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Refinado por: Biblioteca: FM - Fac. Medicina remover
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1
Latency-associated DNA methylation patterns among HIV-1 infected individuals with distinct disease progression courses or antiretroviral virologic response
Latency-associated DNA methylation patterns among HIV-1 infected individuals with distinct disease progression courses or antiretroviral virologic response
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Latency-associated DNA methylation patterns among HIV-1 infected individuals with distinct disease progression courses or antiretroviral virologic response

Nathalia Mantovani Alexandre Defelicibus; Israel Tojal da Silva; Maira Ferreira Cicero; Luiz Claudio Santana; Rafael Arnold; Daniela Funayama de Castro; Rodrigo Lopes Sanz Duro; Milton Yutaka Nishiyama-jr; Inacio Loiola Meirelles Junqueira-de-azevedo; Alberto José da Silva Duarte; Jorge Simão do Rosário Casseb

Scientific reports v. 11, n. 1, article ID 22993, 15p, 2021

Berlin 2021

Acesso online. A biblioteca também possui exemplares impressos.

2
NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia
NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia
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NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia

Carolina Hassibe Thomé Germano Aguiar Ferreira; Diego Antonio Pereira Martins; Guilherme Augusto dos Santos; César Alexander Ortiz; Lucas Eduardo Botelho de Souza; Lays Martins Sobral; Cleide Lúcia Araújo Silva; Priscila Santos Scheucher; Cristiane Damas Gil; Andréia Machado Leopoldino; Douglas Rafaele Almeida Silveira; Juan Luiz Coelho da Silva; Fabiola Traina; Luisa C Koury; Raul A. M Melo; Rosane Bittencourt; Katia Pagnano; Ricardo Pasquini; Elenaide C Nunes; Evandro M Fagundes; Ana Beatriz F Gloria; Fábio Rodrigues kerbauy; Maria de Lourdes Chauffaille; Armand Keating; Martin S Tallman; Raul C Ribeiro; Richard Dillon; Arnold Ganser; Bob Löwenberg; Peter Valk; Francesco Lo-Coco; Miguel A Sanz; Nancy Berliner; Vitor Marcel Faça; Eduardo Magalhaes Rego

Scientific Reports London v. 10, n. 1, art. 10315, 2020

London 2020

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 3032993 Acervo Digital ) e outros locais(Acessar)

3
Sex differences in the genetic architecture of obsessive-compulsive disorder
Sex differences in the genetic architecture of obsessive-compulsive disorder
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Sex differences in the genetic architecture of obsessive-compulsive disorder

Ekaterina A. Khramtsova Raphael Heldman; Eske M Derks; Dongmei Yu; Lea K Davis; Barbara E Stranger; Paul D Arnold; Helena Paula Brentani; Eurípedes Constantino Miguel Filho; Homero Pinto Vallada Filho

American journal of medical genetics part b-neuropsychiatric genetics v. 180, n. 6, Special Issue, p. 351-364, 2019

Hoboken 2019

Acesso online. A biblioteca também possui exemplares impressos.

4
The increasing burden of cancer attributable to high body mass index in Brazil
The increasing burden of cancer attributable to high body mass index in Brazil
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The increasing burden of cancer attributable to high body mass index in Brazil

Leandro Fornias Machado de Rezende Jose Eluf-neto; Melina Arnold; Fabiana Maluf Rabacow; Renata Bertazzi Levy; Rafael Moreira Claro; Edward GIOVANNUCCI

Cancer epidemiology v. 54, p. 63-70, 2018

Oxford 2018

Localização: FM - Fac. Medicina    (OPI/27028 2018 )(Acessar)

5
Time course of safety and efficacy of aflibercept in combination with FOLFIRI in patients with metastatic colorectal cancer who progressed on previous oxaliplatin-based therapy
Time course of safety and efficacy of aflibercept in combination with FOLFIRI in patients with metastatic colorectal cancer who progressed on previous oxaliplatin-based therapy
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Time course of safety and efficacy of aflibercept in combination with FOLFIRI in patients with metastatic colorectal cancer who progressed on previous oxaliplatin-based therapy

Paul Ruff David R Ferry; Radek Lakomỳ; Gael McWalter; Guy A Van Hazel; Paulo M Hoff; David Cunningham; Dirk Arnold; Hans J Schmoll; Vladimir M Moiseyenko; Joseph J McKendrick; Albert J ten Tije; Raghu L Vishwanath; Pankaj Bhargava; Soazig Chevalier; Teresa Macarulla; Eric Van Cutsem

European Journal of Cancer Oxford v. 51, n. 1, p. 18-26, 2015

Oxford 2015

Localização: FM - Fac. Medicina    (BCSEP 043 2015 )(Acessar)

6
COMT and MAO-A Polymorphisms and Obsessive-Compulsive Disorder: A Family-Based Association Study
COMT and MAO-A Polymorphisms and Obsessive-Compulsive Disorder: A Family-Based Association Study
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COMT and MAO-A Polymorphisms and Obsessive-Compulsive Disorder: A Family-Based Association Study

Aline Santos Sampaio Ana Gabriela Hounie; Kátia Petribú; Carolina Cappi; Ivanil Morais; Homero Vallada; Maria Conceição do Rosário; S. Evelyn Stewart; Jesen Fargeness; Carol Mathews; Paul Arnold; Gregory L Hanna; Margaret Richter; James Kennedy; Leonardo Fontenelle; Carlos Alberto de Bragança Pereira 1946-; David L Pauls; Eurípedes Constantino Miguel

PloS ONE San Francisco v. 10, n. 3, 14 p., art. e0119592, Feb., 2015

San Francisco 2015

Acesso online. A biblioteca também possui exemplares impressos.

