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[Indications and anomalies of extended electrocardiogram recording (24 hours) at the Gabriel Toure university hospital in Bamako].

Le Mali medical

Menta I, Ba HO, Diall IB, Coulibaly S, Traoré D, Maiga Y, Sidibé N, Sangaré I, Camara Y, Touré K, Sanogo KM.
PMID: 30049113
Mali Med. 2014;29(4):34-37.

AIM: To specify indications and main anomalies of the 24 hours electrocardiogram in Bamako.METHODOLOGY: The study was retrospective and conducted from 1st January 2008 to 31st July 2013, on patients whose file comprised a readable recording holter. The Holter...

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Menta I, Ba HO, Diall IB, et al. Les indications et anomalies de l'enregistrement de longue duree (24 heures) de l'electrocardiogramme au CHU Gabriel Toure de Bamako. [Indications and anomalies of extended electrocardiogram recording (24 hours) at the Gabriel Toure university hospital in Bamako]. Mali Med. 2014;29(4):34-37
Menta, I., Ba, H. O., Diall, I. B., Coulibaly, S., Traoré, D., Maiga, Y., Sidibé, N., Sangaré, I., Camara, Y., Touré, K., & Sanogo, K. M. (2014). Les indications et anomalies de l'enregistrement de longue duree (24 heures) de l'electrocardiogramme au CHU Gabriel Toure de Bamako. [Indications and anomalies of extended electrocardiogram recording (24 hours) at the Gabriel Toure university hospital in Bamako]. Le Mali medical, 29(4), 34-37.
Menta, I, et al. "Les indications et anomalies de l'enregistrement de longue duree (24 heures) de l'electrocardiogramme au CHU Gabriel Toure de Bamako." [Indications and anomalies of extended electrocardiogram recording (24 hours) at the Gabriel Toure university hospital in Bamako]. Le Mali medical vol. 29,4 (2014): 34-37.
Menta I, Ba HO, Diall IB, Coulibaly S, Traoré D, Maiga Y, Sidibé N, Sangaré I, Camara Y, Touré K, Sanogo KM. Les indications et anomalies de l'enregistrement de longue duree (24 heures) de l'electrocardiogramme au CHU Gabriel Toure de Bamako. [Indications and anomalies of extended electrocardiogram recording (24 hours) at the Gabriel Toure university hospital in Bamako]. Mali Med. 2014;29(4):34-37. French. PMID: 30049113.
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Heat Inactivation of the Alkaline Phosphatase in Human Milk and Colostrum .

Journal of food protection

Odumodu CU, Alford ES, Dill CW, Richter RL, Garza C.
PMID: 31084070
J Food Prot. 1993 Mar;56(3):260-262. doi: 10.4315/0362-028X-56.3.260.

Time-temperature relationships were developed for heat inactivation of alkaline phosphatase in pooled human milk and colostrum. Heat inactivation of the enzyme in human milk proceeds at the same rate as in cows' milk. The heat sensitivity of the enzyme...

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Odumodu CU, Alford ES, Dill CW, et al. Heat Inactivation of the Alkaline Phosphatase in Human Milk and Colostrum . J Food Prot. 1993;56(3):260-262doi: 10.4315/0362-028X-56.3.260.
Odumodu, C. U., Alford, E. S., Dill, C. W., Richter, R. L., & Garza, C. (1993). Heat Inactivation of the Alkaline Phosphatase in Human Milk and Colostrum . Journal of food protection, 56(3), 260-262. https://doi.org/10.4315/0362-028X-56.3.260
Odumodu, C U, et al. "Heat Inactivation of the Alkaline Phosphatase in Human Milk and Colostrum ." Journal of food protection vol. 56,3 (1993): 260-262. doi: https://doi.org/10.4315/0362-028X-56.3.260
Odumodu CU, Alford ES, Dill CW, Richter RL, Garza C. Heat Inactivation of the Alkaline Phosphatase in Human Milk and Colostrum . J Food Prot. 1993 Mar;56(3):260-262. doi: 10.4315/0362-028X-56.3.260. PMID: 31084070.
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Physiology and Pathophysiology of Human Airway Mucus.

