Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Michael Litt"'
Autor:
Chunting Zhang, Steven T. Gossert, Jonathan Williams, Michael Little, Marilia Barros, Barton Dear, Bradley Falk, Ankit D. Kanthe, Robert Garmise, Luciano Mueller, Andrew Ilott, Anuji Abraham
Publikováno v:
mAbs, Vol 15, Iss 1 (2023)
ABSTRACTExcipients are added to biopharmaceutical formulations to enhance protein stability and enable the development of robust formulations with acceptable physicochemical properties, but the mechanism by which they confer stability is not fully un
Externí odkaz:
https://doaj.org/article/d07fb9b5f85d4dc88d56aaec9a92f83e
Autor:
Michael Little
Publikováno v:
AERA Open, Vol 9 (2023)
There is a movement to improve alignment between the early childhood and K–12 education sectors, which I term The Alignment Agenda. This qualitative study provides an in-depth description of this agenda through analysis of data from interviews with
Externí odkaz:
https://doaj.org/article/4b6124cfb95e49ee9afc33ecc43f7f8d
Autor:
Harshit Garg, Dharam Kaushik, Dawn Hui, Zachary Kahlenberg, Emily Vail, Lalithapriya Jayakumar, Hanzhang Wang, Deepak Pruthi, Ahmed M. Mansour, Michael Little
Publikováno v:
BJUI Compass, Vol 3, Iss 5, Pp 327-330 (2022)
Externí odkaz:
https://doaj.org/article/78a535ea00944ec097624611e673920f
Autor:
Xuanji Wang, Michael Littau, Joseph Fahmy, Sean Kisch, M. Alyssa Varsanik, Alexander O'Hara, Jacob Pozin, L. Mark Knab, Gerard Abood
Publikováno v:
Surgery in Practice and Science, Vol 10, Iss , Pp 100106- (2022)
Background: Malnutrition is a significant risk factor for decreased survival in cancer patients undergoing a pancreaticoduodenectomy (PD). Our study aims to investigate the impact of immunonutrition on length of stay (LOS), infection rates, postopera
Externí odkaz:
https://doaj.org/article/448cd5a6aee1499b9ac2e0cd4f871a7f
Publikováno v:
Human Molecular Genetics. 5:1631-1636
High resolution (0.1 cM) CEPH crossover mapping panels were constructed for chromosome 11. These panels will facilitate a transition from top-down physical and genetic mapping strategies to integrated breakpoint mapping strategies. Novel methods, whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d46889b893e9a5c9028b1b77670cbd
https://doi.org/10.1093/hmg/5.10.1631
https://doi.org/10.1093/hmg/5.10.1631
Autor:
David J. Munroe, Marcel M.A.M. Mannens, Manfred Gessler, Rajesh V. Thakker, Stephen J. O'Brien, Marielle Alders, Peter Devilee, Patrick Gaudray, Laura H. Reid, P Cartwright, S Bennett, [No Value] Vorechovsky, Chris Davies, S Chandrasekharappa, Paul R. Cooper, E vanSchothorst, Norma J. Nowak, D Burbee, Daniela S. Gerhard, Glen A. Evans, R Elliott, M Perlin, J. Fantes, A Courseaux, Bernhard H. F. Weber, Peter Little, Holger Hummerich, Dallas M. Swallow, C Wadelius, Charles W. Richard, J Lagercrantz, H Garner, N Parker, Michael Litt, Mike R. James, Bernhard Zabel, [No Value] vanHeyningen, Michael J. Higgins, Devignes, M Sawicki, Thomas B. Shows
Publikováno v:
Cytogenetic and Genome Research. 74:1-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58535d17fc16467c3478550fb9985ea1
https://doi.org/10.1159/000134383
https://doi.org/10.1159/000134383
Autor:
Ewout R. Brunt, Rein P. Stulp, W. J. Lubbers, T.W. van Weerden, Hans Scheffer, Michael Litt, D. L. Browne
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 59:400-405
A sixth family with autosomal dominantly inherited myokymia and paroxysmal ataxia is described. The syndrome in this family is linked to the recently discovered locus for inherited myokymia and paroxysmal ataxia on the human chromosome 12p, and a mis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82fd5ccaccf0e90afe9fd1f2e175913c
https://doi.org/10.1136/jnnp.59.4.400
https://doi.org/10.1136/jnnp.59.4.400
Autor:
Helen Donis-Keller, Diane W. Cox, Michael Litt, G. D. Billingsley, Jean Weissenbach, J.L. Weber, F. Persichetti, Allen E. Bale, J.H. Edwards, Nigel K. Spurr, W. Mcbride, Ray White
Publikováno v:
Cytogenetic and Genome Research. 69:175-178
Families from the linkage panel of Centre d’Etude du Polymorphisme Humain have been used to generate a linkage map containing 68 loci; 13 genes, 33 di- and 4 tetranucleotide repeats, one oligonucleotide ligation assay (OLA), and 17 RFLPs. This map
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d174a97476b2d036949011afac564df
https://doi.org/10.1159/000133955
https://doi.org/10.1159/000133955
Publikováno v:
Genomics. 20:62-67
The voltage-dependent anion channel of the mitochondrial outer membrane (VDAC) is a small, abundant pore-forming protein found in the outer membranes of all eukaryotic mitochondria. The VDAC protein is believed to form the major pathway for movement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8381cddd2d5727370f5384d3e8d40a0a
https://doi.org/10.1006/geno.1994.1127
https://doi.org/10.1006/geno.1994.1127
Autor:
J.L. Weber, A.E. Retief, M.S. Holt, J. Welssenbach, Louise Warnich, S. Mishra, X.Y. Hauge, Patricia L. Kramer, C. Jones, P.J. Wilkle, Helen Donis-Keller, Michael Litt, Z. Wang
Publikováno v:
Human Molecular Genetics. 2:909-913
We have constructed a continuous index map of 25 microsatellite markers on human chromosome 11. The markers have been typed in 40 CEPH families, have heterozygosities of 69% or higher and can be typed by PCR. The odds against inversion of adjacent ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::617177acf66d7e77f81b6fe5ff16c616
https://doi.org/10.1093/hmg/2.7.909
https://doi.org/10.1093/hmg/2.7.909