Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Karen J. Dunn"'
Autor:
Karen J. Dunn, Gareth McCray
Publikováno v:
Frontiers in Psychology, Vol 11 (2020)
For practical and theoretical purposes, tests of second language (L2) ability commonly aim to measure one overarching trait, general language ability, while simultaneously measuring multiple sub-traits (e.g., reading, grammar, etc.). This tension bet
Externí odkaz:
https://doaj.org/article/111a247152714c969f0d4b2301485e8d
Autor:
Janina Iwaniec, Karen J. Dunn
Publikováno v:
The Routledge Handbook of Second Language Acquisition and Language Testing ISBN: 9781351034784
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca8dd8803b928476d5333cdf291d8142
https://doi.org/10.4324/9781351034784-18
https://doi.org/10.4324/9781351034784-18
Autor:
Karen J. Dunn, Carolyn Bradley
Publikováno v:
Forensic Social Work
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56863f35e839278671a2d66159b7dd9e
https://doi.org/10.1891/9780826120670.0005
https://doi.org/10.1891/9780826120670.0005
Publikováno v:
genesis. 30:70-76
Summary: This study describes an in utero approach for overexpressing genes in a cell-type directed manner. It uses an avian leukosis retroviral expression system coupled with a transgenic mouse line expressing the viral receptor tv-a from a tissue-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::353722933bb9f9fd6e2be6e61c69b9c2
https://doi.org/10.1002/gene.1035
https://doi.org/10.1002/gene.1035
Publikováno v:
Human Genetics. 107:1-6
Waardenburg syndrome (WS) is associated with neural crest-derived melanocyte deficiency caused by mutations in either one of three transcription factors: MITF, PAX3, and SOX10. However, the hierarchical relationship of these transcription factors is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4840dfc309a9958ecc5a52bedb9c2038
https://doi.org/10.1007/s004390000328
https://doi.org/10.1007/s004390000328
Autor:
Katsutoshi Suetomi, Zhijian Lu, Tonia Heck, Javier Navarro, Karen J. Dunn, Thomas G. Wood, Deborah Prusak
Publikováno v:
Journal of Biological Chemistry. 274:11768-11772
We have probed an epitope sequence (His18-Pro19-Lys20-Phe21) in interleukin-8 (IL-8) by site-directed mutagenesis. This work shows that single and double Ala substitutions of His18 and Phe21 in IL-8 reduced up to 77-fold the binding affinity to IL-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae063dd1f786e1308dfa6908a62e9284
https://doi.org/10.1074/jbc.274.17.11768
https://doi.org/10.1074/jbc.274.17.11768
Autor:
Suzie Chen, Pamela M. Pollock, Jeffrey J. Martino, Raman Sood, Karen J. Dunn, Kerine R. Mackason, James S. Goydos, Christiane M. Robbins, Kevin Ryan, William J. Pavan, Michael Eckhaus, Steven M. Crespo-Carbone, Christopher L. Graham, Yarí E. Marín, Jun Cheng, Daniel Sinsimer, Jin Namkoong, Arturo Incao, Kenneth R. Reuhl, Jeffrey M. Trent, Izabela Makalowska, Amy Chen, Kathleen G. Roberts, Laura M. Yudt, Aruna Koganti, Heather W. Pinkett, Paul S. Meltzer, Seung Shick Shin, Hua Zhu, Karine A. Cohen-Solal
Publikováno v:
Nature genetics. 34(1)
To gain insight into melanoma pathogenesis, we characterized an insertional mouse mutant, TG3, that is predisposed to develop multiple melanomas. Physical mapping identified multiple tandem insertions of the transgene into intron 3 of Grm1 (encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f92780953cdce9df58bcdf807a24c69
https://pubmed.ncbi.nlm.nih.gov/12704387
https://pubmed.ncbi.nlm.nih.gov/12704387
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 97(18)
Wnt1 signaling has been implicated as one factor involved in neural crest-derived melanocyte (NC-M) development. Mice deficient for both Wnt1 and Wnt3a have a marked deficiency in trunk neural crest derivatives including NC-Ms. We have used cell line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91c6db27f1d52440633f7f6502d56ae4
https://pubmed.ncbi.nlm.nih.gov/10963668
https://pubmed.ncbi.nlm.nih.gov/10963668
Autor:
Francis S. Collins, Nijaguna B. Prasad, Settara C. Chandrasekharappa, Judy S. Crabtree, Kevin D. Brown, William J. Pavan, Allen M. Spiegel, Danny Wangsa, A. Lee Burns, Pachiappan Manickam, Stephen J. Marx, Siradanahalli C. Guru, Karen J. Dunn
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 10(6)
The mouse homolog of the human MEN1 gene, which is defective in a dominant familial cancer syndrome, multiple endocrine neoplasia type 1 (MEN1), has been identified and characterized. The mouse Men1 transcript contains an open reading frame encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f58dc10aeabeb153b999588db7ba3e0c
https://pubmed.ncbi.nlm.nih.gov/10341092
https://pubmed.ncbi.nlm.nih.gov/10341092
Publikováno v:
Virology. 56:152-163
Mouse sarcoma virus-transformed 3T3FL cells (S+L− cells) produced spontaneously and at variable rates flat variants with some properties of nontransformed cells. The frequency of occurrence of such variant cells increased after treatment of S+L−c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6378cb7088d50bf54d10b32f56be8418
https://doi.org/10.1016/0042-6822(73)90294-8
https://doi.org/10.1016/0042-6822(73)90294-8