Physiological reviews

Hill DB, Button B, Rubinstein M, Boucher RC.
PMID: 35001665
Physiol Rev. 2022 Jan 10; doi: 10.1152/physrev.00004.2021. Epub 2022 Jan 10.

The mucus clearance system is the dominant mechanical host defense system of the human lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas liquid pumping and cough-dependent mechanisms, and mucus transport rates are...

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Hill DB, Button B, Rubinstein M, et al. Physiology and Pathophysiology of Human Airway Mucus. Physiol Rev. 2022;doi: 10.1152/physrev.00004.2021.
Hill, D. B., Button, B., Rubinstein, M., & Boucher, R. C. (2022). Physiology and Pathophysiology of Human Airway Mucus. Physiological reviews, . https://doi.org/10.1152/physrev.00004.2021
Hill, David B, et al. "Physiology and Pathophysiology of Human Airway Mucus." Physiological reviews vol. (2022). doi: https://doi.org/10.1152/physrev.00004.2021
Hill DB, Button B, Rubinstein M, Boucher RC. Physiology and Pathophysiology of Human Airway Mucus. Physiol Rev. 2022 Jan 10; doi: 10.1152/physrev.00004.2021. Epub 2022 Jan 10. PMID: 35001665.
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Spatial Stress and Strain Distributions of Viscoelastic Layers in Oscillatory Shear.

Mathematics and computers in simulation

Lindley BS, Forest MG, Smith BD, Mitran SM, Hill DB.
PMID: 22547900
Math Comput Simul. 2012 Mar 01;82(7):1249-1257. doi: 10.1016/j.matcom.2010.07.031. Epub 2010 Aug 10.

One of the standard experimental probes of a viscoelastic material is to measure the response of a layer trapped between parallel surfaces, imposing either periodic stress or strain at one boundary and measuring the other. The relative phase between...

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Lindley BS, Forest MG, Smith BD, et al. Spatial Stress and Strain Distributions of Viscoelastic Layers in Oscillatory Shear. Math Comput Simul. 2010;82(7):1249-1257doi: 10.1016/j.matcom.2010.07.031.
Lindley, B. S., Forest, M. G., Smith, B. D., Mitran, S. M., & Hill, D. B. (2012). Spatial Stress and Strain Distributions of Viscoelastic Layers in Oscillatory Shear. Mathematics and computers in simulation, 82(7), 1249-1257. https://doi.org/10.1016/j.matcom.2010.07.031
Lindley, Brandon S, et al. "Spatial Stress and Strain Distributions of Viscoelastic Layers in Oscillatory Shear." Mathematics and computers in simulation vol. 82,7 (2012): 1249-1257. doi: https://doi.org/10.1016/j.matcom.2010.07.031
Lindley BS, Forest MG, Smith BD, Mitran SM, Hill DB. Spatial Stress and Strain Distributions of Viscoelastic Layers in Oscillatory Shear. Math Comput Simul. 2012 Mar 01;82(7):1249-1257. doi: 10.1016/j.matcom.2010.07.031. Epub 2010 Aug 10. PMID: 22547900; PMCID: PMC3338131.
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Stability of Senecavirus A in animal feed ingredients and infection following consumption of contaminated feed.

Transboundary and emerging diseases

C Caserta L, G Noll JC, Singrey A, Niederwerder MC, Dee S, Nelson EA, Diel DG.
PMID: 34473909
Transbound Emerg Dis. 2022 Jan;69(1):88-96. doi: 10.1111/tbed.14310. Epub 2021 Sep 25.

Animal feed and feed ingredients have recently been investigated as sources of pathogen introduction to farms and as a potential source of infection to animals post-consumption of contaminated feed. Survival of several viruses for a prolonged period has been...

