A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family
Patel, Kunjan, Giese, Arnaud P, Grossheim, J M, Hegde, Rashmi S, Hegde, Rashima S, Delio, Maria, Samanich, Joy, Riazuddin, Saima, Frolenkov, Gregory I, Cai, Jinlu, Ahmed, Zubair M, Morrow, Bernice E
Published in PloS one (01.10.2015)
Published in PloS one (01.10.2015)
Get full text
Journal Article
Whole-Genome Sequencing and iPLEX MassARRAY Genotyping Map an EMS-Induced Mutation Affecting Cell Competition in Drosophila melanogaster
Lee, Chang-Hyun, Rimesso, Gerard, Reynolds, David M, Cai, Jinlu, Baker, Nicholas E
Published in G3 : genes - genomes - genetics (01.10.2016)
Published in G3 : genes - genomes - genetics (01.10.2016)
Get full text
Journal Article
Correction: A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family
Patel, Kunjan, Giese, Arnaud P, Grossheim, J M, Hegde, Rashmi S, Delio, Maria, Samanich, Joy, Riazuddin, Saima, Frolenkov, Gregory I, Cai, Jinlu, Ahmed, Zubair M, Morrow, Bernice E
Published in PloS one (16.10.2015)
Published in PloS one (16.10.2015)
Get full text
Journal Article
The effect of graphitized carbon on the adsorption and photocatalytic degradation of methylene blue over TiO2/C composites
Cai, Jinlu, Hu, Shenghua, Junhuai Xiang, Zhang, Honghua, Men, Dandan
Published in RSC advances (09.11.2020)
Published in RSC advances (09.11.2020)
Get full text
Journal Article
The effect of graphitized carbon on the adsorption and photocatalytic degradation of methylene blue over TiO/C composites
Cai, Jinlu, Hu, Shenghua, Xiang, Junhuai, Zhang, Honghua, Men, Dandan
Published in RSC advances (09.11.2020)
Published in RSC advances (09.11.2020)
Get full text
Journal Article
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
Dougherty, Joseph D, Maloney, Susan E, Wozniak, David F, Rieger, Michael A, Sonnenblick, Lisa, Coppola, Giovanni, Mahieu, Nathaniel G, Zhang, Juliet, Cai, Jinlu, Patti, Gary J, Abrahams, Brett S, Geschwind, Daniel H, Heintz, Nathaniel
Published in The Journal of neuroscience (13.02.2013)
Published in The Journal of neuroscience (13.02.2013)
Get full text
Journal Article
Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations
Chung, Jonathan H., Cai, Jinlu, Suskin, Barrie G., Zhang, Zhengdong, Coleman, Karlene, Morrow, Bernice E.
Published in Human mutation (01.08.2015)
Published in Human mutation (01.08.2015)
Get full text
Journal Article
Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome
Delio, Maria, Pope, Kathleen, Wang, Tao, Samanich, Joy, Haldeman-Englert, Chad R., Kaplan, Paige, Shaikh, Tamim H., Cai, Jinlu, Marion, Robert W., Morrow, Bernice E., Babcock, Melanie
Published in American journal of medical genetics. Part A (01.03.2013)
Published in American journal of medical genetics. Part A (01.03.2013)
Get full text
Journal Article
A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family: e0133082
Patel, Kunjan, Giese, Arnaud P, Grossheim, J M, Hegde, Rashima S, Delio, Maria, Samanich, Joy, Riazuddin, Saima, Frolenkov, Gregory I, Cai, Jinlu, Ahmed, Zubair M
Published in PloS one (01.10.2015)
Published in PloS one (01.10.2015)
Get full text
Journal Article