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Article ; Online: RUS6, a DUF647-containing protein, is essential for early embryonic development in Arabidopsis thaliana

Perry, Nathaniel / Leasure, Colin D. / Tong, Hongyun / Duarte, Elias M. / He, Zheng-Hui

BMC Plant Biol. 2021 Dec., v. 21, no. 1 p.232-232

2021

Abstract: BACKGROUND: The Arabidopsis RUS (ROOT UV-B SENSITIVE) gene family contains six members, each of which encodes a protein containing a DUF647 (domain of unknown function 647) that is commonly found in eukaryotes. Previous studies have demonstrated that ... ...

Abstract	BACKGROUND: The Arabidopsis RUS (ROOT UV-B SENSITIVE) gene family contains six members, each of which encodes a protein containing a DUF647 (domain of unknown function 647) that is commonly found in eukaryotes. Previous studies have demonstrated that RUS1 and RUS2 play critical roles in early seedling development. All six RUS genes are expressed throughout the plant, but little is known about the functional roles of RUS3, RUS4, RUS5 and RUS6. RESULTS: We used a reverse-genetic approach to identify knockout mutants for RUS3, RUS4, RUS5 and RUS6. Each mutant was confirmed by direct DNA sequencing and genetic segregation analysis. No visible phenotypic differences were observed in rus3, rus4, or rus5 knockout mutants under standard growth conditions, but rus6 knockout mutants displayed a strong embryo-lethal phenotype. Two independent knockout lines for RUS6 were characterized. The rus6 mutations could only be maintained through a heterozygote, because rus6 homozygous mutants did not survive. Closer examinations of homozygous rus6 embryos from rus6/ + parent plants revealed that RUS6 is required for early embryo development. Loss of RUS6 resulted in embryo lethality, specifically at the mid-globular stage. The embryo-lethality phenotype was complemented by a RUS6::RUS6-GFP transgene, and GFP signal was detected throughout the embryo. Histological analyses with the β-glucuronidase reporter gene driven by the RUS6 promoter showed tissue- and development-specific expression of RUS6, which was highest in floral tissues. CONCLUSION: Our data revealed that RUS6 is essential for early embryo development in Arabidopsis, and that the RUS gene family functions in multiple stages of plant development.
Keywords	Arabidopsis thaliana ; DNA ; death ; embryogenesis ; eukaryotic cells ; heterozygosity ; histology ; homozygosity ; mutants ; phenotype ; plant development ; reporter genes ; seedlings ; transgenes
Language	English
Dates of publication	2021-12
Size	p. 232.
Publishing place	BioMed Central
Document type	Article ; Online
ZDB-ID	2059868-3
ISSN	1471-2229
ISSN	1471-2229
DOI	10.1186/s12870-021-03011-8
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: RUS6, a DUF647-containing protein, is essential for early embryonic development in Arabidopsis thaliana.

Perry, Nathaniel / Leasure, Colin D / Tong, Hongyun / Duarte, Elias M / He, Zheng-Hui

BMC plant biology

2021 Volume 21, Issue 1, Page(s) 232

Abstract: Background: The Arabidopsis RUS (ROOT UV-B SENSITIVE) gene family contains six members, each of which encodes a protein containing a DUF647 (domain of unknown function 647) that is commonly found in eukaryotes. Previous studies have demonstrated that ... ...

