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Showing 25 to 36 of 915 entries
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Corrigendum to "Structural features underlying raloxifene's biophysical interaction with bone matrix" [Bioorg. Med. Chem. 24 (2016) 759-767].

Bioorganic & medicinal chemistry

Bivi N, Hu H, Chavali B, Chalmers MJ, Reutter CT, Durst GL, Riley A, Sato M, Allen MR, Burr DB, Dodge JA.
PMID: 27544045
Bioorg Med Chem. 2016 Sep 15;24(18):4516. doi: 10.1016/j.bmc.2016.07.014. Epub 2016 Jul 14.

No abstract available.

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Bivi N, Hu H, Chavali B, et al. Corrigendum to "Structural features underlying raloxifene's biophysical interaction with bone matrix" [Bioorg. Med. Chem. 24 (2016) 759-767]. Bioorg Med Chem. 2016;24(18):4516doi: 10.1016/j.bmc.2016.07.014.
Bivi, N., Hu, H., Chavali, B., Chalmers, M. J., Reutter, C. T., Durst, G. L., Riley, A., Sato, M., Allen, M. R., Burr, D. B., & Dodge, J. A. (2016). Corrigendum to "Structural features underlying raloxifene's biophysical interaction with bone matrix" [Bioorg. Med. Chem. 24 (2016) 759-767]. Bioorganic & medicinal chemistry, 24(18), 4516. https://doi.org/10.1016/j.bmc.2016.07.014
Bivi, Nicoletta, et al. "Corrigendum to "Structural features underlying raloxifene's biophysical interaction with bone matrix" [Bioorg. Med. Chem. 24 (2016) 759-767]." Bioorganic & medicinal chemistry vol. 24,18 (2016): 4516. doi: https://doi.org/10.1016/j.bmc.2016.07.014
Bivi N, Hu H, Chavali B, Chalmers MJ, Reutter CT, Durst GL, Riley A, Sato M, Allen MR, Burr DB, Dodge JA. Corrigendum to "Structural features underlying raloxifene's biophysical interaction with bone matrix" [Bioorg. Med. Chem. 24 (2016) 759-767]. Bioorg Med Chem. 2016 Sep 15;24(18):4516. doi: 10.1016/j.bmc.2016.07.014. Epub 2016 Jul 14. PMID: 27544045.
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Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer.

ACS medicinal chemistry letters

Zhang Y, Seigal BA, Terrett NK, Talbott RL, Fargnoli J, Naglich JG, Chaudhry C, Posy SL, Vuppugalla R, Cornelius G, Lei M, Wang C, Zhang Y, Schmidt RJ, Wei DD, Miller MM, Allen MP, Li L, Carter PH, Vite GD, Borzilleri RM.
PMID: 26191364
ACS Med Chem Lett. 2015 May 27;6(7):770-5. doi: 10.1021/acsmedchemlett.5b00091. eCollection 2015 Jul 09.

A series of dimeric macrocyclic compounds were prepared and evaluated as antagonists for inhibitor of apoptosis proteins. The most potent analogue 11, which binds to XIAP and c-IAP proteins with high affinity and induces caspase-3 activation and ultimately cell...