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C Caserta L, G Noll JC, Singrey A, et al. Stability of Senecavirus A in animal feed ingredients and infection following consumption of contaminated feed. Transbound Emerg Dis. 2021;69(1):88-96doi: 10.1111/tbed.14310.
C Caserta, L., G Noll, J. C., Singrey, A., Niederwerder, M. C., Dee, S., Nelson, E. A., & Diel, D. G. (2022). Stability of Senecavirus A in animal feed ingredients and infection following consumption of contaminated feed. Transboundary and emerging diseases, 69(1), 88-96. https://doi.org/10.1111/tbed.14310
C Caserta, Leonardo, et al. "Stability of Senecavirus A in animal feed ingredients and infection following consumption of contaminated feed." Transboundary and emerging diseases vol. 69,1 (2022): 88-96. doi: https://doi.org/10.1111/tbed.14310
C Caserta L, G Noll JC, Singrey A, Niederwerder MC, Dee S, Nelson EA, Diel DG. Stability of Senecavirus A in animal feed ingredients and infection following consumption of contaminated feed. Transbound Emerg Dis. 2022 Jan;69(1):88-96. doi: 10.1111/tbed.14310. Epub 2021 Sep 25. PMID: 34473909.
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Susceptibility of white-tailed deer (.

Journal of virology

Palmer MV, Martins M, Falkenberg S, Buckley A, Caserta LC, Mitchell PK, Cassmann ED, Rollins A, Zylich NC, Renshaw RW, Guarino C, Wagner B, Lager K, Diel DG.
PMID: 33692203
J Virol. 2021 Mar 10; doi: 10.1128/JVI.00083-21. Epub 2021 Mar 10.

The origin of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus causing the global coronavirus disease 19 (COVID-19) pandemic, remains a mystery. Current evidence suggests a likely spillover into humans from an animal reservoir. Understanding the host range...

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Palmer MV, Martins M, Falkenberg S, et al. Susceptibility of white-tailed deer (. J Virol. 2021;doi: 10.1128/JVI.00083-21.
Palmer, M. V., Martins, M., Falkenberg, S., Buckley, A., Caserta, L. C., Mitchell, P. K., Cassmann, E. D., Rollins, A., Zylich, N. C., Renshaw, R. W., Guarino, C., Wagner, B., Lager, K., & Diel, D. G. (2021). Susceptibility of white-tailed deer (. Journal of virology, . https://doi.org/10.1128/JVI.00083-21
Palmer, Mitchell V, et al. "Susceptibility of white-tailed deer (." Journal of virology vol. (2021). doi: https://doi.org/10.1128/JVI.00083-21
Palmer MV, Martins M, Falkenberg S, Buckley A, Caserta LC, Mitchell PK, Cassmann ED, Rollins A, Zylich NC, Renshaw RW, Guarino C, Wagner B, Lager K, Diel DG. Susceptibility of white-tailed deer (. J Virol. 2021 Mar 10; doi: 10.1128/JVI.00083-21. Epub 2021 Mar 10. PMID: 33692203; PMCID: PMC8139686.
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Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS.

Microbiology spectrum

Oftedal TF, Ovchinnikov KV, Hestad KA, Goldbeck O, Porcellato D, Narvhus J, Riedel CU, Kjos M, Diep DB.
PMID: 34643411
Microbiol Spectr. 2021 Oct 31;9(2):e0029921. doi: 10.1128/Spectrum.00299-21. Epub 2021 Oct 13.

Bovine mastitis infection in dairy cattle is a significant economic burden for the dairy industry globally. To reduce the use of antibiotics in treatment of clinical mastitis, new alternative treatment options are needed. Antimicrobial peptides from bacteria, also known...

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Oftedal TF, Ovchinnikov KV, Hestad KA, et al. Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS. Microbiol Spectr. 2021;9(2):e0029921doi: 10.1128/Spectrum.00299-21.
Oftedal, T. F., Ovchinnikov, K. V., Hestad, K. A., Goldbeck, O., Porcellato, D., Narvhus, J., Riedel, C. U., Kjos, M., & Diep, D. B. (2021). Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS. Microbiology spectrum, 9(2), e0029921. https://doi.org/10.1128/Spectrum.00299-21
Oftedal, Thomas F, et al. "Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS." Microbiology spectrum vol. 9,2 (2021): e0029921. doi: https://doi.org/10.1128/Spectrum.00299-21
Oftedal TF, Ovchinnikov KV, Hestad KA, Goldbeck O, Porcellato D, Narvhus J, Riedel CU, Kjos M, Diep DB. Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS. Microbiol Spectr. 2021 Oct 31;9(2):e0029921. doi: 10.1128/Spectrum.00299-21. Epub 2021 Oct 13. PMID: 34643411; PMCID: PMC8515946.
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Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation.

bioRxiv : the preprint server for biology

Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR.
PMID: 33851153
bioRxiv. 2021 Apr 08; doi: 10.1101/2021.04.06.438731.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the agent behind the current COVID-19 pandemic having emerged in Wuhan China in late 2019 from a yet to be determined animal reservoir. SARS-CoV-2 B.1.1.7, a variant identified in the UK...