Abstract	Background: The Arabidopsis RUS (ROOT UV-B SENSITIVE) gene family contains six members, each of which encodes a protein containing a DUF647 (domain of unknown function 647) that is commonly found in eukaryotes. Previous studies have demonstrated that RUS1 and RUS2 play critical roles in early seedling development. All six RUS genes are expressed throughout the plant, but little is known about the functional roles of RUS3, RUS4, RUS5 and RUS6. Results: We used a reverse-genetic approach to identify knockout mutants for RUS3, RUS4, RUS5 and RUS6. Each mutant was confirmed by direct DNA sequencing and genetic segregation analysis. No visible phenotypic differences were observed in rus3, rus4, or rus5 knockout mutants under standard growth conditions, but rus6 knockout mutants displayed a strong embryo-lethal phenotype. Two independent knockout lines for RUS6 were characterized. The rus6 mutations could only be maintained through a heterozygote, because rus6 homozygous mutants did not survive. Closer examinations of homozygous rus6 embryos from rus6/ + parent plants revealed that RUS6 is required for early embryo development. Loss of RUS6 resulted in embryo lethality, specifically at the mid-globular stage. The embryo-lethality phenotype was complemented by a RUS6::RUS6-GFP transgene, and GFP signal was detected throughout the embryo. Histological analyses with the β-glucuronidase reporter gene driven by the RUS6 promoter showed tissue- and development-specific expression of RUS6, which was highest in floral tissues. Conclusion: Our data revealed that RUS6 is essential for early embryo development in Arabidopsis, and that the RUS gene family functions in multiple stages of plant development.
MeSH term(s)	Arabidopsis/embryology ; Arabidopsis/genetics ; Arabidopsis Proteins/genetics ; Arabidopsis Proteins/metabolism ; Intracellular Signaling Peptides and Proteins/genetics ; Intracellular Signaling Peptides and Proteins/metabolism ; Mutation ; Phenotype ; Promoter Regions, Genetic/genetics
Chemical Substances	AT5G49820 protein, Arabidopsis ; Arabidopsis Proteins ; Intracellular Signaling Peptides and Proteins
Language	English
Publishing date	2021-05-25
Publishing country	England
Document type	Journal Article
ISSN	1471-2229
ISSN (online)	1471-2229
DOI	10.1186/s12870-021-03011-8
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Optimization of whole-genome sequencing of Plasmodium falciparum from low-density dried blood spot samples.

Teyssier, Noam B / Chen, Anna / Duarte, Elias M / Sit, Rene / Greenhouse, Bryan / Tessema, Sofonias K

Malaria journal

2021 Volume 20, Issue 1, Page(s) 116

Abstract: Background: Whole-genome sequencing (WGS) is becoming increasingly useful to study the biology, epidemiology, and ecology of malaria parasites. Despite ease of sampling, DNA extracted from dried blood spots (DBS) has a high ratio of human DNA compared ... ...

Abstract	Background: Whole-genome sequencing (WGS) is becoming increasingly useful to study the biology, epidemiology, and ecology of malaria parasites. Despite ease of sampling, DNA extracted from dried blood spots (DBS) has a high ratio of human DNA compared to parasite DNA, which poses a challenge for downstream genetic analyses. The effects of multiple methods for DNA extraction, digestion of methylated DNA, and amplification were evaluated on the quality and fidelity of WGS data recovered from DBS. Methods: Low parasite density mock DBS samples were created, extracted either with Tween-Chelex or QIAamp, treated with or without McrBC, and amplified with one of three different amplification techniques (two sWGA primer sets and one rWGA). Extraction conditions were evaluated on performance of sequencing depth, percentiles of coverage, and expected SNP concordance. Results: At 100 parasites/μL, Chelex-Tween-McrBC samples had higher coverage (5 × depth = 93% genome) than QIAamp extracted samples (5 × depth = 76% genome). The two evaluated sWGA primer sets showed minor differences in overall genome coverage and SNP concordance, with a newly proposed combination of 20 primers showing a modest improvement in coverage over those previously published. Conclusions: Overall, Tween-Chelex extracted samples that were treated with McrBC digestion and are amplified using 6A10AD sWGA conditions had minimal dropout rate, higher percentages of coverage at higher depth, and more accurate SNP concordance than QiaAMP extracted samples. These findings extend the results of previously reported methods, making whole genome sequencing accessible to a larger number of low density samples that are commonly encountered in cross-sectional surveys.
MeSH term(s)	Dried Blood Spot Testing/instrumentation ; Humans ; Plasmodium falciparum/genetics ; Whole Genome Sequencing/instrumentation ; Whole Genome Sequencing/methods
Language	English
Publishing date	2021-02-26
Publishing country	England
Document type	Journal Article
ISSN	1475-2875
ISSN (online)	1475-2875
DOI	10.1186/s12936-021-03630-4
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Protection against symptomatic dengue infection by neutralizing antibodies varies by infection history and infecting serotype.

Bos, Sandra / Graber, Aaron L / Cardona-Ospina, Jaime A / Duarte, Elias M / Zambrana, Jose Victor / Ruíz Salinas, Jorge A / Mercado-Hernandez, Reinaldo / Singh, Tulika / Katzelnick, Leah C / de Silva, Aravinda / Kuan, Guillermina / Balmaseda, Angel / Harris, Eva

Nature communications

2024 Volume 15, Issue 1, Page(s) 382

Abstract: Dengue viruses (DENV1-4) are the most prevalent arboviruses in humans and a major public health concern. Understanding immune mechanisms that modulate DENV infection outcome is critical for vaccine development. Neutralizing antibodies (nAbs) are an ... ...

