Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1225 to 1234 of 1234 entries
Sorted by: Best Match Show Resources per page
Children's Opioid Use at Home After Laparoscopic Appendectomy.

Pain management nursing : official journal of the American Society of Pain Management Nurses

Manworren RCB, Kaduwela N, Mishra T, Cooper J.
PMID: 33812791
Pain Manag Nurs. 2021 Dec;22(6):708-715. doi: 10.1016/j.pmn.2021.02.011. Epub 2021 Mar 31.

BACKGROUND: To combat the opioid epidemic, prescribers need accurate information about pediatric home opioid requirements to manage acute pain after surgery. Current opioid use estimates come from retrospective surveys; this study used medication adherence technology (eCAP) to track home...

Cite
Manworren RCB, Kaduwela N, Mishra T, et al. Children's Opioid Use at Home After Laparoscopic Appendectomy. Pain Manag Nurs. 2021;22(6):708-715doi: 10.1016/j.pmn.2021.02.011.
Manworren, R. C. B., Kaduwela, N., Mishra, T., & Cooper, J. (2021). Children's Opioid Use at Home After Laparoscopic Appendectomy. Pain management nursing : official journal of the American Society of Pain Management Nurses, 22(6), 708-715. https://doi.org/10.1016/j.pmn.2021.02.011
Manworren, Renee C B, et al. "Children's Opioid Use at Home After Laparoscopic Appendectomy." Pain management nursing : official journal of the American Society of Pain Management Nurses vol. 22,6 (2021): 708-715. doi: https://doi.org/10.1016/j.pmn.2021.02.011
Manworren RCB, Kaduwela N, Mishra T, Cooper J. Children's Opioid Use at Home After Laparoscopic Appendectomy. Pain Manag Nurs. 2021 Dec;22(6):708-715. doi: 10.1016/j.pmn.2021.02.011. Epub 2021 Mar 31. PMID: 33812791.
Copy Download .nbib Format: NLM
BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program.

iScience

Drashansky TT, Helm EY, Curkovic N, Cooper J, Cheng P, Chen X, Gautam N, Meng L, Kwiatkowski AJ, Collins WO, Keselowsky BG, Sant'Angelo D, Huo Z, Zhang W, Zhou L, Avram D.
PMID: 33870128
iScience. 2021 Mar 13;24(4):102307. doi: 10.1016/j.isci.2021.102307. eCollection 2021 Apr 23.

Mucosal-associated invariant T (MAIT) cells recognize microbial riboflavin metabolites presented by MR1 and play role in immune responses to microbial infections and tumors. We report here that absence of the transcription factor (TF) Bcl11b in mice alters predominantly MAIT17...

Cite
Drashansky TT, Helm EY, Curkovic N, et al. BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program. iScience. 2021;24(4):102307doi: 10.1016/j.isci.2021.102307.
Drashansky, T. T., Helm, E. Y., Curkovic, N., Cooper, J., Cheng, P., Chen, X., Gautam, N., Meng, L., Kwiatkowski, A. J., Collins, W. O., Keselowsky, B. G., Sant'Angelo, D., Huo, Z., Zhang, W., Zhou, L., & Avram, D. (2021). BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program. iScience, 24(4), 102307. https://doi.org/10.1016/j.isci.2021.102307
Drashansky, Theodore T, et al. "BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program." iScience vol. 24,4 (2021): 102307. doi: https://doi.org/10.1016/j.isci.2021.102307
Drashansky TT, Helm EY, Curkovic N, Cooper J, Cheng P, Chen X, Gautam N, Meng L, Kwiatkowski AJ, Collins WO, Keselowsky BG, Sant'Angelo D, Huo Z, Zhang W, Zhou L, Avram D. BCL11B is positioned upstream of PLZF and RORγt to control thymic development of mucosal-associated invariant T cells and MAIT17 program. iScience. 2021 Mar 13;24(4):102307. doi: 10.1016/j.isci.2021.102307. eCollection 2021 Apr 23. PMID: 33870128; PMCID: PMC8042176.
Copy Download .nbib Format: NLM
Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis.

