.1242/dev.105.1.61openalex-snapshot
A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus
inferredcites →https://doi.org/10.1242/dev.110.2.325openalex-snapshot
Localization of specific mRNAs in Xenopus embryos by whole-mount in situ hybridization
inferredcites →https://doi.org/10.1242/dev.119.1.199openalex-snapshot
FGF-4 maintains polarizing activity of posterior limb bud cells in vivo and in vitro
inferredcites →https://doi.org/10.1242/dev.120.11.3267openalex-snapshot
Relationship between retinoic acid and sonic hedgehog, two polarizing signals in the chick wing bud
inferredcites →https://doi.org/10.1242/dev.121.6.1731openalex-snapshot
Regulation of HoxA expression in developing and regenerating axolotl limbs
inferredcites →https://doi.org/10.1242/dev.125.15.2983openalex-snapshot
Sonic hedgehog is not required for the induction of medial floor plate cells in the zebrafish
inferredcites →https://doi.org/10.1242/dev.125.21.4175openalex-snapshot
Involvement of the Sonic Hedgehog, patched 1 and bmp2 genes in patterning of the zebrafish dermal fin rays
inferredcites →https://doi.org/10.1242/dev.26.2.169openalex-snapshot
Early limb development of Xenopus laevis
inferredcites →https://doi.org/10.1242/dev.32.3.651openalex-snapshot
A quantitative analysis of the effect of excision of the AER from the chick limb-bud
inferredcites →https://doi.org/10.1242/dev.50.1.217openalex-snapshot
The zone of polarizing activity: evidence for a role in normal chick limb morphogenesis
inferredcites →https://doi.org/10.1242/dev.87.1.163openalex-snapshot
Maps of strength of positional signalling activity in the developing chick wing bud
inferredcites →https://doi.org/10.1554/0014-3820(2000)054[1273:mibdci]2.0.co;2openalex-snapshot
MORPHOLOGICAL INTEGRATION BETWEEN DEVELOPMENTAL COMPARTMENTS IN THE DROSOPHILA WING
inferredcites →https://doi.org/10.1668/0003-1569(2000)040[0711:gittso]2.0.co;2openalex-snapshot
General Introduction to the Symposium on EvolutionaryDevelopmental Biology: Paradigms, Problems, and Prospects1Co-organized by Richard Burian, Scott Gilbert, Paula Mabee, and Billie Swalla
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Balfour, Garstang and de Beer: The First Century of Evolutionary Embryology1
inferredcites →https://doi.org/10.1668/0003-1569(2000)040[0770:midawi]2.0.co;2openalex-snapshot
Modularity in Development and Why It Matters to Evo-Devo1
inferredcites →https://doi.org/10.2307/1444854openalex-snapshot
Direct Development in Eleutherodactylus coqui (Anura: Leptodactylidae): A Staging Table
inferredcites →https://doi.org/10.2307/1541765openalex-snapshot
A Practical Guide to the Developmental Biology of Terrestrial-Breeding Frogs
inferredcites →https://doi.org/10.5860/choice.34-1536openalex-snapshot
The shape of life: genes, development, and the evolution of animal form
inferredcites →https://doi.org/10.7208/chicago/9780226256573.001.0001openalex-snapshot
The Shape of Life
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlae162zenodo-depositor-declared
Systematics of minute strabomantid frogs allocated to the genus Noblella (Amphibia: Anura) with description of a new genus, seven new species, and insights into historical biogeography
inferred← citeshttps://doi.org/10.1002/ar.22705openalex-snapshot
Ontogeny of the Vertebral Column of Eleutherodactylus johnstonei (Anura: Eleutherodactylidae) Reveals Heterochronies Relative to Metamorphic Frogs
inferred← citeshttps://doi.org/10.1002/dvdy.21025openalex-snapshot
Inhibition of Sonic hedgehog signaling leads to posterior digit loss in Ambystoma mexicanum: Parallels to natural digit reduction in urodeles
inferred← citeshttps://doi.org/10.1002/dvdy.21220openalex-snapshot
Muscle development in a biphasic animal: The frog
inferred← citeshttps://doi.org/10.1002/dvdy.275openalex-snapshot
Parallel evolution of direct development in frogs ‐ Skin and thyroid gland development in African Squeaker Frogs (Anura: Arthroleptidae: Arthroleptis )
inferred← citeshttps://doi.org/10.1002/dvg.22935openalex-snapshot
Developmental aspects of the direct‐developing frog A delophryne maranguapensis
inferred← citeshttps://doi.org/10.1002/jez.b.19openalex-snapshot
Developmental basis of evolutionary digit loss in the Australian lizard Hemiergis
inferred← citeshttps://doi.org/10.1002/jez.b.22549openalex-snapshot
Development of fore‐ and hindlimb muscles in frogs: Morphogenesis, homeotic transformations, digit reduction, and the forelimb–hindlimb enigma
inferred← citeshttps://doi.org/10.1002/jez.b.23103openalex-snapshot
Time to synchronize our clocks: Connecting developmental mechanisms and evolutionary consequences of heterochrony
inferred← citeshttps://doi.org/10.1002/jmor.20223openalex-snapshot
Cranial muscle development in frogs with different developmental modes: Direct development versus biphasic development
inferred← citeshttps://doi.org/10.1002/wdev.23openalex-snapshot
Developmental diversity of amphibians
inferred← citeshttps://doi.org/10.1007/978-3-319-93560-7_7openalex-snapshot
Diversity of Heads, Jaws, and Cephalic Muscles in Amphibians
