Lista de obras - Kent Lloyd - Dominio Público Uruguay

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

artículo científico publicado en 2017

A metabolome atlas of the aging mouse brain

artículo científico publicado en 2021

Centralized mouse repositories

artículo científico publicado en 2012

Conditional targeting of Ispd using paired Cas9 nickase and a single DNA template in mice

artículo científico publicado en 2014

Corrigendum: High-throughput discovery of novel developmental phenotypes.

artículo científico publicado en 2017

DNA fragmentation index (DFI) as a measure of sperm quality and fertility in mice

artículo científico publicado en 2020

Deficiency of microRNA miR-34a expands cell fate potential in pluripotent stem cells

artículo científico publicado en 2017

Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies.

artículo científico publicado en 2018

Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.

artículo científico publicado en 2017

Efficient mouse genome engineering by CRISPR-EZ technology

artículo científico publicado en 2018

Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts

artículo científico publicado en 2019

Generating mouse models for biomedical research: technological advances

artículo científico publicado en 2019

Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and function

artículo científico publicado en 2019

High-throughput discovery of genetic determinants of circadian misalignment

artículo científico publicado en 2020

Human and mouse essentiality screens as a resource for disease gene discovery

artículo científico publicado en 2020

Identification of genes required for eye development by high-throughput screening of mouse knockouts

artículo científico publicado en 2018

Identification of genetic elements in metabolism by high-throughput mouse phenotyping

artículo científico publicado en 2018

Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen

artículo científico publicado en 2021

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density

artículo científico publicado en 2020

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis

artículo científico publicado en 2017

Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma

artículo científico publicado en 2021

Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo"

artículo científico publicado en 2018

The Deep Genome Project

scientific article published on 03 February 2020

The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA

scientific article published on 27 July 2021

The mammalian gene function resource: the International Knockout Mouse Consortium

artículo científico publicado en 2012

Lista de obras de Kent Lloyd

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.

A metabolome atlas of the aging mouse brain

Centralized mouse repositories

Conditional targeting of Ispd using paired Cas9 nickase and a single DNA template in mice

Corrigendum: High-throughput discovery of novel developmental phenotypes.

DNA fragmentation index (DFI) as a measure of sperm quality and fertility in mice

Deficiency of microRNA miR-34a expands cell fate potential in pluripotent stem cells

Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies.

Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.

Efficient mouse genome engineering by CRISPR-EZ technology

Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts

Generating mouse models for biomedical research: technological advances

Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and function

High-throughput discovery of genetic determinants of circadian misalignment

Human and mouse essentiality screens as a resource for disease gene discovery

Identification of genes required for eye development by high-throughput screening of mouse knockouts

Identification of genetic elements in metabolism by high-throughput mouse phenotyping

Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis

Proteotyping of knockout mouse strains reveals sex- and strain-specific signatures in blood plasma

Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo"

The Deep Genome Project

The Mutant Mouse Resource and Research Center (MMRRC): the NIH-supported National Public Repository and Distribution Archive of Mutant Mouse Models in the USA

The mammalian gene function resource: the International Knockout Mouse Consortium