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  1. Article ; Online: Cervical High-Grade Squamous Intraepithelial Lesion Burden and Standard of Care Treatment Effectiveness and Safety in the United States, 2008-2018: The EACH-WOMAN Project.

    Hughes, Katherine C / Herring, Timothy A / Song, Jennifer N / Gately, Robert V / Przybyl, Lindsey M / Ogilvie, Rachel P / Simon, Keiko / Bhuyan, Prakash K / Kyrgiou, Maria / Seeger, John D

    Journal of lower genital tract disease

    2023  Volume 27, Issue 2, Page(s) 105–112

    Abstract: Objective: Management of cervical high-grade squamous intraepithelial lesions (HSILs), the immediate precursor of cervical cancer, consists largely of surgical treatment for women at higher risk for progression to cancer. The authors' objective was to ... ...

    Abstract Objective: Management of cervical high-grade squamous intraepithelial lesions (HSILs), the immediate precursor of cervical cancer, consists largely of surgical treatment for women at higher risk for progression to cancer. The authors' objective was to describe the occurrence of cervical HSIL in the United States and various outcomes for women who received surgical treatment.
    Methods: From a US commercial health insurer, a cohort of adult women with cervical HSIL diagnoses receiving surgical treatment within 3 months of diagnosis between January 2008 and September 2018 was identified. This cohort was followed for several outcomes, including cervical HSIL recurrence, human papillomavirus clearance, preterm birth, infection, and bleeding.
    Results: The incidence rate of cervical HSIL declined from 2.34 (95% CI = 2.30-2.39) cases per 1,000 person-years in 2008 to 1.39 (95% CI = 1.35-1.43) cases per 1,000 person-years in 2014, remaining near that level through 2018. Among 65,527 women with cervical HSIL, 47,067 (72%) received surgical treatment within 3 months of diagnosis. Among the women receiving surgical treatment, cervical HSIL recurred in 6% of surgically treated women, whereas 45% of surgically treated women underwent subsequent virological testing that indicated human papillomavirus clearance. Preterm birth was observed in 5.9% by 5 years follow-up and bleeding and infection each at 2.2% by 7 days follow-up.
    Conclusions: From 2008 through 2018, the incidence of diagnosed cervical HSIL decreased for several years before stabilizing. Surgical treatment of HSIL may be beneficial in removing the precancerous lesion, but cervical HSIL may recur, and the surgery is associated with complications including preterm birth, infection, and bleeding.
    MeSH term(s) Infant, Newborn ; Adult ; Female ; Humans ; United States/epidemiology ; Uterine Cervical Dysplasia/pathology ; Vaginal Smears ; Premature Birth ; Standard of Care ; Uterine Cervical Neoplasms/epidemiology ; Uterine Cervical Neoplasms/surgery ; Uterine Cervical Neoplasms/diagnosis ; Squamous Intraepithelial Lesions/epidemiology ; Squamous Intraepithelial Lesions/complications ; Carcinoma, Squamous Cell/pathology ; Treatment Outcome ; Carcinoma in Situ ; Papillomavirus Infections/complications ; Papillomavirus Infections/epidemiology ; Papillomavirus Infections/diagnosis ; Papillomaviridae
    Language English
    Publishing date 2023-02-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041332-4
    ISSN 1526-0976 ; 1089-2591
    ISSN (online) 1526-0976
    ISSN 1089-2591
    DOI 10.1097/LGT.0000000000000719
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Lyme disease knowledge, beliefs, and practices of New Hampshire primary care physicians.

    Magri, Julie M / Johnson, Melissa T / Herring, Timothy A / Greenblatt, Jesse F

    The Journal of the American Board of Family Practice

    2002  Volume 15, Issue 4, Page(s) 277–284

    Abstract: Background: Lyme disease is the most commonly reported vectorborne illness in the United States and is endemic in many counties in the Northeast, including counties in New Hampshire. Previous studies conducted elsewhere on Lyme disease have indicated ... ...

