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Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide.

Physical chemistry chemical physics : PCCP

Class CA, Liu M, Vandeputte AG, Green WH.
PMID: 27431650
Phys Chem Chem Phys. 2016 Aug 03;18(31):21651-8. doi: 10.1039/c6cp02202b.

The automated Reaction Mechanism Generator (RMG), using rate parameters derived from ab initio CCSD(T) calculations, is used to build reaction networks for the thermal decomposition of di-tert-butyl sulfide. Simulation results were compared with data from pyrolysis experiments with and...

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Class CA, Liu M, Vandeputte AG, et al. Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide. Phys Chem Chem Phys. 2016;18(31):21651-8doi: 10.1039/c6cp02202b.
Class, C. A., Liu, M., Vandeputte, A. G., & Green, W. H. (2016). Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide. Physical chemistry chemical physics : PCCP, 18(31), 21651-8. https://doi.org/10.1039/c6cp02202b
Class, Caleb A, et al. "Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide." Physical chemistry chemical physics : PCCP vol. 18,31 (2016): 21651-8. doi: https://doi.org/10.1039/c6cp02202b
Class CA, Liu M, Vandeputte AG, Green WH. Automatic mechanism generation for pyrolysis of di-tert-butyl sulfide. Phys Chem Chem Phys. 2016 Aug 03;18(31):21651-8. doi: 10.1039/c6cp02202b. PMID: 27431650.
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[Not Available].

MMW Fortschritte der Medizin

Jansson A, V Liebe A.
PMID: 27368294
MMW Fortschr Med. 2007 Apr;149(16):38-40. doi: 10.1007/BF03365005.

No abstract available.

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Jansson A, V Liebe A. Was steckt hinter dem "Beinweh"? : Serie Kindersprechstunde, Teil 4: Schmerzen in den Kniegelenken. [Not Available]. MMW Fortschr Med. 2007;149(16):38-40doi: 10.1007/BF03365005.
Jansson, A., & V Liebe, A. (2007). Was steckt hinter dem "Beinweh"? : Serie Kindersprechstunde, Teil 4: Schmerzen in den Kniegelenken. [Not Available]. MMW Fortschritte der Medizin, 149(16), 38-40. https://doi.org/10.1007/BF03365005
Jansson, Annette, and V Liebe, A. "Was steckt hinter dem "Beinweh"? : Serie Kindersprechstunde, Teil 4: Schmerzen in den Kniegelenken." [Not Available]. MMW Fortschritte der Medizin vol. 149,16 (2007): 38-40. doi: https://doi.org/10.1007/BF03365005
Jansson A, V Liebe A. Was steckt hinter dem "Beinweh"? : Serie Kindersprechstunde, Teil 4: Schmerzen in den Kniegelenken. [Not Available]. MMW Fortschr Med. 2007 Apr;149(16):38-40. doi: 10.1007/BF03365005. German. PMID: 27368294.
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Mutations in CDK5RAP2 cause Seckel syndrome.

Molecular genetics & genomic medicine

Yigit G, Brown KE, Kayserili H, Pohl E, Caliebe A, Zahnleiter D, Rosser E, Bögershausen N, Uyguner ZO, Altunoglu U, Nürnberg G, Nürnberg P, Rauch A, Li Y, Thiel CT, Wollnik B.
PMID: 26436113
Mol Genet Genomic Med. 2015 Sep;3(5):467-80. doi: 10.1002/mgg3.158. Epub 2015 May 24.

Seckel syndrome is a heterogeneous, autosomal recessive disorder marked by prenatal proportionate short stature, severe microcephaly, intellectual disability, and characteristic facial features. Here, we describe the novel homozygous splice-site mutations c.383+1G>C and c.4005-9A>G in CDK5RAP2 in two consanguineous families...

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Yigit G, Brown KE, Kayserili H, et al. Mutations in CDK5RAP2 cause Seckel syndrome. Mol Genet Genomic Med. 2015;3(5):467-80doi: 10.1002/mgg3.158.
Yigit, G., Brown, K. E., Kayserili, H., Pohl, E., Caliebe, A., Zahnleiter, D., Rosser, E., Bögershausen, N., Uyguner, Z. O., Altunoglu, U., Nürnberg, G., Nürnberg, P., Rauch, A., Li, Y., Thiel, C. T., & Wollnik, B. (2015). Mutations in CDK5RAP2 cause Seckel syndrome. Molecular genetics & genomic medicine, 3(5), 467-80. https://doi.org/10.1002/mgg3.158
Yigit, Gökhan, et al. "Mutations in CDK5RAP2 cause Seckel syndrome." Molecular genetics & genomic medicine vol. 3,5 (2015): 467-80. doi: https://doi.org/10.1002/mgg3.158
Yigit G, Brown KE, Kayserili H, Pohl E, Caliebe A, Zahnleiter D, Rosser E, Bögershausen N, Uyguner ZO, Altunoglu U, Nürnberg G, Nürnberg P, Rauch A, Li Y, Thiel CT, Wollnik B. Mutations in CDK5RAP2 cause Seckel syndrome. Mol Genet Genomic Med. 2015 Sep;3(5):467-80. doi: 10.1002/mgg3.158. Epub 2015 May 24. PMID: 26436113; PMCID: PMC4585455.
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Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients.

