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Sequence of ossification in the skeleton of growing and metamorphosing tadpoles of Rana pipiens
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ar.1090940103openalex-snapshot
Stages in the normal development of Rana pipiens larvae
inferredcites →https://doi.org/10.1002/jez.1401220104openalex-snapshot
Local action of thyroxin on amphibian metamorphosis. I. Local metamorphosis in Rana pipiens larvae effected by thyroxin‐cholesterol implants
inferredcites →https://doi.org/10.1002/jez.1401220105openalex-snapshot
Local action of thyroxin on amphibian metamorphosis. II. Development of the eyelids, nictitating membrane, cornea, and extrinsic ocular muscles in Rana pipiens larvae effected by thyroxin‐cholesterol implants
inferredcites →https://doi.org/10.1002/jmor.1051190207openalex-snapshot
The development of the osteocranium of Pleurodeles waltlii Michahelles
inferredcites →https://doi.org/10.1002/jmor.1051190210openalex-snapshot
The development of the musculature of the hindlimb in the frog, Rana pipiens
inferredcites →https://doi.org/10.1002/jmor.1051210102openalex-snapshot
Early ossification in the skeleton of the sucker (Catostomus macrocheilus) and the guppy (Poecilia reticulata)
inferredcites →https://doi.org/10.1007/bf02118767openalex-snapshot
Zur Entwicklung des knöchernen Skelets von Triton und Rana unter besonderer Berücksichtigung der Zeitfolge der Ossifikationen
inferredcites →https://doi.org/10.1007/bf02170533openalex-snapshot
Über die Einwirkung des Schilddrüsenhormons auf die Ossifikation
inferredcites →https://doi.org/10.1016/0003-9969(61)90120-0openalex-snapshot
Calcification in Biological Systems
inferredcites →https://doi.org/10.1016/0012-1606(63)90110-6openalex-snapshot
Observations on the effect of thyroid and parathyroid secretions on explanted mouse radius rudiments
inferredcites →https://doi.org/10.1016/0012-1606(65)90006-0openalex-snapshot
The role of epithelium and mesenchyme in the production of a collagenolytic enzyme and a hyaluronidase in the anuran tadpole
inferredcites →https://doi.org/10.1016/b978-0-12-395731-3.50017-8openalex-snapshot
PROTEIN SYNTHESIS AND CELLS OF THE SKELETAL SYSTEM
inferredcites →https://doi.org/10.1016/b978-1-4831-6755-8.50013-9openalex-snapshot
