Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Katie Fennell"'
Autor:
Christine Biben, Tom Weber, Kathryn Potts, Jarny Choi, Denise Miles, Amandine Carmagnac, Tobias Sargent, Carolyn de Graaf, Katie Fennell, Alison Farley, Olivia Stonehouse, Mark Dawson, Douglas Hilton, Shalin Naik, Samir Taoudi
Publikováno v:
Experimental Hematology. 100:S35-S36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3980e7cc35732fe0dd96ddf0bdc2ed18
https://doi.org/10.1016/j.exphem.2021.12.382
https://doi.org/10.1016/j.exphem.2021.12.382
Autor:
Gorka Ochoa-Garay, Yolanda Larizgoitia-Martin, Mónica López, Guido Nespoli, Lara Herrera-Del-Val, Montserrat Rubia-Tejero, Tommaso Mancuso, Jorge Monge-Ruiz, Angela Collaretti, Antonella Matteocci, Marianne Stef, Katie Fennell, Izaskun Apraiz, Luca Pierelli
Publikováno v:
TransfusionREFERENCES. 61(3)
Background The most common large-deletion RHD allele (RHD*01N.01) includes the entire coding sequence, intervening regions and untranslated regions. The rest of large-deletion RHD alleles reported to-date consist of single-exon deletions, such as RHD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7144c7a5452741caa3d7848d05f1885e
https://pubmed.ncbi.nlm.nih.gov/33241598
https://pubmed.ncbi.nlm.nih.gov/33241598
Autor:
Cecilia González, Núria Nogués, Marianne Stef, Katie Fennell, Izaskun Apraiz, Gorka Ochoa-Garay, David Arteta
Publikováno v:
TransfusionREFERENCES. 60(11)
Background Conventional sequencing uses gene-specific primers to determine the location of RH variants and permits a qualitative assessment of zygosity. Whole-genome and whole-exome sequencing determine the genetic location of variants and enable a q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::250646e3f50a1ee70387e6a51fe10010
https://pubmed.ncbi.nlm.nih.gov/32871036
https://pubmed.ncbi.nlm.nih.gov/32871036
Autor:
Olivia Stonehouse, Christine Biben, Katie Fennell, Alexandra Garnham, Tom Weber, Samir Taoudi
Publikováno v:
Experimental Hematology. 100:S104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2946098c4b5380167c79d75eb367496f
https://doi.org/10.1016/j.exphem.2021.12.345
https://doi.org/10.1016/j.exphem.2021.12.345
Autor:
Ken Yoshida, Lavendri Govender, Kuben Vather, Margaret A. Keller, Gorka Ochoa-Garay, Katie Fennell, Roser Hoffman, Sadahiko Iwamoto, Ute Jentsch, Ashika Sookraj, Chantale Pambrun, Catherine McAuley
Publikováno v:
Transfusion. 57:2804-2808
BACKGROUND Only a few genetic variants have been reported in regulatory elements of blood group genes. Most of them affect GATA motifs, binding sites for the GATA-1 transcription factor. STUDY DESIGN AND METHODS Samples from two patients and one dono
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c79898d4a028c9a99c72f5d7bd77c8ff
https://doi.org/10.1111/trf.14299
https://doi.org/10.1111/trf.14299
Autor:
Selena Cen, Katie Fennell, Gorka Ochoa-Garay, Donald R. Branch, Jacqueline Cote, Chantale Pambrun
Publikováno v:
Transfusion. 59:2461-2462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede334723cdec289b465bb8b7b180a95
https://doi.org/10.1111/trf.15295
https://doi.org/10.1111/trf.15295
Autor:
Katie, Fennell, Roser, Hoffman, Ken, Yoshida, Sadahiko, Iwamoto, Lavendri, Govender, Kuben, Vather, Ashika, Sookraj, Ute, Jentsch, Chantale, Pambrun, Catherine, McAuley, Margaret A, Keller, Gorka, Ochoa-Garay
Publikováno v:
Transfusion. 57(11)
Only a few genetic variants have been reported in regulatory elements of blood group genes. Most of them affect GATA motifs, binding sites for the GATA-1 transcription factor.Samples from two patients and one donor with unusual or discrepant serology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fce9ef746a28271df8407ba7735341e7
https://pubmed.ncbi.nlm.nih.gov/28815618
https://pubmed.ncbi.nlm.nih.gov/28815618
Autor:
Thomas Yong, J. Nathan Davis, James A. Cardelli, Shari Meyers, Katie Fennell, Adam H. Greer, Marcie Fowler, Floyd Galiano, Yara W. Moustafa, Shu-Wing Ng, Ross S. Berkowitz
Publikováno v:
Journal of Cellular Physiology. 228:2350-2364
Core binding factor (CBF) is a heterodimeric transcription factor containing one of three DNA-binding proteins of the Runt-related transcription factor family (RUNX1-3) and the non-DNA-binding protein, CBFβ. RUNX1 and CBFβ are the most common targe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25aac11f1e59aeb411180876990a8e72
https://doi.org/10.1002/jcp.24406
https://doi.org/10.1002/jcp.24406
Autor:
Adam H, Greer, Thomas, Yong, Katie, Fennell, Yara W, Moustafa, Marcie, Fowler, Floyd, Galiano, Shu-Wing, Ng, Ross S, Berkowitz, James, Cardelli, Shari, Meyers, J Nathan, Davis
Publikováno v:
Journal of cellular physiology. 228(12)
Core binding factor (CBF) is a heterodimeric transcription factor containing one of three DNA-binding proteins of the Runt-related transcription factor family (RUNX1-3) and the non-DNA-binding protein, CBFβ. RUNX1 and CBFβ are the most common targe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5fe728e6b0d33cde1dd04155fa6aeb41
https://pubmed.ncbi.nlm.nih.gov/23813439
https://pubmed.ncbi.nlm.nih.gov/23813439
Autor:
Amanda Sun, Jonathan Glass, Shari Meyers, Bing Cheng, J. Nathan Davis, Katie Fennell, Yara W. Moustafa, J. Michael Mathis, Thomas Yong, B. Jill Williams, Jette S. Jung, Runhua Shi, Lisa K. Adams, Donna Rogers, Erkut Borazanci
Publikováno v:
Journal of cellular physiology. 225(3)
Core binding factor (CBF) is a transcription factor complex that plays roles in development, stem-cell homeostasis, and human disease. CBF is a heterodimer composed of one of three DNA-binding RUNX proteins plus the non-DNA-binding protein, CBFβ. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6ad77645ba5b74448da306d806582dd
https://pubmed.ncbi.nlm.nih.gov/20607802
https://pubmed.ncbi.nlm.nih.gov/20607802