Annals of clinical and translational neurology

Lareau CA, Adrianto I, Levin AM, Iannuzzi MC, Rybicki BA, Montgomery CG.
PMID: 26478897
Ann Clin Transl Neurol. 2015 Oct;2(10):972-7. doi: 10.1002/acn3.229. Epub 2015 Jul 31.

Neurosarcoidosis is a clinical subtype of sarcoidosis characterized by the presence of granulomas in the nervous system. Here, we report a highly significant association with a variant (rs75652600, P = 3.12 × 10(-8), odds ratios = 4.34) within a...

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Lareau CA, Adrianto I, Levin AM, et al. Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients. Ann Clin Transl Neurol. 2015;2(10):972-7doi: 10.1002/acn3.229.
Lareau, C. A., Adrianto, I., Levin, A. M., Iannuzzi, M. C., Rybicki, B. A., & Montgomery, C. G. (2015). Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients. Annals of clinical and translational neurology, 2(10), 972-7. https://doi.org/10.1002/acn3.229
Lareau, Caleb A, et al. "Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients." Annals of clinical and translational neurology vol. 2,10 (2015): 972-7. doi: https://doi.org/10.1002/acn3.229
Lareau CA, Adrianto I, Levin AM, Iannuzzi MC, Rybicki BA, Montgomery CG. Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients. Ann Clin Transl Neurol. 2015 Oct;2(10):972-7. doi: 10.1002/acn3.229. Epub 2015 Jul 31. PMID: 26478897; PMCID: PMC4603380.
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Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines.

Dalton transactions (Cambridge, England : 2003)

Brown CA, Nile TA, Mahon MF, Webster RL.
PMID: 25730705
Dalton Trans. 2015 Jul 21;44(27):12189-95. doi: 10.1039/c5dt00112a. Epub 2015 Mar 02.

Monophosphines prepared by iron catalysed hydrophosphination have been used as pro-ligands in iron catalysed Negishi cross-coupling of alkyl bromides and diphenyl zinc reagents. The cross-coupling has been investigated with monophosphines with varying electronic properties and we find the simplest,...

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Brown CA, Nile TA, Mahon MF, et al. Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton Trans. 2015;44(27):12189-95doi: 10.1039/c5dt00112a.
Brown, C. A., Nile, T. A., Mahon, M. F., & Webster, R. L. (2015). Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton transactions (Cambridge, England : 2003), 44(27), 12189-95. https://doi.org/10.1039/c5dt00112a
Brown, Caleb A, et al. "Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines." Dalton transactions (Cambridge, England : 2003) vol. 44,27 (2015): 12189-95. doi: https://doi.org/10.1039/c5dt00112a
Brown CA, Nile TA, Mahon MF, Webster RL. Iron catalysed Negishi cross-coupling using simple ethyl-monophosphines. Dalton Trans. 2015 Jul 21;44(27):12189-95. doi: 10.1039/c5dt00112a. Epub 2015 Mar 02. PMID: 25730705.
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[A new health strategy for Europe].

Gaceta sanitaria

Calvete A.
PMID: 11578574
Gac Sanit. 2001 Jul-Aug;15(4):371.

No abstract available.

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Calvete A. La nueva estrategia europea de salud. [A new health strategy for Europe]. Gac Sanit. 2001;15(4):371
Calvete, A. (2001). La nueva estrategia europea de salud. [A new health strategy for Europe]. Gaceta sanitaria, 15(4), 371.
Calvete, A. "La nueva estrategia europea de salud." [A new health strategy for Europe]. Gaceta sanitaria vol. 15,4 (2001): 371.
Calvete A. La nueva estrategia europea de salud. [A new health strategy for Europe]. Gac Sanit. 2001 Jul-Aug;15(4):371. Spanish. PMID: 11578574.
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Cavity dynamics and particle alignment in the wake of a supersonic projectile penetrating a dusty plasma.

Physical review. E, Statistical, nonlinear, and soft matter physics

Arp O, Caliebe D, Piel A.
PMID: 21797495
Phys Rev E Stat Nonlin Soft Matter Phys. 2011 Jun;83(6):066404. doi: 10.1103/PhysRevE.83.066404. Epub 2011 Jun 10.

