Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Kathryn L. Lovell"'
Autor:
Karen Vignare, Kathryn L. Lovell
Publikováno v:
Online Learning. 13
At Michigan State University the two medical schools, College of Human Medicine (CHM; M.D. degree) and College of Osteopathic Medicine (COM; D.O. degree), have offered the same science courses to first year students for many years. Science department
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef50865b86e2f16f50c5ff6dbf98898f
https://doi.org/10.24059/olj.v13i1.1677
https://doi.org/10.24059/olj.v13i1.1677
Autor:
Kathryn L. Lovell
Interactive neuropathology computer-based teaching modules and other neuroscience computer-based resources were developed to provide individualized self-paced content information accompanied by images and self-assessment questions with feedback, alon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116140fbf0b4d2af56b3ddcd6cfcd75c
https://doi.org/10.4018/978-1-5225-5478-3.ch011
https://doi.org/10.4018/978-1-5225-5478-3.ch011
Publikováno v:
Teaching and Learning in Medicine. 18:130-136
Background: In an effort to expand preclinical formative assessments, our medical school has implemented additional simulated encounters using faculty members and students in addition to actors to portray standardized patients (SP). This report focus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc5b02e15d264fb6467b5761ee8f16c5
https://doi.org/10.1207/s15328015tlm1802_7
https://doi.org/10.1207/s15328015tlm1802_7
Autor:
Kathryn L. Lovell, Mei Zhu, Elizabeth D. Hughes, Thomas L. Saunders, Karen H. Friderici, Jon S. Patterson
Publikováno v:
Human Molecular Genetics. 15:493-500
Beta-mannosidase, a lysosomal enzyme which acts exclusively at the last step of oligosaccharide catabolism in glycoprotein degradation, functions to cleave the unique beta-linked mannose sugar found in all N-linked oligosaccharides of glycoproteins.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4867ddff39ed09d428d2f2de67c6aa4
https://doi.org/10.1093/hmg/ddi465
https://doi.org/10.1093/hmg/ddi465
Autor:
Stacey A. Kraemer, Kathryn L. Lovell, Jodi Nichols-Torrez, Margaret Z. Jones, Kawanaa D. Carter, N. Kent Ames, Jeffrey R. Leipprandt, D.J. Sprecher, Darush K. Rahmani
Publikováno v:
Fetal Diagnosis and Therapy. 16:13-17
Objectives: We explored the feasibility and efficacy of in utero hematopoietic stem cell transplantation in the caprine animal model system with the objectives of determining procedures for transplantation and establishing methods for detecting engra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54d10b95180f0a98075e1e0b4c203d86
https://doi.org/10.1159/000053873
https://doi.org/10.1159/000053873
Publikováno v:
Advances in Health Sciences Education. 3:165-176
When second year medical students were less successful than expected in solving an OSCE neurologic case, a subsequent performance-based assessment was modified to permit testing of four hypotheses related to knowledge application, ability decay over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7492c7ec4476895cd402cae6dd2783f9
https://doi.org/10.1023/a:1009794026466
https://doi.org/10.1023/a:1009794026466
Autor:
Kathryn L. Lovell, Jon S. Patterson, N. K. Ames, F. Matsuura, G. Baeverfjord, Margaret Z. Jones
Publikováno v:
Prenatal Diagnosis. 17:551-557
Lysosomal storage diseases associated with early-onset pathological changes may require prenatal therapy to avert the profound effects of the metabolic error on organs, especially the central nervous system. The present investigation determined the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56dd2e59db8bb9ae5c6c01cb57d90264
https://doi.org/10.1002/(sici)1097-0223(199706)17:6<551::aid-pd109>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199706)17:6<551::aid-pd109>3.0.co
Publikováno v:
JIMD Reports ISBN: 9783642541483
Neurological dysfunction is common in humans and animals with lysosomal storage diseases. β-Mannosidosis, an autosomal recessive inherited disorder of glycoprotein catabolism caused by deficiency of the lysosomal enzyme β-mannosidase, is characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b23d0854729ed91a965a1bafd7175ea
https://doi.org/10.1007/8904_2013_258
https://doi.org/10.1007/8904_2013_258
Publikováno v:
Molecular and Chemical Neuropathology. 21:61-74
Goats affected with beta-mannosidosis, an autosomal recessive disease of glycoprotein catabolism, have deficient tissue and plasma levels of the lysosomal enzyme beta-mannosidase. Pathological characteristics include cytoplasmic vacuolation in the ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45956cea1deb0243f5bb728fd077a33
https://doi.org/10.1007/bf03160085
https://doi.org/10.1007/bf03160085
Publikováno v:
Brain Research. 620:127-132
Caprine β-mannosidosis is an inherited lysosomal storage disorder due to a deficiency of β-mannosidase which cleaves β-linked mannose residues from the ends of N-asparagine linked oligosaccharides of glycoproteins. Histological and chemical examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::936b32751cde363883720b56450bfe4f
https://doi.org/10.1016/0006-8993(93)90278-u
https://doi.org/10.1016/0006-8993(93)90278-u