Abstract	Dengue viruses (DENV1-4) are the most prevalent arboviruses in humans and a major public health concern. Understanding immune mechanisms that modulate DENV infection outcome is critical for vaccine development. Neutralizing antibodies (nAbs) are an essential component of the protective immune response, yet their measurement often relies on a single cellular substrate and partially mature virions, which does not capture the full breadth of neutralizing activity and may lead to biased estimations of nAb potency. Here, we analyze 125 samples collected after one or more DENV infections but prior to subsequent symptomatic or inapparent DENV1, DENV2, or DENV3 infections from a long-standing pediatric cohort study in Nicaragua. By assessing nAb responses using Vero cells with or without DC-SIGN and with mature or partially mature virions, we find that nAb potency and the protective NT50 cutoff are greatly influenced by cell substrate and virion maturation state. Additionally, the correlation between nAb titer and protection from disease depends on prior infection history and infecting serotype. Finally, we uncover variations in nAb composition that contribute to protection from symptomatic infection differently after primary and secondary prior infection. These findings have important implications for identifying antibody correlates of protection for vaccines and natural infections.
MeSH term(s)	Chlorocebus aethiops ; Animals ; Humans ; Child ; Antibodies, Neutralizing ; Cohort Studies ; Serogroup ; Vero Cells ; Coinfection ; Dengue/prevention & control
Chemical Substances	Antibodies, Neutralizing
Language	English
Publishing date	2024-01-09
Publishing country	England
Document type	Journal Article
ZDB-ID	2553671-0
ISSN	2041-1723 ; 2041-1723
ISSN (online)	2041-1723
ISSN	2041-1723
DOI	10.1038/s41467-023-44330-8
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article: The association of neutralizing antibodies with protection against symptomatic dengue virus infection varies by serotype, prior infection history, and assay condition.

medRxiv : the preprint server for health sciences

2023

Abstract: The four dengue virus serotypes (DENV1-4) are the most prevalent arboviruses in humans and a major public health concern worldwide. Understanding immune mechanisms that modulate DENV infection outcome is critical for epidemic preparedness and development ...

Abstract	The four dengue virus serotypes (DENV1-4) are the most prevalent arboviruses in humans and a major public health concern worldwide. Understanding immune mechanisms that modulate DENV infection outcome is critical for epidemic preparedness and development of a safe and effective vaccine. Neutralizing antibodies (nAbs) are an essential component of the protective response, yet their measurement often relies on a single cellular substrate and partially mature virions, which do not capture the full breadth of neutralizing activity and may lead to biased estimations of nAb potency. Here, we investigated the characteristics of nAbs associated with protection against dengue cases using samples collected after one or more DENV infections but prior to subsequent symptomatic or inapparent DENV1, DENV2, or DENV3 infections from a long- standing pediatric cohort study in Nicaragua. By assessing nAb responses using Vero cells with or without the attachment factor DC-SIGN and with mature or partially mature virions, we found that nAb potency and the protective NT
Language	English
Publishing date	2023-10-13
Publishing country	United States
Document type	Preprint
DOI	10.1101/2023.06.20.23291522
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Sensitive, Highly Multiplexed Sequencing of Microhaplotypes From the Plasmodium falciparum Heterozygome.

Tessema, Sofonias K / Hathaway, Nicholas J / Teyssier, Noam B / Murphy, Maxwell / Chen, Anna / Aydemir, Ozkan / Duarte, Elias M / Simone, Wilson / Colborn, James / Saute, Francisco / Crawford, Emily / Aide, Pedro / Bailey, Jeffrey A / Greenhouse, Bryan

The Journal of infectious diseases

2020 Volume 225, Issue 7, Page(s) 1227–1237

Abstract: Background: Targeted next-generation sequencing offers the potential for consistent, deep coverage of information-rich genomic regions to characterize polyclonal Plasmodium falciparum infections. However, methods to identify and sequence these genomic ... ...

