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Poly(3-alkylthiophene)- block-poly(3-alkylselenophene)s: Conjugated Diblock Co-polymers with Atypical Self-Assembly Behavior.

ACS applied materials & interfaces

Kynaston EL, Winchell KJ, Yee PY, Manion JG, Hendsbee AD, Li Y, Huettner S, Tolbert SH, Seferos DS.
PMID: 30720263
ACS Appl Mater Interfaces. 2019 Feb 20;11(7):7174-7183. doi: 10.1021/acsami.8b18795. Epub 2019 Feb 05.

Understanding self-assembly behavior and resulting morphologies in block co-polymer films is an essential aspect of chemistry and materials science. Although the self-assembly of amorphous coil-coil block co-polymers is relatively well understood, that of semicrystalline block co-polymers where each block...

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Kynaston EL, Winchell KJ, Yee PY, et al. Poly(3-alkylthiophene)- block-poly(3-alkylselenophene)s: Conjugated Diblock Co-polymers with Atypical Self-Assembly Behavior. ACS Appl Mater Interfaces. 2019;11(7):7174-7183doi: 10.1021/acsami.8b18795.
Kynaston, E. L., Winchell, K. J., Yee, P. Y., Manion, J. G., Hendsbee, A. D., Li, Y., Huettner, S., Tolbert, S. H., & Seferos, D. S. (2019). Poly(3-alkylthiophene)- block-poly(3-alkylselenophene)s: Conjugated Diblock Co-polymers with Atypical Self-Assembly Behavior. ACS applied materials & interfaces, 11(7), 7174-7183. https://doi.org/10.1021/acsami.8b18795
Kynaston, Emily L, et al. "Poly(3-alkylthiophene)- block-poly(3-alkylselenophene)s: Conjugated Diblock Co-polymers with Atypical Self-Assembly Behavior." ACS applied materials & interfaces vol. 11,7 (2019): 7174-7183. doi: https://doi.org/10.1021/acsami.8b18795
Kynaston EL, Winchell KJ, Yee PY, Manion JG, Hendsbee AD, Li Y, Huettner S, Tolbert SH, Seferos DS. Poly(3-alkylthiophene)- block-poly(3-alkylselenophene)s: Conjugated Diblock Co-polymers with Atypical Self-Assembly Behavior. ACS Appl Mater Interfaces. 2019 Feb 20;11(7):7174-7183. doi: 10.1021/acsami.8b18795. Epub 2019 Feb 05. PMID: 30720263.
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Advance care planning re-imagined: a needed shift for COVID times and beyond.

Palliative care and social practice

Abel J, Kellehear A, Millington Sanders C, Taubert M, Kingston H.
PMID: 32924012
Palliat Care Soc Pract. 2020 Aug 13;14:2632352420934491. doi: 10.1177/2632352420934491. eCollection 2020.

No abstract available.

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Abel J, Kellehear A, Millington Sanders C, et al. Advance care planning re-imagined: a needed shift for COVID times and beyond. Palliat Care Soc Pract. 2020;14:2632352420934491doi: 10.1177/2632352420934491.
Abel, J., Kellehear, A., Millington Sanders, C., Taubert, M., & Kingston, H. (2020). Advance care planning re-imagined: a needed shift for COVID times and beyond. Palliative care and social practice, 142632352420934491. https://doi.org/10.1177/2632352420934491
Abel, Julian, et al. "Advance care planning re-imagined: a needed shift for COVID times and beyond." Palliative care and social practice vol. 14 (2020): 2632352420934491. doi: https://doi.org/10.1177/2632352420934491
Abel J, Kellehear A, Millington Sanders C, Taubert M, Kingston H. Advance care planning re-imagined: a needed shift for COVID times and beyond. Palliat Care Soc Pract. 2020 Aug 13;14:2632352420934491. doi: 10.1177/2632352420934491. eCollection 2020. PMID: 32924012; PMCID: PMC7446254.
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Community engagement and education: addressing the needs of South Asian families with genetic disorders.

Journal of community genetics

Khan N, Kerr G, Kingston H.
PMID: 27614444
J Community Genet. 2016 Oct;7(4):317-323. doi: 10.1007/s12687-016-0278-0. Epub 2016 Sep 10.

Consanguineous marriage is common among the South Asian heritage community in the UK. While conferring social and cultural benefits, consanguinity is associated with an increased risk of autosomal recessive disorders and an increase in childhood death and disability. We...

