Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Niels Wacher Rodarte"'
Autor:
Odessica Hughes, Amy R. Bentley, Charles E. Breeze, Francois Aguet, Xiaoguang Xu, Girish Nadkarni, Quan Sun, Bridget M. Lin, Thomas Gilliland, Mariah C. Meyer, Jiawen Du, Laura M. Raffield, Holly Kramer, Robert W. Morton, Mateus H. Gouveia, Elizabeth G. Atkinson, Adan Valladares-Salgado, Niels Wacher-Rodarte, Nicole D. Dueker, Xiuqing Guo, Yang Hai, Adebowale Adeyemo, Lyle G. Best, Jianwen Cai, Guanjie Chen, Michael Chong, Ayo Doumatey, James Eales, Mark O. Goodarzi, Eli Ipp, Marguerite Ryan Irvin, Minzhi Jiang, Alana C. Jones, Charles Kooperberg, Jose E. Krieger, Ethan M. Lange, Matthew B. Lanktree, James P. Lash, Paulo A. Lotufo, Ruth J.F. Loos, Vy Thi Ha My, Jesús Peralta-Romero, Lihong Qi, Leslie J. Raffel, Stephen S. Rich, Erik J. Rodriquez, Eduardo Tarazona-Santos, Kent D. Taylor, Jason G. Umans, Jia Wen, Bessie A. Young, Zhi Yu, Ying Zhang, Yii-Der Ida Chen, Tanja Rundek, Jerome I. Rotter, Miguel Cruz, Myriam Fornage, Maria Fernanda Lima-Costa, Alexandre C. Pereira, Guillaume Paré, Pradeep Natarajan, Shelley A. Cole, April P. Carson, Leslie A. Lange, Yun Li, Eliseo J. Perez-Stable, Ron Do, Fadi J. Charchar, Maciej Tomaszewski, Josyf C. Mychaleckyj, Charles Rotimi, Andrew P. Morris, Nora Franceschini
Publikováno v:
Cell Genomics, Vol 4, Iss 1, Pp 100468- (2024)
Summary: Chronic kidney disease is a leading cause of death and disability globally and impacts individuals of African ancestry (AFR) or with ancestry in the Americas (AMS) who are under-represented in genome-wide association studies (GWASs) of kidne
Externí odkaz:
https://doaj.org/article/975974e930614de28f7b1b95b70b9859
Autor:
Miguel Vázquez-Moreno, Daniel Locia-Morales, Adan Valladares-Salgado, Tanmay Sharma, Aleyda Perez-Herrera, Roxana Gonzalez-Dzib, Francisco Rodríguez-Ruíz, Niels Wacher-Rodarte, Miguel Cruz, David Meyre
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract We investigated the association between the loss-of-function mutation MC4R p.Ile269Asn and T2D risk in the Mexican population. We enrolled 6929 adults [3175 T2D cases and 3754 normal glucose tolerant (NGT) controls] and 994 NGT children in t
Externí odkaz:
https://doaj.org/article/1876f4c9831d41798d9cb65071b717a1
Autor:
Keiko Taniguchi-Ponciano, Eduardo Vadillo, Héctor Mayani, César Raúl Gonzalez-Bonilla, Javier Torres, Abraham Majluf, Guillermo Flores-Padilla, Niels Wacher-Rodarte, Juan Carlos Galan, Eduardo Ferat-Osorio, Francisco Blanco-Favela, Constantino Lopez-Macias, Aldo Ferreira-Hermosillo, Claudia Ramirez-Renteria, Eduardo Peña-Martínez, Gloria Silva-Román, Sandra Vela-Patiño, Carlos Mata-Lozano, Roberto Carvente-Garcia, Lourdes Basurto-Acevedo, Renata Saucedo, Patricia Piña-Sanchez, Antonieta Chavez-Gonzalez, Daniel Marrero-Rodríguez, Moisés Mercado
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 197-207 (2021)
AbstractBackground COVID-19 counts 46 million people infected and killed more than 1.2 million. Hypoxaemia is one of the main clinical manifestations, especially in severe cases. HIF1α is a master transcription factor involved in the cellular respon
Externí odkaz:
https://doaj.org/article/d7d5cbc7ec954c4fbfb9590414a7248c
Autor:
Andrew P. Morris, Thu H. Le, Haojia Wu, Artur Akbarov, Peter J. van der Most, Gibran Hemani, George Davey Smith, Anubha Mahajan, Kyle J. Gaulton, Girish N. Nadkarni, Adan Valladares-Salgado, Niels Wacher-Rodarte, Josyf C. Mychaleckyj, Nicole D. Dueker, Xiuqing Guo, Yang Hai, Jeffrey Haessler, Yoichiro Kamatani, Adrienne M. Stilp, Gu Zhu, James P. Cook, Johan Ärnlöv, Susan H. Blanton, Martin H. de Borst, Erwin P. Bottinger, Thomas A. Buchanan, Sylvia Cechova, Fadi J. Charchar, Pei-Lun Chu, Jeffrey Damman, James Eales, Ali G. Gharavi, Vilmantas Giedraitis, Andrew C. Heath, Eli Ipp, Krzysztof Kiryluk, Holly J. Kramer, Michiaki Kubo, Anders Larsson, Cecilia M. Lindgren, Yingchang Lu, Pamela A. F. Madden, Grant W. Montgomery, George J. Papanicolaou, Leslie J. Raffel, Ralph L. Sacco, Elena Sanchez, Holger Stark, Johan Sundstrom, Kent D. Taylor, Anny H. Xiang, Aleksandra Zivkovic, Lars Lind, Erik Ingelsson, Nicholas G. Martin, John B. Whitfield, Jianwen Cai, Cathy C. Laurie, Yukinori Okada, Koichi Matsuda, Charles Kooperberg, Yii-Der Ida Chen, Tatjana Rundek, Stephen S. Rich, Ruth J. F. Loos, Esteban J. Parra, Miguel Cruz, Jerome I. Rotter, Harold Snieder, Maciej Tomaszewski, Benjamin D. Humphreys, Nora Franceschini