Abstract	Background: Targeted next-generation sequencing offers the potential for consistent, deep coverage of information-rich genomic regions to characterize polyclonal Plasmodium falciparum infections. However, methods to identify and sequence these genomic regions are currently limited. Methods: A bioinformatic pipeline and multiplex methods were developed to identify and simultaneously sequence 100 targets and applied to dried blood spot (DBS) controls and field isolates from Mozambique. For comparison, whole-genome sequencing data were generated for the same controls. Results: Using publicly available genomes, 4465 high-diversity genomic regions suited for targeted sequencing were identified, representing the P. falciparum heterozygome. For this study, 93 microhaplotypes with high diversity (median expected heterozygosity = 0.7) were selected along with 7 drug resistance loci. The sequencing method achieved very high coverage (median 99%), specificity (99.8%), and sensitivity (90% for haplotypes with 5% within sample frequency in dried blood spots with 100 parasites/µL). In silico analyses revealed that microhaplotypes provided much higher resolution to discriminate related from unrelated polyclonal infections than biallelic single-nucleotide polymorphism barcodes. Conclusions: The bioinformatic and laboratory methods outlined here provide a flexible tool for efficient, low-cost, high-throughput interrogation of the P. falciparum genome, and can be tailored to simultaneously address multiple questions of interest in various epidemiological settings.
MeSH term(s)	Haplotypes ; High-Throughput Nucleotide Sequencing/methods ; Humans ; Malaria, Falciparum/epidemiology ; Plasmodium falciparum/genetics ; Whole Genome Sequencing/methods
Language	English
Publishing date	2020-08-18
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	3019-3
ISSN	1537-6613 ; 0022-1899
ISSN (online)	1537-6613
ISSN	0022-1899
DOI	10.1093/infdis/jiaa527
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Article: Rapid deployment of SARS-CoV-2 testing: The CLIAHUB

Crawford, Emily D / Acosta, Irene / Ahyong, Vida / Anderson, Erika C / Arevalo, Shaun / Asarnow, Daniel / Axelrod, Shannon / Ayscue, Patrick / Azimi, Camillia S / Azumaya, Caleigh M / Bachl, Stefanie / Bachmutsky, Iris / Bhaduri, Aparna / Brown, Jeremy Bancroft / Batson, Joshua / Behnert, Astrid / Boileau, Ryan M / Bollam, Saumya R / Bonny, Alain R /

PLoS Pathog

Keywords	covid19
Publisher	WHO
Document type	Article
Note	WHO #Covidence: #895085
Database	COVID19

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Article ; Online: Rapid deployment of SARS-CoV-2 testing: The CLIAHUB.

