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The effect of growth rate on the three‐dimensional orientation of vascular canals in the cortical bone of broiler chickens
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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/(sici)1097-4687(199906)240:3<237::aid-jmor3>3.0.co;2-nopenalex-snapshot
Experimental alteration of limb posture in the chicken (Gallus gallus) and its bearing on the use of birds as analogs for dinosaur locomotion
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The “new bone”: Some anthropological potentials
inferredcites →https://doi.org/10.1002/ajpa.23297openalex-snapshot
Occurrence of osteon banding in adult human cortical bone
inferredcites →https://doi.org/10.1002/ar.b.10024openalex-snapshot
Quantitative 3D analysis of the canal network in cortical bone by micro‐computed tomography
inferredcites →https://doi.org/10.1002/jbmr.1643openalex-snapshot
The amount of periosteal apposition required to maintain bone strength during aging depends on adult bone morphology and tissue-modulus degradation rate
inferredcites →https://doi.org/10.1002/jbmr.2012openalex-snapshot
3D Assessment of Cortical Bone Porosity and Tissue Mineral Density Using High-Resolution µCT: Effects of Resolution and Threshold Method
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Relationships between body size and some life history parameters
inferredcites →https://doi.org/10.1007/s00198-002-1345-4openalex-snapshot
Bone strength and its determinants
inferredcites →https://doi.org/10.1007/s00223-002-2124-0openalex-snapshot
Bone Strength During Growth: Influence of Growth Rate on Cortical Porosity and Mineralization
inferredcites →https://doi.org/10.1007/s00223-005-0274-6openalex-snapshot
Effect of Voxel Size on 3D Micro-CT Analysis of Cortical Bone Porosity
inferredcites →https://doi.org/10.1007/s00339-006-3507-2openalex-snapshot
Applications of X-ray synchrotron microtomography for non-destructive 3D studies of paleontological specimens
inferredcites →https://doi.org/10.1007/s11914-014-0233-0openalex-snapshot
Micro- and Nano-CT for the Study of Bone Ultrastructure
inferredcites →https://doi.org/10.1007/s11914-016-0319-yopenalex-snapshot
Cortical Bone Porosity: What Is It, Why Is It Important, and How Can We Detect It?
inferredcites →https://doi.org/10.1016/0021-9290(94)00035-2openalex-snapshot
Spatial organization of the haversian bone in man
inferredcites →https://doi.org/10.1016/8756-3282(94)90288-7openalex-snapshot
Osteon orientation of the diaphysis of the long bones in man
inferredcites →https://doi.org/10.1016/j.bone.2009.04.243openalex-snapshot
Genetic selection for fast growth generates bone architecture characterised by enhanced periosteal expansion and limited consolidation of the cortices but a diminution in the early responses to mechanical loading
inferredcites →https://doi.org/10.1016/j.bone.2012.09.010openalex-snapshot
Variation in osteocyte lacunar morphology and density in the human femur — a synchrotron radiation micro-CT study
inferredcites →https://doi.org/10.1016/j.micron.2016.10.006openalex-snapshot
A method for measuring the three-dimensional orientation of cortical canals with implications for comparative analysis of bone microstructure in vertebrates
inferredcites →https://doi.org/10.1016/j.nima.2007.08.087openalex-snapshot
Beamlines of the biomedical imaging and therapy facility at the Canadian light source—Part 1
inferredcites →https://doi.org/10.1016/j.nima.2014.11.088openalex-snapshot
Beamlines of the biomedical imaging and therapy facility at the Canadian light source – part 3
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Bone typology and growth rate: testing and quantifying ‘Amprino’s rule’ in the mallard (Anas platyrhynchos)
inferredcites →https://doi.org/10.1017/s0094837300020108openalex-snapshot
Locomotion in non-avian dinosaurs: integrating data from hindlimb kinematics, in vivo strains, and bone morphology
inferredcites →https://doi.org/10.1017/s1431927612001079openalex-snapshot
Three-Dimensional Synchrotron Virtual Paleohistology: A New Insight into the World of Fossil Bone Microstructures
inferredcites →https://doi.org/10.1046/j.1469-7580.2002.00118.xopenalex-snapshot
