An extended set of yeast-based functional assays accurately identifies human disease mutations

Por Sun, Song, Yang, Fan, Tan, Guihong, Costanzo, Michael, Oughtred, Rose, Hirschman, Jodi, Theesfeld, Chandra L., Bansal, Pritpal, Sahni, Nidhi, Yi, Song, Yu, Analyn, Tyagi, Tanya, Tie, Cathy, Hill, David E., Vidal, Marc, Andrews, Brenda J., Boone, Charles, Dolinski, Kara, Roth, Frederick P.
Publicado no Genome Res (2016)

Stroke mimic diagnoses presenting to a hyperacute stroke unit

Por Dawson, Ang, Cloud, Geoffrey C, Pereira, Anthony C, Moynihan, Barry J
Publicado no Clin Med (Lond) (2016)

HSV-NIS, an oncolytic herpes simplex virus type 1 encoding human sodium iodide symporter for preclinical prostate cancer radiovirotherapy

Por Li, H, Nakashima, H, Decklever, T D, Nace, R A, Russell, S J
Publicado em 2013

Sodium 3D COncentration MApping (COMA 3D) Using (23)Na and Proton MRI

Por Truong, Milton L., Harrington, Michael G., Schepkin, Victor D., Chekmenev, Eduard Y.
Publicado em 2014

Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis

Por Caminsky, Natasha, Mucaki, Eliseos J., Rogan, Peter K.
Publicado no F1000Res (2014)

Validation of Algorithm to Identify Persons with Non-traumatic Spinal Cord Dysfunction in Canada Using Administrative Health Data

Por Ho, Chester, Guilcher, Sara J.T., McKenzie, Nicole, Mouneimne, Magda, Williams, Anita, Voth, Jennifer, Chen, Yan, Cronin, Shawna, Noonan, Vanessa K., Jaglal, Susan B.
Publicado no Top Spinal Cord Inj Rehabil (2017)

GENCODE: The reference human genome annotation for The ENCODE Project

Por Harrow, Jennifer, Frankish, Adam, Gonzalez, Jose M., Tapanari, Electra, Diekhans, Mark, Kokocinski, Felix, Aken, Bronwen L., Barrell, Daniel, Zadissa, Amonida, Searle, Stephen, Barnes, If, Bignell, Alexandra, Boychenko, Veronika, Hunt, Toby, Kay, Mike, Mukherjee, Gaurab, Rajan, Jeena, Despacio-Reyes, Gloria, Saunders, Gary, Steward, Charles, Harte, Rachel, Lin, Michael, Howald, Cédric, Tanzer, Andrea, Derrien, Thomas, Chrast, Jacqueline, Walters, Nathalie, Balasubramanian, Suganthi, Pei, Baikang, Tress, Michael, Rodriguez, Jose Manuel, Ezkurdia, Iakes, van Baren, Jeltje, Brent, Michael, Haussler, David, Kellis, Manolis, Valencia, Alfonso, Reymond, Alexandre, Gerstein, Mark, Guigó, Roderic, Hubbard, Tim J.
Publicado em 2012

MFCompress: a compression tool for FASTA and multi-FASTA data

Por Pinho, Armando J., Pratas, Diogo
Publicado em 2014

In silico identification of novel selenoproteins in the Drosophila melanogaster genome

Por Castellano, Sergi, Morozova, Nadya, Morey, Marta, Berry, Marla J., Serras, Florenci, Corominas, Montserrat, Guigó, Roderic
Publicado em 2001

A Pan-Cancer Analysis of Enhancer Expression in Nearly 9000 Patient Samples

Por Chen, Han, Li, Chunyan, Peng, Xinxin, Zhou, Zhicheng, Weinstein, John N., Liang, Han
Publicado no Cell (2018)

Efficient Inference of Recent and Ancestral Recombination within Bacterial Populations

Por Mostowy, Rafal, Croucher, Nicholas J., Andam, Cheryl P., Corander, Jukka, Hanage, William P., Marttinen, Pekka
Publicado no Mol Biol Evol (2017)

Detection of Genetic Markers Related to High Pathogenicity in Influenza by SERS

Por Negri, Pierre, Dluhy, Richard A.
Publicado em 2013

NORMALIZATION OF TRANSPOSON-MUTANT LIBRARY SEQUENCING DATASETS TO IMPROVE IDENTIFICATION OF CONDITIONALLY ESSENTIAL GENES

Por DeJesus, Michael A., Ioerger, Thomas R.
Publicado no J Bioinform Comput Biol (2016)

Functional analysis of synonymous substitutions predicted to affect splicing of the CFTR gene

Por Scott, Alexandra, Petrykowska, Hanna M., Hefferon, Timothy, Gotea, Valer, Elnitski, Laura
Publicado em 2012

A mesh-based model of liver vasculature: implications for improved radiation dosimetry to liver parenchyma for radiopharmaceuticals

Por Camilo M. Correa-Alfonso, Julia D. Withrow, Sean J. Domal, Shu Xing, Jungwook Shin, Clemens Grassberger, Harald Paganetti, Wesley E. Bolch
Publicado em 2022-04-01

False Positive Marks on Unsuspicious Screening Mammography with Computer-Aided Detection

Por Mahoney, Mary C., Meganathan, Karthikeyan
Publicado em 2011

Machine Learning Model to Predict Osteoporotic Spine with Hounsfield Units on Lumbar Computed Tomography

Por Nam, Kyoung Hyup, Seo, Il, Kim, Dong Hwan, Lee, Jae Il, Choi, Byung Kwan, Han, In Ho
Publicado no J Korean Neurosurg Soc (2019)

An Integrated Platform for Genome-wide Mapping of Chromatin States Using High-throughput ChIP-sequencing in Tumor Tissues

Por Terranova, Christopher, Tang, Ming, Orouji, Elias, Maitituoheti, Mayinuer, Raman, Ayush, Amin, Samirkumar, Liu, Zhiyi, Rai, Kunal
Publicado no J Vis Exp (2018)

High-Throughput Sequencing of Arabidopsis microRNAs: Evidence for Frequent Birth and Death of MIRNA Genes

Por Fahlgren, Noah, Howell, Miya D., Kasschau, Kristin D., Chapman, Elisabeth J., Sullivan, Christopher M., Cumbie, Jason S., Givan, Scott A., Law, Theresa F., Grant, Sarah R., Dangl, Jeffery L., Carrington, James C.
Publicado em 2007

The Use of Resveratrol as an Adjuvant Treatment of Pain in Endometriosis: A Randomized Clinical Trial

Por Mendes da Silva, Daniel, Gross, Luiza Azevedo, Neto, Ernesto de Paula Guedes, Lessey, Bruce A., Savaris, Ricardo Francalacci
Publicado no J Endocr Soc (2017)