Calcification of Skeletal Tissues
inferredcites →https://doi.org/10.1038/142004a0openalex-snapshot
The Development of the Vertebrate Skull
inferredcites →https://doi.org/10.1083/jcb.26.3.747openalex-snapshot
COLLAGENOLYTIC ACTIVITY IN RAT BONE CELLS
inferredcites →https://doi.org/10.1093/icb/1.1.107openalex-snapshot
MECHANISMS OF AMPHIBIAN METAMORPHOSIS: HORMONES
inferredcites →https://doi.org/10.1097/00000441-196208000-00033openalex-snapshot
A TEXTBOOK OF COMPARATIVE ENDOCRINOLOGY
inferredcites →https://doi.org/10.1097/00005053-193111000-00026openalex-snapshot
STUDIES ON THE STRUCTURE AND DEVELOPMENT OF VERTEBRATES
inferredcites →https://doi.org/10.1098/rstl.1871.0009openalex-snapshot
VIII. On the structure and development of the skull of the common frog ( Rana temporaria , L.)
inferredcites →https://doi.org/10.1098/rstl.1876.0024openalex-snapshot
XXIV. On the structure and development of the skull in the batrachia.—Part II
inferredcites →https://doi.org/10.1098/rstl.1881.0001openalex-snapshot
I. On the structure and development of the the skull in the batrachia. —Part III
inferredcites →https://doi.org/10.1113/jphysiol.1955.sp005269openalex-snapshot
The biological action of thyroxine on embryonic bones grown in tissue culture
inferredcites →https://doi.org/10.1113/jphysiol.1956.sp005568openalex-snapshot
The effect of L‐triiodothyronine on the growth and development of embryonic chick limb bones in tissue culture
inferredcites →https://doi.org/10.1136/pgmj.44.511.347openalex-snapshot
Biochemistry of hyperthyroidism and hypothyroidism
inferredcites →https://doi.org/10.1210/endo-70-6-774openalex-snapshot
Effects of Thyroxine Upon Strontium and Calcium Metabolism of Embryonic Bone Grownin Vitro
inferredcites →https://doi.org/10.2307/1439196openalex-snapshot
The Progress of Ossification in the Skull of the Cricketfrog Pseudacris nigrita triseriata
inferredcites →https://doi.org/10.2307/1441083openalex-snapshot
Morphology and Development of the Skull in the Frog Hyla septentrionalis
inferredcites →https://doi.org/10.2307/3223872openalex-snapshot
Observations on the Development of the Anuran Urostyle
inferredcites →https://doi.org/10.5962/bhl.title.12399openalex-snapshot
On the structure and development of the skull in the Batrachia.
inferredcites →https://doi.org/10.5962/bhl.title.6376openalex-snapshot
The vertebrate skeleton from the developmental standpoint
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Strange Tadpoles from the Lower Miocene of Turkey: Is Paedogenesis Possible in Anurans?
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Anatomy of rat semaphorin III collapsin‐1 mRNA expression and relationship to developing nerve tracts during neuroembryogenesis
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Postembryonic ontogeny of the spadefoot toad, Scaphiopus intermontanus (Anura: Pelobatidae): Skeletal morphology
inferred← citeshttps://doi.org/10.1002/(sici)1097-4687(199904)240:1<49::aid-jmor5>3.0.co;2-zopenalex-snapshot
Osteology and skeletal development ofPyxicephalus adspersus (Anura: Ranidae: Raninae)
inferred← citeshttps://doi.org/10.1002/(sici)1097-4687(199905)240:2<143::aid-jmor5>3.0.co;2-lopenalex-snapshot
Development of the suprarostral plate of Pipoid Frogs
inferred← citeshttps://doi.org/10.1002/(sici)1097-4687(200001)243:1<75::aid-jmor4>3.0.co;2-lopenalex-snapshot
Ontogeny of the bizarre: an osteological description ofPipa pipa (Anura: Pipidae), with an account of skeletal development in the species
inferred← citeshttps://doi.org/10.1002/.22599openalex-snapshot
Amphibian skull evolution: The developmental and functional context of simplification, bone loss and heterotopy
inferred← citeshttps://doi.org/10.1002/aja.1001960305openalex-snapshot
Ablation of various regions within the avian vagal neural crest has differential effects on ganglion formation in the fore‐, mid‐ and hindgut
inferred← citeshttps://doi.org/10.1002/ar.1092280211openalex-snapshot
Myotome and early neurogenesis in chick embryos
inferred← citeshttps://doi.org/10.1002/ar.20958openalex-snapshot
Neurovascular Anatomy of the Embryonic Quail Hindlimb
inferred← citeshttps://doi.org/10.1002/ar.22544openalex-snapshot
Heterochronic Protein Expression Patterns in the Developing Embryonic Chick Cerebellum
inferred← citeshttps://doi.org/10.1002/ar.23341openalex-snapshot
Patterns of Cranial Development in Larval Rana macrocnemis: Chondrocranial Size and Shape Relationship With Pelophylax bedriagae (Anura: Ranidae)
inferred← citeshttps://doi.org/10.1002/bdrc.20091openalex-snapshot
Genetic analysis of molecular oscillators in mammalian somitogenesis: Clues for studies of human vertebral disorders
inferred← citeshttps://doi.org/10.1002/bdrc.20093openalex-snapshot
Disruption of the somitic molecular clock causes abnormal vertebral segmentation
inferred← citeshttps://doi.org/10.1002/bies.1084openalex-snapshot
Mechanisms and molecules in motor neuron specification and axon pathfinding
inferred← citeshttps://doi.org/10.1002/bies.950130103openalex-snapshot
Growth cone inhibition – an important mechanism in neural development?
