Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Bruno Batista, de Souza"'
Autor:
Sueli Matilde da Silva Costa, Mirta Tomie Ito, Pedro Rodrigues Sousa da Cruz, Bruno Batista De Souza, Vinicius Mandolesi Rios, Victor de Haidar e Bertozzo, Ana Carolina Lima Camargo, Marina Gonçalves Monteiro Viturino, Carolina Lanaro, Dulcinéia Martins de Albuquerque, Amanda Morato do Canto, Sara Teresinha Olalla Saad, Stephanie Ospina-Prieto, Margareth Castro Ozelo, Fernando Ferreira Costa, Mônica Barbosa de Melo
Publikováno v:
Experimental Biology and Medicine, Vol 249 (2024)
HbSC disease, a less severe form of sickle cell disease, affects the retina more frequently and patients have higher rates of proliferative retinopathy that can progress to vision loss. This study aimed to identify differences in the expression of en
Externí odkaz:
https://doaj.org/article/fa1706a357894d4bbcbdf5ba1859ce6d
Autor:
Thiago Adalton Rosa Rodrigues, Bruno Batista de Souza, Victor de Haidar e Bertozzo, Júlia Nicoliello Pereira de Castro, Ana Carolina Lima Camargo, Fernando Ferreira Costa, Rui Barroso Schimiti, Vital Paulino Costa, José Paulo Cabral de Vasconcellos, Mônica Barbosa de Melo
Publikováno v:
Ophthalmic Genetics. 44:246-252
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1eb04a685a0c6230add8b9d140727f9
https://doi.org/10.1080/13816810.2023.2191704
https://doi.org/10.1080/13816810.2023.2191704
Autor:
Fernando Ferreira Costa, Aderson S Araujo, Sara Teresinha Olalla Saad, Igor de Farias Domingos, Mônica Barbosa de Melo, Iscia Lopes-Cendes, Diego Arruda Falcão, Mirta Tomie Ito, Bruno Batista de Souza, Marcos André Cavalcanti Bezerra, Murilo Guimarães Borges, Sueli Matilde da Silva-Costa, Galina Ananina, Gabriela Queila de Carvalho-Siqueira, Marilda Souza Goncalves, Antonio R. Lucena-Araujo
Publikováno v:
Experimental Biology and Medicine. 244:932-939
Although sickle cell anemia results from homozygosity for a single mutation at position 7 of the β-globin chain, the clinical aspects of this condition are very heterogeneous. Complications include leg ulcers, which have a negative impact on patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93b1912fda6f36cfaf30035ea54c3b70
https://doi.org/10.1177/1535370219849592
https://doi.org/10.1177/1535370219849592
Autor:
Mônica Barbosa de Melo, Let ıcia C Baptista, Kleber Yotsumoto Fertrin, Maria Laura Costa, Camilla O. Figueira, Arthur Antolini, Bruno Batista de Souza, Fernando Ferreira Costa
Publikováno v:
Experimental Biology and Medicine. 244:395-403
Environmentally induced changes in placental morphological and molecular phenotypes may provide relevant insight towards pathophysiology of diseases. Sickle cell disease (SCD) is a common inherited hemoglobin disorder characterized by chronic hemolyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f2ebe92f5e17d7fdf4b98a6ca2c5297
https://doi.org/10.1177/1535370219834305
https://doi.org/10.1177/1535370219834305
Autor:
Manoel Vinicius Rocha, Araki, Yuri Carvalho Oiamore, Silva, Thiago Adalton Rosa, Rodrigues, Flavia Fialho, Bajano, Bruno Batista, de Souza, Fernando Ferreira, Costa, Vital Paulino, Costa, Mônica Barbosa, de Melo, José Paulo Cabral, de Vasconcellos
Publikováno v:
Molecular vision. 28
Glaucoma is the world's leading cause of irreversible blindness, with primary open-angle glaucoma (POAG) being the most prevalent subtype. In recent years, there have been advances in knowledge about the genetics involved in POAG, but genetic studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbe4f6d4ece71b5348ffd90b22933c46
