Pesquisas alternativas:
present native » present nation (Expandir a Pesquisa), presenting native (Expandir a Pesquisa), preserve native (Expandir a Pesquisa)
absence gene » absence genes (Expandir a Pesquisa), absence genree (Expandir a Pesquisa), absent gene (Expandir a Pesquisa)
genes serve » levels serve (Expandir a Pesquisa)
native cyst » native cystic (Expandir a Pesquisa), negative cyst (Expandir a Pesquisa), native cas9 (Expandir a Pesquisa)
serve cyst » nerve cyst (Expandir a Pesquisa), nerve cystic (Expandir a Pesquisa)
1 absence » _ absence (Expandir a Pesquisa), 2 absence (Expandir a Pesquisa)
gene case » gene cause (Expandir a Pesquisa), gene causes (Expandir a Pesquisa), gene caused (Expandir a Pesquisa)
_ present » _ presence (Expandir a Pesquisa)
cyst dis » cyst d (Expandir a Pesquisa), cyst dna (Expandir a Pesquisa)
case di » case did (Expandir a Pesquisa), case dti (Expandir a Pesquisa), case de (Expandir a Pesquisa)
j genes » j gene (Expandir a Pesquisa), j geddes (Expandir a Pesquisa), j genuis (Expandir a Pesquisa)
present native » present nation (Expandir a Pesquisa), presenting native (Expandir a Pesquisa), preserve native (Expandir a Pesquisa)
absence gene » absence genes (Expandir a Pesquisa), absence genree (Expandir a Pesquisa), absent gene (Expandir a Pesquisa)
genes serve » levels serve (Expandir a Pesquisa)
native cyst » native cystic (Expandir a Pesquisa), negative cyst (Expandir a Pesquisa), native cas9 (Expandir a Pesquisa)
serve cyst » nerve cyst (Expandir a Pesquisa), nerve cystic (Expandir a Pesquisa)
1 absence » _ absence (Expandir a Pesquisa), 2 absence (Expandir a Pesquisa)
gene case » gene cause (Expandir a Pesquisa), gene causes (Expandir a Pesquisa), gene caused (Expandir a Pesquisa)
_ present » _ presence (Expandir a Pesquisa)
cyst dis » cyst d (Expandir a Pesquisa), cyst dna (Expandir a Pesquisa)
case di » case did (Expandir a Pesquisa), case dti (Expandir a Pesquisa), case de (Expandir a Pesquisa)
j genes » j gene (Expandir a Pesquisa), j geddes (Expandir a Pesquisa), j genuis (Expandir a Pesquisa)
1
Por Obal, Gonzalo, Ramos, Ana Lía, Silva, Valeria, Lima, Analía, Batthyany, Carlos, Bessio, María Inés, Ferreira, Fernando, Salinas, Gustavo, Ferreira, Ana María
Publicado em 2012
“... homology with a group of hydrophobic ligand binding proteins (HLBPs) present exclusively in cestode...”Publicado em 2012
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2
Por Zhang, Chao, Balbo, Bruno, Ma, Ming, Zhao, Jun, Tian, Xin, Kluger, Yuval, Somlo, Stefan
Publicado no J Am Soc Nephrol (2021)
“... alone. CONCLUSIONS: Dysregulation of Cdk1 is an early driver of cyst cell proliferation in ADPKD due...”Publicado no J Am Soc Nephrol (2021)
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3
“... and native cattle. The present study was performed during 2011–2012. 2,657 and 525 imported and native cattle...”
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4
Por Di Micco, Pierpaolo, Di Fiore, Rosanna, Niglio, Alferio, Quaranta, Sandro, Angiolillo, Antonella, Cardillo, Giuseppe, Castaldo, Giuseppe
Publicado em 2008
“... strongly heterogeneous clinical outcome. Case 1, a female of 27 years, developed a full thrombosis...”Publicado em 2008
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5
Por Angiolillo Antonella, Quaranta Sandro, Niglio Alferio, Di Fiore Rosanna, Di Micco Pierpaolo, Cardillo Giuseppe, Castaldo Giuseppe
Publicado em 2008-07-01
“... that displayed a strongly heterogeneous clinical outcome. Case 1, a female of 27 years, developed a full...”Publicado em 2008-07-01
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6
Por Papi, Giampaolo, Paragliola, Rosa Maria, Concolino, Paola, Di Donato, Carlo, Pontecorvi, Alfredo, Corsello, Salvatore Maria
Publicado no Case Rep Endocrinol (2018)
Assuntos:
“...Case Report...”Publicado no Case Rep Endocrinol (2018)
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7
Por Alghamdi, Malak, Al Khalifah, Reem, Al Homyani, Doua K, Alkhamis, Waleed H, Arold, Stefan T, Ekhzaimy, Aishah, El-Wetidy, Mohammed, Kashour, Tarek, Halwani, Rabih
Publicado no J Endocr Soc (2019)
“... in development. Haploinsufficiency of the TBX1 gene is reported to cause features similar to DiGeorge syndrome...”Publicado no J Endocr Soc (2019)
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8
Por Magro, Gaetano, Broggi, Giuseppe, Zin, Angelica, Di Benedetto, Vincenzo, Meli, Mariaclaudia, Di Cataldo, Andrea, Alaggio, Rita, Salvatorelli, Lucia
