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Mentoring portfolio use in undergraduate and postgraduate medical education

Undergraduate training programs

Driessen E, Scheele F.
GSID: FXGfxF9eJWEJ
H Dekker, E Driessen, ET Braak, F Scheele… - Medical …, 2009 - Taylor & Francis

… programmes in undergraduate and postgraduate settings. … programmes included staff development training to support mentors; however, the content of these training programmes …

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Dekker, H., Driessen, E., Braak, E. T., Scheele, F., Slaets, J., Van Der Molen, T., & Cohen-Schotanus, J. (2009). Mentoring portfolio use in undergraduate and postgraduate medical education. Medical Teacher, 31(10), 903-909.
Dekker, Hanke, et al. "Mentoring portfolio use in undergraduate and postgraduate medical education." Medical Teacher 31.10 (2009): 903-909.
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Genome-wide association studies in pediatric chronic kidney disease.

Pediatric nephrology (Berlin, Germany)

Gupta J, Kanetsky PA, Wuttke M, Köttgen A, Schaefer F, Wong CS.
PMID: 26490952
Pediatr Nephrol. 2016 Aug;31(8):1241-52. doi: 10.1007/s00467-015-3235-y. Epub 2015 Oct 21.

The genome-wide association study (GWAS) has become an established scientific method that provides an unbiased screen for genetic loci potentially associated with phenotypes of clinical interest, such as chronic kidney disease (CKD). Thus, GWAS provides opportunities to gain new...

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Gupta J, Kanetsky PA, Wuttke M, et al. Genome-wide association studies in pediatric chronic kidney disease. Pediatr Nephrol. 2015;31(8):1241-52doi: 10.1007/s00467-015-3235-y.
Gupta, J., Kanetsky, P. A., Wuttke, M., Köttgen, A., Schaefer, F., & Wong, C. S. (2016). Genome-wide association studies in pediatric chronic kidney disease. Pediatric nephrology (Berlin, Germany), 31(8), 1241-52. https://doi.org/10.1007/s00467-015-3235-y
Gupta, Jayanta, et al. "Genome-wide association studies in pediatric chronic kidney disease." Pediatric nephrology (Berlin, Germany) vol. 31,8 (2016): 1241-52. doi: https://doi.org/10.1007/s00467-015-3235-y
Gupta J, Kanetsky PA, Wuttke M, Köttgen A, Schaefer F, Wong CS. Genome-wide association studies in pediatric chronic kidney disease. Pediatr Nephrol. 2016 Aug;31(8):1241-52. doi: 10.1007/s00467-015-3235-y. Epub 2015 Oct 21. PMID: 26490952; PMCID: PMC5287054.
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Averting the legacy of kidney disease: focus on childhood.

Current opinion in organ transplantation

Ingelfinger JR, Kalantar-Zadeh K, Schaefer F.
PMID: 27077601
Curr Opin Organ Transplant. 2016 Jun;21(3):343-8. doi: 10.1097/MOT.0000000000000287.

No abstract available.

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Ingelfinger JR, Kalantar-Zadeh K, Schaefer F. Averting the legacy of kidney disease: focus on childhood. Curr Opin Organ Transplant. 2016;21(3):343-8doi: 10.1097/MOT.0000000000000287.
Ingelfinger, J. R., Kalantar-Zadeh, K., Schaefer, F. (2016). Averting the legacy of kidney disease: focus on childhood. Current opinion in organ transplantation, 21(3), 343-8. https://doi.org/10.1097/MOT.0000000000000287
Ingelfinger, Julie R, et al. "Averting the legacy of kidney disease: focus on childhood." Current opinion in organ transplantation vol. 21,3 (2016): 343-8. doi: https://doi.org/10.1097/MOT.0000000000000287
Ingelfinger JR, Kalantar-Zadeh K, Schaefer F. Averting the legacy of kidney disease: focus on childhood. Curr Opin Organ Transplant. 2016 Jun;21(3):343-8. doi: 10.1097/MOT.0000000000000287. PMID: 27077601.
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Corrigendum: Organocatalytic removal of formaldehyde adducts from RNA and DNA bases.