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Lubinski B, Fernandes MHV, Frazier L, et al. Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv. 2021;doi: 10.1101/2021.04.06.438731.
Lubinski, B., Fernandes, M. H. V., Frazier, L., Tang, T., Daniel, S., Diel, D. G., Jaimes, J. A., & Whittaker, G. R. (2021). Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv : the preprint server for biology, . https://doi.org/10.1101/2021.04.06.438731
Lubinski, Bailey, et al. "Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation." bioRxiv : the preprint server for biology vol. (2021). doi: https://doi.org/10.1101/2021.04.06.438731
Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR. Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv. 2021 Apr 08; doi: 10.1101/2021.04.06.438731. PMID: 33851153; PMCID: PMC8043443.
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The Role of Peritoneal Dialysis in the Treatment of Acute Kidney Injury in Patients With Acute-on-Chronic Liver Failure: A Prospective Brazilian Study.

Frontiers in medicine

Ponce D, Zamoner W, Dias DB, Pires da Rocha E, Kojima C, Balbi AL.
PMID: 34631735
Front Med (Lausanne). 2021 Sep 23;8:713160. doi: 10.3389/fmed.2021.713160. eCollection 2021.

This study aimed to explore the role of peritoneal dialysis (PD) in acute-on-chronic liver disease (ACLD) in relation to metabolic and fluid control and outcome. Fifty-three patients were treated by PD (prescribed Kt/V = 0.40/session), with a flexible catheter,...

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Ponce D, Zamoner W, Dias DB, et al. The Role of Peritoneal Dialysis in the Treatment of Acute Kidney Injury in Patients With Acute-on-Chronic Liver Failure: A Prospective Brazilian Study. Front Med (Lausanne). 2021;8:713160doi: 10.3389/fmed.2021.713160.
Ponce, D., Zamoner, W., Dias, D. B., Pires da Rocha, E., Kojima, C., & Balbi, A. L. (2021). The Role of Peritoneal Dialysis in the Treatment of Acute Kidney Injury in Patients With Acute-on-Chronic Liver Failure: A Prospective Brazilian Study. Frontiers in medicine, 8713160. https://doi.org/10.3389/fmed.2021.713160
Ponce, Daniela, et al. "The Role of Peritoneal Dialysis in the Treatment of Acute Kidney Injury in Patients With Acute-on-Chronic Liver Failure: A Prospective Brazilian Study." Frontiers in medicine vol. 8 (2021): 713160. doi: https://doi.org/10.3389/fmed.2021.713160
Ponce D, Zamoner W, Dias DB, Pires da Rocha E, Kojima C, Balbi AL. The Role of Peritoneal Dialysis in the Treatment of Acute Kidney Injury in Patients With Acute-on-Chronic Liver Failure: A Prospective Brazilian Study. Front Med (Lausanne). 2021 Sep 23;8:713160. doi: 10.3389/fmed.2021.713160. eCollection 2021. PMID: 34631735; PMCID: PMC8496932.
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Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike.

iScience

Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR.
PMID: 34909610
iScience. 2022 Jan 21;25(1):103589. doi: 10.1016/j.isci.2021.103589. Epub 2021 Dec 10.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the agent causing the COVID-19 pandemic. SARS-CoV-2 B.1.1.7 (Alpha), a WHO variant of concern first identified in the United Kingdom in late 2020, contains several mutations including P681H in the spike...

