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Maiella, Sylvie
27  results:
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1

Coding undiagnosed rare disease patients in health informat..:

Angin, Céline ; Mazzucato, Monica ; Weber, Stefanie...
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

ORPHAcodes use for the coding of rare diseases: comparison ..:

Mazzucato, Monica ; Pozza, Laura Visonà Dalla ; Facchin, Paola...
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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3

Correction: Phenotate: crowdsourcing phenotype annotations ..:

Chang, Willie H. ; Mashouri, Pouria ; Lozano, Alexander X....
Genetics in Medicine.  22 (2020)  8 - p. 1427 , 2020
Link: https://doi.org/10.1038/..
 
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4

Phenotate: crowdsourcing phenotype annotations as exercises..:

Chang, Willie H. ; Mashouri, Pouria ; Lozano, Alexander X....
Genetics in Medicine.  22 (2020)  8 - p. 1391-1400 , 2020
Link: https://doi.org/10.1038/..
 
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5

Characterization of paralogous uncx transcription factor en..:

Nittoli, Valeria ; Fortunato, Antonio Emidio ; Fasano, Giulia...
Gene.  721 (2019)  - p. 100011 , 2019
Link: https://doi.org/10.1016/..
 
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6

Harmonising phenomics information for a better interoperabi..:

Maiella, Sylvie ; Olry, Annie ; Hanauer, Marc...
European Journal of Medical Genetics.  61 (2018)  11 - p. 706-714 , 2018
Link: https://doi.org/10.1016/..
 
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7

Single-cell gene profiling of human regulatory T cell subse..:

Dong, Shen ; Maiella, Sylvie ; Xhaard, Aliénor...
Journal of Translational Medicine.  9 (2011)  S2 - p. , 2011
Link: https://doi.org/10.1186/..
 
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8

In vivo expansion of naive and activated CD4⁺CD25⁺FOXP3⁺ re..:

Weiss, Laurence ; Letimier, Fabrice A. ; Carriere, Matthieu...
Proceedings of the National Academy of Sciences of the United States of America.  107 (2010)  23 - p. 10632-10637 , 2010
Link: https://www.jstor.org/st..
 
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9

In vivo expansion of naive and activated CD4+CD25+FOXP3+reg..:

Weiss, Laurence ; Letimier, Fabrice A. ; Carriere, Matthieu...
Proceedings of the National Academy of Sciences.  107 (2010)  23 - p. 10632-10637 , 2010
Link: https://doi.org/10.1073/..
 
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10

Genetic and epigenetic networks controlling T helper 1 cell..:

Placek, Katarzyna ; Coffre, Maryaline ; Maiella, Sylvie..
Immunology.  127 (2009)  2 - p. 155-162 , 2009
Link: https://doi.org/10.1111/..
 
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11

Natural Variation of Model Mutant Phenotypes in Ciona intes..:

Sordino, Paolo ; Andreakis, Nikos ; Brown, Euan R....
PLoS ONE.  3 (2008)  6 - p. e2344 , 2008
Link: https://doi.org/10.1371/..
 
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12

ORPHAcodes use for the coding of rare diseases: comparison ..:

Mazzucato, Monica ; Pozza, Laura Visonà Dalla ; Facchin, Paola...
https://repository.publisso.de/resource/frl:6472868.  , 2023
Link: https://repository.publi..
 
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13

ORPHAcodes use for the coding of rare diseases: comparison ..:

Mazzucato, Monica ; Pozza, Laura Visonà Dalla ; Facchin, Paola...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476382/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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14

Characterization of paralogous uncx transcription factor en..:

Nittoli, Valeria ; Fortunato, Antonio Emidio ; Fasano, Giulia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543554/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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15

Single-cell gene profiling of human regulatory T cell subse..:

Dong, Shen ; Maiella, Sylvie ; Xhaard, Aliénor...
info:eu-repo/semantics/altIdentifier/doi/10.1186/1479-5876-9-S2-P28.  , 2011
Link: https://inserm.hal.scien..
 
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