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Zhang Y, Seigal BA, Terrett NK, et al. Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer. ACS Med Chem Lett. 2015;6(7):770-5doi: 10.1021/acsmedchemlett.5b00091.
Zhang, Y., Seigal, B. A., Terrett, N. K., Talbott, R. L., Fargnoli, J., Naglich, J. G., Chaudhry, C., Posy, S. L., Vuppugalla, R., Cornelius, G., Lei, M., Wang, C., Zhang, Y., Schmidt, R. J., Wei, D. D., Miller, M. M., Allen, M. P., Li, L., Carter, P. H., Vite, G. D., & Borzilleri, R. M. (2015). Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer. ACS medicinal chemistry letters, 6(7), 770-5. https://doi.org/10.1021/acsmedchemlett.5b00091
Zhang, Yong, et al. "Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer." ACS medicinal chemistry letters vol. 6,7 (2015): 770-5. doi: https://doi.org/10.1021/acsmedchemlett.5b00091
Zhang Y, Seigal BA, Terrett NK, Talbott RL, Fargnoli J, Naglich JG, Chaudhry C, Posy SL, Vuppugalla R, Cornelius G, Lei M, Wang C, Zhang Y, Schmidt RJ, Wei DD, Miller MM, Allen MP, Li L, Carter PH, Vite GD, Borzilleri RM. Dimeric Macrocyclic Antagonists of Inhibitor of Apoptosis Proteins for the Treatment of Cancer. ACS Med Chem Lett. 2015 May 27;6(7):770-5. doi: 10.1021/acsmedchemlett.5b00091. eCollection 2015 Jul 09. PMID: 26191364; PMCID: PMC4499820.
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Soil biota responses to long-term atmospheric CO.

Oecologia

Rillig MC, Field CB, Allen MF.
PMID: 28307716
Oecologia. 1999 Jun;119(4):572-577. doi: 10.1007/s004420050821.

Root, arbuscular-mycorrhizal (AM), soil faunal (protozoa and microarthropods), and microbial responses to field exposure to CO

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Rillig MC, Field CB, Allen MF. Soil biota responses to long-term atmospheric CO. Oecologia. 1999;119(4):572-577doi: 10.1007/s004420050821.
Rillig, M. C., Field, C. B., & Allen, M. F. (1999). Soil biota responses to long-term atmospheric CO. Oecologia, 119(4), 572-577. https://doi.org/10.1007/s004420050821
Rillig, Matthias C, et al. "Soil biota responses to long-term atmospheric CO." Oecologia vol. 119,4 (1999): 572-577. doi: https://doi.org/10.1007/s004420050821
Rillig MC, Field CB, Allen MF. Soil biota responses to long-term atmospheric CO. Oecologia. 1999 Jun;119(4):572-577. doi: 10.1007/s004420050821. PMID: 28307716.
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Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species.

Oecologia

Allen MT, Pearcy RW.
PMID: 28308339
Oecologia. 2000 Mar;122(4):479-486. doi: 10.1007/s004420050969.

Photosynthetic performance under dynamic light regimes was assessed in four different species of tropical shrubs from the family Rubiaceae via field gas exchange measurements conducted on Barro Colorado Island, Panamá. Rates of photosynthetic induction and induction loss were assessed...

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Allen MT, Pearcy RW. Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species. Oecologia. 2000;122(4):479-486doi: 10.1007/s004420050969.
Allen, M. T., & Pearcy, R. W. (2000). Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species. Oecologia, 122(4), 479-486. https://doi.org/10.1007/s004420050969
Allen, M T, and Pearcy, R W. "Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species." Oecologia vol. 122,4 (2000): 479-486. doi: https://doi.org/10.1007/s004420050969
Allen MT, Pearcy RW. Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species. Oecologia. 2000 Mar;122(4):479-486. doi: 10.1007/s004420050969. PMID: 28308339.
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The metabolic bone disease associated with the .

Bone reports

Hum JM, Clinkenbeard EL, Ip C, Cass TA, Allen M, White KE.
PMID: 28377980
Bone Rep. 2017 Jan 17;6:38-43. doi: 10.1016/j.bonr.2017.01.003. eCollection 2017 Jun.

Fibroblast growth factor-23 (FGF23) controls key responses to systemic phosphate increases through its phosphaturic actions on the kidney. In addition to stimulation by phosphate, FGF23 positively responds to iron deficiency anemia and hypoxia in rodent models and in humans....