Booth, David / Borja, Michael Jerico B / Brown, David / Buie, Bryan / Burnett, Cassandra E / Byrnes, Lauren E / Cabral, Katelyn A / Cabrera, Joana P / Caldera, Saharai / Canales, Gabriela / Castañeda, Gloria R / Chan, Agnes Protacio / Chang, Christopher R / Charles-Orszag, Arthur / Cheung, Carly / Chio, Unseng / Chow, Eric D / Citron, Y Rose / Cohen, Allison / Cohn, Lillian B / Chiu, Charles / Cole, Mitchel A / Conrad, Daniel N / Constantino, Angela / Cote, Andrew / Crayton-Hall, Tre'Jon / Darmanis, Spyros / Detweiler, Angela M / Dial, Rebekah L / Dong, Shen / Duarte, Elias M / Dynerman, David / Egger, Rebecca / Fanton, Alison / Frumm, Stacey M / Fu, Becky Xu Hua / Garcia, Valentina E / Garcia, Julie / Gladkova, Christina / Goldman, Miriam / Gomez-Sjoberg, Rafael / Gordon, M Grace / Grove, James C R / Gupta, Shweta / Haddjeri-Hopkins, Alexis / Hadley, Pierce / Haliburton, John / Hao, Samantha L / Hartoularos, George / Herrera, Nadia / Hilberg, Melissa / Ho, Kit Ying E / Hoppe, Nicholas / Hosseinzadeh, Shayan / Howard, Conor J / Hussmann, Jeffrey A / Hwang, Elizabeth / Ingebrigtsen, Danielle / Jackson, Julia R / Jowhar, Ziad M / Kain, Danielle / Kim, James Y S / Kistler, Amy / Kreutzfeld, Oriana / Kulsuptrakul, Jessie / Kung, Andrew F / Langelier, Charles / Laurie, Matthew T / Lee, Lena / Leng, Kun / Leon, Kristoffer E / Leonetti, Manuel D / Levan, Sophia R / Li, Sam / Li, Aileen W / Liu, Jamin / Lubin, Heidi S / Lyden, Amy / Mann, Jennifer / Mann, Sabrina / Margulis, Gorica / Marquez, Diana M / Marsh, Bryan P / Martyn, Calla / McCarthy, Elizabeth E / McGeever, Aaron / Merriman, Alexander F / Meyer, Lauren K / Miller, Steve / Moore, Megan K / Mowery, Cody T / Mukhtar, Tanzila / Mwakibete, Lusajo L / Narez, Noelle / Neff, Norma F / Osso, Lindsay A / Oviedo, Diter / Peng, Suping / Phelps, Maira / Phong, Kiet / Picard, Peter / Pieper, Lindsey M / Pincha, Neha / Pisco, Angela Oliveira / Pogson, Angela / Pourmal, Sergei / Puccinelli, Robert R / Puschnik, Andreas S / Rackaityte, Elze / Raghavan, Preethi / Raghavan, Madhura / Reese, James / Replogle, Joseph M / Retallack, Hanna / Reyes, Helen / Rose, Donald / Rosenberg, Marci F / Sanchez-Guerrero, Estella / Sattler, Sydney M / Savy, Laura / See, Stephanie K / Sellers, Kristin K / Serpa, Paula Hayakawa / Sheehy, Maureen / Sheu, Jonathan / Silas, Sukrit / Streithorst, Jessica A / Strickland, Jack / Stryke, Doug / Sunshine, Sara / Suslow, Peter / Sutanto, Renaldo / Tamura, Serena / Tan, Michelle / Tan, Jiongyi / Tang, Alice / Tato, Cristina M / Taylor, Jack C / Tenvooren, Iliana / Thompson, Erin M / Thornborrow, Edward C / Tse, Eric / Tung, Tony / Turner, Marc L / Turner, Victoria S / Turnham, Rigney E / Turocy, Mary J / Vaidyanathan, Trisha V / Vainchtein, Ilia D / Vanaerschot, Manu / Vazquez, Sara E / Wandler, Anica M / Wapniarski, Anne / Webber, James T / Weinberg, Zara Y / Westbrook, Alexandra / Wong, Allison W / Wong, Emily / Worthington, Gajus / Xie, Fang / Xu, Albert / Yamamoto, Terrina / Yang, Ying / Yarza, Fauna / Zaltsman, Yefim / Zheng, Tina / DeRisi, Joseph L

PLoS pathogens

2020 Volume 16, Issue 10, Page(s) e1008966

MeSH term(s)	Betacoronavirus ; COVID-19 ; COVID-19 Testing ; California ; Clinical Laboratory Services/supply & distribution ; Clinical Laboratory Techniques/methods ; Coronavirus Infections/diagnosis ; Humans ; Pandemics ; Pneumonia, Viral/diagnosis ; SARS-CoV-2 ; Workflow
Keywords	covid19
Language	English
Publishing date	2020-10-28
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2205412-1
ISSN	1553-7374 ; 1553-7374
ISSN (online)	1553-7374
ISSN	1553-7374
DOI	10.1371/journal.ppat.1008966
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Rapid deployment of SARS-CoV-2 testing

Crawford, Emily D. / Acosta, Irene / Ahyong, Vida / Anderson, Erika C. / Arevalo, Shaun / Asarnow, Daniel / Axelrod, Shannon / Ayscue, Patrick / Azimi, Camillia S. / Azumaya, Caleigh M. / Bachl, Stefanie / Bachmutsky, Iris / Bhaduri, Aparna / Brown, Jeremy Bancroft / Batson, Joshua / Behnert, Astrid / Boileau, Ryan M. / Bollam, Saumya R. / Bonny, Alain R. /