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Khan N, Kerr G, Kingston H. Community engagement and education: addressing the needs of South Asian families with genetic disorders. J Community Genet. 2016;7(4):317-323doi: 10.1007/s12687-016-0278-0.
Khan, N., Kerr, G., & Kingston, H. (2016). Community engagement and education: addressing the needs of South Asian families with genetic disorders. Journal of community genetics, 7(4), 317-323. https://doi.org/10.1007/s12687-016-0278-0
Khan, Nasaim, et al. "Community engagement and education: addressing the needs of South Asian families with genetic disorders." Journal of community genetics vol. 7,4 (2016): 317-323. doi: https://doi.org/10.1007/s12687-016-0278-0
Khan N, Kerr G, Kingston H. Community engagement and education: addressing the needs of South Asian families with genetic disorders. J Community Genet. 2016 Oct;7(4):317-323. doi: 10.1007/s12687-016-0278-0. Epub 2016 Sep 10. PMID: 27614444; PMCID: PMC5138164.
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Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England.

Journal of community genetics

Salway S, Ali P, Ratcliffe G, Such E, Khan N, Kingston H, Quarrell O.
PMID: 27311843
J Community Genet. 2016 Jul;7(3):215-28. doi: 10.1007/s12687-016-0269-1. Epub 2016 Jun 16.

Populations practising customary consanguineous marriage have a higher incidence of autosomal recessive genetic disorders than those in which reproductive partners are usually unrelated. In the absence of any national-level response, English service developments to address the additional needs of...

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Salway S, Ali P, Ratcliffe G, et al. Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England. J Community Genet. 2016;7(3):215-28doi: 10.1007/s12687-016-0269-1.
Salway, S., Ali, P., Ratcliffe, G., Such, E., Khan, N., Kingston, H., & Quarrell, O. (2016). Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England. Journal of community genetics, 7(3), 215-28. https://doi.org/10.1007/s12687-016-0269-1
Salway, Sarah, et al. "Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England." Journal of community genetics vol. 7,3 (2016): 215-28. doi: https://doi.org/10.1007/s12687-016-0269-1
Salway S, Ali P, Ratcliffe G, Such E, Khan N, Kingston H, Quarrell O. Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England. J Community Genet. 2016 Jul;7(3):215-28. doi: 10.1007/s12687-016-0269-1. Epub 2016 Jun 16. PMID: 27311843; PMCID: PMC4960028.
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Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions.

SAGE open medicine

Daker-White G, Ealing J, Greenfield J, Kingston H, Sanders C, Payne K.
PMID: 26770684
SAGE Open Med. 2013 Sep 28;1:2050312113505560. doi: 10.1177/2050312113505560. eCollection 2013.

OBJECTIVES: An exploratory investigation of diagnosis and management in progressive ataxias: rare neurological conditions usually affecting balance, mobility and speech.METHODS: A longitudinal qualitative study into the experiences of people with ataxia and neurologists. Thematic analysis and follow-up interviews were...

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Daker-White G, Ealing J, Greenfield J, et al. Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions. SAGE Open Med. 2013;1:2050312113505560doi: 10.1177/2050312113505560.
Daker-White, G., Ealing, J., Greenfield, J., Kingston, H., Sanders, C., & Payne, K. (2013). Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions. SAGE open medicine, 12050312113505560. https://doi.org/10.1177/2050312113505560
Daker-White, Gavin, et al. "Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions." SAGE open medicine vol. 1 (2013): 2050312113505560. doi: https://doi.org/10.1177/2050312113505560
Daker-White G, Ealing J, Greenfield J, Kingston H, Sanders C, Payne K. Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions. SAGE Open Med. 2013 Sep 28;1:2050312113505560. doi: 10.1177/2050312113505560. eCollection 2013. PMID: 26770684; PMCID: PMC4687766.
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Feelings Associated with Being a Carrier and Characteristics of Reproductive Decision Making in Women Known to Be Carriers of X-linked Conditions.

Journal of health psychology

Kay E, Kingston H.
PMID: 22114236
J Health Psychol. 2002 Mar;7(2):169-81. doi: 10.1177/1359105302007002456.

Qualitative data were collected from 14 women known to be carriers of an X-linked condition associated with 'serious' disability on feelings about being a carrier and impact on reproductive decisions. Guilt and responsibility were commonly expressed by carriers about...