    Abstract Background: Lyme disease is the most commonly reported vectorborne illness in the United States and is endemic in many counties in the Northeast, including counties in New Hampshire. Previous studies conducted elsewhere on Lyme disease have indicated substantial differences between physician practices and published consensus guidelines for diagnosis and treatment.
    Methods: During 1999, we mailed a 21-item questionnaire to 600 randomly selected family practice physicians, internists, and pediatricians in New Hampshire.
    Results: Respondents answered a median of 10 (76.9%) of 13 knowledge items correctly. Most physicians (73.6%) underestimated the incidence of erythema migrans among Lyme disease patients, and 41.2% would either test or offer treatment to an asymptomatic patient with deer-tick bite. When surveyed, most respondents (72.4%) planned to recommend Lyme disease vaccine to high-risk persons. Approximately one half (44.8%) reported giving empiric antibiotic treatment of Lyme disease solely because of patient concern.
    Conclusions: New Hampshire primary care physicians indicated good knowledge about Lyme disease. Lack of awareness about Lyme disease diagnostic criteria, however, could contribute to misdiagnosis through overreliance on laboratory testing. Lyme disease vaccine appeared to be well accepted by physicians, although the vaccine has since been withdrawn from the US market. Both inappropriate management of tick bite and empiric treatment of unsubstantiated Lyme disease diagnoses were common.
    MeSH term(s) Antigens, Surface/administration & dosage ; Bacterial Outer Membrane Proteins/administration & dosage ; Bacterial Vaccines ; Clinical Competence ; Cross-Sectional Studies ; Health Knowledge, Attitudes, Practice ; Health Services Research ; Humans ; Incidence ; Lipoproteins ; Lyme Disease/diagnosis ; Lyme Disease/epidemiology ; Lyme Disease/therapy ; New Hampshire/epidemiology ; Physicians, Family/psychology ; Physicians, Family/standards ; Practice Patterns, Physicians' ; Risk Factors ; Surveys and Questionnaires
    Chemical Substances Antigens, Surface ; Bacterial Outer Membrane Proteins ; Bacterial Vaccines ; Lipoproteins ; OspA protein
    Language English
    Publishing date 2002-07
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1036289-7
    ISSN 0893-8652
    ISSN 0893-8652
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Safety, efficacy, and immunogenicity of VGX-3100, a therapeutic synthetic DNA vaccine targeting human papillomavirus 16 and 18 E6 and E7 proteins for cervical intraepithelial neoplasia 2/3: a randomised, double-blind, placebo-controlled phase 2b trial.

    Trimble, Cornelia L / Morrow, Matthew P / Kraynyak, Kimberly A / Shen, Xuefei / Dallas, Michael / Yan, Jian / Edwards, Lance / Parker, R Lamar / Denny, Lynette / Giffear, Mary / Brown, Ami Shah / Marcozzi-Pierce, Kathleen / Shah, Divya / Slager, Anna M / Sylvester, Albert J / Khan, Amir / Broderick, Kate E / Juba, Robert J / Herring, Timothy A /
    Boyer, Jean / Lee, Jessica / Sardesai, Niranjan Y / Weiner, David B / Bagarazzi, Mark L

    Lancet (London, England)

    2015  Volume 386, Issue 10008, Page(s) 2078–2088

    Abstract: Background: Despite preventive vaccines for oncogenic human papillomaviruses (HPVs), cervical intraepithelial neoplasia (CIN) is common, and current treatments are ablative and can lead to long-term reproductive morbidity. We assessed whether VGX-3100, ... ...