The penetration of a projectile into a strongly coupled dusty plasma was studied in a radio-frequency discharge under microgravity conditions. A supersonic projectile produces an elongated dust-free cavity in its wake. The dynamics of the cavity is analyzed and...

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Arp O, Caliebe D, Piel A. Cavity dynamics and particle alignment in the wake of a supersonic projectile penetrating a dusty plasma. Phys Rev E Stat Nonlin Soft Matter Phys. 2011;83(6):066404doi: 10.1103/PhysRevE.83.066404.
Arp, O., Caliebe, D., & Piel, A. (2011). Cavity dynamics and particle alignment in the wake of a supersonic projectile penetrating a dusty plasma. Physical review. E, Statistical, nonlinear, and soft matter physics, 83(6), 066404. https://doi.org/10.1103/PhysRevE.83.066404
Arp, O, et al. "Cavity dynamics and particle alignment in the wake of a supersonic projectile penetrating a dusty plasma." Physical review. E, Statistical, nonlinear, and soft matter physics vol. 83,6 (2011): 066404. doi: https://doi.org/10.1103/PhysRevE.83.066404
Arp O, Caliebe D, Piel A. Cavity dynamics and particle alignment in the wake of a supersonic projectile penetrating a dusty plasma. Phys Rev E Stat Nonlin Soft Matter Phys. 2011 Jun;83(6):066404. doi: 10.1103/PhysRevE.83.066404. Epub 2011 Jun 10. PMID: 21797495.
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No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control.

Molecular cytogenetics

Frohnauer J, Caliebe A, Gesk S, Partsch CJ, Siebert R, Pankau R, Jenderny J.
PMID: 21054846
Mol Cytogenet. 2010 Nov 05;3:21. doi: 10.1186/1755-8166-3-21.

BACKGROUND: Typical Williams-Beuren syndrome (WBS) is commonly caused by a ~1.5 Mb - ~1.8 Mb heterozygous deletion of contiguous genes at chromosome region 7q11.23. The majority of WBS cases occurs sporadically but few familial cases of autosomal dominant inheritance...

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Frohnauer J, Caliebe A, Gesk S, et al. No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control. Mol Cytogenet. 2010;3:21doi: 10.1186/1755-8166-3-21.
Frohnauer, J., Caliebe, A., Gesk, S., Partsch, C. J., Siebert, R., Pankau, R., & Jenderny, J. (2010). No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control. Molecular cytogenetics, 321. https://doi.org/10.1186/1755-8166-3-21
Frohnauer, Judith, et al. "No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control." Molecular cytogenetics vol. 3 (2010): 21. doi: https://doi.org/10.1186/1755-8166-3-21
Frohnauer J, Caliebe A, Gesk S, Partsch CJ, Siebert R, Pankau R, Jenderny J. No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control. Mol Cytogenet. 2010 Nov 05;3:21. doi: 10.1186/1755-8166-3-21. PMID: 21054846; PMCID: PMC2993725.
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The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation.

Indian pacing and electrophysiology journal

Murdock DK, Overton N, Kersten M, Kaliebe J, Devecchi F.
PMID: 18679523
Indian Pacing Electrophysiol J. 2008 Aug 01;8(3):175-81.

BACKGROUND: Atrial fibrillation (AF) may arise out of anomalous impulse activity at atrial venous junctions. Triggered activity may be a source of abnormal impulse activity. Ranolazine is an anti-anginal agent, which inhibits normal and abnormal late Na+ channel current...

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Murdock DK, Overton N, Kersten M, et al. The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation. Indian Pacing Electrophysiol J. 2008;8(3):175-81
Murdock, D. K., Overton, N., Kersten, M., Kaliebe, J., & Devecchi, F. (2008). The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation. Indian pacing and electrophysiology journal, 8(3), 175-81.
Murdock, David K, et al. "The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation." Indian pacing and electrophysiology journal vol. 8,3 (2008): 175-81.
Murdock DK, Overton N, Kersten M, Kaliebe J, Devecchi F. The effect of ranolazine on maintaining sinus rhythm in patients with resistant atrial fibrillation. Indian Pacing Electrophysiol J. 2008 Aug 01;8(3):175-81. PMID: 18679523; PMCID: PMC2490806.
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Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain.

Molecular syndromology

Naik S, Thomas NS, Davies JH, Lever M, Raponi M, Baralle D, Temple IK, Caliebe A.
PMID: 22511895
Mol Syndromol. 2012 Jan;2(2):76-80. doi: 10.1159/000335220. Epub 2012 Jan 04.