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Lubinski B, Fernandes MHV, Frazier L, et al. Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike. iScience. 2021;25(1):103589doi: 10.1016/j.isci.2021.103589.
Lubinski, B., Fernandes, M. H. V., Frazier, L., Tang, T., Daniel, S., Diel, D. G., Jaimes, J. A., & Whittaker, G. R. (2022). Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike. iScience, 25(1), 103589. https://doi.org/10.1016/j.isci.2021.103589
Lubinski, Bailey, et al. "Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike." iScience vol. 25,1 (2022): 103589. doi: https://doi.org/10.1016/j.isci.2021.103589
Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR. Functional evaluation of the P681H mutation on the proteolytic activation of the SARS-CoV-2 variant B.1.1.7 (Alpha) spike. iScience. 2022 Jan 21;25(1):103589. doi: 10.1016/j.isci.2021.103589. Epub 2021 Dec 10. PMID: 34909610; PMCID: PMC8662955.
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Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation.

bioRxiv : the preprint server for biology

Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR.
PMID: 33851153
bioRxiv. 2021 Apr 08; doi: 10.1101/2021.04.06.438731.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the agent behind the current COVID-19 pandemic having emerged in Wuhan China in late 2019 from a yet to be determined animal reservoir. SARS-CoV-2 B.1.1.7, a variant identified in the UK...

Cite
Lubinski B, Fernandes MHV, Frazier L, et al. Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv. 2021;doi: 10.1101/2021.04.06.438731.
Lubinski, B., Fernandes, M. H. V., Frazier, L., Tang, T., Daniel, S., Diel, D. G., Jaimes, J. A., & Whittaker, G. R. (2021). Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv : the preprint server for biology, . https://doi.org/10.1101/2021.04.06.438731
Lubinski, Bailey, et al. "Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation." bioRxiv : the preprint server for biology vol. (2021). doi: https://doi.org/10.1101/2021.04.06.438731
Lubinski B, Fernandes MHV, Frazier L, Tang T, Daniel S, Diel DG, Jaimes JA, Whittaker GR. Functional evaluation of proteolytic activation for the SARS-CoV-2 variant B.1.1.7: role of the P681H mutation. bioRxiv. 2021 Apr 08; doi: 10.1101/2021.04.06.438731. PMID: 33851153; PMCID: PMC8043443.
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Recombinant production of the lantibiotic nisin using Corynebacterium glutamicum in a two-step process.

Microbial cell factories

Weixler D, Berghoff M, Ovchinnikov KV, Reich S, Goldbeck O, Seibold GM, Wittmann C, Bar NS, Eikmanns BJ, Diep DB, Riedel CU.
PMID: 35033086
Microb Cell Fact. 2022 Jan 15;21(1):11. doi: 10.1186/s12934-022-01739-y.

BACKGROUND: The bacteriocin nisin is naturally produced by Lactococcus lactis as an inactive prepeptide that is modified posttranslationally resulting in five (methyl-)lanthionine rings characteristic for class Ia bacteriocins. Export and proteolytic cleavage of the leader peptide results in release...

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Weixler D, Berghoff M, Ovchinnikov KV, et al. Recombinant production of the lantibiotic nisin using Corynebacterium glutamicum in a two-step process. Microb Cell Fact. 2022;21(1):11doi: 10.1186/s12934-022-01739-y.
Weixler, D., Berghoff, M., Ovchinnikov, K. V., Reich, S., Goldbeck, O., Seibold, G. M., Wittmann, C., Bar, N. S., Eikmanns, B. J., Diep, D. B., & Riedel, C. U. (2022). Recombinant production of the lantibiotic nisin using Corynebacterium glutamicum in a two-step process. Microbial cell factories, 21(1), 11. https://doi.org/10.1186/s12934-022-01739-y
Weixler, Dominik, et al. "Recombinant production of the lantibiotic nisin using Corynebacterium glutamicum in a two-step process." Microbial cell factories vol. 21,1 (2022): 11. doi: https://doi.org/10.1186/s12934-022-01739-y
Weixler D, Berghoff M, Ovchinnikov KV, Reich S, Goldbeck O, Seibold GM, Wittmann C, Bar NS, Eikmanns BJ, Diep DB, Riedel CU. Recombinant production of the lantibiotic nisin using Corynebacterium glutamicum in a two-step process. Microb Cell Fact. 2022 Jan 15;21(1):11. doi: 10.1186/s12934-022-01739-y. PMID: 35033086.
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