Nature chemistry

Karmakar S, Harcourt EM, Hewings DS, Scherer F, Lovejoy AF, Kurtz DM, Ehrenschwender T, Barandun LJ, Roost C, Alizadeh AA, Kool ET.
PMID: 26587722
Nat Chem. 2015 Dec;7(12):1033. doi: 10.1038/nchem.2401.

No abstract available.

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Karmakar S, Harcourt EM, Hewings DS, et al. Corrigendum: Organocatalytic removal of formaldehyde adducts from RNA and DNA bases. Nat Chem. 2015;7(12):1033doi: 10.1038/nchem.2401.
Karmakar, S., Harcourt, E. M., Hewings, D. S., Scherer, F., Lovejoy, A. F., Kurtz, D. M., Ehrenschwender, T., Barandun, L. J., Roost, C., Alizadeh, A. A., & Kool, E. T. (2015). Corrigendum: Organocatalytic removal of formaldehyde adducts from RNA and DNA bases. Nature chemistry, 7(12), 1033. https://doi.org/10.1038/nchem.2401
Karmakar, Saswata, et al. "Corrigendum: Organocatalytic removal of formaldehyde adducts from RNA and DNA bases." Nature chemistry vol. 7,12 (2015): 1033. doi: https://doi.org/10.1038/nchem.2401
Karmakar S, Harcourt EM, Hewings DS, Scherer F, Lovejoy AF, Kurtz DM, Ehrenschwender T, Barandun LJ, Roost C, Alizadeh AA, Kool ET. Corrigendum: Organocatalytic removal of formaldehyde adducts from RNA and DNA bases. Nat Chem. 2015 Dec;7(12):1033. doi: 10.1038/nchem.2401. PMID: 26587722.
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WITHDRAWN: Efficacy and Safety of Mycophenolate Mofetil Versus Levamisole in Children and Adolescents With Idiopathic Nephrotic Syndrome: Results of a Randomized Clinical Trial.

American journal of kidney diseases : the official journal of the National Kidney Foundation

Basu B, Pandey R, Mahapatra TK, Mondal N, Schaefer F.
PMID: 26071057
Am J Kidney Dis. 2015 Jun 09; doi: 10.1053/j.ajkd.2015.04.048. Epub 2015 Jun 09.

This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy.

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Basu B, Pandey R, Mahapatra TK, et al. WITHDRAWN: Efficacy and Safety of Mycophenolate Mofetil Versus Levamisole in Children and Adolescents With Idiopathic Nephrotic Syndrome: Results of a Randomized Clinical Trial. Am J Kidney Dis. 2015;doi: 10.1053/j.ajkd.2015.04.048.
Basu, B., Pandey, R., Mahapatra, T. K., Mondal, N., & Schaefer, F. (2015). WITHDRAWN: Efficacy and Safety of Mycophenolate Mofetil Versus Levamisole in Children and Adolescents With Idiopathic Nephrotic Syndrome: Results of a Randomized Clinical Trial. American journal of kidney diseases : the official journal of the National Kidney Foundation, . https://doi.org/10.1053/j.ajkd.2015.04.048
Basu, Biswanath, et al. "WITHDRAWN: Efficacy and Safety of Mycophenolate Mofetil Versus Levamisole in Children and Adolescents With Idiopathic Nephrotic Syndrome: Results of a Randomized Clinical Trial." American journal of kidney diseases : the official journal of the National Kidney Foundation vol. (2015). doi: https://doi.org/10.1053/j.ajkd.2015.04.048
Basu B, Pandey R, Mahapatra TK, Mondal N, Schaefer F. WITHDRAWN: Efficacy and Safety of Mycophenolate Mofetil Versus Levamisole in Children and Adolescents With Idiopathic Nephrotic Syndrome: Results of a Randomized Clinical Trial. Am J Kidney Dis. 2015 Jun 09; doi: 10.1053/j.ajkd.2015.04.048. Epub 2015 Jun 09. PMID: 26071057.
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Agdc1p - a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast .

Frontiers in microbiology

Meier AK, Worch S, Böer E, Hartmann A, Mascher M, Marzec M, Scholz U, Riechen J, Baronian K, Schauer F, Bode R, Kunze G.
PMID: 28966611
Front Microbiol. 2017 Sep 15;8:1777. doi: 10.3389/fmicb.2017.01777. eCollection 2017.

Tannins and hydroxylated aromatic acids, such as gallic acid (3,4,5-trihydroxybenzoic acid), are plant secondary metabolites which protect plants against herbivores and plant-associated microorganisms. Some microbes, such as the yeast

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Meier AK, Worch S, Böer E, et al. Agdc1p - a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast . Front Microbiol. 2017;8:1777doi: 10.3389/fmicb.2017.01777.
Meier, A. K., Worch, S., Böer, E., Hartmann, A., Mascher, M., Marzec, M., Scholz, U., Riechen, J., Baronian, K., Schauer, F., Bode, R., & Kunze, G. (2017). Agdc1p - a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast . Frontiers in microbiology, 81777. https://doi.org/10.3389/fmicb.2017.01777
Meier, Anna K, et al. "Agdc1p - a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast ." Frontiers in microbiology vol. 8 (2017): 1777. doi: https://doi.org/10.3389/fmicb.2017.01777
Meier AK, Worch S, Böer E, Hartmann A, Mascher M, Marzec M, Scholz U, Riechen J, Baronian K, Schauer F, Bode R, Kunze G. Agdc1p - a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast . Front Microbiol. 2017 Sep 15;8:1777. doi: 10.3389/fmicb.2017.01777. eCollection 2017. PMID: 28966611; PMCID: PMC5605622.
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Averting the legacy of kidney disease-Focus on childhood.

Nephrologie & therapeutique

Ingelfinger JR, Kalantar-Zadeh K, Schaefer F, Kam Tao Li P, Garcia-Garcia G, Couser WG, Erk T, Ingelfinger JR, Kalantar-Zadeh K, Kernahan C, Osafo C, Riella MC, Segantini L, Zakharova E.
PMID: 26822334
Nephrol Ther. 2016 Feb;12(1):1-5. doi: 10.1016/j.nephro.2015.11.001. Epub 2016 Jan 26.

No abstract available.

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Ingelfinger JR, Kalantar-Zadeh K, Schaefer F. Averting the legacy of kidney disease-Focus on childhood. Nephrol Ther. 2016;12(1):1-5doi: 10.1016/j.nephro.2015.11.001.
Ingelfinger, J. R., Kalantar-Zadeh, K., Schaefer, F., Kam Tao Li, P., Garcia-Garcia, G., Couser, W. G., Erk, T., Ingelfinger, J. R., Kalantar-Zadeh, K., Kernahan, C., Osafo, C., Riella, M. C., Segantini, L., & Zakharova, E. (2016). Averting the legacy of kidney disease-Focus on childhood. Nephrologie & therapeutique, 12(1), 1-5. https://doi.org/10.1016/j.nephro.2015.11.001
Ingelfinger, Julie R, et al. "Averting the legacy of kidney disease-Focus on childhood." Nephrologie & therapeutique vol. 12,1 (2016): 1-5. doi: https://doi.org/10.1016/j.nephro.2015.11.001
Ingelfinger JR, Kalantar-Zadeh K, Schaefer F, Kam Tao Li P, Garcia-Garcia G, Couser WG, Erk T, Ingelfinger JR, Kalantar-Zadeh K, Kernahan C, Osafo C, Riella MC, Segantini L, Zakharova E. Averting the legacy of kidney disease-Focus on childhood. Nephrol Ther. 2016 Feb;12(1):1-5. doi: 10.1016/j.nephro.2015.11.001. Epub 2016 Jan 26. PMID: 26822334.
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Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease.

Frontiers in pediatrics

Ebner K, Schaefer F, Liebau MC.
PMID: 28296980
Front Pediatr. 2017 Feb 16;5:18. doi: 10.3389/fped.2017.00018. eCollection 2017.

Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phenotype often presenting prenatally or in early childhood. With its obligate renal and hepatic involvement, ARPKD is one of the most important indications for liver...

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Ebner K, Schaefer F, Liebau MC. Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease. Front Pediatr. 2017;5:18doi: 10.3389/fped.2017.00018.
Ebner, K., Schaefer, F., Liebau, M. C. (2017). Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease. Frontiers in pediatrics, 518. https://doi.org/10.3389/fped.2017.00018
Ebner, Kathrin, et al. "Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease." Frontiers in pediatrics vol. 5 (2017): 18. doi: https://doi.org/10.3389/fped.2017.00018
Ebner K, Schaefer F, Liebau MC. Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease. Front Pediatr. 2017 Feb 16;5:18. doi: 10.3389/fped.2017.00018. eCollection 2017. PMID: 28296980; PMCID: PMC5327862.
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International Charter of principles for sharing bio-specimens and data.

European journal of human genetics : EJHG

Mascalzoni D, Dove ES, Rubinstein Y, Dawkins HJ, Kole A, McCormack P, Woods S, Riess O, Schaefer F, Lochmüller H, Knoppers BM, Hansson M.
PMID: 27307116
Eur J Hum Genet. 2016 Jul;24(7):1096. doi: 10.1038/ejhg.2015.237.

No abstract available.

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Mascalzoni D, Dove ES, Rubinstein Y, et al. International Charter of principles for sharing bio-specimens and data. Eur J Hum Genet. 2016;24(7):1096doi: 10.1038/ejhg.2015.237.
Mascalzoni, D., Dove, E. S., Rubinstein, Y., Dawkins, H. J., Kole, A., McCormack, P., Woods, S., Riess, O., Schaefer, F., Lochmüller, H., Knoppers, B. M., & Hansson, M. (2016). International Charter of principles for sharing bio-specimens and data. European journal of human genetics : EJHG, 24(7), 1096. https://doi.org/10.1038/ejhg.2015.237
Mascalzoni, Deborah, et al. "International Charter of principles for sharing bio-specimens and data." European journal of human genetics : EJHG vol. 24,7 (2016): 1096. doi: https://doi.org/10.1038/ejhg.2015.237
Mascalzoni D, Dove ES, Rubinstein Y, Dawkins HJ, Kole A, McCormack P, Woods S, Riess O, Schaefer F, Lochmüller H, Knoppers BM, Hansson M. International Charter of principles for sharing bio-specimens and data. Eur J Hum Genet. 2016 Jul;24(7):1096. doi: 10.1038/ejhg.2015.237. PMID: 27307116; PMCID: PMC5070889.
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Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss.

PeerJ

Pique LM, Brennan ML, Davidson CJ, Schaefer F, Greinwald J, Schrijver I.
PMID: 24860705
PeerJ. 2014 May 08;2:e384. doi: 10.7717/peerj.384. eCollection 2014.

Pendred syndrome (PDS) and DFNB4 comprise a phenotypic spectrum of sensorineural hearing loss disorders that typically result from biallelic mutations of the SLC26A4 gene. Although PDS and DFNB4 are recessively inherited, sequencing of the coding regions and splice sites...

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Pique LM, Brennan ML, Davidson CJ, et al. Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss. PeerJ. 2014;2:e384doi: 10.7717/peerj.384.
Pique, L. M., Brennan, M. L., Davidson, C. J., Schaefer, F., Greinwald, J., & Schrijver, I. (2014). Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss. PeerJ, 2e384. https://doi.org/10.7717/peerj.384
Pique, Lynn M, et al. "Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss." PeerJ vol. 2 (2014): e384. doi: https://doi.org/10.7717/peerj.384
Pique LM, Brennan ML, Davidson CJ, Schaefer F, Greinwald J, Schrijver I. Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss. PeerJ. 2014 May 08;2:e384. doi: 10.7717/peerj.384. eCollection 2014. PMID: 24860705; PMCID: PMC4017815.
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Signal transduction in the footsteps of goethe and schiller.

