Molecular Biology & Genetics
Listando 16 trabajos del autor/autora 38
Lista de trabajos en el área Molecular Biology & Genetics
Mentions
661
Twitter
6
Wikipedia
417
News
0
Policy
Article
Interspecies Chimerism with Mammalian Pluripotent Stem Cells
Wu, Jun; Platero-Luengo, Aida; Sakurai, Masahiro; Sugawara, Atsushi; Antonia Gil, Maria; Yamauchi, Takayoshi; Suzuki, Keiichiro; Bogliotti, Yanina Soledad; Cuello, Cristina; Valencia, Mariana Morales; Okumura, Daiji; Luo, Jingping; Vilarino, Marcela; Parri
CELL
0092-8674 (2017)
DOI /
10.1016/j.cell.2016.12.036
Green accepted, Bronze, Green published
Mentions
721
Twitter
3
Wikipedia
57
News
0
Policy
Article
In Vivo Target Gene Activation via CRISPR/Cas9-Mediated Trans-epigenetic Modulation
Liao, Hsin-Kai; Hatanaka, Fumiyuki; Araoka, Toshikazu; Reddy, Pradeep; Wu, Min-Zu; Sui, Yinghui; Yamauchi, Takayoshi; Sakurai, Masahiro; O'Keefe, David D.; Nunez-Delicado, Estrella; Guillen, Pedro; Campistol, Josep M.; Wu, Cheng-Jang; Lu, Li-Fan; Rodriguez
CELL
0092-8674 (2017)
DOI /
10.1016/j.cell.2017.10.025
Green accepted, Bronze
Mentions
20
Twitter
4
Wikipedia
31
News
0
Policy
Review
The complete European guidelines on phenylketonuria: diagnosis and treatment
van Wegberg, A. M. J.; Macdonald, A.; Ahring, K.; Belanger-Quintana, A.; Blau, N.; Bosch, A. M.; Burlina, A.; Campistol, J.; Feillet, F.; Gizewska, M.; Huijbregts, S. C.; Kearney, S.; Leuzzi, V.; Maillot, F.; Muntau, A. C.; van Rijn, M.; Trefz, F.; Walter,
ORPHANET JOURNAL OF RARE DISEASES
(2017)
DOI /
10.1186/s13023-017-0685-2
Green published, Green accepted, Gold
Mentions
16
Twitter
0
Wikipedia
16
News
0
Policy
Letter
alpha KLOTHO and sTGF beta R2 treatment counteract the osteoarthritic phenotype developed in a rat model
Martinez-Redondo, Paloma; Guillen-Guillen, Isabel; Davidsohn, Noah; Wang, Chao; Prieto, Javier; Kurita, Masakazu; Hatanaka, Fumiyuki; Zhong, Cuiqing; Hernandez-Benitez, Reyna; Hishida, Tomoaki; Lezaki, Takashi; Sakamoto, Akihisa; Nemeth, Amy N.; Hishida, Y
PROTEIN & CELL
1674-800X (2020)
DOI /
10.1007/s13238-019-00685-7
Gold DOAJ, Green published
Mentions
43
Twitter
0
Wikipedia
14
News
0
Policy
Article
Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction
Suzuki, Keiichiro; Yamamoto, Mako; Hernandez-Benitez, Reyna; Li, Zhe; Wei, Christopher; Devi Soligalla, Rupa; Aizawa, Emi; Hatanaka, Fumiyuki; Kurita, Masakazu; Reddy, Pradeep; Ocampo, Alejandro; Hishida, Tomoaki; Sakurai, Masahiro; Nemeth, Amy N.; Nunez D
CELL RESEARCH
1001-0602 (2019)
DOI /
10.1038/s41422-019-0213-0
Green published, Bronze
Mentions
60
Twitter
0
Wikipedia
1
News
0
Policy
Review
PKU dietary handbook to accompany PKU guidelines
Macdonald, A.; van Wegberg, A. M. J.; Ahring, K.; Beblo, S.; Belanger-Quintana, A.; Burlina, A.; Campistol, J.; Coskun, T.; Feillet, F.; Gizewska, M.; Huijbregts, S. C.; Leuzzi, V.; Maillot, F.; Muntau, A. C.; Rocha, J. C.; Romani, C.; Trefz, F.; van Spron
ORPHANET JOURNAL OF RARE DISEASES
(2020)
DOI /
10.1186/s13023-020-01391-y
Gold other, Green published, Green accepted
Mentions
7
Twitter
0
Wikipedia
0
News
0
Policy
Article
A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis
Coelho, Teresa; Adams, David; Conceicao, Isabel; Waddington-Cruz, Marcia; Schmidt, Hartmut H.; Buades, Juan; Campistol, Josep; Berk, John L.; Polydefkis, Michael; Wang, Jing Jing; Chen, Jihong; Sweetser, Marianne T.; Gollob, Jared; Suhr, Ole B.