Laminar bone as an adaptation to torsional loads in flapping flight
inferredcites →https://doi.org/10.1080/00071668.2012.659652openalex-snapshot
Impact of daylength on the productivity of two commercial broiler strains
inferredcites →https://doi.org/10.1080/00071669208417536openalex-snapshot
Composition, cortical structure and mechanical properties of chicken tibiotarsi: Effect of growth rate
inferredcites →https://doi.org/10.1080/713654918openalex-snapshot
Skeletal development in the meat-type chicken
inferredcites →https://doi.org/10.1088/0031-9155/56/16/012openalex-snapshot
Imaging the 3D structure of secondary osteons in human cortical bone using phase-retrieval tomography
inferredcites →https://doi.org/10.1088/0031-9155/60/1/211openalex-snapshot
In vivo imaging of rat cortical bone porosity by synchrotron phase contrast micro computed tomography
inferredcites →https://doi.org/10.1111/j.0021-8782.2004.00275.xopenalex-snapshot
Histological organization and its relationship to function in the femur of Alligator mississippiensis
inferredcites →https://doi.org/10.1111/j.0021-8782.2004.00318.xopenalex-snapshot
Does the degree of laminarity correlate with site‐specific differences in collagen fibre orientation in primary bone? An evaluation in the turkey ulna diaphysis
inferredcites →https://doi.org/10.1111/j.1365-2656.2006.01081.xopenalex-snapshot
Self‐regulation within outbreak populations of feral house mice: a test of alternative models
inferredcites →https://doi.org/10.1111/j.1365-2818.2007.01785.xopenalex-snapshot
Imaging applications of synchrotron X‐ray phase‐contrast microtomography in biological morphology and biomaterials science. I. General aspects of the technique and its advantages in the analysis of millimetre‐sized arthropod structure
inferredcites →https://doi.org/10.1111/j.1469-7580.2011.01398.xopenalex-snapshot
Visualization of 3D osteon morphology by synchrotron radiation micro‐CT
inferredcites →https://doi.org/10.1111/j.1469-7580.2011.01450.xopenalex-snapshot
The effects of immobilization on vascular canal orientation in rat cortical bone
inferredcites →https://doi.org/10.1111/j.1556-4029.2005.00001.xopenalex-snapshot
The Effects of Chemical and Heat Maceration Techniques on the Recovery of Nuclear and Mitochondrial DNA from Bone*
inferredcites →https://doi.org/10.1111/j.1556-4029.2010.01387.xopenalex-snapshot
The Effects of Different Maceration Techniques on Nuclear DNA Amplification Using Human Bone
inferredcites →https://doi.org/10.1111/joa.12357openalex-snapshot
Does 3D orientation account for variation in osteon morphology assessed by 2D histology?
inferredcites →https://doi.org/10.1111/joa.12430openalex-snapshot
Three‐dimensional reconstruction of Haversian systems in human cortical bone using synchrotron radiation‐based micro‐ CT : morphology and quantification of branching and transverse connections across age
inferredcites →https://doi.org/10.1111/joa.12803openalex-snapshot
Interpreting the three‐dimensional orientation of vascular canals and cross‐sectional geometry of cortical bone in birds and bats
inferredcites →https://doi.org/10.1139/z06-195openalex-snapshot
Bone microstructure: quantifying bone vascular orientation
inferredcites →https://doi.org/10.1242/jeb.00841openalex-snapshot
Assessing a relationship between bone microstructure and growth rate: a fluorescent labelling study in the king penguin chick (Aptenodytes patagonicus)
inferredcites →https://doi.org/10.1371/journal.pone.0001545openalex-snapshot
Leg Disorders in Broiler Chickens: Prevalence, Risk Factors and Prevention
inferredcites →https://doi.org/10.1525/california/9780520273528.003.0008openalex-snapshot
Analysis of Growth Rates
inferredcites →https://doi.org/10.3382/ps.2011-01968openalex-snapshot
The effects of growth rate on leg morphology and tibia breaking strength, mineral density, mineral content, and bone ash in broilers
inferredcites →https://doi.org/10.3389/fendo.2015.00122openalex-snapshot
Modalities for Visualization of Cortical Bone Remodeling: The Past, Present, and Future
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00435-025-00751-1openalex-snapshot