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Kay E, Kingston H. Feelings Associated with Being a Carrier and Characteristics of Reproductive Decision Making in Women Known to Be Carriers of X-linked Conditions. J Health Psychol. 2002;7(2):169-81doi: 10.1177/1359105302007002456.
Kay, E., & Kingston, H. (2002). Feelings Associated with Being a Carrier and Characteristics of Reproductive Decision Making in Women Known to Be Carriers of X-linked Conditions. Journal of health psychology, 7(2), 169-81. https://doi.org/10.1177/1359105302007002456
Kay, Elizabeth, and Kingston, Helen. "Feelings Associated with Being a Carrier and Characteristics of Reproductive Decision Making in Women Known to Be Carriers of X-linked Conditions." Journal of health psychology vol. 7,2 (2002): 169-81. doi: https://doi.org/10.1177/1359105302007002456
Kay E, Kingston H. Feelings Associated with Being a Carrier and Characteristics of Reproductive Decision Making in Women Known to Be Carriers of X-linked Conditions. J Health Psychol. 2002 Mar;7(2):169-81. doi: 10.1177/1359105302007002456. PMID: 22114236.
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Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient.

Frontiers in endocrinology

Raffan E, Hurst LA, Turki SA, Carpenter G, Scott C, Daly A, Coffey A, Bhaskar S, Howard E, Khan N, Kingston H, Palotie A, Savage DB, O'Driscoll M, Smith C, O'Rahilly S, Barroso I, Semple RK.
PMID: 22654791
Front Endocrinol (Lausanne). 2011 Mar 29;2:8. doi: 10.3389/fendo.2011.00008. eCollection 2011.

Genetic diagnosis of inherited metabolic disease is conventionally achieved through syndrome recognition and targeted gene sequencing, but many patients receive no specific diagnosis. Next-generation sequencing allied to capture of expressed sequences from genomic DNA now offers a powerful new...

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Raffan E, Hurst LA, Turki SA, et al. Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. Front Endocrinol (Lausanne). 2011;2:8doi: 10.3389/fendo.2011.00008.
Raffan, E., Hurst, L. A., Turki, S. A., Carpenter, G., Scott, C., Daly, A., Coffey, A., Bhaskar, S., Howard, E., Khan, N., Kingston, H., Palotie, A., Savage, D. B., O'Driscoll, M., Smith, C., O'Rahilly, S., Barroso, I., & Semple, R. K. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. Frontiers in endocrinology, 28. https://doi.org/10.3389/fendo.2011.00008
Raffan, Eleanor, et al. "Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient." Frontiers in endocrinology vol. 2 (2011): 8. doi: https://doi.org/10.3389/fendo.2011.00008
Raffan E, Hurst LA, Turki SA, Carpenter G, Scott C, Daly A, Coffey A, Bhaskar S, Howard E, Khan N, Kingston H, Palotie A, Savage DB, O'Driscoll M, Smith C, O'Rahilly S, Barroso I, Semple RK. Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. Front Endocrinol (Lausanne). 2011 Mar 29;2:8. doi: 10.3389/fendo.2011.00008. eCollection 2011. PMID: 22654791; PMCID: PMC3356119.
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Should Finasteride Be Routinely Given Preoperatively for TURP?.

ISRN urology

Aboumarzouk OM, Aslam MZ, Wedderburn A, Turner K, Hughes O, Kynaston HG.
PMID: 23984104
ISRN Urol. 2013 Jul 29;2013:458353. doi: 10.1155/2013/458353. eCollection 2013.

Objective. The aim of the review was to compare the use of finasteride to placebo in patients undergoing TURP procedures. Material & Methods. We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE (1966-November 2011), EMBASE (1980-November 2011),...

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Aboumarzouk OM, Aslam MZ, Wedderburn A, et al. Should Finasteride Be Routinely Given Preoperatively for TURP?. ISRN Urol. 2013;2013:458353doi: 10.1155/2013/458353.
Aboumarzouk, O. M., Aslam, M. Z., Wedderburn, A., Turner, K., Hughes, O., & Kynaston, H. G. (2013). Should Finasteride Be Routinely Given Preoperatively for TURP?. ISRN urology, 2013458353. https://doi.org/10.1155/2013/458353
Aboumarzouk, O M, et al. "Should Finasteride Be Routinely Given Preoperatively for TURP?." ISRN urology vol. 2013 (2013): 458353. doi: https://doi.org/10.1155/2013/458353
Aboumarzouk OM, Aslam MZ, Wedderburn A, Turner K, Hughes O, Kynaston HG. Should Finasteride Be Routinely Given Preoperatively for TURP?. ISRN Urol. 2013 Jul 29;2013:458353. doi: 10.1155/2013/458353. eCollection 2013. PMID: 23984104; PMCID: PMC3747465.
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Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families.