Human mutation

Hamada S, Masson E, Chen JM, Sakaguchi R, Rebours V, Buscail L, Matsumoto R, Tanaka Y, Kikuta K, Kataoka F, Sasaki A, Le Rhun M, Audin H, Lachaux A, Caumont B, Lorenzo D, Billiemaz K, Besnard R, Koch S, Lamireau T, De Koninck X, Génin E, Cooper DN, Mori Y, Masamune A, Férec C.
PMID: 34923708
Hum Mutat. 2021 Dec 19; doi: 10.1002/humu.24315. Epub 2021 Dec 19.

The recent discovery of TRPV6 as a pancreatitis susceptibility gene served to identify a novel mechanism of chronic pancreatitis (CP) due to Ca

Cite
Hamada S, Masson E, Chen JM, et al. Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis. Hum Mutat. 2021;doi: 10.1002/humu.24315.
Hamada, S., Masson, E., Chen, J. M., Sakaguchi, R., Rebours, V., Buscail, L., Matsumoto, R., Tanaka, Y., Kikuta, K., Kataoka, F., Sasaki, A., Le Rhun, M., Audin, H., Lachaux, A., Caumont, B., Lorenzo, D., Billiemaz, K., Besnard, R., Koch, S., Lamireau, T., De Koninck, X., Génin, E., Cooper, D. N., Mori, Y., Masamune, A., & Férec, C. (2021). Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis. Human mutation, . https://doi.org/10.1002/humu.24315
Hamada, Shin, et al. "Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis." Human mutation vol. (2021). doi: https://doi.org/10.1002/humu.24315
Hamada S, Masson E, Chen JM, Sakaguchi R, Rebours V, Buscail L, Matsumoto R, Tanaka Y, Kikuta K, Kataoka F, Sasaki A, Le Rhun M, Audin H, Lachaux A, Caumont B, Lorenzo D, Billiemaz K, Besnard R, Koch S, Lamireau T, De Koninck X, Génin E, Cooper DN, Mori Y, Masamune A, Férec C. Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis. Hum Mutat. 2021 Dec 19; doi: 10.1002/humu.24315. Epub 2021 Dec 19. PMID: 34923708.
Copy Download .nbib Format: NLM
Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting.

British journal of haematology

Gabelli M, Ademokun C, Cooper N, Amrolia PI.
PMID: 34195990
Br J Haematol. 2022 Jan;196(1):45-62. doi: 10.1111/bjh.17648. Epub 2021 Jun 30.

Autoimmune haemolytic anaemia (AIHA) is a rare complication of allogeneic haematopoietic stem cell transplantation (HSCT), observed with an incidence of 1-5%. Paediatric age, diagnosis of non-malignant disease, lympho-depleting agents in the conditioning regimen, use of unrelated donor, graft versus...

Cite
Gabelli M, Ademokun C, Cooper N, et al. Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting. Br J Haematol. 2021;196(1):45-62doi: 10.1111/bjh.17648.
Gabelli, M., Ademokun, C., Cooper, N., & Amrolia, P. I. (2022). Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting. British journal of haematology, 196(1), 45-62. https://doi.org/10.1111/bjh.17648
Gabelli, Maria, et al. "Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting." British journal of haematology vol. 196,1 (2022): 45-62. doi: https://doi.org/10.1111/bjh.17648
Gabelli M, Ademokun C, Cooper N, Amrolia PI. Pathogenesis, risk factors and therapeutic options for autoimmune haemolytic anaemia in the post-transplant setting. Br J Haematol. 2022 Jan;196(1):45-62. doi: 10.1111/bjh.17648. Epub 2021 Jun 30. PMID: 34195990.
Copy Download .nbib Format: NLM
Statistics: a learning needs assessment.