    Abstract Background: Despite preventive vaccines for oncogenic human papillomaviruses (HPVs), cervical intraepithelial neoplasia (CIN) is common, and current treatments are ablative and can lead to long-term reproductive morbidity. We assessed whether VGX-3100, synthetic plasmids targeting HPV-16 and HPV-18 E6 and E7 proteins, delivered by electroporation, would cause histopathological regression in women with CIN2/3.
    Methods: Efficacy, safety, and immunogenicity of VGX-3100 were assessed in CIN2/3 associated with HPV-16 and HPV-18, in a randomised, double-blind, placebo-controlled phase 2b study. Patients from 36 academic and private gynaecology practices in seven countries were randomised (3:1) to receive 6 mg VGX-3100 or placebo (1 mL), given intramuscularly at 0, 4, and 12 weeks. Randomisation was stratified by age (<25 vs ≥25 years) and CIN2 versus CIN3 by computer-generated allocation sequence (block size 4). Funder and site personnel, participants, and pathologists were masked to treatment. The primary efficacy endpoint was regression to CIN1 or normal pathology 36 weeks after the first dose. Per-protocol and modified intention-to-treat analyses were based on patients receiving three doses without protocol violations, and on patients receiving at least one dose, respectively. The safety population included all patients who received at least one dose. The trial is registered at ClinicalTrials.gov (number NCT01304524) and EudraCT (number 2012-001334-33).
    Findings: Between Oct 19, 2011, and July 30, 2013, 167 patients received either VGX-3100 (n=125) or placebo (n=42). In the per-protocol analysis 53 (49·5%) of 107 VGX-3100 recipients and 11 (30·6%) of 36 placebo recipients had histopathological regression (percentage point difference 19·0 [95% CI 1·4-36·6]; p=0·034). In the modified intention-to-treat analysis 55 (48·2%) of 114 VGX-3100 recipients and 12 (30·0%) of 40 placebo recipients had histopathological regression (percentage point difference 18·2 [95% CI 1·3-34·4]; p=0·034). Injection-site reactions occurred in most patients, but only erythema was significantly more common in the VGX-3100 group (98/125, 78·4%) than in the placebo group (24/42, 57·1%; percentage point difference 21·3 [95% CI 5·3-37·8]; p=0·007).
    Interpretation: VGX-3100 is the first therapeutic vaccine to show efficacy against CIN2/3 associated with HPV-16 and HPV-18. VGX-3100 could present a non-surgical therapeutic option for CIN2/3, changing the treatment outlook for this common disease.
    Funding: Inovio Pharmaceuticals.
    MeSH term(s) Adult ; Cancer Vaccines/immunology ; Cancer Vaccines/therapeutic use ; Cervical Intraepithelial Neoplasia/drug therapy ; Cervical Intraepithelial Neoplasia/virology ; DNA-Binding Proteins/genetics ; DNA-Binding Proteins/immunology ; Double-Blind Method ; Female ; Human papillomavirus 16/genetics ; Human papillomavirus 16/immunology ; Human papillomavirus 18/genetics ; Human papillomavirus 18/immunology ; Humans ; Oncogene Proteins, Viral/genetics ; Oncogene Proteins, Viral/immunology ; Papillomavirus E7 Proteins/genetics ; Papillomavirus E7 Proteins/immunology ; Papillomavirus Infections/drug therapy ; Papillomavirus Infections/virology ; Papillomavirus Vaccines/immunology ; Papillomavirus Vaccines/therapeutic use ; Repressor Proteins/genetics ; Repressor Proteins/immunology ; Treatment Outcome ; Uterine Cervical Neoplasms/drug therapy ; Uterine Cervical Neoplasms/virology ; Vaccines, DNA/immunology ; Vaccines, DNA/therapeutic use ; Young Adult
    Chemical Substances Cancer Vaccines ; DNA-Binding Proteins ; E6 protein, Human papillomavirus type 16 ; E6 protein, Human papillomavirus type 18 ; E7 protein, Human papillomavirus type 18 ; Oncogene Proteins, Viral ; Papillomavirus E7 Proteins ; Papillomavirus Vaccines ; Repressor Proteins ; VGX-3100 ; Vaccines, DNA ; oncogene protein E7, Human papillomavirus type 16
    Language English
    Publishing date 2015-11-21
    Publishing country England
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(15)00239-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Immunogenicity of a DNA vaccine candidate for COVID-19.

    Smith, Trevor R F / Patel, Ami / Ramos, Stephanie / Elwood, Dustin / Zhu, Xizhou / Yan, Jian / Gary, Ebony N / Walker, Susanne N / Schultheis, Katherine / Purwar, Mansi / Xu, Ziyang / Walters, Jewell / Bhojnagarwala, Pratik / Yang, Maria / Chokkalingam, Neethu / Pezzoli, Patrick / Parzych, Elizabeth / Reuschel, Emma L / Doan, Arthur /
    Tursi, Nicholas / Vasquez, Miguel / Choi, Jihae / Tello-Ruiz, Edgar / Maricic, Igor / Bah, Mamadou A / Wu, Yuanhan / Amante, Dinah / Park, Daniel H / Dia, Yaya / Ali, Ali Raza / Zaidi, Faraz I / Generotti, Alison / Kim, Kevin Y / Herring, Timothy A / Reeder, Sophia / Andrade, Viviane M / Buttigieg, Karen / Zhao, Gan / Wu, Jiun-Ming / Li, Dan / Bao, Linlin / Liu, Jiangning / Deng, Wei / Qin, Chuan / Brown, Ami Shah / Khoshnejad, Makan / Wang, Nianshuang / Chu, Jacqueline / Wrapp, Daniel / McLellan, Jason S / Muthumani, Kar / Wang, Bin / Carroll, Miles W / Kim, J Joseph / Boyer, Jean / Kulp, Daniel W / Humeau, Laurent M P F / Weiner, David B / Broderick, Kate E

    Nature communications

    2020  Volume 11, Issue 1, Page(s) 2601

    Abstract: The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a ... ...