7
Primary age-related tauopathy (PART) a common pathology associated with human aging
Primary age-related tauopathy (PART) a common pathology associated with human aging
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Primary age-related tauopathy (PART) a common pathology associated with human aging

John F. Crary John Q Trojanowski; Julie A Schneider; Jose F Abisambra; Erin L Abner; Irina Alafuzoff; Steven E Arnold; Johannes Attems; Thomas G Beach; Eileen H Bigio; Nigel J Cairns; Dennis W Dickson; Marla Gearing; Lea T Grinberg; Patrick R Hof; Bradley T Hyman; Kurt Jellinger; Gregory A Jicha; Gabor G Kovacs; David S Knopman; Julia Kofler; Walter A Kukull; Ian R Mackenzie; Eliezer Masliah; Ann McKee; Thomas J Montine; Melissa E Murray; Janna H Neltner; Ismael Santa-Maria; William W Seeley; Alberto Serrano-Pozo; Michael L Shelanski; Thor Stein; Masaki Takao; Dietmar R Thal; Jonathan B Toledo; Juan C Troncoso; Jean Paul Vonsattel; Charles L White; Thomas Wisniewski; Randall L Woltjer; Masahito Yamada; Peter T Nelson

Acta Neuropathologica Berlin v. 128, n. 6, p. 755-766, 2014

Berlin 2014

Localização: FM - Fac. Medicina    (BCSEP 090 2014 )(Acessar)

8
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Material Type:
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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Lea K. Davis Dongomei Yu; Clare L Keenan; Eric R Gamazon; Anuar I Konkashbaev; Eske M Derks; Benjamin M Neale; Jian Yang; S. Hong Lee; Patrick Evans; Cathy L Barr; Laura Bellodi; Fortu Benarroch; Gabriel Bedova Berrio; Oscar J Bienvenu; Michael H Bloch; Rianne M Blom; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Desmond Campbell; Carolina Cappi; Julio C. Cardona Salgado; Danielle C Cath; Maria C Cavallini; Denise A Chavira; Sylvain Chouinard; David V Conti; Edwin H Cook; Vladimir Coric; Bernadette A Cullen; Dieter Deforce; Richard Delorne; Yves Dion; Christopher K Edlund; Karin Egberts; Peter Falkai; Thomas V Fernandez; Patience J Gallagher; Helena Garrido; Daniel Geller; Simon L Girard; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross Tsur; Stephen Haddad; Gary A Heiman; Sian M. J Hemmings; Ana G Hounie; Cornelia Illmann; Joseph Jankovic; Michael A Jenike; Robert A King; Barbara Kremeyer; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennerts; Chunyu Liu; Christine Lochner; Thomas L Lowe; Fabio Macciardi; James T McCracken; Lauren MacGrant; Sandra C. Mesa Restrepo; Rainald Moessner; Jubel Morgan; Heike Muller; Dennis L Murphy; Allan L Naarden; William Cornejo Ochoa; Roel A Ophoff; Lisa Osieck; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Scott L Rauch; Tobias J Renner; Victor I Reus; Mark A Riddle; Mary M Robertson; Roxana Romero; Maria C Rosàrio; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Andres Ruiz Linares; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; E Strengman; Jay A Tischfield; Ana V. Valencia Duarte; Homero Pinto Vallada Filho; Filip Van Nieuwerburgh; Jeremy Veenstra VanderWeele; Susanne Walitza; Ying Wang; Jens R Wendland; Herman G. M Westenberg; Yin Yao Shugart; Eurípedes Constantino Miguel; William McMahon; Michael Wagner; Humberto Nicolini; Danielle Posthuma; Gregory L Hanna; Peter Heutink; Damiaan Denys; Paul D Arnold; Ben A Oostra; Gerald Nestadt; Nelson B Freimer; David L Pauls; Naomi R Wray; S. Evelyn Stewart; Carol A Mathews; James A Knowles; Nancy J Cox; Jeremiah M Scharf

Plos genetics San Francisco v. 9, n. 10, p. e1003864, 2013

San Francisco 2013

Localização: FM - Fac. Medicina    (BCSEP 483 2013 )(Acessar)

9
Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants
Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants
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Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants

Marian Kroos Marianne Hoogeveen-westerveld; Helen Michelakakis; Robert Pomponio; Ans Van der Ploeg; Dicky Halley; Arnold Reuser; Suely Kazue Nagahashi Marie

Human mutation v. 33, n. 8, p. 1161-1165, 2012

Hoboken 2012

Acesso online. A biblioteca também possui exemplares impressos.

10
Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation
Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation
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Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation

Sorahia Domenice Vinicius N Brito; Priscila Cukier; Ivo J. P Arnold; Mirian Y Nishi; Ana C Latronico; Berenice B Mendonca; ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo 94 2012 Houston, Texas

Endocrine Reviews Chevy Chase v. 33, 03_meetingAbstracts, Res. SUN-622, 2012

Chevy Chase 2012

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Arnold, P
  2. Anderson, W
  3. Cappi, C
  4. Katz, A
  5. Mathews, C

Neste Assunto:

  1. Patologia
  2. Pathology
  3. Transtorno Obsessivo-Compulsivo
  4. Biologia Molecular
  5. Fatores De Risco

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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