Comparative analysis of histological and vascular adaptations in the humeral diaphysis of fossil and recent Anas platyrhynchos: insights from the Late Pleistocene Binagadi asphalt deposits
inferred← citeshttps://doi.org/10.1016/j.bone.2024.117073openalex-snapshot
Vascular study of decellularized porcine long bones: Characterization of a tissue engineering model
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105343openalex-snapshot
Necrotic enteritis affects bone growth and bone microstructure in non-selected conventional and modern meat-type chicken strains
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105812openalex-snapshot
Growth performance and body composition of Eimeria-infected broiler fed berry pomaces and a Limosilactobacillus reuteri isolate
inferred← citeshttps://doi.org/10.1016/j.vas.2025.100485openalex-snapshot
Bone development of broiler chickens supplemented with chondroitin sulfate and manganese
inferred← citeshttps://doi.org/10.1038/s41598-021-93547-4openalex-snapshot
Labelling experiments in red deer provide a general model for early bone growth dynamics in ruminants
inferred← citeshttps://doi.org/10.1080/00071668.2025.2489059openalex-snapshot
Skeletal disorders in laying hens: a systematic review with a focus on non-cage housing systems and hemp-based dietary interventions for bone health
inferred← citeshttps://doi.org/10.1080/08912963.2021.1960323openalex-snapshot
Dichotomy in formation and growth of bones of Yanornis martini (Pygostylia, Ornithuromorpha): study of thermal regime in an extinct bird
inferred← citeshttps://doi.org/10.1080/08912963.2023.2228335openalex-snapshot
Bone microstructure of bony-toothed birds (Odontopterygiformes) from the Eocene of Ikove, Ukraine: preliminary paleobiological implications
inferred← citeshttps://doi.org/10.1111/azo.12396openalex-snapshot
The osteohistological variability in the evolution of basal avialans
inferred← citeshttps://doi.org/10.1111/azo.12402openalex-snapshot
Synchrotron microtomography‐based osteohistology ofGansus yumenensis: new data on the evolution of uninterrupted bone deposition in basal birds
inferred← citeshttps://doi.org/10.1111/joa.13325openalex-snapshot
Quantifying intracortical bone microstructure: A critical appraisal of 2D and 3D approaches for assessing vascular canals and osteocyte lacunae
inferred← citeshttps://doi.org/10.1111/joa.13741openalex-snapshot
Ontogenetic changes in cortical bone vascular microstructure in the domestic duck (Anas platyrhynchos) and ring‐necked pheasant (Phasianus colchicus)
inferred← citeshttps://doi.org/10.22099/ijvr.2022.40936.5935openalex-snapshot
Different litter compositions influence broiler chicken locomotion.
inferred← citeshttps://doi.org/10.3382/ps/pez375openalex-snapshot
The efficacy of 2 phytases on inositol phosphate degradation in different segments of the gastrointestinal tract, calcium and phosphorus digestibility, and bone quality of broilers
inferred← citeshttps://doi.org/10.3382/ps/pez400openalex-snapshot
Effects of reducing growth rate via diet dilution on bone mineralization, performance and carcass yield of coccidia-infected broilers
inferred← citeshttps://doi.org/10.36380/jwpr.2019.15openalex-snapshot
Model Estimation for LongitudinalBone Growth Based on Age in Male and Female Commercial Broiler Chickens
inferred← citeshttps://doi.org/10.5115/acb.19.189openalex-snapshot
Three-dimensional microstructures of the intracortical canals in the animal model of osteoporosis
inferred← citeshttps://doi.org/10.7287/peerj.7616v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The effects of growth rate and biomechanical loading on bone laminarity within the emu skeleton (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7616v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The effects of growth rate and biomechanical loading on bone laminarity within the emu skeleton (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7616v0.2/reviews/1openalex-snapshot
Peer Review #1 of "The effects of growth rate and biomechanical loading on bone laminarity within the emu skeleton (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.7616openalex-snapshot
The effects of growth rate and biomechanical loading on bone laminarity within the emu skeleton
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