Medical teacher

Creanor S, Cooper N, Creanor SL.
PMID: 21966689
Med Teach. 2011;33(9):775-6.

No abstract available.

Cite
Creanor S, Cooper N, Creanor SL. Statistics: a learning needs assessment. Med Teach. 2011;33(9):775-6
Creanor, S., Cooper, N., & Creanor, S. L. (2011). Statistics: a learning needs assessment. Medical teacher, 33(9), 775-6.
Creanor, Siobhan, et al. "Statistics: a learning needs assessment." Medical teacher vol. 33,9 (2011): 775-6.
Creanor S, Cooper N, Creanor SL. Statistics: a learning needs assessment. Med Teach. 2011;33(9):775-6. PMID: 21966689.
Copy Download .nbib Format: NLM
Use of Lateral Flow Immunoassay to Characterize SARS-CoV-2 RBD-Specific Antibodies and Their Ability to React with the UK, SA and BR P.1 Variant RBDs.

Diagnostics (Basel, Switzerland)

Tan E, Frew E, Cooper J, Humphrey J, Holden M, Mand AR, Li J, Anderson S, Bi M, Hatler J, Person A, Mortari F, Gould K, Barry S.
PMID: 34208912
Diagnostics (Basel). 2021 Jun 30;11(7). doi: 10.3390/diagnostics11071190.

Identifying anti-spike antibodies that exhibit strong neutralizing activity against current dominant circulating variants, and antibodies that are escaped by these variants, has important implications in the development of therapeutic and diagnostic solutions and in improving understanding of the humoral...

Cite
Tan E, Frew E, Cooper J, et al. Use of Lateral Flow Immunoassay to Characterize SARS-CoV-2 RBD-Specific Antibodies and Their Ability to React with the UK, SA and BR P.1 Variant RBDs. Diagnostics (Basel). 2021;11(7)doi: 10.3390/diagnostics11071190.
Tan, E., Frew, E., Cooper, J., Humphrey, J., Holden, M., Mand, A. R., Li, J., Anderson, S., Bi, M., Hatler, J., Person, A., Mortari, F., Gould, K., & Barry, S. (2021). Use of Lateral Flow Immunoassay to Characterize SARS-CoV-2 RBD-Specific Antibodies and Their Ability to React with the UK, SA and BR P.1 Variant RBDs. Diagnostics (Basel, Switzerland), 11(7), . https://doi.org/10.3390/diagnostics11071190
Tan, Enqing, et al. "Use of Lateral Flow Immunoassay to Characterize SARS-CoV-2 RBD-Specific Antibodies and Their Ability to React with the UK, SA and BR P.1 Variant RBDs." Diagnostics (Basel, Switzerland) vol. 11,7 (2021). doi: https://doi.org/10.3390/diagnostics11071190
Tan E, Frew E, Cooper J, Humphrey J, Holden M, Mand AR, Li J, Anderson S, Bi M, Hatler J, Person A, Mortari F, Gould K, Barry S. Use of Lateral Flow Immunoassay to Characterize SARS-CoV-2 RBD-Specific Antibodies and Their Ability to React with the UK, SA and BR P.1 Variant RBDs. Diagnostics (Basel). 2021 Jun 30;11(7). doi: 10.3390/diagnostics11071190. PMID: 34208912; PMCID: PMC8303872.
Copy Download .nbib Format: NLM
Chimeric Antigen Receptor T Cell Therapy and Its Significance in Multiple Myeloma.

Cureus

Padda J, Khalid K, Zubair U, Peethala MM, Kakani V, Goriparthi L, Almanie AH, Cooper AC, Jean-Charles G.
PMID: 34322356
Cureus. 2021 Jun 25;13(6):e15917. doi: 10.7759/cureus.15917. eCollection 2021 Jun.

Multiple myeloma (MM) has a five-year prevalence worldwide of 230,000 people and is known as the second most common hematological malignancy within the United States. Extensive research has been conducted to gain a wide range of treatment strategies, providing...