Journal of community genetics

Khan N, Benson J, Macleod R, Kingston H.
PMID: 22460207
J Community Genet. 2010 Jun;1(2):73-81. doi: 10.1007/s12687-010-0012-2. Epub 2010 Aug 20.

Blackburn with Darwen Primary Care Trust (PCT) provides services to a substantial Asian population in which the practice of consanguineous marriage is common and there is a high incidence of autosomal recessive disorders. The aim was to provide and...

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Khan N, Benson J, Macleod R, et al. Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families. J Community Genet. 2010;1(2):73-81doi: 10.1007/s12687-010-0012-2.
Khan, N., Benson, J., Macleod, R., & Kingston, H. (2010). Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families. Journal of community genetics, 1(2), 73-81. https://doi.org/10.1007/s12687-010-0012-2
Khan, Nasaim, et al. "Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families." Journal of community genetics vol. 1,2 (2010): 73-81. doi: https://doi.org/10.1007/s12687-010-0012-2
Khan N, Benson J, Macleod R, Kingston H. Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families. J Community Genet. 2010 Jun;1(2):73-81. doi: 10.1007/s12687-010-0012-2. Epub 2010 Aug 20. PMID: 22460207; PMCID: PMC3185987.
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Management of lower urinary tract symptoms in men.

British journal of hospital medicine (London, England : 2005)

Jefferies M, Cox A, Bennett A, Kynaston H.
PMID: 24022553
Br J Hosp Med (Lond). 2013 Sep;74(9):518-22. doi: 10.12968/hmed.2013.74.9.518.

Lower urinary tract symptoms in men are common, increase with age and can become bothersome, causing significant morbidity such as urinary retention or the need for surgery. This article outlines how to assess a man with lower urinary tract...

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Jefferies M, Cox A, Bennett A, et al. Management of lower urinary tract symptoms in men. Br J Hosp Med (Lond). 2013;74(9):518-22doi: 10.12968/hmed.2013.74.9.518.
Jefferies, M., Cox, A., Bennett, A., & Kynaston, H. (2013). Management of lower urinary tract symptoms in men. British journal of hospital medicine (London, England : 2005), 74(9), 518-22. https://doi.org/10.12968/hmed.2013.74.9.518
Jefferies, Matthew, et al. "Management of lower urinary tract symptoms in men." British journal of hospital medicine (London, England : 2005) vol. 74,9 (2013): 518-22. doi: https://doi.org/10.12968/hmed.2013.74.9.518
Jefferies M, Cox A, Bennett A, Kynaston H. Management of lower urinary tract symptoms in men. Br J Hosp Med (Lond). 2013 Sep;74(9):518-22. doi: 10.12968/hmed.2013.74.9.518. PMID: 24022553.
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Erratum to 'Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received' [European Urology 77 (2020) 320-330].

European urology

Neal DE, Metcalfe C, Donovan JL, Lane JA, Davis M, Young GJ, Dutton SJ, Walsh EI, Martin RM, Peters TJ, Turner EL, Mason M, Bryant R, Bollina P, Catto J, Doherty A, Gillatt D, Gnanapragasam V, Holding P, Hughes O, Kockelbergh R, Kynaston H, Oxley J, Paul A, Paez E, Rosario DJ, Rowe E, Staffurth J, Altman DG, Hamdy FC.
PMID: 32624282
Eur Urol. 2020 Sep;78(3):e139-e143. doi: 10.1016/j.eururo.2020.05.030. Epub 2020 Jul 03.

No abstract available.

