about
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Deficiency of microRNA miR-34a expands cell fate potential in pluripotent stem cells.A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis.Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies.Identification of genes required for eye development by high-throughput screening of mouse knockoutsGenerating mouse models for biomedical research: technological advancesErratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsResponse to "Unexpected mutations after CRISPR-Cas9 editing in vivo"Efficient mouse genome engineering by CRISPR-EZ technologyHuman and mouse essentiality screens as a resource for disease gene discoveryDNA fragmentation index (DFI) as a measure of sperm quality and fertility in miceGenome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and functionHigh-throughput discovery of genetic determinants of circadian misalignment
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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type
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Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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K.C. Kent Lloyd
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K.C.K. Lloyd
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Kent Lloyd KC
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Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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Kent Lloyd
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P106
P31
P4012
P496
0000-0002-5318-4144