Booth, David / Borja, Michael Jerico B. / Brown, David / Buie, Bryan / Burnett, Cassandra E. / Byrnes, Lauren E. / Cabral, Katelyn A. / Cabrera, Joana P. / Caldera, Saharai / Canales, Gabriela / Castañeda, Gloria R. / Chan, Agnes Protacio / Chang, Christopher R. / Charles-Orszag, Arthur / Cheung, Carly / Chio, Unseng / Chow, Eric D. / Citron, Y. Rose / Cohen, Allison / Cohn, Lillian B. / Chiu, Charles / Cole, Mitchel A. / Conrad, Daniel N. / Constantino, Angela / Cote, Andrew / Crayton-Hall, Tre’Jon / Darmanis, Spyros / Detweiler, Angela M. / Dial, Rebekah L. / Dong, Shen / Duarte, Elias M. / Dynerman, David / Egger, Rebecca / Fanton, Alison / Frumm, Stacey M. / Fu, Becky Xu Hua / Garcia, Valentina E. / Garcia, Julie / Gladkova, Christina / Goldman, Miriam / Gomez-Sjoberg, Rafael / Gordon, M. Grace / Grove, James C. R. / Gupta, Shweta / Haddjeri-Hopkins, Alexis / Hadley, Pierce / Haliburton, John / Hao, Samantha L. / Hartoularos, George / Herrera, Nadia / Hilberg, Melissa / Ho, Kit Ying E. / Hoppe, Nicholas / Hosseinzadeh, Shayan / Howard, Conor J. / Hussmann, Jeffrey A. / Hwang, Elizabeth / Ingebrigtsen, Danielle / Jackson, Julia R. / Jowhar, Ziad M. / Kain, Danielle / Kim, James Y. S. / Kistler, Amy / Kreutzfeld, Oriana / Kulsuptrakul, Jessie / Kung, Andrew F. / Langelier, Charles / Laurie, Matthew T. / Lee, Lena / Leng, Kun / Leon, Kristoffer E. / Leonetti, Manuel D. / Levan, Sophia R. / Li, Sam / Li, Aileen W. / Liu, Jamin / Lubin, Heidi S. / Lyden, Amy / Mann, Jennifer / Mann, Sabrina / Margulis, Gorica / Marquez, Diana M. / Marsh, Bryan P. / Martyn, Calla / McCarthy, Elizabeth E. / McGeever, Aaron / Merriman, Alexander F. / Meyer, Lauren K. / Miller, Steve / Moore, Megan K. / Mowery, Cody T. / Mukhtar, Tanzila / Mwakibete, Lusajo L. / Narez, Noelle / Neff, Norma F. / Osso, Lindsay A. / Oviedo, Diter / Peng, Suping / Phelps, Maira / Phong, Kiet / Picard, Peter / Pieper, Lindsey M. / Pincha, Neha / Pisco, Angela Oliveira / Pogson, Angela / Pourmal, Sergei / Puccinelli, Robert R. / Puschnik, Andreas S. / Rackaityte, Elze / Raghavan, Preethi / Raghavan, Madhura / Reese, James / Replogle, Joseph M. / Retallack, Hanna / Reyes, Helen / Rose, Donald / Rosenberg, Marci F. / Sanchez-Guerrero, Estella / Sattler, Sydney M. / Savy, Laura / See, Stephanie K. / Sellers, Kristin K. / Serpa, Paula Hayakawa / Sheehy, Maureen / Sheu, Jonathan / Silas, Sukrit / Streithorst, Jessica A. / Strickland, Jack / Stryke, Doug / Sunshine, Sara / Suslow, Peter / Sutanto, Renaldo / Tamura, Serena / Tan, Michelle / Tan, Jiongyi / Tang, Alice / Tato, Cristina M. / Taylor, Jack C. / Tenvooren, Iliana / Thompson, Erin M. / Thornborrow, Edward C. / Tse, Eric / Tung, Tony / Turner, Marc L. / Turner, Victoria S. / Turnham, Rigney E. / Turocy, Mary J. / Vaidyanathan, Trisha V. / Vainchtein, Ilia D. / Vanaerschot, Manu / Vazquez, Sara E. / Wandler, Anica M. / Wapniarski, Anne / Webber, James T. / Weinberg, Zara Y. / Westbrook, Alexandra / Wong, Allison W. / Wong, Emily / Worthington, Gajus / Xie, Fang / Xu, Albert / Yamamoto, Terrina / Yang, Ying / Yarza, Fauna / Zaltsman, Yefim / Zheng, Tina / DeRisi, Joseph L.

PLOS Pathogens

The CLIAHUB

2020 Volume 16, Issue 10, Page(s) e1008966

Keywords	Immunology ; Genetics ; Molecular Biology ; Microbiology ; Parasitology ; Virology ; covid19
Language	English
Publisher	Public Library of Science (PLoS)
Publishing country	us
Document type	Article ; Online
ZDB-ID	2205412-1
ISSN	1553-7374 ; 1553-7366
ISSN (online)	1553-7374
ISSN	1553-7366
DOI	10.1371/journal.ppat.1008966
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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