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Hum JM, Clinkenbeard EL, Ip C, et al. The metabolic bone disease associated with the . Bone Rep. 2017;6:38-43doi: 10.1016/j.bonr.2017.01.003.
Hum, J. M., Clinkenbeard, E. L., Ip, C., Cass, T. A., Allen, M., & White, K. E. (2017). The metabolic bone disease associated with the . Bone reports, 638-43. https://doi.org/10.1016/j.bonr.2017.01.003
Hum, Julia M, et al. "The metabolic bone disease associated with the ." Bone reports vol. 6 (2017): 38-43. doi: https://doi.org/10.1016/j.bonr.2017.01.003
Hum JM, Clinkenbeard EL, Ip C, Cass TA, Allen M, White KE. The metabolic bone disease associated with the . Bone Rep. 2017 Jan 17;6:38-43. doi: 10.1016/j.bonr.2017.01.003. eCollection 2017 Jun. PMID: 28377980; PMCID: PMC5365303.
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Response to Courtney et al.

Bone

Bajaj D, Geissler JR, Allen MR, Burr DB, Fritton JC.
PMID: 25813582
Bone. 2016 Aug;89:77-79. doi: 10.1016/j.bone.2015.03.007. Epub 2015 Mar 24.

No abstract available.

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Bajaj D, Geissler JR, Allen MR, et al. Response to Courtney et al. Bone. 2015;89:77-79doi: 10.1016/j.bone.2015.03.007.
Bajaj, D., Geissler, J. R., Allen, M. R., Burr, D. B., & Fritton, J. C. (2016). Response to Courtney et al. Bone, 8977-79. https://doi.org/10.1016/j.bone.2015.03.007
Bajaj, Devendra, et al. "Response to Courtney et al." Bone vol. 89 (2016): 77-79. doi: https://doi.org/10.1016/j.bone.2015.03.007
Bajaj D, Geissler JR, Allen MR, Burr DB, Fritton JC. Response to Courtney et al. Bone. 2016 Aug;89:77-79. doi: 10.1016/j.bone.2015.03.007. Epub 2015 Mar 24. PMID: 25813582.
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Comparisons of MN.

Dalton transactions (Cambridge, England : 2003)

Lunsford AM, Goldstein KF, Cohan MA, Denny JA, Bhuvanesh N, Ding S, Hall MB, Darensbourg MY.
PMID: 28322401
Dalton Trans. 2017 Apr 19;46(16):5175-5182. doi: 10.1039/c7dt00600d.

The bipyridine ligand is renowned as a photo- and redox-active ligand in catalysis; the latter has been particularly explored in the complex Re(bipy)(CO)

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Lunsford AM, Goldstein KF, Cohan MA, et al. Comparisons of MN. Dalton Trans. 2017;46(16):5175-5182doi: 10.1039/c7dt00600d.
Lunsford, A. M., Goldstein, K. F., Cohan, M. A., Denny, J. A., Bhuvanesh, N., Ding, S., Hall, M. B., & Darensbourg, M. Y. (2017). Comparisons of MN. Dalton transactions (Cambridge, England : 2003), 46(16), 5175-5182. https://doi.org/10.1039/c7dt00600d
Lunsford, Allen M, et al. "Comparisons of MN." Dalton transactions (Cambridge, England : 2003) vol. 46,16 (2017): 5175-5182. doi: https://doi.org/10.1039/c7dt00600d
Lunsford AM, Goldstein KF, Cohan MA, Denny JA, Bhuvanesh N, Ding S, Hall MB, Darensbourg MY. Comparisons of MN. Dalton Trans. 2017 Apr 19;46(16):5175-5182. doi: 10.1039/c7dt00600d. PMID: 28322401.
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Diagnostic Approach to Hepatic Mass Lesions and Role of Immunohistochemistry.

Surgical pathology clinics

Marginean EC, Gown AM, Jain D.
PMID: 26838978
Surg Pathol Clin. 2013 Jun;6(2):333-65. doi: 10.1016/j.path.2013.03.005. Epub 2013 May 04.

This review provides an overview of various hepatic mass lesions and a practical diagnostic approach, including most recent immunohistochemical stains used in clinical practice. A wide variety of benign and malignant lesions present as hepatic masses, and the differential...

