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Showing 1 to 12 of 12 entries
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Overexpression of CXCL16 in lesional psoriatic skin.

Dermato-endocrinology

Oh ST, Schramme A, Tilgen W, Gutwein P, Reichrath J.
PMID: 20224694
Dermatoendocrinol. 2009 Mar;1(2):114-8. doi: 10.4161/derm.1.2.7750.

BACKGROUND: Psoriasis is characterized as an autoimmune disease resulting in an exaggerated innate immune response. The CXC-chemokine ligand 16 (CXCL16) is described to function as an adhesion molecule, a scavenger receptor or as a soluble molecule it acts as...

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Oh ST, Schramme A, Tilgen W, et al. Overexpression of CXCL16 in lesional psoriatic skin. Dermatoendocrinol. 2009;1(2):114-8doi: 10.4161/derm.1.2.7750.
Oh, S. T., Schramme, A., Tilgen, W., Gutwein, P., & Reichrath, J. (2009). Overexpression of CXCL16 in lesional psoriatic skin. Dermato-endocrinology, 1(2), 114-8. https://doi.org/10.4161/derm.1.2.7750
Oh, Shin-Taek, et al. "Overexpression of CXCL16 in lesional psoriatic skin." Dermato-endocrinology vol. 1,2 (2009): 114-8. doi: https://doi.org/10.4161/derm.1.2.7750
Oh ST, Schramme A, Tilgen W, Gutwein P, Reichrath J. Overexpression of CXCL16 in lesional psoriatic skin. Dermatoendocrinol. 2009 Mar;1(2):114-8. doi: 10.4161/derm.1.2.7750. PMID: 20224694; PMCID: PMC2835901.
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sim2.71828.

Science (New York, N.Y.)

Borwein P.
PMID: 17794079
Science. 1994 Jun 24;264(5167):1952-3. doi: 10.1126/science.264.5167.1952-a.

No abstract available.

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Borwein P. sim2.71828. Science. 1994;264(5167):1952-3doi: 10.1126/science.264.5167.1952-a.
Borwein, P. (1994). sim2.71828. Science (New York, N.Y.), 264(5167), 1952-3. https://doi.org/10.1126/science.264.5167.1952-a
Borwein, P. "sim2.71828." Science (New York, N.Y.) vol. 264,5167 (1994): 1952-3. doi: https://doi.org/10.1126/science.264.5167.1952-a
Borwein P. sim2.71828. Science. 1994 Jun 24;264(5167):1952-3. doi: 10.1126/science.264.5167.1952-a. PMID: 17794079.
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Live cell imaging reveals marked variability in myoblast proliferation and fate.

Skeletal muscle

Gross SM, Rotwein P.
PMID: 23638706
Skelet Muscle. 2013 May 02;3(1):10. doi: 10.1186/2044-5040-3-10.

BACKGROUND: During the process of muscle regeneration, activated stem cells termed satellite cells proliferate, and then differentiate to form new myofibers that restore the injured area. Yet not all satellite cells contribute to muscle repair. Some continue to proliferate,...

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Gross SM, Rotwein P. Live cell imaging reveals marked variability in myoblast proliferation and fate. Skelet Muscle. 2013;3(1):10doi: 10.1186/2044-5040-3-10.
Gross, S. M., & Rotwein, P. (2013). Live cell imaging reveals marked variability in myoblast proliferation and fate. Skeletal muscle, 3(1), 10. https://doi.org/10.1186/2044-5040-3-10
Gross, Sean M, and Rotwein, Peter. "Live cell imaging reveals marked variability in myoblast proliferation and fate." Skeletal muscle vol. 3,1 (2013): 10. doi: https://doi.org/10.1186/2044-5040-3-10
Gross SM, Rotwein P. Live cell imaging reveals marked variability in myoblast proliferation and fate. Skelet Muscle. 2013 May 02;3(1):10. doi: 10.1186/2044-5040-3-10. PMID: 23638706; PMCID: PMC3712004.
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Gene Mapping by RNA-sequencing: A Direct Way to Characterize Genes and Gene Expression through Targeted Queries of Large Public Databases.