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Neal DE, Metcalfe C, Donovan JL, et al. Erratum to 'Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received' [European Urology 77 (2020) 320-330]. Eur Urol. 2020;78(3):e139-e143doi: 10.1016/j.eururo.2020.05.030.
Neal, D. E., Metcalfe, C., Donovan, J. L., Lane, J. A., Davis, M., Young, G. J., Dutton, S. J., Walsh, E. I., Martin, R. M., Peters, T. J., Turner, E. L., Mason, M., Bryant, R., Bollina, P., Catto, J., Doherty, A., Gillatt, D., Gnanapragasam, V., Holding, P., Hughes, O., Kockelbergh, R., Kynaston, H., Oxley, J., Paul, A., Paez, E., Rosario, D. J., Rowe, E., Staffurth, J., Altman, D. G., Hamdy, F. C. (2020). Erratum to 'Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received' [European Urology 77 (2020) 320-330]. European urology, 78(3), e139-e143. https://doi.org/10.1016/j.eururo.2020.05.030
Neal, David E, et al. "Erratum to 'Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received' [European Urology 77 (2020) 320-330]." European urology vol. 78,3 (2020): e139-e143. doi: https://doi.org/10.1016/j.eururo.2020.05.030
Neal DE, Metcalfe C, Donovan JL, Lane JA, Davis M, Young GJ, Dutton SJ, Walsh EI, Martin RM, Peters TJ, Turner EL, Mason M, Bryant R, Bollina P, Catto J, Doherty A, Gillatt D, Gnanapragasam V, Holding P, Hughes O, Kockelbergh R, Kynaston H, Oxley J, Paul A, Paez E, Rosario DJ, Rowe E, Staffurth J, Altman DG, Hamdy FC. Erratum to 'Ten-year Mortality, Disease Progression, and Treatment-related Side Effects in Men with Localised Prostate Cancer from the ProtecT Randomised Controlled Trial According to Treatment Received' [European Urology 77 (2020) 320-330]. Eur Urol. 2020 Sep;78(3):e139-e143. doi: 10.1016/j.eururo.2020.05.030. Epub 2020 Jul 03. PMID: 32624282.
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Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments.

Microbiology resource announcements

Rodriguez-Medina J, Kim HG, Castro J, Contreras CM, Glon CL, Goyal A, Guo BY, Knowles S, Lin JC, McGuiness CL, Sorkin E, Stefani J, Yegireddi SJ, Chaganti S, Cui D, Deck SL, Deokule Y, Douglas H, Kenaston M, O'Brien A, Patterson E, Schoppa N, Tran Vo D, Tran K, Tran TL, Pérez-Irizarry V, Carrasquillo-Nieves K, Montalvo-Rodriguez R, Yao AI, Albeck JG, Facciotti MT, Nord AS, Furrow RE.
PMID: 32079635
Microbiol Resour Announc. 2020 Feb 20;9(8). doi: 10.1128/MRA.01540-19.

Halophile-specific enzymes have wide-ranging industrial and commercial applications. Despite their importance, there is a paucity of available halophile whole-genome sequences. Here, we report the draft genome sequences of 16 diverse salt-tolerant strains of bacteria and archaea isolated from a...

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Rodriguez-Medina J, Kim HG, Castro J, et al. Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments. Microbiol Resour Announc. 2020;9(8)doi: 10.1128/MRA.01540-19.
Rodriguez-Medina, J., Kim, H. G., Castro, J., Contreras, C. M., Glon, C. L., Goyal, A., Guo, B. Y., Knowles, S., Lin, J. C., McGuiness, C. L., Sorkin, E., Stefani, J., Yegireddi, S. J., Chaganti, S., Cui, D., Deck, S. L., Deokule, Y., Douglas, H., Kenaston, M., O'Brien, A., Patterson, E., Schoppa, N., Tran Vo, D., Tran, K., Tran, T. L., Pérez-Irizarry, V., Carrasquillo-Nieves, K., Montalvo-Rodriguez, R., Yao, A. I., Albeck, J. G., Facciotti, M. T., Nord, A. S., & Furrow, R. E. (2020). Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments. Microbiology resource announcements, 9(8), . https://doi.org/10.1128/MRA.01540-19
Rodriguez-Medina, Joel, et al. "Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments." Microbiology resource announcements vol. 9,8 (2020). doi: https://doi.org/10.1128/MRA.01540-19
Rodriguez-Medina J, Kim HG, Castro J, Contreras CM, Glon CL, Goyal A, Guo BY, Knowles S, Lin JC, McGuiness CL, Sorkin E, Stefani J, Yegireddi SJ, Chaganti S, Cui D, Deck SL, Deokule Y, Douglas H, Kenaston M, O'Brien A, Patterson E, Schoppa N, Tran Vo D, Tran K, Tran TL, Pérez-Irizarry V, Carrasquillo-Nieves K, Montalvo-Rodriguez R, Yao AI, Albeck JG, Facciotti MT, Nord AS, Furrow RE. Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments. Microbiol Resour Announc. 2020 Feb 20;9(8). doi: 10.1128/MRA.01540-19. PMID: 32079635; PMCID: PMC7033272.
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