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Refinado por: assunto: eng remover Base de dados/Biblioteca: Wiley Online Library remover
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1
A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer
A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer
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A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer

Hesterberg, Amanda B ; Rios, Brenda L ; Wolf, Elysa M ; Tubbs, Colby ; Wong, Hong Yuen ; Schaffer, Kerry R ; Lotan, Tamara L ; Giannico, Giovanna A ; Gordetsky, Jennifer B ; Hurley, Paula J

The Journal of Pathology: Clinical Research, 2021-05, Vol.7 (3), p.271-286 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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2
Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia
Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia
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Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia

Zhao, Yali ; Zhang, Yuan ; Wang, Xiangdong ; Zhang, Luo

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e893-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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3
Band Edge Engineering of Oxide Photoanodes for Photoelectrochemical Water Splitting: Integration of Subsurface Dipoles with Atomic-Scale Control
Band Edge Engineering of Oxide Photoanodes for Photoelectrochemical Water Splitting: Integration of Subsurface Dipoles with Atomic-Scale Control
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Band Edge Engineering of Oxide Photoanodes for Photoelectrochemical Water Splitting: Integration of Subsurface Dipoles with Atomic-Scale Control

Hikita, Yasuyuki ; Nishio, Kazunori ; Seitz, Linsey C. ; Chakthranont, Pongkarn ; Tachikawa, Takashi ; Jaramillo, Thomas F. ; Hwang, Harold Y.

Advanced energy materials, 2016-04, Vol.6 (7), p.np-n/a [Periódico revisado por pares]

Weinheim: Blackwell Publishing Ltd

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4
Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects
Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects
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Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

Machado, Rajiv D. ; Southgate, Laura ; Eichstaedt, Christina A. ; Aldred, Micheala A. ; Austin, Eric D. ; Best, D. Hunter ; Chung, Wendy K. ; Benjamin, Nicola ; Elliott, C. Gregory ; Eyries, Mélanie ; Fischer, Christine ; Gräf, Stefan ; Hinderhofer, Katrin ; Humbert, Marc ; Keiles, Steven B. ; Loyd, James E. ; Morrell, Nicholas W. ; Newman, John H. ; Soubrier, Florent ; Trembath, Richard C. ; Viales, Rebecca Rodríguez ; Grünig, Ekkehard

Human mutation, 2015-12, Vol.36 (12), p.1113-1127 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension
Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension
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Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension

Chen, Yan-Jun ; Yang, Qing-Hui ; Liu, Dong ; Liu, Qian-Qian ; Eyries, Mélanie ; Wen, Liang ; Wu, Wen-Hui ; Jiang, Xin ; Yuan, Ping ; Zhang, Rui ; Soubrier, Florent ; Jing, Zhi-Cheng

European journal of clinical investigation, 2013-10, Vol.43 (10), p.1016-1024 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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6
Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis
Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis
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Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis

McDonald, J ; Damjanovich, K ; Millson, A ; Wooderchak, W ; Chibuk, JM ; Stevenson, DA ; Gedge, F ; Bayrak-Toydemir, P

Clinical genetics, 2011-04, Vol.79 (4), p.335-344 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia
Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia
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Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia

Shoukier, M ; Teske, U ; Weise, A ; Engel, W ; Argyriou, L

Clinical genetics, 2008-04, Vol.73 (4), p.320-330 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers
Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers
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Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers

SABBÀ, C. ; PASCULLI, G. ; LENATO, G. M. ; SUPPRESSA, P. ; LASTELLA, P. ; MEMEO, M. ; DICUONZO, F. ; GUANTI, G.

Journal of thrombosis and haemostasis, 2007-06, Vol.5 (6), p.1149-1157 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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9
Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients
Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients
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Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients

Lesca, Gaëtan ; Burnichon, Nelly ; Raux, Grégory ; Tosi, Mario ; Pinson, Stéphane ; Marion, Marie-Jeanne ; Babin, Emmanuel ; Gilbert-Dussardier, Brigitte ; Rivière, Sophie ; Goizet, Cyril ; Faivre, Laurence ; Plauchu, Henri ; Frébourg, Thierry ; Calender, Alain ; Giraud, Sophie

Human mutation, 2006-06, Vol.27 (6), p.598-598 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1
Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1
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Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1

Fernandez-L, Africa ; Sanz-Rodriguez, Francisco ; Zarrabeitia, Roberto ; Perez-Molino, Alfonso ; Morales, Carmelo ; Restrepo, Carlos M. ; Ramirez, Jose R. ; Coto, Eliecer ; Lenato, Gennaro M. ; Bernabeu, Carmelo ; Botella, Luisa M.

Human mutation, 2006-03, Vol.27 (3), p.295-295 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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