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Showing results (131-140 of 235) with videos related to

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Journal of Cellular and Molecular Medicine|June 5, 2014
Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cellsAnnalucia Carbone, Stefano Castellani, Maria Favia, et al.
The European Journal of Neuroscience|September 16, 2018
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years onLuiz G Guidi, Antonio Velayos-Baeza, Isabel Martinez-Garay, et al.
Human Genetics|November 1, 2006
Y-chromosomal insights into the genetic impact of the caste system in IndiaTatiana Zerjal, Arpita Pandya, Kumarasamy Thangaraj, et al.
Haemostasis|January 1, 1984
Acquired factor VIII inhibitor in a non-haemophilic patient: successful treatment with plasma exchange associated with factor VIII concentrate and immunosuppressorsM L Paracchini, G M Rocchini, P Renoldi, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 27, 2025
Artificial intelligence in the operating room: A systematic review of AI models for surgical phase, instruments and anatomical structure identificationSara Paracchini, Cristina Taliento, Giulia Pellecchia, et al.
American Journal of Human Genetics|June 18, 2004
A predominantly neolithic origin for Y-chromosomal DNA variation in North AfricaBarbara Arredi, Estella S Poloni, Silvia Paracchini, et al.
Environment International|June 1, 2014
Comparing measured and modelled PFOS concentrations in a UK freshwater catchment and estimating emission ratesMark R Earnshaw, Alexander G Paul, Robert Loos, et al.
Plos One|January 26, 2016
Towards Plant Species Identification in Complex Samples: A Bioinformatics Pipeline for the Identification of Novel Nuclear Barcode CandidatesAlexandre Angers-Loustau, Mauro Petrillo, Valentina Paracchini, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Human Genetics|September 5, 2023
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twinsCheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, et al.
Pageof 24

Showing results (131-140 of 235) with videos related to

Sort By:
Pageof 24
Journal of Cellular and Molecular Medicine|June 5, 2014
Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cellsAnnalucia Carbone, Stefano Castellani, Maria Favia, et al.
The European Journal of Neuroscience|September 16, 2018
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years onLuiz G Guidi, Antonio Velayos-Baeza, Isabel Martinez-Garay, et al.
Human Genetics|November 1, 2006
Y-chromosomal insights into the genetic impact of the caste system in IndiaTatiana Zerjal, Arpita Pandya, Kumarasamy Thangaraj, et al.
Haemostasis|January 1, 1984
Acquired factor VIII inhibitor in a non-haemophilic patient: successful treatment with plasma exchange associated with factor VIII concentrate and immunosuppressorsM L Paracchini, G M Rocchini, P Renoldi, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 27, 2025
Artificial intelligence in the operating room: A systematic review of AI models for surgical phase, instruments and anatomical structure identificationSara Paracchini, Cristina Taliento, Giulia Pellecchia, et al.
American Journal of Human Genetics|June 18, 2004
A predominantly neolithic origin for Y-chromosomal DNA variation in North AfricaBarbara Arredi, Estella S Poloni, Silvia Paracchini, et al.
Environment International|June 1, 2014
Comparing measured and modelled PFOS concentrations in a UK freshwater catchment and estimating emission ratesMark R Earnshaw, Alexander G Paul, Robert Loos, et al.
Plos One|January 26, 2016
Towards Plant Species Identification in Complex Samples: A Bioinformatics Pipeline for the Identification of Novel Nuclear Barcode CandidatesAlexandre Angers-Loustau, Mauro Petrillo, Valentina Paracchini, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Human Genetics|September 5, 2023
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twinsCheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, et al.
Pageof 24