inferred← citeshttps://doi.org/10.1002/bies.950130104openalex-snapshot
Cells and cell‐interactions that guide motor axons in the developing chick embryo
inferred← citeshttps://doi.org/10.1002/bies.950150402openalex-snapshot
Mechanisms of neural crest cell migration
inferred← citeshttps://doi.org/10.1002/cne.903280309openalex-snapshot
A nonrandom interneuronal pattern in the developing frog spinal cord
inferred← citeshttps://doi.org/10.1002/dvdy.10492openalex-snapshot
Long‐distance cue from emerging dermis stimulates neural crest melanoblast migration
inferred← citeshttps://doi.org/10.1002/dvdy.20919openalex-snapshot
Lineage specification in neural crest cell pathfinding
inferred← citeshttps://doi.org/10.1002/dvdy.24055openalex-snapshot
Hox genes and region‐specific sensorimotor circuit formation in the hindbrain and spinal cord
inferred← citeshttps://doi.org/10.1002/dvdy.24669openalex-snapshot
Endochondral ossification in hindlimbs during bufo gargarizans metamorphosis: A model of studying skeletal development in vertebrates
inferred← citeshttps://doi.org/10.1002/dvdy.407openalex-snapshot
Postembryonic development and aging of the appendicular skeleton in Ambystoma mexicanum
inferred← citeshttps://doi.org/10.1002/glia.440130402openalex-snapshot
Boundaries and inhibitory molecules in developing neural tissues
inferred← citeshttps://doi.org/10.1002/jez.1134openalex-snapshot
Early development of amphioxus nervous system with special reference to segmental cell organization and putative sensory cell precursors: A study based on the expression of pan‐neuronal marker gene Hu/elav
inferred← citeshttps://doi.org/10.1002/jez.1136openalex-snapshot
Limb development in a “nonmodel” vertebrate, the direct‐developing frog Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1002/jez.1402510211openalex-snapshot
Different subsets of axonal guidance cues are essential for sensory neurite outgrowth to cutaneous and muscle targets in the dorsal ramus of the embryonic chick
inferred← citeshttps://doi.org/10.1002/jez.b.21182openalex-snapshot
Deconstructing the pharyngeal metamere
inferred← citeshttps://doi.org/10.1002/jez.b.22599openalex-snapshot
Amphibian skull evolution: The developmental and functional context of simplification, bone loss and heterotopy
inferred← citeshttps://doi.org/10.1002/jez.b.23280openalex-snapshot
Skull Ossification in the Andean Toad Rhinella spinulosa (Bufonidae) and the Genetic Model Organism Xenopus tropicalis (Pipidae) Reveals Heterochrony Phenomena and Frontoparietal Suture Modifications
inferred← citeshttps://doi.org/10.1002/jmor.10313openalex-snapshot
Ontogeny, phylogeny, and morphology in anuran larvae: Morphometric analysis of cranial development and evolution inRana tadpoles (Anura: Ranidae)
inferred← citeshttps://doi.org/10.1002/jmor.10344openalex-snapshot
Development and growth of long bones in European water frogs (Amphibia: Anura: Ranidae), with remarks on age determination
inferred← citeshttps://doi.org/10.1002/jmor.1051590303openalex-snapshot
Development of the urostyle during metamorphosis in five species of anurans
inferred← citeshttps://doi.org/10.1002/jmor.1051820302openalex-snapshot
Variation and timing of the cranial ossification sequence of the oriental fire‐bellied toad, Bombina orientalis (Amphibia, Discoglossidae)
inferred← citeshttps://doi.org/10.1002/jmor.1051950303openalex-snapshot
Skull development during anuran metamorphosis: I. Early development of the first three bones to form—the exoccipital, the parasphenoid, and the frontoparietal
inferred← citeshttps://doi.org/10.1002/jmor.1052000305openalex-snapshot
Ontogeny of bone and the role of heterochrony in the myobatrachine genera Uperoleia, Crinia, and Pseudophryne (anura: Leptodactylidae: Myobatrachinae)
inferred← citeshttps://doi.org/10.1002/jmor.1052020104openalex-snapshot
Ontogeny of the skeleton of Spea bombifrons (anura: Pelobatidae)
inferred← citeshttps://doi.org/10.1002/jmor.1052090206openalex-snapshot
Distribution and expression of two interactive extracellular matrix proteins, cytotactin and cytotactin‐binding proteoglycan, during development of Xenopus laevis. I. Embryonic development
