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Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial DysostosisA transcriptional profile of human fetal cartilage.Comparative transcriptomic analysis indicates genes associated with local and systemic resistance to Colletotrichum graminicola in maize.Shedding some light over the floral metabolism by arum lily (Zantedeschia aethiopica) spathe de novo transcriptome assemblyUse of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal DisordersBMP signaling in the cartilage growth plate.Use of microRNAs in directing therapy and evaluating treatment response in colorectal cancer.Plant storage proteins with antimicrobial activity: novel insights into plant defense mechanisms.The exon 3 polymorphism of the growth hormone receptor is a severity-related factor for osteoporosis.BMPs regulate multiple aspects of growth-plate chondrogenesis through opposing actions on FGF pathways.Rare genetic diseases: update on diagnosis, treatment and online resources.Computational Investigation of Growth Hormone Receptor Trp169Arg Heterozygous Mutation in a Child With Short Stature.Short stature, unusual face, delta phalanx, and abnormal vertebrae and ribs in a girl born to half-siblings.Partial trisomy 17q and partial monosomy 20q in a boy with craniosynostosisBreaking the frontiers of cosmetology with antimicrobial peptidesSecondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencingProbable identity-by-descent for a mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia (Dymeclin) gene among patients from Guam, Chile, Argentina, and SpainHuman iPSC-Derived Retinal Pigment Epithelium: A Model System for Prioritizing and Functionally Characterizing Causal Variants at AMD Risk Loci.Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyCardiomyopathy in duchenne, becker, and sarcoglycanopathies: a role for coronary dysfunction?Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophiesThe phenotype of calpainopathy: diagnosis based on a multidisciplinary approachMultiplex SSCP and heteroduplex analysis with Southern hybridization for large-scale mutation detectionPathogenic variants in the TRIP11 gene cause a skeletal dysplasia spectrum from odontochondrodysplasia to achondrogenesis 1AIDR-1018 induces cell proliferation, migration, and reparative gene expression in 2D culture and 3D human skin equivalentsIntraovarian injection of mesenchymal stem cells improves oocyte yield and in vitro embryo production in a bovine model of fertility loss
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Robert Pogue
@ast
Robert Pogue
@en
Robert Pogue
@es
Robert Pogue
@nl
Robert Pogue
@sl
type
label
Robert Pogue
@ast
Robert Pogue
@en
Robert Pogue
@es
Robert Pogue
@nl
Robert Pogue
@sl
prefLabel
Robert Pogue
@ast
Robert Pogue
@en
Robert Pogue
@es
Robert Pogue
@nl
Robert Pogue
@sl
P106
P1153
55924164500
P21
P31
P496
0000-0002-8789-3512