Cite
Padda J, Khalid K, Zubair U, et al. Chimeric Antigen Receptor T Cell Therapy and Its Significance in Multiple Myeloma. Cureus. 2021;13(6):e15917doi: 10.7759/cureus.15917.
Padda, J., Khalid, K., Zubair, U., Peethala, M. M., Kakani, V., Goriparthi, L., Almanie, A. H., Cooper, A. C., & Jean-Charles, G. (2021). Chimeric Antigen Receptor T Cell Therapy and Its Significance in Multiple Myeloma. Cureus, 13(6), e15917. https://doi.org/10.7759/cureus.15917
Padda, Jaskamal, et al. "Chimeric Antigen Receptor T Cell Therapy and Its Significance in Multiple Myeloma." Cureus vol. 13,6 (2021): e15917. doi: https://doi.org/10.7759/cureus.15917
Padda J, Khalid K, Zubair U, Peethala MM, Kakani V, Goriparthi L, Almanie AH, Cooper AC, Jean-Charles G. Chimeric Antigen Receptor T Cell Therapy and Its Significance in Multiple Myeloma. Cureus. 2021 Jun 25;13(6):e15917. doi: 10.7759/cureus.15917. eCollection 2021 Jun. PMID: 34322356; PMCID: PMC8310625.
Copy Download .nbib Format: NLM
A Population-Based Study of the Incidence, Medical Care, and Medical Expenditures for Pediatric Traumatic Brain Injury.

The Journal of surgical research

Shen J, Shi J, Cooper J, Chen C, Taylor HG, Xiang H.
PMID: 34298211
J Surg Res. 2021 Jul 19;268:87-96. doi: 10.1016/j.jss.2021.06.025. Epub 2021 Jul 19.

BACKGROUND: Traumatic brain injury (TBI) is one of the leading causes of pediatric trauma morbidity and mortality around the world. However, limited research exists regarding disparities in the incidence of TBI and medical care seeking behaviors and medical expenditures...

Cite
Shen J, Shi J, Cooper J, et al. A Population-Based Study of the Incidence, Medical Care, and Medical Expenditures for Pediatric Traumatic Brain Injury. J Surg Res. 2021;268:87-96doi: 10.1016/j.jss.2021.06.025.
Shen, J., Shi, J., Cooper, J., Chen, C., Taylor, H. G., & Xiang, H. (2021). A Population-Based Study of the Incidence, Medical Care, and Medical Expenditures for Pediatric Traumatic Brain Injury. The Journal of surgical research, 26887-96. https://doi.org/10.1016/j.jss.2021.06.025
Shen, Jiabin, et al. "A Population-Based Study of the Incidence, Medical Care, and Medical Expenditures for Pediatric Traumatic Brain Injury." The Journal of surgical research vol. 268 (2021): 87-96. doi: https://doi.org/10.1016/j.jss.2021.06.025
Shen J, Shi J, Cooper J, Chen C, Taylor HG, Xiang H. A Population-Based Study of the Incidence, Medical Care, and Medical Expenditures for Pediatric Traumatic Brain Injury. J Surg Res. 2021 Jul 19;268:87-96. doi: 10.1016/j.jss.2021.06.025. Epub 2021 Jul 19. PMID: 34298211.
Copy Download .nbib Format: NLM
Pig husbandry in Papua New Guinea A bibliography 1863-1979.

Annales de genetique et de selection animale

Cooper AB, Lauvergne J, Malynicz G, Quartermain A.
PMID: 22896209
Ann Genet Sel Anim. 1981;13(3):301-30. doi: 10.1186/1297-9686-13-3-301.

No abstract available.