    Abstract The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a synthetic DNA vaccine targeting the MERS coronavirus Spike (S) protein, the major surface antigen of coronaviruses, which is currently in clinical study. Here we build on this prior experience to generate a synthetic DNA-based vaccine candidate targeting SARS-CoV-2 S protein. The engineered construct, INO-4800, results in robust expression of the S protein in vitro. Following immunization of mice and guinea pigs with INO-4800 we measure antigen-specific T cell responses, functional antibodies which neutralize the SARS-CoV-2 infection and block Spike protein binding to the ACE2 receptor, and biodistribution of SARS-CoV-2 targeting antibodies to the lungs. This preliminary dataset identifies INO-4800 as a potential COVID-19 vaccine candidate, supporting further translational study.
    MeSH term(s) Angiotensin-Converting Enzyme 2 ; Animals ; Antibodies, Neutralizing/immunology ; Antigens, Viral/chemistry ; Antigens, Viral/immunology ; COVID-19 Vaccines ; Coronavirus Infections/immunology ; Coronavirus Infections/prevention & control ; Epitope Mapping ; Guinea Pigs ; Immunity, Humoral ; Immunoglobulin G/immunology ; Lung/immunology ; Mice ; Mice, Inbred BALB C ; Middle East Respiratory Syndrome Coronavirus ; Models, Animal ; Peptidyl-Dipeptidase A/metabolism ; Spike Glycoprotein, Coronavirus/chemistry ; Spike Glycoprotein, Coronavirus/immunology ; Vaccines, DNA/immunology ; Viral Vaccines/chemistry ; Viral Vaccines/immunology
    Chemical Substances Antibodies, Neutralizing ; Antigens, Viral ; COVID-19 Vaccines ; Immunoglobulin G ; Spike Glycoprotein, Coronavirus ; Vaccines, DNA ; Viral Vaccines ; spike protein, SARS-CoV-2 ; Peptidyl-Dipeptidase A (EC 3.4.15.1) ; Ace2 protein, mouse (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Keywords covid19
    Language English
    Publishing date 2020-05-20
    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/s41467-020-16505-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Immunogenicity of a DNA vaccine candidate for COVID-19

    Smith, Trevor R F / Patel, Ami / Ramos, Stephanie / Elwood, Dustin / Zhu, Xizhou / Yan, Jian / Gary, Ebony N / Walker, Susanne N / Schultheis, Katherine / Purwar, Mansi / Xu, Ziyang / Walters, Jewell / Bhojnagarwala, Pratik / Yang, Maria / Chokkalingam, Neethu / Pezzoli, Patrick / Parzych, Elizabeth / Reuschel, Emma L / Doan, Arthur /
    Tursi, Nicholas / Vasquez, Miguel / Choi, Jihae / Tello-Ruiz, Edgar / Maricic, Igor / Bah, Mamadou A / Wu, Yuanhan / Amante, Dinah / Park, Daniel H / Dia, Yaya / Ali, Ali Raza / Zaidi, Faraz I / Generotti, Alison / Kim, Kevin Y / Herring, Timothy A / Reeder, Sophia / Andrade, Viviane M / Buttigieg, Karen / Zhao, Gan / Wu, Jiun-Ming / Li, Dan / Bao, Linlin / Liu, Jiangning / Deng, Wei / Qin, Chuan / Brown, Ami Shah / Khoshnejad, Makan / Wang, Nianshuang / Chu, Jacqueline / Wrapp, Daniel / McLellan, Jason S

    Nat Commun

    Abstract: The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a ... ...

    Abstract The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a synthetic DNA vaccine targeting the MERS coronavirus Spike (S) protein, the major surface antigen of coronaviruses, which is currently in clinical study. Here we build on this prior experience to generate a synthetic DNA-based vaccine candidate targeting SARS-CoV-2 S protein. The engineered construct, INO-4800, results in robust expression of the S protein in vitro. Following immunization of mice and guinea pigs with INO-4800 we measure antigen-specific T cell responses, functional antibodies which neutralize the SARS-CoV-2 infection and block Spike protein binding to the ACE2 receptor, and biodistribution of SARS-CoV-2 targeting antibodies to the lungs. This preliminary dataset identifies INO-4800 as a potential COVID-19 vaccine candidate, supporting further translational study.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #326048
    Database COVID19

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  6. Article ; Online: Immunogenicity of a DNA vaccine candidate for COVID-19