Cell communication and signaling : CCS

Friedrich K, Lindquist JA, Entschladen F, Serfling E, Thiel G, Kieser A, Giehl K, Ehrhardt C, Feller SM, Ullrich O, Schaper F, Janssen O, Hass R.
PMID: 19193215
Cell Commun Signal. 2009 Feb 04;7:2. doi: 10.1186/1478-811X-7-2.

The historical town of Weimar in Thuringia, the "green heart of Germany" was the sphere of Goethe and Schiller, the two most famous representatives of German literature's classic era. Not yet entirely as influential as those two cultural icons,...

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Friedrich K, Lindquist JA, Entschladen F, et al. Signal transduction in the footsteps of goethe and schiller. Cell Commun Signal. 2009;7:2doi: 10.1186/1478-811X-7-2.
Friedrich, K., Lindquist, J. A., Entschladen, F., Serfling, E., Thiel, G., Kieser, A., Giehl, K., Ehrhardt, C., Feller, S. M., Ullrich, O., Schaper, F., Janssen, O., & Hass, R. (2009). Signal transduction in the footsteps of goethe and schiller. Cell communication and signaling : CCS, 72. https://doi.org/10.1186/1478-811X-7-2
Friedrich, Karlheinz, et al. "Signal transduction in the footsteps of goethe and schiller." Cell communication and signaling : CCS vol. 7 (2009): 2. doi: https://doi.org/10.1186/1478-811X-7-2
Friedrich K, Lindquist JA, Entschladen F, Serfling E, Thiel G, Kieser A, Giehl K, Ehrhardt C, Feller SM, Ullrich O, Schaper F, Janssen O, Hass R. Signal transduction in the footsteps of goethe and schiller. Cell Commun Signal. 2009 Feb 04;7:2. doi: 10.1186/1478-811X-7-2. PMID: 19193215; PMCID: PMC2645404.
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Magnetism and superconductivity driven by identical 4f states in a heavy-fermion metal.

Proceedings of the National Academy of Sciences of the United States of America

Nair S, Stockert O, Witte U, Nicklas M, Schedler R, Kiefer K, Thompson JD, Bianchi AD, Fisk Z, Wirth S, Steglich F.
PMID: 20457945
Proc Natl Acad Sci U S A. 2010 May 25;107(21):9537-40. doi: 10.1073/pnas.1004958107. Epub 2010 May 10.

The apparently inimical relationship between magnetism and superconductivity has come under increasing scrutiny in a wide range of material classes, where the free energy landscape conspires to bring them in close proximity to each other. Particularly enigmatic is the...

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Nair S, Stockert O, Witte U, et al. Magnetism and superconductivity driven by identical 4f states in a heavy-fermion metal. Proc Natl Acad Sci U S A. 2010;107(21):9537-40doi: 10.1073/pnas.1004958107.
Nair, S., Stockert, O., Witte, U., Nicklas, M., Schedler, R., Kiefer, K., Thompson, J. D., Bianchi, A. D., Fisk, Z., Wirth, S., & Steglich, F. (2010). Magnetism and superconductivity driven by identical 4f states in a heavy-fermion metal. Proceedings of the National Academy of Sciences of the United States of America, 107(21), 9537-40. https://doi.org/10.1073/pnas.1004958107
Nair, Sunil, et al. "Magnetism and superconductivity driven by identical 4f states in a heavy-fermion metal." Proceedings of the National Academy of Sciences of the United States of America vol. 107,21 (2010): 9537-40. doi: https://doi.org/10.1073/pnas.1004958107
Nair S, Stockert O, Witte U, Nicklas M, Schedler R, Kiefer K, Thompson JD, Bianchi AD, Fisk Z, Wirth S, Steglich F. Magnetism and superconductivity driven by identical 4f states in a heavy-fermion metal. Proc Natl Acad Sci U S A. 2010 May 25;107(21):9537-40. doi: 10.1073/pnas.1004958107. Epub 2010 May 10. PMID: 20457945; PMCID: PMC2906831.
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Showing 1 to 12 of 321 entries