Cite
Cooper AB, Lauvergne J, Malynicz G, et al. Pig husbandry in Papua New Guinea A bibliography 1863-1979. Ann Genet Sel Anim. 1981;13(3):301-30doi: 10.1186/1297-9686-13-3-301.
Cooper, A. B., Lauvergne, J., Malynicz, G., & Quartermain, A. (1981). Pig husbandry in Papua New Guinea A bibliography 1863-1979. Annales de genetique et de selection animale, 13(3), 301-30. https://doi.org/10.1186/1297-9686-13-3-301
Cooper, A B, et al. "Pig husbandry in Papua New Guinea A bibliography 1863-1979." Annales de genetique et de selection animale vol. 13,3 (1981): 301-30. doi: https://doi.org/10.1186/1297-9686-13-3-301
Cooper AB, Lauvergne J, Malynicz G, Quartermain A. Pig husbandry in Papua New Guinea A bibliography 1863-1979. Ann Genet Sel Anim. 1981;13(3):301-30. doi: 10.1186/1297-9686-13-3-301. PMID: 22896209; PMCID: PMC2718009.
Copy Download .nbib Format: NLM
The functional spectrum of low-frequency coding variation.

Marth GT, Yu FL, Indap AR, Garimella K, Gravel S, Leong WF, Tyler-Smith C, Bainbridge M, Blackwell T, Zheng-Bradley X, Chen Y, Challis D, Clarke L, Ball EV, Cibulskis K, Cooper DN, Fulton B, Hartl C, Koboldt D, Muzny D, Smith R, Sougnez C, Stewart C, Ward A, Yu J, Xue YL, Altshuler D, Bustamante CD, Clark AG, Daly M, DePristo M, Flicek P, Gabriel S, Mardis E, Palotie A, Gibbs R, Genomes Project.
UIID-AD: 715
2011;12. doi: 10.1186/gb-2011-12-9-r84.

Background: Rare coding variants constitute an important class of human genetic variation, but are underrepresented in current databases that are based on small population samples. Recent studies show that variants altering amino acid sequence and protein function are enriched...

Cite
Marth GT, Yu FL, Indap AR, et al. The functional spectrum of low-frequency coding variation. 2011;12doi: 10.1186/gb-2011-12-9-r84.
Marth, G. T., Yu, F. L., Indap, A. R., Garimella, K., Gravel, S., Leong, W. F., Tyler-Smith, C., Bainbridge, M., Blackwell, T., Zheng-Bradley, X., Chen, Y., Challis, D., Clarke, L., Ball, E. V., Cibulskis, K., Cooper, D. N., Fulton, B., Hartl, C., Koboldt, D., Muzny, D., Smith, R., Sougnez, C., Stewart, C., Ward, A., Yu, J., Xue, Y. L., Altshuler, D., Bustamante, C. D., Clark, A. G., Daly, M., DePristo, M., Flicek, P., Gabriel, S., Mardis, E., Palotie, A., Gibbs, R., & Genomes, P. r. o. j. e. c. t. (2011). The functional spectrum of low-frequency coding variation. 12. https://doi.org/10.1186/gb-2011-12-9-r84
Marth, G T, et al. "The functional spectrum of low-frequency coding variation." vol. 12 (2011). doi: https://doi.org/10.1186/gb-2011-12-9-r84
Marth GT, Yu FL, Indap AR, Garimella K, Gravel S, Leong WF, Tyler-Smith C, Bainbridge M, Blackwell T, Zheng-Bradley X, Chen Y, Challis D, Clarke L, Ball EV, Cibulskis K, Cooper DN, Fulton B, Hartl C, Koboldt D, Muzny D, Smith R, Sougnez C, Stewart C, Ward A, Yu J, Xue YL, Altshuler D, Bustamante CD, Clark AG, Daly M, DePristo M, Flicek P, Gabriel S, Mardis E, Palotie A, Gibbs R, Genomes Project. The functional spectrum of low-frequency coding variation. 2011;12. doi: 10.1186/gb-2011-12-9-r84. UIID-AD: 715.
Copy Download .nbib Format: NLM
Showing 1225 to 1234 of 1234 entries