https://pubmed.ncbi.nlm.nih.gov/35400990
https://pubmed.ncbi.nlm.nih.gov/35400990
Autor:
Mônica Barbosa de Melo, Letícia C. Baptista, Fernando Ferreira Costa, Fernanda Garanhani Surita, Maria Laura Costa, Bruno Batista de Souza, Cristiane S. Rocha, Iscia Lopes-Cendes
Publikováno v:
Blood cells, moleculesdiseases. 84
Sickle cell disease (SCD) is a group of disorders whose common characteristic is the presence of hemoglobin (Hb) S in erythrocytes. The main consequence of this abnormality is vaso-occlusion, which can affect almost all organs including the placenta.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd950cacfa9a4a6ad5f610759098c0c8
https://pubmed.ncbi.nlm.nih.gov/32562953
https://pubmed.ncbi.nlm.nih.gov/32562953
Autor:
Dulcineia M. Albuquerque, Carolina Lanaro, Fernando Ferreira Costa, Jersey Heitor da Silva Maués, Flávia Peixoto Albuquerque, Ingrid Grazielle Sousa, Bruno Batista de Souza
Publikováno v:
Blood. 138:944-944
Patients with homozygous beta thalassemia and the β⁰β⁰ genotype produce almost only fetal hemoglobin and a small proportion of hemoglobin A2. However, in the bone marrow of these patients there are descriptions of two different subpopulations o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5498e89ffd90f16e55fa4da50fb81cf
https://doi.org/10.1182/blood-2021-153601
https://doi.org/10.1182/blood-2021-153601
Autor:
Flávia Peixoto Albuquerque, Jhs Maués, F. F. Costa, Bruno Batista de Souza, Dulcineia M. Albuquerque, Carolina Lanaro, Ingrid Grazielle Sousa
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S24-(2021)
Pacientes com β-talassemia homozigótica e genótipo β0β0 produzem apenas hemoglobina fetal (HbF) e uma pequena proporção de hemoglobina A2. No entanto, na medula óssea desses pacientes foram descritas duas subpopulações de eritroblastos, uma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a35864aea1783126dbe34d0d61cae5ce
https://doi.org/10.1016/j.htct.2021.10.041
https://doi.org/10.1016/j.htct.2021.10.041
Autor:
Bruno Batista de Souza
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientador: Mônica Barbosa de Melo Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia Resumo: O glaucoma é a principal causa de cegueira irreversível no mundo, acometendo cerca de 70 milhões de indivíduos, com pelo menos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e436d371067310448ec6c0ade3510f
Autor:
Tina T. Wong, Yaan Fun Chong, Kathryn P. Burdon, Sancy Low, Ningli Wang, Tuan Anh Tran, Emma Rusmayani, Alexander C Day, Kei Tashiro, Tam Thi Luu, Aye Thi Han, Christine A. Kiire, Nay Lin Oo, Hiroshi Sakai, Ewa Kosior-Jarecka, Sripriya Sarangapani, Mimiwati Zahari, Widya Artini Wiyogo, Seng-Chee Loon, Rigo Daniel Reyes, Rrima Dada, Robert Ritch, E-Shyong Tai, Jin-Xin Bei, Ren-Yi Wu, Balekudaru Shantha, Leyla Al-Jasim, Giulia Consolandi, Ya Xing Wang, Saleh A. Al-Obeidan, Tomasz Zarnowski, Shazia Micheal, Maria Luisa Guevara-Fujita, Raquel Quino, Yuzhen Jiang, Monisha E. Nongpiur, Yik Y. Teo, Francesca Pasutto, Hailin Meng, Mani Baskaran, Shigeru Kinoshita, Sunee Chansangpetch, Clement C Y Tham, Eranga N. Vithana, Paul J. Foster, Greet J. Boland, Deepak P. Edward, Young Hoon Hwang, Daniel H. Su, Ricardo Fujita, Huan Nguyen Pham, Yong Ho Sohn, Mark Seielstad, Rengaraj Venkatesh, Paul Mitchell, Morio Ueno, Chaw Chaw Khaing, Thanh Thu Nguyen, Celso Tello, Anita S. Chan, Muhammad Imran Khan, Vernon Yong, Eileen Png, Takanori Mizoguchi, Nguyen Van Vinh Chau, Soo Hong Chew, Laura