Bio-protocol

Rotwein P.
PMID: 32699811
Bio Protoc. 2019 Jan 05;9(1). doi: 10.21769/BioProtoc.3129.

Recent advances in genomics present new opportunities for enhancing knowledge about gene regulation and function across a wide spectrum of organisms and species. Understanding and evaluating this information at the individual gene level is challenging, and not only requires...

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Rotwein P. Gene Mapping by RNA-sequencing: A Direct Way to Characterize Genes and Gene Expression through Targeted Queries of Large Public Databases. Bio Protoc. 2019;9(1)doi: 10.21769/BioProtoc.3129.
Rotwein, P. (2019). Gene Mapping by RNA-sequencing: A Direct Way to Characterize Genes and Gene Expression through Targeted Queries of Large Public Databases. Bio-protocol, 9(1), . https://doi.org/10.21769/BioProtoc.3129
Rotwein, Peter. "Gene Mapping by RNA-sequencing: A Direct Way to Characterize Genes and Gene Expression through Targeted Queries of Large Public Databases." Bio-protocol vol. 9,1 (2019). doi: https://doi.org/10.21769/BioProtoc.3129
Rotwein P. Gene Mapping by RNA-sequencing: A Direct Way to Characterize Genes and Gene Expression through Targeted Queries of Large Public Databases. Bio Protoc. 2019 Jan 05;9(1). doi: 10.21769/BioProtoc.3129. PMID: 32699811; PMCID: PMC7375414.
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Revisiting the Population Genetics of Human Height.

Journal of the Endocrine Society

Rotwein P.
PMID: 32232182
J Endocr Soc. 2020 Mar 05;4(4):bvaa025. doi: 10.1210/jendso/bvaa025. eCollection 2020 Apr 01.

CONTEXT: Recent advances in genetics and genomics present unique opportunities for enhancing knowledge of human physiology and disease susceptibility. An outstanding example of these new insights may be seen in the study of human height, of which it has...

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Rotwein P. Revisiting the Population Genetics of Human Height. J Endocr Soc. 2020;4(4):bvaa025doi: 10.1210/jendso/bvaa025.
Rotwein, P. (2020). Revisiting the Population Genetics of Human Height. Journal of the Endocrine Society, 4(4), bvaa025. https://doi.org/10.1210/jendso/bvaa025
Rotwein, Peter. "Revisiting the Population Genetics of Human Height." Journal of the Endocrine Society vol. 4,4 (2020): bvaa025. doi: https://doi.org/10.1210/jendso/bvaa025
Rotwein P. Revisiting the Population Genetics of Human Height. J Endocr Soc. 2020 Mar 05;4(4):bvaa025. doi: 10.1210/jendso/bvaa025. eCollection 2020 Apr 01. PMID: 32232182; PMCID: PMC7093090.
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Mathematical malaises.

Science (New York, N.Y.)

Borwein J, Borwein P.
PMID: 17836254
Science. 1993 Mar 26;259(5103):1928-30. doi: 10.1126/science.259.5103.1928.

No abstract available.

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Borwein J, Borwein P. Mathematical malaises. Science. 1993;259(5103):1928-30doi: 10.1126/science.259.5103.1928.
Borwein, J., & Borwein, P. (1993). Mathematical malaises. Science (New York, N.Y.), 259(5103), 1928-30. https://doi.org/10.1126/science.259.5103.1928
Borwein, J, and Borwein, P. "Mathematical malaises." Science (New York, N.Y.) vol. 259,5103 (1993): 1928-30. doi: https://doi.org/10.1126/science.259.5103.1928
Borwein J, Borwein P. Mathematical malaises. Science. 1993 Mar 26;259(5103):1928-30. doi: 10.1126/science.259.5103.1928. PMID: 17836254.
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Evaluation of a 'breaking bad news' course at the Charité, Berlin.

Medical education

Schildmann J, Brunklaus A, Herrmann E, Klambeck A, Ortwein H, Schwarz C.
PMID: 11489113
Med Educ. 2001 Aug;35(8):806-7. doi: 10.1046/j.1365-2923.2001.1014b.x.