ORPHANET JOURNAL OF RARE DISEASES
(2020)
DOI /
10.1186/s13023-020-01399-4
Gold other, Green published
Mentions
16
Twitter
0
Wikipedia
0
News
0
Policy
Article
White matter microstructural damage in early treated phenylketonuric patients
Julieta Gonzalez, Maria; Rebollo Polo, Monica; Ripolles, Pablo; Gassio, Rosa; Ormazabal, Aida; Sierra, Cristina; Colome Roura, Roser; Artuch, Rafael; Campistol, Jaume
ORPHANET JOURNAL OF RARE DISEASES
(2018)
DOI /
10.1186/s13023-018-0912-5
Gold, Green published
Mentions
8
Twitter
0
Wikipedia
0
News
0
Policy
Article
Encephalopathies with intracranial calcification in children: clinical and genetic characterization
Tonduti, Davide; Panteghini, Celeste; Pichiecchio, Anna; Decio, Alice; Carecchio, Miryam; Reale, Chiara; Moroni, Isabella; Nardocci, Nardo; Campistol, Jaume; Garcia-Cazorla, Angela; Perez Duenas, Belen; Chiapparini, Luisa; Garavaglia, Barbara; Orcesi, Simo
ORPHANET JOURNAL OF RARE DISEASES
(2018)
DOI /
10.1186/s13023-018-0854-y
Gold DOAJ, Green published
Mentions
6
Twitter
0
Wikipedia
0
News
0
Policy
Article
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia
Gallego, Diana; Leal, Fatima; Gamez, Alejandra; Castro, Margarita; Navarrete, Rosa; Sanchez-Lijarcio, Obdulia; Vitoria, Isidro; Bueno-Delgado, Maria; Belanger-Quintana, Amaya; Morais, Ana; Pedron-Giner, Consuelo; Garcia, Inmaculada; Campistol, Jaume; Artuc
HUMAN MUTATION
1059-7794 (2020)
DOI /
10.1002/humu.24026
Mentions
4
Twitter
0
Wikipedia
0
News
0
Policy
Article
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countries
Evers, R. A. F.; van Wegberg, A. M. J.; Ahring, K.; Beblo, S.; Belanger-Quintana, A.; Bosch, A. M.; Burlina, A.; Campistol, J.; Coskun, T.; Feillet, F.; Gizewska, M.; Huijbregts, S. C. J.; Kearney, S.; Langeveld, M.; Leuzzi, V; Maillot, F.; Muntau, A. C.;
MOLECULAR GENETICS AND METABOLISM
1096-7192 (2021)
DOI /
10.1016/j.ymgme.2021.01.013
Gold other, Green accepted
Mentions
9
Twitter
0
Wikipedia
0
News
0
Policy
Article
Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients
Tenorio, Jair; Alarcon, Pablo; Arias, Pedro; Dapia, Irene; Garcia-Minaur, Sixto; Bralo, Maria Palomares; Campistol, Jaume; Climent, Salvador; Valenzuela, Irene; Ramos, Sergio; Monseny, Antonio Martinez; Grondona, Fermina Lopez; Botet, Javier; Serrano, Merc
EUROPEAN JOURNAL OF HUMAN GENETICS
1018-4813 (2020)
DOI /
10.1038/s41431-019-0485-3
Mentions
3
Twitter
0
Wikipedia
0
News
0
Policy
Article
Nephroprotective Potential of Mesenchymal Stromal Cells and Their Extracellular Vesicles in a Murine Model of Chronic Cyclosporine Nephrotoxicity
Ramirez-Bajo, Maria Jose; Martin-Ramirez, Javier; Bruno, Stefania; Pasquino, Chiara; Banon-Maneus, Elisenda; Rovira, Jordi; Moya-Rull, Daniel; Lazo-Rodriguez, Marta; Campistol, Josep M.; Camussi, Giovanni; Diekmann, Fritz
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
2296-634X (2020)
DOI /
10.3389/fcell.2020.00296
Gold DOAJ, Green published
Mentions
2
Twitter
0
Wikipedia
0
News
0
Policy
Article
MRX93 syndrome (BRWD3 gene): five new patients with novel mutations
Tenorio, Jair; Alarcon, Pablo; Arias, Pedro; Ramos, Feliciano J.; Campistol, Jaume; Climent, Salvador; Garcia-Minaur, Sixto; Dapia, Irene; Hernandez, Alicia; Nevado, Julian; Solis, Mario; Ruiz-Perez, Victor L.; Lapunzina, Pablo
CLINICAL GENETICS
0009-9163 (2019)
DOI /
10.1111/cge.13504
Mentions
2
Twitter
0
Wikipedia
0
News
0
Policy
Article
Mutations in foregut SOX2(+) cells induce efficient proliferation via CXCR2 pathway
Hishida, Tomoaki; Vazquez-Ferrer, Eric; Hishida-Nozaki, Yuriko; Sancho-Martinez, Ignacio; Takahashi, Yuta; Hatanaka, Fumiyuki; Wu, Jun; Ocampo, Alejandro; Reddy, Pradeep; Wu, Min-Zu; Gerken, Laurie; Shaw, Reuben J.; Rodriguez Esteban, Concepcion; Benner, C
PROTEIN & CELL
1674-800X (2019)
DOI /
10.1007/s13238-019-0630-3
Gold DOAJ, Green published
Mentions
4
Twitter
0
Wikipedia
0
News
0
Policy
Article
Impact of Mesenchymal Stromal Cells and Their Extracellular Vesicles in a Rat Model of Kidney Rejection
Jose Ramirez-Bajo, Maria; Rovira, Jordi; Lazo-Rodriguez, Marta; Banon-Maneus, Elisenda; Tubita, Valeria; Moya-Rull, Daniel; Hierro-Garcia, Natalia; Ventura-Aguiar, Pedro; Oppenheimer, Federico; Campistol, Josep M.; Diekmann, Fritz
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
2296-634X (2020)
DOI /
10.3389/fcell.2020.00010
Gold DOAJ, Green published