inferred← citeshttps://doi.org/10.1002/jmor.1052090307openalex-snapshot
Osteology, skeletal development, and chondrocranial structure ofHamptophryne boliviana(Anura: Microhylidae)
inferred← citeshttps://doi.org/10.1002/jmor.1052140102openalex-snapshot
Skeletal development in Xenopus laevis (Anura: Pipidae)
inferred← citeshttps://doi.org/10.1002/jmor.1052230204openalex-snapshot
Skeletal morphogenesis in the urodele skull: II. Effect of developmental stage in thyroid hormone‐induced remodeling
inferred← citeshttps://doi.org/10.1002/jmor.10545openalex-snapshot
Cranial ontogeny in Philautus silus (Anura: Ranidae: Rhacophorinae) reveals few similarities with other direct‐developing anurans
inferred← citeshttps://doi.org/10.1002/jmor.20855openalex-snapshot
Growth and cranial development in the Andean frogs of the genus Telmatobius (Anura: Telmatobiidae): Exploring the relation of heterochrony and skeletal diversity
inferred← citeshttps://doi.org/10.1002/jmor.21264openalex-snapshot
Variation in the growth and development of the hind limbs in frogs of the genus Telmatobius (Anura: Telmatobiidae)
inferred← citeshttps://doi.org/10.1002/jmor.21664openalex-snapshot
Epichordal vertebral column formation in Xenopus laevis
inferred← citeshttps://doi.org/10.1002/jmor.70044openalex-snapshot
Perichordal Vertebral Column Formation in Rana kobai
inferred← citeshttps://doi.org/10.1002/jnr.490210206openalex-snapshot
Distribution and function of tenascin during cranial neural crest development in the chick
inferred← citeshttps://doi.org/10.1002/jnr.490210232openalex-snapshot
Projection‐neurons that send axons through the lumbar spinal cord of the chick embryo are not obviously distributed in a segmentally repetitive pattern
inferred← citeshttps://doi.org/10.1002/neu.10113openalex-snapshot
Chondroitin sulfate disrupts axon pathfinding in the optic tract and alters growth cone dynamics
inferred← citeshttps://doi.org/10.1002/neu.480230302openalex-snapshot
A positive correlation between permissiveness of mesoderm to neural crest migration and early DRG growth
inferred← citeshttps://doi.org/10.1002/neu.480240209openalex-snapshot
Environmental influences on neural crest cell migration
inferred← citeshttps://doi.org/10.1002/neu.480240309openalex-snapshot
Selective fasciculation as a mechanism for the formation of specific chemical connections between Aplysia neurons in vitro
inferred← citeshttps://doi.org/10.1002/neu.480241207openalex-snapshot
Neurotrophin‐3 affects proliferation and differentiation of distinct neural crest cells and is present in the early neural tube of avian embryos
inferred← citeshttps://doi.org/10.1002/tera.10033openalex-snapshot
Homocysteine modifies development of neurulation and dorsal root ganglia in chick embryos
inferred← citeshttps://doi.org/10.1007/978-1-4613-3246-6_12openalex-snapshot
Biological Basis of Tissue Regression and Synthesis
inferred← citeshttps://doi.org/10.1007/bf00318225openalex-snapshot
Skull development during anuran metamorphosis
inferred← citeshttps://doi.org/10.1007/s00442-015-3504-2openalex-snapshot
Stoichiometric implications of a biphasic life cycle
inferred← citeshttps://doi.org/10.1007/s00442-016-3746-7openalex-snapshot
Ontogenetic changes in sensitivity to nutrient limitation of tadpole growth
inferred← citeshttps://doi.org/10.1016/0003-9969(74)90131-9openalex-snapshot
Ultrastructure of the enamel layer in developing teeth of the shark Carcharhinus menisorrah
inferred← citeshttps://doi.org/10.1016/0012-1606(72)90179-0openalex-snapshot
Hemolytic effect of phenylhydrazine during amphibian metamorphosis
inferred← citeshttps://doi.org/10.1016/0012-1606(81)90455-3openalex-snapshot
Thyroid-hormone-induced differentiation and development of anuran tadpole hind limbs: Detection and quantitation of M-line protein and α-actinin synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-452801-7.50006-7openalex-snapshot
Hormonal Responses in Amphibian Metamorphosis
inferred← citeshttps://doi.org/10.1016/b978-012730935-4/50007-9openalex-snapshot
Hormonal Control in Larval Development and Evolution—Amphibians
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.735727openalex-snapshot