No abstract available.

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Schildmann J, Brunklaus A, Herrmann E, et al. Evaluation of a 'breaking bad news' course at the Charité, Berlin. Med Educ. 2001;35(8):806-7doi: 10.1046/j.1365-2923.2001.1014b.x.
Schildmann, J., Brunklaus, A., Herrmann, E., Klambeck, A., Ortwein, H., & Schwarz, C. (2001). Evaluation of a 'breaking bad news' course at the Charité, Berlin. Medical education, 35(8), 806-7. https://doi.org/10.1046/j.1365-2923.2001.1014b.x
Schildmann, J, et al. "Evaluation of a 'breaking bad news' course at the Charité, Berlin." Medical education vol. 35,8 (2001): 806-7. doi: https://doi.org/10.1046/j.1365-2923.2001.1014b.x
Schildmann J, Brunklaus A, Herrmann E, Klambeck A, Ortwein H, Schwarz C. Evaluation of a 'breaking bad news' course at the Charité, Berlin. Med Educ. 2001 Aug;35(8):806-7. doi: 10.1046/j.1365-2923.2001.1014b.x. PMID: 11489113.
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Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms.

The Journal of biological chemistry

Rotwein P.
PMID: 29196571
J Biol Chem. 2017 Dec 01;292(48):19608. doi: 10.1074/jbc.AAC117.000854.

No abstract available.

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Rotwein P. Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms. J Biol Chem. 2017;292(48):19608doi: 10.1074/jbc.AAC117.000854.
Rotwein, P. (2017). Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms. The Journal of biological chemistry, 292(48), 19608. https://doi.org/10.1074/jbc.AAC117.000854
Rotwein, Peter. "Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms." The Journal of biological chemistry vol. 292,48 (2017): 19608. doi: https://doi.org/10.1074/jbc.AAC117.000854
Rotwein P. Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms. J Biol Chem. 2017 Dec 01;292(48):19608. doi: 10.1074/jbc.AAC117.000854. PMID: 29196571; PMCID: PMC5712604.
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Hair-cycle dependent differential expression of ADAM 10 and ADAM 12: An immunohistochemical analysis in human hair follicles in situ.

Dermato-endocrinology

Oh ST, Cho BK, Schramme A, Gutwein P, Tilgen W, Reichrath J.
PMID: 20046589
Dermatoendocrinol. 2009 Jan;1(1):46-53. doi: 10.4161/derm.1.1.7497.

BACKGROUND: ADAM proteases play important roles in processes of development and differentiation. However, no report has been found in the literature addressing the expression and function of ADAM proteases during hair cycling.RESULTS: Cytoplasmic expression pattern of ADAM 10, 12...

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Oh ST, Cho BK, Schramme A, et al. Hair-cycle dependent differential expression of ADAM 10 and ADAM 12: An immunohistochemical analysis in human hair follicles in situ. Dermatoendocrinol. 2009;1(1):46-53doi: 10.4161/derm.1.1.7497.
Oh, S. T., Cho, B. K., Schramme, A., Gutwein, P., Tilgen, W., & Reichrath, J. (2009). Hair-cycle dependent differential expression of ADAM 10 and ADAM 12: An immunohistochemical analysis in human hair follicles in situ. Dermato-endocrinology, 1(1), 46-53. https://doi.org/10.4161/derm.1.1.7497
Oh, Shin-Taek, et al. "Hair-cycle dependent differential expression of ADAM 10 and ADAM 12: An immunohistochemical analysis in human hair follicles in situ." Dermato-endocrinology vol. 1,1 (2009): 46-53. doi: https://doi.org/10.4161/derm.1.1.7497
Oh ST, Cho BK, Schramme A, Gutwein P, Tilgen W, Reichrath J. Hair-cycle dependent differential expression of ADAM 10 and ADAM 12: An immunohistochemical analysis in human hair follicles in situ. Dermatoendocrinol. 2009 Jan;1(1):46-53. doi: 10.4161/derm.1.1.7497. PMID: 20046589; PMCID: PMC2715197.
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Anthraquinone Content in Noni (Morinda citrifolia L.).

