Cargando…

CRISPR/CAS9-mediated amino acid substitution reveals phosphorylation residues of RSPH6A are not essential for male fertility in mice

Detalles Bibliográficos
Autores principales:	Miyata, Haruhiko, Abbasi, Ferheen, Visconti, Pablo E, Ikawa, Masahito
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609874/ https://www.ncbi.nlm.nih.gov/pubmed/32901808 http://dx.doi.org/10.1093/biolre/ioaa161

Ejemplares similares

Revolutionizing male fertility factor research in mice by using the genome editing tool CRISPR/Cas9
por: Abbasi, Ferheen, et al.
Publicado: (2017)

CRISPR/Cas9-Mediated Genome Editing Reveals Oosp Family Genes are Dispensable for Female Fertility in Mice
por: Abbasi, Ferheen, et al.
Publicado: (2020)

CRISPR/Cas9-mediated genome editing reveals 12 testis-enriched genes dispensable for male fertility in mice
por: Oyama, Yuki, et al.
Publicado: (2021)

CRISPR/Cas9-Mediated Rapid Generation of Multiple Mouse Lines Identified Ccdc63 as Essential for Spermiogenesis
por: Young, Samantha A. M., et al.
Publicado: (2015)

CRISPR/Cas9-based genome editing in mice uncovers 13 testis- or epididymis-enriched genes individually dispensable for male reproduction(†)
por: Sun, Jiang, et al.
Publicado: (2020)

FAM71F1 binds to RAB2A and RAB2B and is essential for acrosome formation and male fertility in mice
por: Morohoshi, Akane, et al.
Publicado: (2021)

SPATA33 localizes calcineurin to the mitochondria and regulates sperm motility in mice
por: Miyata, Haruhiko, et al.
Publicado: (2021)

CRISPR/Cas9 mediated genome editing in ES cells and its application for chimeric analysis in mice
por: Oji, Asami, et al.
Publicado: (2016)

The motor domain of testis-enriched kinesin KIF9 is essential for its localization in the mouse flagellum
por: Miyata, Haruhiko, et al.
Publicado: (2021)

Glycerol kinase 2 is essential for proper arrangement of crescent-like mitochondria to form the mitochondrial sheath during mouse spermatogenesis
por: SHIMADA, Keisuke, et al.
Publicado: (2019)

Generation of mutant mice by pronuclear injection of circular plasmid expressing Cas9 and single guided RNA
por: Mashiko, Daisuke, et al.
Publicado: (2013)

CRISPR/Cas9-mediated genome editing reveals 30 testis-enriched genes dispensable for male fertility in mice
por: Lu, Yonggang, et al.
Publicado: (2019)

Rsph4a is essential for the triplet radial spoke head assembly of the mouse motile cilia
por: Yoke, Hiroshi, et al.
Publicado: (2020)

The RSPH4A Gene in Primary Ciliary Dyskinesia
por: De Jesús-Rojas, Wilfredo, et al.
Publicado: (2023)

CCDC183 is essential for cytoplasmic invagination around the flagellum during spermiogenesis and male fertility
por: Shimada, Keisuke, et al.
Publicado: (2023)

FBXO24 ensures male fertility by preventing abnormal accumulation of membraneless granules in sperm flagella
por: Kaneda, Yuki, et al.
Publicado: (2023)

Testis-enriched ferlin, FER1L5, is required for Ca(2+)-activated acrosome reaction and male fertility
por: Morohoshi, Akane, et al.
Publicado: (2023)

ARMC12 regulates spatiotemporal mitochondrial dynamics during spermiogenesis and is required for male fertility
por: Shimada, Keisuke, et al.
Publicado: (2021)

Factors controlling sperm migration through the oviduct revealed by gene-modified mouse models
por: Fujihara, Yoshitaka, et al.
Publicado: (2018)

Analysis of the sperm flagellar axoneme using gene-modified mice
por: Miyata, Haruhiko, et al.
Publicado: (2020)

Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility
por: Aprea, I., et al.
Publicado: (2023)

Advantages of using the CRISPR/Cas9 system of genome editing to investigate male reproductive mechanisms using mouse models
por: Young, Samantha AM, et al.
Publicado: (2015)

RSPH and IFH call for a clean-up of public understanding and attitudes to hygiene
por: Bloomfield, Sally F
Publicado: (2019)

Structural insights into the cause of human RSPH4A primary ciliary dyskinesia
por: Zhao, Yanhe, et al.
Publicado: (2021)

Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice
por: Morohoshi, Akane, et al.
Publicado: (2020)

CIB4 is essential for the haploid phase of spermatogenesis in mice
por: Xu, Zoulan, et al.
Publicado: (2020)

Chimeric analysis with newly established EGFP/DsRed2-tagged ES cells identify HYDIN as essential for spermiogenesis in mice
por: Oura, Seiya, et al.
Publicado: (2018)

Human Globozoospermia-Related Gene Spata16 Is Required for Sperm Formation Revealed by CRISPR/Cas9-Mediated Mouse Models
por: Fujihara, Yoshitaka, et al.
Publicado: (2017)

Ultra-superovulation for the CRISPR-Cas9-mediated production of gene-knockout, single-amino-acid-substituted, and floxed mice
por: Nakagawa, Yoshiko, et al.
Publicado: (2016)

Loss of Rsph9 causes neonatal hydrocephalus with abnormal development of motile cilia in mice
por: Zou, Wenzheng, et al.
Publicado: (2020)

CRISPR-sub: Analysis of DNA substitution mutations caused by CRISPR-Cas9 in human cells
por: Hwang, Gue-Ho, et al.
Publicado: (2020)

CRISPR/Cas9 Essential Gene Editing in Drosophila
por: Osadchiy, I. S., et al.
Publicado: (2023)

CRISPR-Cas9 screen identifies oxidative phosphorylation as essential for cancer cell survival at low extracellular pH
por: Michl, Johanna, et al.
Publicado: (2022)

Impaired male fertility and abnormal epididymal epithelium differentiation in mice lacking CRISP1 and CRISP4
por: Carvajal, Guillermo, et al.
Publicado: (2018)

Single-step generation of rabbits carrying a targeted allele of the tyrosinase gene using CRISPR/Cas9
por: Honda, Arata, et al.
Publicado: (2014)

CRISPR/Cas9-mediated gene manipulation to create single-amino-acid-substituted and floxed mice with a cloning-free method
por: Ma, Xiaolong, et al.
Publicado: (2017)

CRISPR/Cas12a Mediated Genome Editing To Introduce Amino Acid Substitutions into the Mechanosensitive Channel MscCG of Corynebacterium glutamicum
por: Krumbach, Karin, et al.
Publicado: (2019)

Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia
por: Lin, Jianfeng, et al.
Publicado: (2014)

Primary Ciliary Dyskinesia: Ancestral Haplotypes Analysis of the RSPH4A Founder Mutation in Puerto Rico
por: De Jesús-Rojas, Wilfredo, et al.
Publicado: (2021)

Expression of RSPH6A in the first wave of rat spermatogenesis and oxidative stress conditions: Attenuation by melatonin
por: Romano, Maria Zelinda, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_un642jsn5frki6kel0t31vj3g8