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Marginean EC, Gown AM, Jain D. Diagnostic Approach to Hepatic Mass Lesions and Role of Immunohistochemistry. Surg Pathol Clin. 2013;6(2):333-65doi: 10.1016/j.path.2013.03.005.
Marginean, E. C., Gown, A. M., & Jain, D. (2013). Diagnostic Approach to Hepatic Mass Lesions and Role of Immunohistochemistry. Surgical pathology clinics, 6(2), 333-65. https://doi.org/10.1016/j.path.2013.03.005
Marginean, Esmeralda Celia, et al. "Diagnostic Approach to Hepatic Mass Lesions and Role of Immunohistochemistry." Surgical pathology clinics vol. 6,2 (2013): 333-65. doi: https://doi.org/10.1016/j.path.2013.03.005
Marginean EC, Gown AM, Jain D. Diagnostic Approach to Hepatic Mass Lesions and Role of Immunohistochemistry. Surg Pathol Clin. 2013 Jun;6(2):333-65. doi: 10.1016/j.path.2013.03.005. Epub 2013 May 04. PMID: 26838978.
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Inducible ternary control of transgene expression and cell ablation in Drosophila.

Development genes and evolution

Smith HK, Roberts IJ, Allen MJ, Connolly JB, Moffat KG, O'Kane CJ.
PMID: 24173393
Dev Genes Evol. 1996 Jun;206(1):14-24. doi: 10.1007/s004270050026.

In Drosophila, P-GAL4 enhancer trap lines can target expression of a cloned gene, under control of a UASGAL element, to any cells of interest. However, additional expression of GAL4 in other cells can produce unwanted lethality or side-effects, particularly...

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Smith HK, Roberts IJ, Allen MJ, et al. Inducible ternary control of transgene expression and cell ablation in Drosophila. Dev Genes Evol. 1996;206(1):14-24doi: 10.1007/s004270050026.
Smith, H. K., Roberts, I. J., Allen, M. J., Connolly, J. B., Moffat, K. G., & O'Kane, C. J. (1996). Inducible ternary control of transgene expression and cell ablation in Drosophila. Development genes and evolution, 206(1), 14-24. https://doi.org/10.1007/s004270050026
Smith, H K, et al. "Inducible ternary control of transgene expression and cell ablation in Drosophila." Development genes and evolution vol. 206,1 (1996): 14-24. doi: https://doi.org/10.1007/s004270050026
Smith HK, Roberts IJ, Allen MJ, Connolly JB, Moffat KG, O'Kane CJ. Inducible ternary control of transgene expression and cell ablation in Drosophila. Dev Genes Evol. 1996 Jun;206(1):14-24. doi: 10.1007/s004270050026. PMID: 24173393.
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Nanopatterned surfaces based on template-assisted multilayer electrodeposition.

Small (Weinheim an der Bergstrasse, Germany)

Kim M, Kim J, Allen M.
PMID: 25504916
Small. 2015 Apr 24;11(16):1912-8. doi: 10.1002/smll.201402584. Epub 2014 Dec 15.

Selective, template-assisted growth of electrodeposited, layered materials leads to the top-down designable realization of nanopatterned surfaces with a large surface area (>1 cm(2)) comprised of multi-dimensional, multiscale (10 nm-1 μm) features, without the need of standard nanolithography. This process...

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Kim M, Kim J, Allen M. Nanopatterned surfaces based on template-assisted multilayer electrodeposition. Small. 2014;11(16):1912-8doi: 10.1002/smll.201402584.
Kim, M., Kim, J., & Allen, M. (2015). Nanopatterned surfaces based on template-assisted multilayer electrodeposition. Small (Weinheim an der Bergstrasse, Germany), 11(16), 1912-8. https://doi.org/10.1002/smll.201402584
Kim, Minsoo, et al. "Nanopatterned surfaces based on template-assisted multilayer electrodeposition." Small (Weinheim an der Bergstrasse, Germany) vol. 11,16 (2015): 1912-8. doi: https://doi.org/10.1002/smll.201402584
Kim M, Kim J, Allen M. Nanopatterned surfaces based on template-assisted multilayer electrodeposition. Small. 2015 Apr 24;11(16):1912-8. doi: 10.1002/smll.201402584. Epub 2014 Dec 15. PMID: 25504916.
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The relationship between blood pressure and sciatic nerve blood flow velocity in rats with insulin-treated experimental diabetes.