Metamorphosis and skeletal development of hybrid Epinephelus awoara (♀) and Epinephelus tukula (♂) progenies
inferred← citeshttps://doi.org/10.1016/j.bbagen.2018.07.032openalex-snapshot
Transcriptome analyses reveal molecular mechanisms that regulate endochondral ossification in amphibian Bufo gargarizans during metamorphosis
inferred← citeshttps://doi.org/10.1016/j.zool.2013.03.002openalex-snapshot
Old and new hypotheses about the homology of the compound bones from the cheek and otico-occipital regions of the anuran skull
inferred← citeshttps://doi.org/10.1016/s0736-5748(00)00030-7openalex-snapshot
Cadherins: molecular codes for axon guidance and synapse formation
inferred← citeshttps://doi.org/10.1021/acs.est.5c09489openalex-snapshot
Influence of Amphibian Metamorphosis on the Biokinetics and Biodistribution of Radionuclides Cesium and Strontium
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Patterning of the cranial nerves in the chick embryo is dependent on cranial mesoderm and rhombomeric metamerism
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Rhombomere origin plays a role in the specificity of cranial motor axon projections in the chick
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Ancient ontogenies: larval development of the Lower Cretaceous anuran Shomronella jordanica (Amphibia: Pipoidea)
inferred← citeshttps://doi.org/10.1080/02705060.2019.1602569openalex-snapshot
The stoichiometry of larval anuran development in natural wetlands
inferred← citeshttps://doi.org/10.1086/684205openalex-snapshot
Differential consumption and assimilation of leaf litter by wetland herbivores: alternative pathways for decomposition and trophic transfer
inferred← citeshttps://doi.org/10.1086/687047openalex-snapshot
Influence of Physiological Stress on Nutrient Stoichiometry in Larval Amphibians
inferred← citeshttps://doi.org/10.1093/icb/41.3.538openalex-snapshot
Comparative Development of Anurans: Using Phylogeny to Understand Ontogeny
inferred← citeshttps://doi.org/10.1101/2021.03.05.434057openalex-snapshot
Post-embryonic development and aging of the appendicular skeleton in Ambystoma mexicanum
inferred← citeshttps://doi.org/10.1101/352609openalex-snapshot
What do ossification sequences tell us about the origin of extant amphibians?
inferred← citeshttps://doi.org/10.1111/brv.12578openalex-snapshot
Development and evolution of the tetrapod skull–neck boundary
inferred← citeshttps://doi.org/10.1111/ede.12043openalex-snapshot
Ossification sequence heterochrony among amphibians
inferred← citeshttps://doi.org/10.1111/ede.12092openalex-snapshot
Variation in timing of ossification affects inferred heterochrony of cranial bones in Lissamphibia
inferred← citeshttps://doi.org/10.1111/fwb.13216openalex-snapshot
Understanding variation in salamander ionomes: A nutrient balance approach
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AN EXPERIMENTAL STUDY OF INTRASPECIFIC VARIATION, DEVELOPMENTAL TIMING, AND HETEROCHRONY IN FISHES
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THE EVOLUTION OF DEVELOPMENT: TWO PORTRAITS OF SKULL OSSIFICATION IN PIPOID FROGS
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2002.tb01372.xopenalex-snapshot
THE EFFECT OF MINIATURIZED BODY SIZE ON SKELETAL MORPHOLOGY IN FROGS
inferred← citeshttps://doi.org/10.1111/j.1439-0469.2010.00570.xopenalex-snapshot
A large-scale survey of heterochrony in anuran cranial ossification patterns
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1990.00091.xopenalex-snapshot
Do Peanut Agglutinin Receptors on Somites Control the Behavior of Neural Cells?
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1992.00553.xopenalex-snapshot
Regulation of Cell Number in Formation of the Dorsal Root Ganglion Revealed by Transplantation of Quail Neural Crest Cells into Chick Embryos
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1994.00621.xopenalex-snapshot
Transient Calretinin Expression during Intervertebral Disc Formation of the Chick Embryo
inferred← citeshttps://doi.org/10.1111/j.1460-9568.1996.tb01593.xopenalex-snapshot
The Semaphorins: A Family of Axonal Guidance Molecules?
