Fluorescent PCR–based Screening Methods for Precise Knock-in of Small DNA Fragments and Point Mutations in Zebrafish

por Carrington, Blake, Sood, Raman
Publicado 2023

Novel Insights into the Genetic Controls of Primitive and Definitive Hematopoiesis from Zebrafish Models

por Sood, Raman, Liu, Paul
Publicado 2012

Idiopathic hyperzincemia with associated copper deficiency anemia: a diagnostic dilemma

por Merza, Hussein, Sood, Neha, Sood, Raman
Publicado 2015

A Comprehensive Review of Indel Detection Methods for Identification of Zebrafish Knockout Mutants Generated by Genome-Editing Nucleases

por Carrington, Blake, Bishop, Kevin, Sood, Raman
Publicado 2022

BE4max and AncBE4max Are Efficient in Germline Conversion of C:G to T:A Base Pairs in Zebrafish

por Carrington, Blake, Weinstein, Rachel N., Sood, Raman
Publicado 2020

CRISPR-STAT: an easy and reliable PCR-based method to evaluate target-specific sgRNA activity

por Carrington, Blake, Varshney, Gaurav K., Burgess, Shawn M., Sood, Raman
Publicado 2015

A robust pipeline for efficient knock-in of point mutations and epitope tags in zebrafish using fluorescent PCR based screening

por Carrington, Blake, Ramanagoudr-Bhojappa, Ramanagouda, Bresciani, Erica, Han, Tae-Un, Sood, Raman
Publicado 2022

Human SHPRH suppresses genomic instability through proliferating cell nuclear antigen polyubiquitination

por Motegi, Akira, Sood, Raman, Moinova, Helen, Markowitz, Sanford D., Liu, Pu Paul, Myung, Kyungjae
Publicado 2006

Transient knockdown and overexpression reveal a developmental role for the zebrafish enosf1b gene

por Finckbeiner, Steve, Ko, Pin-Joe, Carrington, Blake, Sood, Raman, Gross, Kenneth, Dolnick, Bruce, Sufrin, Janice, Liu, Paul
Publicado 2011

Efficient Methods for Targeted Mutagenesis in Zebrafish Using Zinc-Finger Nucleases: Data from Targeting of Nine Genes Using CompoZr or CoDA ZFNs

por Sood, Raman, Carrington, Blake, Bishop, Kevin, Jones, MaryPat, Rissone, Alberto, Candotti, Fabio, Chandrasekharappa, Settara C., Liu, Paul
Publicado 2013

A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress

por Rissone, Alberto, Jimenez, Erin, Bishop, Kevin, Carrington, Blake, Slevin, Claire, Wincovitch, Stephen M., Sood, Raman, Candotti, Fabio, Burgess, Shawn M.
Publicado 2019

SNPdetector: A Software Tool for Sensitive and Accurate SNP Detection

por Zhang, Jinghui, Wheeler, David A, Yakub, Imtiaz, Wei, Sharon, Sood, Raman, Rowe, William, Liu, Paul P, Gibbs, Richard A, Buetow, Kenneth H
Publicado 2005

Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects

por Veleri, Shobi, Bishop, Kevin, Dalle Nogare, Damian E., English, Milton A., Foskett, Trevor J., Chitnis, Ajay, Sood, Raman, Liu, Paul, Swaroop, Anand
Publicado 2012

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis

por Justice, Cristina M., Bishop, Kevin, Carrington, Blake, Mullikin, Jim C., Swindle, Kandice, Marosy, Beth, Sood, Raman, Miller, Nancy H., Wilson, Alexander F.
Publicado 2016

Zrsr2 Is Essential for the Embryonic Development and Splicing of Minor Introns in RNA and Protein Processing Genes in Zebrafish

por Weinstein, Rachel, Bishop, Kevin, Broadbridge, Elizabeth, Yu, Kai, Carrington, Blake, Elkahloun, Abdel, Zhen, Tao, Pei, Wuhong, Burgess, Shawn M., Liu, Paul, Bresciani, Erica, Sood, Raman
Publicado 2022

Clinical and genomic analysis of a large Chinese family with familial cortical myoclonic tremor with epilepsy and SAMD12 intronic repeat expansion

por Zhou, Yongxing, Sood, Raman, Wang, Qun, Carrington, Blake, Park, Morgan, Young, Alice C., Birnbaum, Daniel, Liu, Zhao, Ashizawa, Tetsuo, Mullikin, James C., Koubeissi, Mohamad Z., Liu, Paul
Publicado 2021

Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility

por Ramanagoudr-Bhojappa, Ramanagouda, Carrington, Blake, Ramaswami, Mukundhan, Bishop, Kevin, Robbins, Gabrielle M., Jones, MaryPat, Harper, Ursula, Frederickson, Stephen C., Kimble, Danielle C., Sood, Raman, Chandrasekharappa, Settara C.
Publicado 2018

CRISPRz: a database of zebrafish validated sgRNAs

por Varshney, Gaurav K., Zhang, Suiyuan, Pei, Wuhong, Adomako-Ankomah, Ashrifia, Fohtung, Jacob, Schaffer, Katherine, Carrington, Blake, Maskeri, Anoo, Slevin, Claire, Wolfsberg, Tyra, Ledin, Johan, Sood, Raman, Burgess, Shawn M.
Publicado 2016

A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly

por Simpson, Claire L., Kimble, Danielle C., Chandrasekharappa, Settara C., Alqosayer, Khalid, Holzinger, Emily, Carrington, Blake, McElderry, John, Sood, Raman, Al‐Souqi, Ghiath, Albacha‐Hejazi, Hasan, Bailey‐Wilson, Joan E.
Publicado 2023

Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly

por Roessler, Erich, Hu, Ping, Hong, Sung-Kook, Srivastava, Kshitij, Carrington, Blake, Sood, Raman, Petrykowska, Hanna, Elnitski, Laura, Ribeiro, Lucilene A., Richieri-Costa, Antonio, Feldman, Benjamin, Odenwald, Ward F., Muenke, Maximilian
Publicado 2012