Dallorto, Chunyan Qiao, Donald T.H. Tan, Norlina Ramli, Mei Chin Lee, Rahat Husain, Kar Seng Sim, Sarah J. Dunstan, Kyu Hyung Park, Stephen A Vernon, Thi Nguyen, Rodolfo A. Perez-Grossmann, Jelinar Mohamed-Noor, Jeeyun Ahn, David Lozano-Giral, Tan Do, Yin Mon Aung, Prin Rojanapongpun, Naris Kitnarong, Martin L. Hibberd, Chan-Yun Kim, Mineo Ozaki, Manchima Makornwattana, Ronnie George, José Paulo Cabral de Vasconcellos, Huong T T Bui, Chona S Liao, Saw Htoo Set, Chi Pui Pang, Paul T K Chew, Aliza Jap, Naushin Waseem, Toshiaki Kubota, Tanuj Dada, Hyoung Won Bae, Tin Aung, Ricardo Y. Abe, Khin Thida Oo, Periasamy Sundaresan, Jose Maria Martinez, Visanee Tantisevi, Shomi S. Bhattacharya, Anneke I. den Hollander, Vira Wardhana Istiantoro, Rohit Shetty, Boonsong Wanichwecharungruang, Liang Xu, Seng Kheong Fang, Masakazu Nakano, E. Randy Craven, Richard P. Ebstein, Ching-Lin Ho, Arkasubhra Ghosh, Jeanne J. Ogle, Hongyan Jia, Muneeb A. Faiq, Yasuo Kurimoto, Michiko Yonahara, Richard Stead, Li Jia Chen, Satoko Nakano, Anavaj Sakuntabhai, Masako Kuroda, Thayanithi Sandragasu, Leonard W. Yip, Lerprat Mangkornkanokpong, Pancy O. S. Tam, Seang-Mei Saw, Ching-Yu Cheng, Saravanan Vijayan, Jia Nee Foo, M B Melo, Wing Lau Ho, Ahmad Tajudin Liza-Sharmini, Alex W. Hewitt, Mary Ann T Catacutan, Carlo Lavia, Curt Hartleben-Matkin, Hon-Tym Wong, Daniela Paoli, Srinivasan Kavitha, Su Nyunt Zaw, Soon Thye Lim, Owen Hee, Yee Yee Aung, Shuang Ru Goh, Chiea Chuen Khor, Maria Cecilia Aquino, Jonathan C.H. Chan, Buddha Basnyat, Zeiras Eka Djamal, Nhu Hon Do, Tuyet Bach Trinh, John H. Fingert, Z. Xie, Thi Lam Huong Dao, Urszula Lukasik, Bruno Batista de Souza, Khaled K. Abu-Amero, Yoko Ikeda, Guillermo Barreto Fong, Eng Hui Gan, Guangxian Tang, Sami Al-Shahwan, Tien Dat Tran, Jost B. Jonas, Xiao Yin Chen, Nagaswamy Soumittra, David Goh, Ramanjit Sihota, Xiao-Yu Ng, Ki Ho Park, Mona S Awadalla, Sujie Fan, Edgar U Leuenberger, Hlaing May Than, Jimmy S. M. Lai, Yi Xin Zeng, Shamira A. Perera, Bonnie Nga Kwan Choy, Jie Jin Wang, Roopam Duvesh, Antonio Maria Fea, Anita Manassakorn, Victor H. K. Yong, Abhilasha Karkey, John F Salmon, Kessara Pathanapitoon, Raheel Qamar, Juan Carlos Zenteno, Jin Wook Jeoung, Jovell Ian M Peregrino, Harm Snippe, Yaakub Azhany, Humaira Ayub, Vania Castro Tamanaja, Paolo Frezzotti, Tung S Hoan, Rajesh S. Kumar, Chelvin C A Sng, Jamie E Craig, Anuwat Prutthipongsit, Vital Paulino Costa, Subbiah. R. Krishnadas, Kuldeep Mohanty, Michael A. Hauser, Vi Huyen Doan, Irene R Felarca, Lingam Vijaya, Jennifer W. H. Shum, Farah Akhtar, R. Rand Allingham, Nuttamon Srisamran, Desmond Quek, Huaizhou Wang, Thipnapa Patthanathamrongkasem, Giulia Pignata, Suman S Thapa, Kazuhiko Mori, Jamil Miguel Neto, Tien Yin Wong, Boon-Ang Lim, Zheng Li
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2016, 48 (5), pp.556-562. ⟨10.1038/ng.3540⟩
Nature Genetics, 2016, 48 (5), pp.556-562. ⟨10.1038/ng.3540⟩
Nature Genetics, Nature Publishing Group, 2016, 48 (5), pp.556-562. ⟨10.1038/ng.3540⟩
Nature Genetics, 2016, 48 (5), pp.556-562. ⟨10.1038/ng.3540⟩
International audience; Primary angle closure glaucoma (PACG) is a major cause of blindness worldwide. We conducted a genome-wide association study (GWAS) followed by replication in a combined total of 10,503 PACG cases and 29,567 controls drawn from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0185d28484b54cebde1cf79b10107d89
https://hal-pasteur.archives-ouvertes.fr/pasteur-02083054
https://hal-pasteur.archives-ouvertes.fr/pasteur-02083054