Publicado no Diagnostics (Basel) (2021)
Assuntos:
“...Case Report...”Publicado no Diagnostics (Basel) (2021)
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9
Por Conti, Francesca, Catelli, Arianna, Cifaldi, Cristina, Leonardi, Lucia, Mulè, Rita, Fusconi, Marco, Stefoni, Vittorio, Chiriaco, Maria, Rivalta, Beatrice, Di Cesare, Silvia, Schifino, Gioacchino, Sbrega, Fabiana, Di Matteo, Gigliola, Ferrari, Simona, Cancrini, Caterina, Pession, Andrea
Publicado no Front Pediatr (2021)
“... regulatory disorder caused by heterozygous gain of function mutation in the PIK3R1 gene encoding PI3Kδ...”Publicado no Front Pediatr (2021)
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10
Por Pisani, Antonio, Daniele, Aurora, Di Domenico, Carmela, Nigro, Ersilia, Salvatore, Francesco, Riccio, Eleonora
Publicado no BMC Res Notes (2015)
Assuntos:
“...Case Report...”Publicado no BMC Res Notes (2015)
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11
Por Catanzano, Francesca, Ombrone, Daniela, Di Stefano, Cristina, Rossi, Anna, Nosari, Norberto, Scolamiero, Emanuela, Tandurella, Igor, Frisso, Giulia, Parenti, Giancarlo, Ruoppolo, Margherita, Andria, Generoso, Salvatore, Francesco
Publicado em 2010
Assuntos:
“...Case Report...”Publicado em 2010
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12
Por Li, Peining, Pomianowski, Pawel, DiMaio, Miriam S., Florio, Joanne R., Rossi, Michael R., Xiang, Bixia, Xu, Fang, Yang, Hui, Geng, Qian, Xie, Jiansheng, Mahoney, Maurice J.
Publicado em 2011
“.... An absence of pathogenic copy number changes was noted in one case with a de novo 11q/14q translocation...”Publicado em 2011
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13
Por Mbaye, Aminata, Gaye, Amy, Dieye, Baba, Ndiaye, Yaye D., Bei, Amy K., Affara, Muna, Deme, Awa B., Yade, Mamadou S., Diongue, Khadim, Ndiaye, Ibrahima M., Ndiaye, Tolla, Sy, Mouhamed, Sy, Ngayo, Koita, Ousmane, Krogstad, Donald J., Volkman, Sarah, Nwakanma, Davis, Ndiaye, Daouda
Publicado no Malar J (2017)
“... for genotyping of pfdhps, pfdhfr, pfmdr1, and pfcrt genes. RESULTS: The mean IC(50)s of chloroquine, amodiaquine...”Publicado no Malar J (2017)
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14
Assuntos:
“...Case Report...”
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15
Por Schmid, Sabine, Omlin, Aurelius, Higano, Celestia, Sweeney, Christopher, Martinez Chanza, Nieves, Mehra, Niven, Kuppen, Malou C. P., Beltran, Himisha, Condeduca, Vincenza, Vargas Pivato de Almeida, Daniel, Cotait Maluf, Fernando, Oh, William K., Tsao, Che-Kai, Sartor, Oliver, Ledet, Elisa, Di Lorenzo, Giuseppe, Yip, Steven M., Chi, Kim N., Bianchini, Diletta, De Giorgi, Ugo, Hansen, Aaron R., Beer, Tomasz M., Pernelle, Lavaud, Morales-Barrera, Rafael, Tucci, Marcello, Castro, Elena, Karalis, Kostas, Bergman, Andries M., Le, Mo Linh, Zürrer-Härdi, Ursina, Pezaro, Carmel, Suzuki, Hiroyoshi, Zivi, Andrea, Klingbiel, Dirk, Schär, Sämi, Gillessen, Silke
Publicado no JAMA Netw Open (2020)
“... repair gene aberrations (ie, cohort 1, present; cohort 2, not detected; and cohort 3, not tested). Data...”Publicado no JAMA Netw Open (2020)
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16
Por Cruz-Muñoz, William, Desidero, Teresa Di, Man, Shan, Xu, Ping, Jaramillo, Maria Luz, Hashimoto, Kae, Collins, Catherine, Banville, Myriam, O’Connor-McCourt, Maureen D, Kerbel, Robert S.
Publicado no Angiogenesis (2014)
“..., in the absence of overt toxicity, especially when combined with targeted antiangiogenic drugs. However, similar...”Publicado no Angiogenesis (2014)
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17
“... and pose a substantial health and socioeconomic burden worldwide. They are responsible for at least 1...”
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18
Publicado no Cell Prolif
(2002)
“...) , I. J. Koerner (2) , J. Gerlach (1) and P. Neuhaus (1) (1) Department of Surgery and (2) Department...”Obter o texto integral
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19
Publicado no Mol Cell Proteomics
(2019)
“... including: 1) absence of ERBB2 amplification (false-ERBB2+); 2) insufficient ERBB2 activity for therapeutic...”Obter o texto integral
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20
Publicado no Mol Cell Proteomics
(2017)
“...3 Weimin Ni(1), Shou-Ling Xu(2), Eduardo González-Grandío(1), Robert J. Chalkley(3), Andreas F. R...”Obter o texto integral
Artigo