inferred← citeshttps://doi.org/10.1111/j.1463-6395.2007.00317.xopenalex-snapshot
The chondrocrania of North American Rana larvae (Anura: Ranidae): a morphological comparison
inferred← citeshttps://doi.org/10.1111/j.1463-6395.2011.00520.xopenalex-snapshot
Chondrocranial ontogeny of Pelodytes punctatus (Anura: Pelodytidae). Response to competition: geometric morphometric and allometric change analysis
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The generation of vertebral segmental patterning in the chick embryo
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The influence of variation in larval period on adult cranial diversity in Pelobates fuscus (Anura: Pelobatidae)
inferred← citeshttps://doi.org/10.1111/j.1502-3931.2009.00192.xopenalex-snapshot
Exceptionally preserved tadpoles from the Miocene of Libros, Spain: ecomorphological reconstruction and the impact of ontogeny upon taphonomy
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2012.00543.xopenalex-snapshot
Development of the head and trunk mesoderm in the dogfish, Scyliorhinus torazame: II. Comparison of gene expression between the head mesoderm and somites with reference to the origin of the vertebrate head
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1991.tb15615.xopenalex-snapshot
Myelin‐Associated Inhibitors of Neurite Outgrowth and Their Role in CNS Regeneration
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1991.tb15661.xopenalex-snapshot
A Growth Cone Collapsing Activity in Chicken Gray Matter
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1998.tb10103.xopenalex-snapshot
Inhibitory Interactions in the Patterning of Trunk Neural Crest Migration
inferred← citeshttps://doi.org/10.1111/joa.12714openalex-snapshot
Patterning spinal nerves and vertebral bones
inferred← citeshttps://doi.org/10.1134/s0031030115140178openalex-snapshot
Experimental approach to the hypotheses of heterochronic evolution in lower vertebrates
inferred← citeshttps://doi.org/10.1134/s003103012211017xopenalex-snapshot
Amphibian Ontogeny: Major Trends, Mechanisms, and Paradoxes of Evolution
inferred← citeshttps://doi.org/10.1242/jeb.246419openalex-snapshot
Femoral bone structure and mechanics at the edge and core of an expanding population of the invasive frog Xenopus laevis
inferred← citeshttps://doi.org/10.1371/journal.pone.0171669openalex-snapshot
Morphological comparison of five species of poison dart frogs of the genus Ranitomeya (Anura: Dendrobatidae) including the skeleton, the muscle system and inner organs
inferred← citeshttps://doi.org/10.14720/abs.60.1.15670openalex-snapshot
Vzorec osifikacije skeleta pri ličinkah navadne krastače Bufo bufo
inferred← citeshttps://doi.org/10.1668/0003-1569(2001)041[0538:cdoaup]2.0.co;2openalex-snapshot
Comparative Development of Anurans: Using Phylogeny to Understand Ontogeny1
inferred← citeshttps://doi.org/10.1670/246-01nopenalex-snapshot
Intraspecific Variation in Cranial Ossification in the Tailed Frog, Ascaphus truei
inferred← citeshttps://doi.org/10.2307/1563611openalex-snapshot
The Sequence of Cranial Ossification in the California Toad, Bufo boreas (Amphibia, Anura, Bufonidae)
inferred← citeshttps://doi.org/10.2307/1565693openalex-snapshot
Temporal Dissociation between the Development of the Cranial and Appendicular Skeletons in Bufo bufo (Amphibia: Bufonidae)
inferred← citeshttps://doi.org/10.30906/1026-2296-2009-16-3-167-176openalex-snapshot
Number of Ossification Centers in the Anuran Cranial Bones Depends upon the Rate of Development: Experimental Evidence
inferred← citeshttps://doi.org/10.30906/1026-2296-2011-18-3-203-209openalex-snapshot
Thyroid Hormone Mediation in Skull Development of Siberian Newt, Salamandrella keyserlingi (Urodela: Hynobiidae), with Comparison to Other Species
inferred← citeshttps://doi.org/10.31390/gradschool_disstheses.8257openalex-snapshot
Comparative Ontogeny of Cranial Ossification in the Spotted Salamander, Ambystoma Maculatum, and the Tailed Frog, Ascaphus Truei
inferred← citeshttps://doi.org/10.3389/fevo.2021.620971openalex-snapshot
Amphibian Hormones, Calcium Physiology, Bone Weight, and Lung Use Call for a More Inclusive Approach to Understanding Ossification Sequence Evolution
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