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Proceedings of the 10th International Symposium on Superalloy 718 and Derivatives

1, 2023

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MiR‐497∼195 Cluster MicroRNAs Regulate Osteoblast Differentiation by Targeting BMP Signaling

Journal of bone and mineral research, 2015-05, Vol.30 (5), p.796-808

2015

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Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms

Journal of cardiovascular electrophysiology, 2020-06, Vol.31 (6), p.1527-1535

2020

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Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study

Journal of medical Internet research, 2024-03, Vol.26 (2), p.e42904-e42904

2024

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Prognostic significance of prenatal ultrasound in fetal arthrogryposis multiplex congenita

Archives of gynecology and obstetrics, 2021-04, Vol.303 (4), p.943-953

2021

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A novel mutation in CDH11, encoding cadherin‐11, cause Branchioskeletogenital (Elsahy‐Waters) syndrome

American journal of medical genetics. Part A, 2018-09, Vol.176 (9), p.2028-2033

2018

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Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

American journal of human genetics, 2007-02, Vol.80 (2), p.232-240

2007

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The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta

Journal of vascular surgery, 2013-06, Vol.57 (6), p.1628-1636.e3

2013

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Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders

American journal of human genetics, 2008-02, Vol.82 (2), p.464-476

2008

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Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing

BMC genomics, 2011-03, Vol.12 (1), p.158-158, Article 158

2011

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The Interaction of BMP2-Induced Defect Healing in Rat and Fixator Stiffness Modulates Matrix Alignment and Contraction

JBMR plus, 2018-05, Vol.2 (3), p.174-186

2018

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Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1

Bone (New York, N.Y.), 2013-08, Vol.55 (2), p.292-297

2013

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Promiscuous and Depolarization‐Induced Immediate‐Early Response Genes Are Induced by Mechanical Strain of Osteoblasts

Journal of bone and mineral research, 2009-07, Vol.24 (7), p.1247-1262

2009

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MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3' UTR and coding-sequence binding sites

PloS one, 2011-01, Vol.6 (1), p.e16250-e16250

2011

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miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling molecules

The international journal of biochemistry & cell biology, 2013-03, Vol.45 (3), p.696-705

2013

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Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?

Journal of human genetics, 2015-08, Vol.60 (8), p.419-425

2015

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Proceedings of the 9th International Symposium on Superalloy 718 & Derivatives: Energy, Aerospace, and Industrial Applications

1st ed. 2018 edition., 2018

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Metal Injection Molding of Alloy 718 for Aerospace Applications

JOM (1989), 2012-02, Vol.64 (2), p.252-256

2012

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Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study

Journal of medical Internet research, 2020-10, Vol.22 (10), p.e19263-e19263

2020

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BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation

Scientific reports, 2017-12, Vol.7 (1), p.17192-13, Article 17192

2017

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Transcriptional profiling of murine osteoblast differentiation based on RNA-seq expression analyses

Bone (New York, N.Y.), 2018-08, Vol.113, p.29-40

2018

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A machine learning-based screening tool for genetic syndromes in children

The Lancet. Digital health, 2022-05, Vol.4 (5), p.e295-e295

2022

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HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families

Genetics in medicine, 2023-11, Vol.25 (11), p.100928-100928, Article 100928

2023

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Proceedings of the 10th International Symposium on Superalloy 718 and Derivatives

MiR‐497∼195 Cluster MicroRNAs Regulate Osteoblast Differentiation by Targeting BMP Signaling

Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms

Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study

SARS-CoV-2 clade dynamics and their associations with hospitalisations during the first two years of the COVID-19 pandemic

Prognostic significance of prenatal ultrasound in fetal arthrogryposis multiplex congenita

A novel mutation in CDH11, encoding cadherin‐11, cause Branchioskeletogenital (Elsahy‐Waters) syndrome

Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica

Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome

The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta

Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders

Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing

The Interaction of BMP2-Induced Defect Healing in Rat and Fixator Stiffness Modulates Matrix Alignment and Contraction

Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1

Promiscuous and Depolarization‐Induced Immediate‐Early Response Genes Are Induced by Mechanical Strain of Osteoblasts

MicroRNAs differentially expressed in postnatal aortic development downregulate elastin via 3' UTR and coding-sequence binding sites

miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling molecules

Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?

Proceedings of the 9th International Symposium on Superalloy 718 & Derivatives: Energy, Aerospace, and Industrial Applications

Metal Injection Molding of Alloy 718 for Aerospace Applications

Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study

BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation

Transcriptional profiling of murine osteoblast differentiation based on RNA-seq expression analyses

A machine learning-based screening tool for genetic syndromes in children

HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families

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