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Molecular Genetics & Genomic Medicine
|
March 29, 2021
Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant
David Marx, Sophie Caillard, Jérôme Olagne, et al.
BMC Plant Biology
|
April 12, 2019
Extensive nuclear reprogramming and endoreduplication in mature leaf during floral induction
Stefania Del Prete, Anne Molitor, Delphine Charif, et al.
Iscience
|
February 3, 2025
Endothelial calcium firing mediates the extravasation of metastatic tumor cells
Marina Peralta, Amandine Dupas, Annabel Larnicol, et al.
Archives of Dermatological Research
|
April 8, 2025
A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review
Leyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, et al.
Journal of Translational Autoimmunity
|
January 19, 2026
Systemic lupus pregnancies are characterized by an intrinsic pro-inflammatory monocyte transcriptome, driven by an aberrant miRNA signature
Marc Scherlinger, Eloi Schmauch, Raphaël Carapito, et al.
EMBO Reports
|
November 16, 2023
Blood flow diverts extracellular vesicles from endothelial degradative compartments to promote angiogenesis
Benjamin Mary, Nandini Asokan, Katerina Jerabkova-Roda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex Dystonia
Amjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
August 14, 2020
Progressive multifocal leukoencephalopathy and sarcoidosis under interleukin 7: The price of healing
Aurélien Guffroy, Morgane Solis, Vincent Gies, et al.
BMC Immunology
|
July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel cases
Erta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Scandinavian Journal of Immunology
|
June 27, 2023
Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient
Shaghayegh Tajik, Mohsen Badalzadeh, Massoud Houshmand, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Molecular Genetics & Genomic Medicine
|
March 29, 2021
Atypical focal segmental glomerulosclerosis associated with a new PODXL nonsense variant
David Marx, Sophie Caillard, Jérôme Olagne, et al.
BMC Plant Biology
|
April 12, 2019
Extensive nuclear reprogramming and endoreduplication in mature leaf during floral induction
Stefania Del Prete, Anne Molitor, Delphine Charif, et al.
Iscience
|
February 3, 2025
Endothelial calcium firing mediates the extravasation of metastatic tumor cells
Marina Peralta, Amandine Dupas, Annabel Larnicol, et al.
Archives of Dermatological Research
|
April 8, 2025
A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review
Leyla Norouzi-Barough, Nasrin Alipour Olyaei, Raphael Carapito, et al.
Journal of Translational Autoimmunity
|
January 19, 2026
Systemic lupus pregnancies are characterized by an intrinsic pro-inflammatory monocyte transcriptome, driven by an aberrant miRNA signature
Marc Scherlinger, Eloi Schmauch, Raphaël Carapito, et al.
EMBO Reports
|
November 16, 2023
Blood flow diverts extracellular vesicles from endothelial degradative compartments to promote angiogenesis
Benjamin Mary, Nandini Asokan, Katerina Jerabkova-Roda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex Dystonia
Amjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
August 14, 2020
Progressive multifocal leukoencephalopathy and sarcoidosis under interleukin 7: The price of healing
Aurélien Guffroy, Morgane Solis, Vincent Gies, et al.
BMC Immunology
|
July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel cases
Erta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.
Scandinavian Journal of Immunology
|
June 27, 2023
Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient
Shaghayegh Tajik, Mohsen Badalzadeh, Massoud Houshmand, et al.
Page
of 5