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Frontiers in Cell and Developmental Biology
|
August 15, 2024
Unveiling the human fetal-maternal interface during the first trimester: biophysical knowledge and gaps
Alice Masserdotti, Michael Gasik, Regina Grillari-Voglauer, et al.
Bone
|
May 4, 2020
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis
Araceli Cuellar, Krithi Bala, Lorena Di Pietro, et al.
Regenerative Biomaterials
|
February 6, 2026
A smart nanocomposite bioactive ink for controlled siRNA delivery in calvarial mesenchymal stromal cells as a minimally invasive treatment for craniosynostosis
Martina Salvati, Federica Tiberio, Noah Giacon, et al.
Bone
|
April 21, 2018
BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche
Marta Barba, Lorena Di Pietro, Luca Massimi, et al.
Journal of Medical Genetics
|
December 30, 2018
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol
Francesco Danilo Tiziano, Rosa Lomastro, Emanuela Abiusi, et al.
Scientific Reports
|
April 12, 2024
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2012
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study
Francesco D Tiziano, Rosa Lomastro, Lorena Di Pietro, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Nature Genetics
|
July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
Erin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
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Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Frontiers in Cell and Developmental Biology
|
August 15, 2024
Unveiling the human fetal-maternal interface during the first trimester: biophysical knowledge and gaps
Alice Masserdotti, Michael Gasik, Regina Grillari-Voglauer, et al.
Bone
|
May 4, 2020
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis
Araceli Cuellar, Krithi Bala, Lorena Di Pietro, et al.
Regenerative Biomaterials
|
February 6, 2026
A smart nanocomposite bioactive ink for controlled siRNA delivery in calvarial mesenchymal stromal cells as a minimally invasive treatment for craniosynostosis
Martina Salvati, Federica Tiberio, Noah Giacon, et al.
Bone
|
April 21, 2018
BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche
Marta Barba, Lorena Di Pietro, Luca Massimi, et al.
Journal of Medical Genetics
|
December 30, 2018
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol
Francesco Danilo Tiziano, Rosa Lomastro, Emanuela Abiusi, et al.
Scientific Reports
|
April 12, 2024
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, et al.
European Journal of Human Genetics : EJHG
|
October 18, 2012
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study
Francesco D Tiziano, Rosa Lomastro, Lorena Di Pietro, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Nature Genetics
|
July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
Erin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
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