A deletion in 15q11.2 involving the SNURF/SNRPN gene is the typical finding in patients with Prader-Willi syndrome. Apart from translocations disrupting this gene, no other mutation types have been described so far. We report a patient in whom a...

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Naik S, Thomas NS, Davies JH, et al. Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain. Mol Syndromol. 2012;2(2):76-80doi: 10.1159/000335220.
Naik, S., Thomas, N. S., Davies, J. H., Lever, M., Raponi, M., Baralle, D., Temple, I. K., & Caliebe, A. (2012). Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain. Molecular syndromology, 2(2), 76-80. https://doi.org/10.1159/000335220
Naik, S, et al. "Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain." Molecular syndromology vol. 2,2 (2012): 76-80. doi: https://doi.org/10.1159/000335220
Naik S, Thomas NS, Davies JH, Lever M, Raponi M, Baralle D, Temple IK, Caliebe A. Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain. Mol Syndromol. 2012 Jan;2(2):76-80. doi: 10.1159/000335220. Epub 2012 Jan 04. PMID: 22511895; PMCID: PMC3326282.
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Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applications.

The Review of scientific instruments

Khalid S, Caliebe W, Siddons P, So I, Clay B, Lenhard T, Hanson J, Wang Q, Frenkel AI, Marinkovic N, Hould N, Ginder-Vogel M, Landrot GL, Sparks DL, Ganjoo A.
PMID: 20113127
Rev Sci Instrum. 2010 Jan;81(1):015105. doi: 10.1063/1.3276679.

In order to learn about in situ structural changes in materials at subseconds time scale, we have further refined the techniques of quick extended x-ray absorption fine structure (QEXAFS) and quick x-ray absorption near edge structure (XANES) spectroscopies at...

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Khalid S, Caliebe W, Siddons P, et al. Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applications. Rev Sci Instrum. 2010;81(1):015105doi: 10.1063/1.3276679.
Khalid, S., Caliebe, W., Siddons, P., So, I., Clay, B., Lenhard, T., Hanson, J., Wang, Q., Frenkel, A. I., Marinkovic, N., Hould, N., Ginder-Vogel, M., Landrot, G. L., Sparks, D. L., & Ganjoo, A. (2010). Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applications. The Review of scientific instruments, 81(1), 015105. https://doi.org/10.1063/1.3276679
Khalid, S, et al. "Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applications." The Review of scientific instruments vol. 81,1 (2010): 015105. doi: https://doi.org/10.1063/1.3276679
Khalid S, Caliebe W, Siddons P, So I, Clay B, Lenhard T, Hanson J, Wang Q, Frenkel AI, Marinkovic N, Hould N, Ginder-Vogel M, Landrot GL, Sparks DL, Ganjoo A. Quick extended x-ray absorption fine structure instrument with millisecond time scale, optimized for in situ applications. Rev Sci Instrum. 2010 Jan;81(1):015105. doi: 10.1063/1.3276679. PMID: 20113127.
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Prevalence, pattern and impact of depression on quality of life of stroke survivors.

International journal of psychiatry in clinical practice

Gbiri CA, Akinpelu AO, Odole AC.
PMID: 24917320
Int J Psychiatry Clin Pract. 2010 Sep;14(3):198-203. doi: 10.3109/13651501003797633. Epub 2010 Jul 20.

Abstract Objective. This study documented the incidence, pattern and impact of depression on QoL of stroke-survivors within 6-month post-stroke. Methods. This study involved 65 stroke survivors consecutively recruited at ictus from a tertiary health institution in Nigeria. The National...

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Gbiri CA, Akinpelu AO, Odole AC. Prevalence, pattern and impact of depression on quality of life of stroke survivors. Int J Psychiatry Clin Pract. 2010;14(3):198-203doi: 10.3109/13651501003797633.
Gbiri, C. A., Akinpelu, A. O., & Odole, A. C. (2010). Prevalence, pattern and impact of depression on quality of life of stroke survivors. International journal of psychiatry in clinical practice, 14(3), 198-203. https://doi.org/10.3109/13651501003797633
Gbiri, Caleb A, et al. "Prevalence, pattern and impact of depression on quality of life of stroke survivors." International journal of psychiatry in clinical practice vol. 14,3 (2010): 198-203. doi: https://doi.org/10.3109/13651501003797633
Gbiri CA, Akinpelu AO, Odole AC. Prevalence, pattern and impact of depression on quality of life of stroke survivors. Int J Psychiatry Clin Pract. 2010 Sep;14(3):198-203. doi: 10.3109/13651501003797633. Epub 2010 Jul 20. PMID: 24917320.
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Showing 1 to 12 of 156 entries