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Estimated glomerular filtration rate (eGFR) is a measure of kidney function used to define chronic kidney disease. Here, Morris et al. perform trans-ethnic genome-wide meta-analyses for eGFR in 312,468 individuals and identify novel loci and downstre
Externí odkaz:
https://doaj.org/article/b8a9cf68600449b683542f422dc012d2
Autor:
Luis Antonio Moreno-Ruiz, Luis Chávez-Sánchez, Wendy Vazquez-González, Alejandra Madrid-Miller, Noe Zamorano-Velázquez, Enrique Martinez-Flores, Niels Wacher-Rodarte, Antonio González-Hermosillo, Francisco Blanco-Favela
Publikováno v:
Archives of medical research. 53(7)
Activation of the renin-angiotensin-aldosterone axis with elevation of inflammatory markers and the resulting fibrosis play a very important role in atrial remodeling in patients with atrial fibrillation (AF), which is associated with post-cardiovers
Autor:
Eduardo Ferat-Osorio, Eduardo Peña-Martínez, Niels Wacher-Rodarte, Carlos Mata-Lozano, Constantino López-Macías, César González-Bonilla, Javier Torres, Moisés Mercado, Abraham Majluf, Aldo Ferreira-Hermosillo, Eduardo Vadillo, Guillermo Flores-Padilla, Patricia Piña-Sánchez, Lourdes Basurto-Acevedo, Daniel Marrero-Rodríguez, Keiko Taniguchi-Ponciano, Antonieta Chávez-González, Gloria Silva-Román, Roberto Carvente-Garcia, Renata Saucedo, Francisco Blanco-Favela, Hector Mayani, Claudia Ramírez-Rentería, Sandra Vela-Patiño, Juan Carlos Galan
Publikováno v:
Annals of Medicine
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Background COVID-19 counts 46 million people infected and killed more than 1.2 million. Hypoxaemia is one of the main clinical manifestations, especially in severe cases. HIF1α is a master transcription factor involved in the cellular response to ox
Autor:
Salomón Waizel-Haiat, Tania Colin-Martínez, José Luis Martínez-Ordaz, Guadalupe Vargas-Ortega, Alfredo Anaya‐Dyck, Baldomero González-Virla, Eduardo Ferat-Osorio, Mayra Alejandra López-Moreno, Niels Wacher Rodarte, Carlos Alfonso Romero-Gameros, Eulalio Vivar-Acevedo, Victoria Mendoza-Zubieta
Publikováno v:
Laryngoscope Investigative Otolaryngology
Objectives At the end of 2019, SARS‐CoV‐2 was identified, the one responsible for the COVID‐19 disease. Between a 5.1% and a 98% of COVID‐19 patients present some form of alteration in their sense of smell. The objective of this study is to d
Autor:
Miguel Cruz, Fernando Suarez-Sanchez, Adriana L. Valdez-González, Niels Wacher-Rodarte, Daniel Locia-Morales, Eugenia Flores-Alfaro, Perla Corona-Salazar, Rita A. Gómez-Díaz, Aleyda Pérez-Herrera, Adan Valladares-Salgado, Miguel Vázquez-Moreno, Jaime Gomez-Zamudio, Roxana Gonzalez-Dzib, David Meyre
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:e2501-e2510
Context Little is known about the association between haptoglobin level and cardiometabolic traits. A previous genome-wide association study identified rs2000999 in the HP gene as the stronger genetic contributor to serum haptoglobin level in Europea
Autor:
Miguel Cruz, David Meyre, Jesús Peralta-Romero, Hamza Asif, Miguel Vázquez-Moreno, Niels Wacher-Rodarte, Gloria Patricia Sosa-Bustamante, Vivian W.Y. Tam, Helen Zeng, Daniel Locia-Morales, Arjuna Maharaj, Socorro Méndez-Martínez, María del Socorro Romero-Figueroa, Adan Valladares-Salgado, Aurora Mejía-Benítez
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:e1468-e1477
Context Rare partial/complete loss-of-function mutations in the melanocortin-4 receptor (MC4R) gene are the most common cause of Mendelian obesity in European populations, but their contribution to obesity in the Mexican population is unclear. Object
Autor:
Daniel Locia-Morales, Francisco Rodríguez-Ruíz, Aleyda Pérez-Herrera, Niels Wacher-Rodarte, Adan Valladares-Salgado, Roxana Gonzalez-Dzib, Miguel Vázquez-Moreno, David Meyre, Miguel Cruz, Tanmay Sharma
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Scientific Reports
Scientific Reports
We investigated the association between the loss-of-function mutation MC4R p.Ile269Asn and T2D risk in the Mexican population. We enrolled 6929 adults [3175 T2D cases and 3754 normal glucose tolerant (NGT) controls] and 994 NGT children in the study.