    Smith, Trevor R.F. / Patel, Ami / Ramos, Stephanie / Elwood, Dustin / Zhu, Xizhou / Yan, Jian / Gary, Ebony N. / Walker, Susanne N. / Schultheis, Katherine / Purwar, Mansi / Xu, Ziyang / Walters, Jewell / Bhojnagarwala, Pratik / Yang, Maria / Chokkalingam, Neethu / Pezzoli, Patrick / Parzych, Elizabeth / Reuschel, Emma L. / Doan, Arthur /
    Tursi, Nicholas / Vasquez, Miguel / Choi, Jihae / Tello-Ruiz, Edgar / Maricic, Igor / Bah, Mamadou A. / Wu, Yuanhan / Amante, Dinah / Park, Daniel H. / Dia, Yaya / Ali, Ali Raza / Zaidi, Faraz I. / Generotti, Alison / Kim, Kevin Y. / Herring, Timothy A. / Reeder, Sophia / Andrade, Viviane M. / Buttigieg, Karen / Zhao, Gan / Wu, Jiun Ming / Li, Dan / Bao, Linlin / Liu, Jiangning / Deng, Wei / Qin, Chuan / Brown, Ami Shah / Khoshnejad, Makan / Wang, Nianshuang / Chu, Jacqueline / Wrapp, Daniel / McLellan, Jason S. / Muthumani, Kar / Wang, Bin / Carroll, Miles W. / Kim, J. Joseph / Boyer, Jean / Kulp, Daniel W. / Humeau, Laurent M.P.F. / Weiner, David B. / Broderick, Kate E.

    reponame:Expeditio Repositorio Institucional UJTL ; instname:Universidad de Bogotá Jorge Tadeo Lozano

    2020  

    Abstract: The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a ... ...

    Abstract The coronavirus family member, SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19. At this time, no vaccine is available to control further dissemination of the disease. We have previously engineered a synthetic DNA vaccine targeting the MERS coronavirus Spike (S) protein, the major surface antigen of coronaviruses, which is currently in clinical study. Here we build on this prior experience to generate a synthetic DNA-based vaccine candidate targeting SARS-CoV-2 S protein. The engineered construct, INO-4800, results in robust expression of the S protein in vitro. Following immunization of mice and guinea pigs with INO-4800 we measure antigen-specific T cell responses, functional antibodies which neutralize the SARS-CoV-2 infection and block Spike protein binding to the ACE2 receptor, and biodistribution of SARS-CoV-2 targeting antibodies to the lungs. This preliminary dataset identifies INO-4800 as a potential COVID-19 vaccine candidate, supporting further translational study.
    Keywords Vacunación ; Síndrome respiratorio agudo grave ; COVID-19 ; SARS-CoV-2 ; Coronavirus ; covid19
    Publishing date 2020-05-20
    Publisher Science Direct
    Publishing country co
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Immunogenicity of a DNA vaccine candidate for COVID-19

    Smith, Trevor R. F. / Patel, Ami / Ramos, Stephanie / Elwood, Dustin / Zhu, Xizhou / Yan, Jian / Gary, Ebony N. / Walker, Susanne N. / Schultheis, Katherine / Purwar, Mansi / Xu, Ziyang / Walters, Jewell / Bhojnagarwala, Pratik / Yang, Maria / Chokkalingam, Neethu / Pezzoli, Patrick / Parzych, Elizabeth / Reuschel, Emma L. / Doan, Arthur /
    Tursi, Nicholas / Vasquez, Miguel / Choi, Jihae / Tello-Ruiz, Edgar / Maricic, Igor / Bah, Mamadou A. / Wu, Yuanhan / Amante, Dinah / Park, Daniel H. / Dia, Yaya / Ali, Ali Raza / Zaidi, Faraz I. / Generotti, Alison / Kim, Kevin Y. / Herring, Timothy A. / Reeder, Sophia / Andrade, Viviane M. / Buttigieg, Karen / Zhao, Gan / Wu, Jiun-Ming / Li, Dan / Bao, Linlin / Liu, Jiangning / Deng, Wei / Qin, Chuan / Brown, Ami Shah / Khoshnejad, Makan / Wang, Nianshuang / Chu, Jacqueline / Wrapp, Daniel / McLellan, Jason S. / Muthumani, Kar / Wang, Bin / Carroll, Miles W. / Kim, J. Joseph / Boyer, Jean / Kulp, Daniel W. / Humeau, Laurent M. P. F. / Weiner, David B. / Broderick, Kate E.

    Nature Communications

    2020  Volume 11, Issue 1

    Keywords General Biochemistry, Genetics and Molecular Biology ; General Physics and Astronomy ; General Chemistry ; covid19
    Language English
    Publisher Springer Science and Business Media LLC
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2553671-0
    ISSN 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-020-16505-0
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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