St. Mary's Hospital, Manchester

Tekijä Foster, Joseph
Julkaistu 1857

Report of the Committee of the American Society of Dental Surgeons, on the Propriety of Rescinding the Amalgam Pledge

Tekijä Townsend, Elisha, Foster, Joseph H.
Julkaisussa Am J Dent Sci (1850)

Photolysis Accompanying Peptide Absorption in Proteins: Electrophoresis and Optical Rotary Dispersion Studies

Tekijä Wilson, W. David, Foster, Joseph F.
Julkaistu 1972

KBG syndrome

Tekijä Morel Swols, Dayna, Foster, Joseph, Tekin, Mustafa
Julkaisussa Orphanet J Rare Dis (2017)

Proteomics data repositories: Providing a safe haven for your data and acting as a springboard for further research

Tekijä Vizcaíno, Juan Antonio, Foster, Joseph M., Martens, Lennart
Julkaistu 2010

RELIABILITY, AVAILABILITY AND MAINTAINABILITY ; THE ASSURANCE TECHNOLOGIES APPLIED TO THE PROCUREMENT OF PRODUCTION SYSTEMS.

Tekijä FOSTER, JOSEPH W, PHILLIPS, DON T, ROGERS, THOMAS R
Julkaistu C1981

PRIDE Cluster: building the consensus of proteomics data

Tekijä Griss, Johannes, Foster, Joseph M., Hermjakob, Henning, Vizcaíno, Juan Antonio
Julkaistu 2013

HHS/CDC Legal Response to SARS Outbreak

Tekijä Misrahi, James J., Foster, Joseph A., Shaw, Frederic E., Cetron, Martin S.
Julkaistu 2004

Common Genes for Non-syndromic Deafness are uncommon in Sub Saharan Africa: A report from Nigeria

Tekijä Lasisi, Akeem O., Bademci, Guney, Foster, Joseph, Blanton, Susan, Tekin, Mustafa
Julkaistu 2014

Comprehensive Genetic Testing Can Save Lives in Hereditary Hearing Loss

Tekijä Tekin, Demet, Tutar, Ercan, Akay, Hatice Ozturkmen, Blanton, Susan, Foster, Joseph, Tekin, Mustafa
Julkaisussa Clin Genet (2014)

An Amino Acid Deletion in SZT2 in a Family with Non-Syndromic Intellectual Disability

Tekijä Falcone, Michelle, Yariz, Kemal O., Ross, David B., Foster, Joseph, Menendez, Ibis, Tekin, Mustafa
Julkaistu 2013

PRIDE: Quality control in a proteomics data repository

Tekijä Csordas, Attila, Ovelleiro, David, Wang, Rui, Foster, Joseph M., Ríos, Daniel, Vizcaíno, Juan Antonio, Hermjakob, Henning
Julkaistu 2012

Dominant deafness–onychodystrophy syndrome caused by an ATP6V1B2 mutation

Tekijä Menendez, Ibis, Carranza, Claudia, Herrera, Mariana, Marroquin, Nely, Foster, Joseph, Cengiz, Filiz Basak, Bademci, Guney, Tekin, Mustafa
Julkaisussa Clin Case Rep (2017)

The Proteomics Identifications database: 2010 update

Tekijä Vizcaíno, Juan Antonio, Côté, Richard, Reisinger, Florian, Barsnes, Harald, Foster, Joseph M., Rameseder, Jonathan, Hermjakob, Henning, Martens, Lennart
Julkaistu 2010

A guide to the Proteomics Identifications Database proteomics data repository

Tekijä Vizcaíno, Juan Antonio, Côté, Richard, Reisinger, Florian, M. Foster, Joseph, Mueller, Michael, Rameseder, Jonathan, Hermjakob, Henning, Martens, Lennart
Julkaistu 2009

A NEXT-GENERATION SEQUENCING GENE PANEL (MIAMI OTOGENES) FOR COMPREHENSIVE ANALYSIS OF DEAFNESS GENES

Tekijä Tekin, Demet, Yan, Denise, Bademci, Guney, Feng, Yong, Guo, Shengru, Foster, Joseph, Blanton, Susan, Tekin, Mustafa, Liu, Xuezhong
Julkaisussa Hear Res (2016)

From Peptidome to PRIDE: Public proteomics data migration at a large scale

Tekijä Csordas, Attila, Wang, Rui, Ríos, Daniel, Reisinger, Florian, Foster, Joseph M, Slotta, Douglas J, Vizcaíno, Juan Antonio, Hermjakob, Henning
Julkaistu 2013

LipidHome: A Database of Theoretical Lipids Optimized for High Throughput Mass Spectrometry Lipidomics

Tekijä Foster, Joseph M., Moreno, Pablo, Fabregat, Antonio, Hermjakob, Henning, Steinbeck, Christoph, Apweiler, Rolf, Wakelam, Michael J. O., Vizcaíno, Juan Antonio
Julkaistu 2013

Genetic screening revealed usher syndrome in a paediatric Chinese patient

Tekijä Qu, Chunyan, Liang, Fenghe, Long, Qin, Zhao, Min, Shang, Haiqiong, Fan, Lynn, Wang, Li, Foster, Joseph, Yan, Denise, Liu, Xuezhong
Julkaisussa Hearing Balance Commun (2017)

Novel Causative Variants in DYRK1A, KARS, and KAT6A Associated with Intellectual Disability and Additional Phenotypic Features

Tekijä Murray, Clark R., Abel, Samantha N., McClure, Matthew B., Foster, Joseph, Walke, Maria I., Jayakar, Parul, Bademci, Guney, Tekin, Mustafa
Julkaisussa J Pediatr Genet (2017)