Diabetes & vascular disease research

Olver TD, Grisé KN, McDonald MW, Dey A, Allen MD, Rice CL, Lacefield JC, Melling CJ, Noble EG, Shoemaker JK.
PMID: 24853907
Diab Vasc Dis Res. 2014 Jul;11(4):281-289. doi: 10.1177/1479164114533357. Epub 2014 May 22.

Peripheral nerve blood flow (NBF) does not autoregulate but, instead, responds passively to changes in mean arterial pressure (MAP). How this relationship is impacted by insulin-treated experimental diabetes (ITED) is unknown. We tested the hypothesis that ITED will reduce...

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Olver TD, Grisé KN, McDonald MW, et al. The relationship between blood pressure and sciatic nerve blood flow velocity in rats with insulin-treated experimental diabetes. Diab Vasc Dis Res. 2014;11(4):281-289doi: 10.1177/1479164114533357.
Olver, T. D., Grisé, K. N., McDonald, M. W., Dey, A., Allen, M. D., Rice, C. L., Lacefield, J. C., Melling, C. J., Noble, E. G., & Shoemaker, J. K. (2014). The relationship between blood pressure and sciatic nerve blood flow velocity in rats with insulin-treated experimental diabetes. Diabetes & vascular disease research, 11(4), 281-289. https://doi.org/10.1177/1479164114533357
Olver, T Dylan, et al. "The relationship between blood pressure and sciatic nerve blood flow velocity in rats with insulin-treated experimental diabetes." Diabetes & vascular disease research vol. 11,4 (2014): 281-289. doi: https://doi.org/10.1177/1479164114533357
Olver TD, Grisé KN, McDonald MW, Dey A, Allen MD, Rice CL, Lacefield JC, Melling CJ, Noble EG, Shoemaker JK. The relationship between blood pressure and sciatic nerve blood flow velocity in rats with insulin-treated experimental diabetes. Diab Vasc Dis Res. 2014 Jul;11(4):281-289. doi: 10.1177/1479164114533357. Epub 2014 May 22. PMID: 24853907.
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Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging.

Pathobiology of aging & age related diseases

Springer DA, Allen M, Hoffman V, Brinster L, Starost MF, Bryant M, Eckhaus M.
PMID: 25143818
Pathobiol Aging Age Relat Dis. 2014 Aug 01;4. doi: 10.3402/pba.v4.24932. eCollection 2014.

Laboratory mice develop naturally occurring lesions that affect biomedical research. Hydronephrosis is a recognized pathologic abnormality of the mouse kidney. Acquired hydronephrosis can affect any mouse, as it is caused by any naturally occurring disease that impairs free urine...

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Springer DA, Allen M, Hoffman V, et al. Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging. Pathobiol Aging Age Relat Dis. 2014;4doi: 10.3402/pba.v4.24932.
Springer, D. A., Allen, M., Hoffman, V., Brinster, L., Starost, M. F., Bryant, M., & Eckhaus, M. (2014). Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging. Pathobiology of aging & age related diseases, 4. https://doi.org/10.3402/pba.v4.24932
Springer, Danielle A, et al. "Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging." Pathobiology of aging & age related diseases vol. 4 (2014). doi: https://doi.org/10.3402/pba.v4.24932
Springer DA, Allen M, Hoffman V, Brinster L, Starost MF, Bryant M, Eckhaus M. Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging. Pathobiol Aging Age Relat Dis. 2014 Aug 01;4. doi: 10.3402/pba.v4.24932. eCollection 2014. PMID: 25143818; PMCID: PMC4119937.
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Showing 25 to 36 of 915 entries