Evidence-based complementary and alternative medicine : eCAM

Bussmann RW, Hennig L, Giannis A, Ortwein J, Kutchan TM, Feng X.
PMID: 24062780
Evid Based Complement Alternat Med. 2013;2013:208378. doi: 10.1155/2013/208378. Epub 2013 Aug 26.

Noni has been used in traditional medicine and as food for thousands of years. While the fruits serve as food and internal medicine, leaves were traditionally used only topically. In recent years, concern regarding the possible content of anthraquinones...

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Bussmann RW, Hennig L, Giannis A, et al. Anthraquinone Content in Noni (Morinda citrifolia L.). Evid Based Complement Alternat Med. 2013;2013:208378doi: 10.1155/2013/208378.
Bussmann, R. W., Hennig, L., Giannis, A., Ortwein, J., Kutchan, T. M., & Feng, X. (2013). Anthraquinone Content in Noni (Morinda citrifolia L.). Evidence-based complementary and alternative medicine : eCAM, 2013208378. https://doi.org/10.1155/2013/208378
Bussmann, Rainer W, et al. "Anthraquinone Content in Noni (Morinda citrifolia L.)." Evidence-based complementary and alternative medicine : eCAM vol. 2013 (2013): 208378. doi: https://doi.org/10.1155/2013/208378
Bussmann RW, Hennig L, Giannis A, Ortwein J, Kutchan TM, Feng X. Anthraquinone Content in Noni (Morinda citrifolia L.). Evid Based Complement Alternat Med. 2013;2013:208378. doi: 10.1155/2013/208378. Epub 2013 Aug 26. PMID: 24062780; PMCID: PMC3770026.
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[No title available]

Evolutionary bioinformatics online

Baral K, Rotwein P.
PMID: 32952394
Evol Bioinform Online. 2020 Sep 02;16:1176934320941500. doi: 10.1177/1176934320941500. eCollection 2020.

Recent advances in genetics present unique opportunities for enhancing our understanding of human physiology and disease predisposition through detailed analysis of gene structure, expression, and population variation via examination of data in publicly accessible genome and gene expression repositories....

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Baral K, Rotwein P. . Evol Bioinform Online. 2020;16:1176934320941500doi: 10.1177/1176934320941500.
Baral, K., & Rotwein, P. (2020). . Evolutionary bioinformatics online, 161176934320941500. https://doi.org/10.1177/1176934320941500
Baral, Kabita, and Rotwein, Peter. "." Evolutionary bioinformatics online vol. 16 (2020): 1176934320941500. doi: https://doi.org/10.1177/1176934320941500
Baral K, Rotwein P. . Evol Bioinform Online. 2020 Sep 02;16:1176934320941500. doi: 10.1177/1176934320941500. eCollection 2020. PMID: 32952394; PMCID: PMC7485168.
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Hospitalizations for Injury Among Medicaid Children: California, 1992.

Health care financing review

Baugh DK, Rotwein S, Hakim RB, Boschert R.
PMID: 25372466
Health Care Financ Rev. 1998;19(4):129-147.

Little is known about the incidence and cost of injuries for Medicaid children. This article provides data on hospital utilization and payments for injuries among Medicaid children, using the Health Care Financing Administration's (HCFA) State Medicaid Research Files. During...

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Baugh DK, Rotwein S, Hakim RB, et al. Hospitalizations for Injury Among Medicaid Children: California, 1992. Health Care Financ Rev. 1998;19(4):129-147
Baugh, D. K., Rotwein, S., Hakim, R. B., & Boschert, R. (1998). Hospitalizations for Injury Among Medicaid Children: California, 1992. Health care financing review, 19(4), 129-147.
Baugh, David K, et al. "Hospitalizations for Injury Among Medicaid Children: California, 1992." Health care financing review vol. 19,4 (1998): 129-147.
Baugh DK, Rotwein S, Hakim RB, Boschert R. Hospitalizations for Injury Among Medicaid Children: California, 1992. Health Care Financ Rev. 1998;19(4):129-147. PMID: 25372466; PMCID: PMC4194513.
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Showing 1 to 12 of 12 entries