inferred← citeshttps://doi.org/10.1007/s00427-009-0314-8openalex-snapshot
Lbx1 expression and frog limb development
inferred← citeshttps://doi.org/10.1007/s00429-002-0291-4openalex-snapshot
Mosaic evolution of neural development in anurans: acceleration of spinal cord development in the direct developing frog Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1007/s00429-005-0022-8openalex-snapshot
Ontogeny of central serotonergic neurons in the directly developing frog, Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1007/s13127-020-00467-8openalex-snapshot
Skeleton in the closet: hidden diversity in patterns of cranial and postcranial ontogeny in Neotropical direct-developing frogs (Anura: Brachycephaloidea)
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.05.025openalex-snapshot
Environmental Oxygen Exposure Allows for the Evolution of Interdigital Cell Death in Limb Patterning
inferred← citeshttps://doi.org/10.1016/j.gep.2013.02.005openalex-snapshot
Expression of cyclin D1, cyclin D2, and N-myc in embryos of the direct developing frog Eleutherodactylus coqui, with a focus on limbs
inferred← citeshttps://doi.org/10.1016/j.semcdb.2005.11.001openalex-snapshot
There's more than one frog in the pond: A survey of the Amphibia and their contributions to developmental biology
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.09.010openalex-snapshot
Of chicken wings and frog legs: A smorgasbord of evolutionary variation in mechanisms of tetrapod limb development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.11.005openalex-snapshot
Saunders's framework for understanding limb development as a platform for investigating limb evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2005.03.006openalex-snapshot
Cenozoic biogeography and evolution in direct-developing frogs of Central America (Leptodactylidae: Eleutherodactylus) as inferred from a phylogenetic analysis of nuclear and mitochondrial genes
inferred← citeshttps://doi.org/10.1016/j.zool.2012.03.003openalex-snapshot
Embryonic development of the fossorial gymnophthalmid lizards Nothobachia ablephara and Calyptommatus sinebrachiatus
inferred← citeshttps://doi.org/10.1023/b:rudo.0000029710.32325.bcopenalex-snapshot
Evolutionary Transformations of Ontogenesis in Anuran Amphibians
inferred← citeshttps://doi.org/10.1078/0944-2006-00051openalex-snapshot
Cranial neural crest-cell migration in the direct-developing frog, Eleutherodactylus coqui: molecular heterogeneity within and among migratory streams
inferred← citeshttps://doi.org/10.1111/ede.12250openalex-snapshot
Early limb patterning in the direct‐developing salamander Plethodon cinereus revealed by sox9 and col2a1
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2004.tb00468.xopenalex-snapshot
A TEST FOR PATTERNS OF MODULARITY IN SEQUENCES OF DEVELOPMENTAL EVENTS
inferred← citeshttps://doi.org/10.1111/j.1463-6395.2008.00349.xopenalex-snapshot
The apical ectodermal ridge in the pectoral fin of the Australian Lungfish (Neoceratodus forsteri): keeping the fin to limb transition in the fold
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2008.00255.xopenalex-snapshot
Gene expression reveals unique skeletal patterning in the limb of the direct‐developing frog, Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2011.00500.xopenalex-snapshot
Molecular anatomy of the developing limb in the coquí frog, E leutherodactylus coqui
inferred← citeshttps://doi.org/10.1111/joa.12150openalex-snapshot
Is salamander hindlimb regeneration similar to that of the forelimb? Anatomical and morphogenetic analysis of hindlimb muscle regeneration in GFP ‐transgenic axolotls as a basis for regenerative and developmental studies
inferred← citeshttps://doi.org/10.1111/joa.13737openalex-snapshot
Diversity and function of the fused anuran radioulna
inferred← citeshttps://doi.org/10.1163/157075603322539426openalex-snapshot
Reproductive modes, ontogenies, and the evolution of body form
inferred← citeshttps://doi.org/10.1186/1477-7827-2-6openalex-snapshot
Induced ovulation and egg deposition in the direct developing anuran Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1186/1477-7827-2-60openalex-snapshot
In vitro fertilization and artificial activation of eggs of the direct-developing anuran Eleutherodactylus coqui.
inferred← citeshttps://doi.org/10.1186/1742-9994-5-9openalex-snapshot
Development of the retinotectal system in the direct-developing frog Eleutherodactylus coqui in comparison with other anurans
inferred← citeshttps://doi.org/10.17077/etd.r5skoi5gopenalex-snapshot
The patterning and determinants of craniofacial robusticity in extant Homo sapiens
inferred← citeshttps://doi.org/10.2984/049.063.0301openalex-snapshot
Biology and Impacts of Pacific Island Invasive Species. 5.Eleutherodactylus coqui, the Coqui Frog (Anura: Leptodactylidae)
inferred← citeshttps://doi.org/10.7554/elife.73401openalex-snapshot
The big potential of the small frog Eleutherodactylus coqui
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