Publications by authors named "Jorge Martin"

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Cancer risk in Sjögren's disease: A longitudinal cohort study on incidence, predictors, and mortality impact.
Olga Rusinovich-Lovgach, Zulema Plaza, Mónica Fernández Castro, Jose Rosas-Gómez de Salazar, Victot Manuel Martínez Taboada, Jorge Juan Gonzalez Martin

Semin Arthritis Rheum· August 2025

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Long-Range Proton Channels Constructed via Hierarchical Peptide Self-Assembly.
Semion Censor, Jorge Vega Martin, Ohad Silberbush, Samala Murali Mohan Reddy, Ran Zalk

Adv Mater· December 2024

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Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfecta.
Alexander Kot, Cora Chun, Jorge H Martin, Davis Wachtell, David Hudson

J Bone Miner Res· September 2024

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Altered Sox9 and FGF signaling gene expression in Aga2 OI mice negatively affects linear growth.
Jennifer Zieba, Lisette Nevarez, Davis Wachtell, Jorge H Martin, Alexander Kot

JCI Insight· November 2023

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Enantioselective synthesis of 3-hydroxy- and 3-amino-3-alkynyl-2-oxindoles by the dimethylzinc-mediated addition of terminal alkynes to isatins and isatin-derived ketimines.
Elena Prieto, Jorge D Martín, Javier Nieto, Celia Andrés

Org Biomol Chem· August 2023

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Skeletal diseases caused by mutations in show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR.
Fabiana Csukasi, Michaela Bosakova, Tomas Barta, Jorge H Martin, Jesus Arcedo

Front Cell Dev Biol· January 2023

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Novel Anti-Neuroinflammatory Properties of a Thiosemicarbazone-Pyridylhydrazone Copper(II) Complex.
Xin Yi Choo, Lachlan E McInnes, Alexandra Grubman, Joanna M Wasielewska, Irina Belaya

Int J Mol Sci· September 2022

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4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.
Ivan Duran, Jennifer Zieba, Fabiana Csukasi, Jorge H Martin, Davis Wachtell

J Bone Miner Res· April 2022

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Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model.
Jennifer Zieba, Kimberly N Forlenza, Kelly Heard, Jorge H Martin, Michaela Bosakova

Bone Res· April 2022

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Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia.
Maya Barad, Fabiana Csukasi, Michaela Bosakova, Jorge H Martin, Wenjuan Zhang

EBioMedicine· December 2020

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Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling.
Michaela Bosakova, Sara P Abraham, Alexandru Nita, Eva Hruba, Marcela Buchtova, Jorge Martin

EMBO Mol Med· November 2020

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Assessing uncertainty of voter transitions estimated from aggregated data. Application to the 2017 French presidential election.
Rafael Romero, Jose M Pavía, Jorge Martín, Gerardo Romero

J Appl Stat· August 2020

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RISK FACTORS FOR HYPOGLYCEMIA IN INPATIENTS WITH TOTAL PARENTERAL NUTRITION AND TYPE 2 DIABETES: A POST HOC ANALYSIS OF THE INSUPAR STUDY.
Gabriel Olveira, Jose Abuín, Rafael López, Sandra Herranz, Jose M García-Almeida

Endocr Pract· June 2020

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Regular insulin added to total parenteral nutrition vs subcutaneous glargine in non-critically ill diabetic inpatients, a multicenter randomized clinical trial: INSUPAR trial.
Gabriel Olveira, Jose Abuín, Rafael López, Sandra Herranz, Jose M García-Almeida

Clin Nutr· February 2020

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Dominant-negative SOX9 mutations in campomelic dysplasia.
Fabiana Csukasi, Ivan Duran, Wenjuan Zhang, Jorge H Martin, Maya Barad

Hum Mutat· December 2019

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The α2 chain of type IX collagen is essential for type IX collagen biosynthesis.
Karthika Balasubramanian, MaryAnn Weis, David R Eyre, Jorge Martin, Jorge Ortiz-Sanchez

Am J Med Genet A· August 2019

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The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling.
Fabiana Csukasi, Ivan Duran, Maya Barad, Tomas Barta, Iva Gudernova, Jorge H Martin

Sci Transl Med· September 2018

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Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathies.
Michaela Kunova Bosakova, Miroslav Varecha, Marek Hampl, Ivan Duran, Alexandru Nita, Jorge H Martin

Hum Mol Genet· March 2018

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A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen.
Ivan Duran, Jorge H Martin, Mary Ann Weis, Pavel Krejci, Peter Konik

J Bone Miner Res· June 2017

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Effects of the application of therapeutic massage in children with cancer: a systematic review.
Juan Rodríguez-Mansilla, Blanca González-Sánchez, Silvia Torres-Piles, Jorge Guerrero Martín, María Jiménez-Palomares

Rev Lat Am Enfermagem· June 2017

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Mutations in IFT-A satellite core component genes and produce short rib polydactyly syndrome with distinctive campomelia.
Ivan Duran, S Paige Taylor, Wenjuan Zhang, Jorge Martin, Faisal Qureshi

Cilia· April 2017

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A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
Jennifer Zieba, Wenjuan Zhang, Jessica X Chong, Kimberly N Forlenza, Jorge H Martin

Sci Rep· February 2017

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Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis.
Felipe Marques, Jessica Tenney, Ivan Duran, Jorge Martin, Lisette Nevarez

PLoS Genet· December 2016

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Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis.
Felipe Marques, Jessica Tenney, Ivan Duran, Jorge Martin, Lisette Nevarez

PLoS Genet· September 2016

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Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
Ivan Duran, S Paige Taylor, Wenjuan Zhang, Jorge Martin, Kimberly N Forlenza

Sci Rep· September 2016

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