Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Gorka Ochoa-Garay"'
Autor:
Sunitha Vege, Aline Floch, Anna Burgos, Toufik Tahiri, Julie Kirkegaard, Megan Dupont, Gorka Ochoa‐Garay, Christine Lomas‐Francis, Connie M. Westhoff
Publikováno v:
Transfusion. 63
Autor:
Toufik Tahiri, Sunitha Vege, Aline Floch, Christine Lomas‐Francis, Gorka Ochoa‐Garay, Connie M. Westhoff
Publikováno v:
TransfusionREFERENCES. 62(12)
Publikováno v:
Immunohematology. 36:123-128
In recent years, polymerase chain reaction–based genotyping platforms, which provide a predicted phenotype, have increased in both patient and high-throughput donor testing, especially in situations where serologic methods or reagents are limited.
Autor:
Aline Floch, Sunitha Vege, Philip Berardi, Judith Hannon, Gorka Ochoa‐Garay, Christine Lomas‐Francis, Connie M. Westhoff
Publikováno v:
TransfusionREFERENCES. 62(2)
Autor:
Gregory A. Denomme, Madeline Knier, Noorah Salman Almarry, Danielle Biese, Gorka Ochoa-Garay, Omar Alsuhaibani, Kathleen M. Bensing, Jasem Albasri
Publikováno v:
Transfusion. 61
Autor:
Jasem, Albasri, Omar, Alsuhaibani, Noorah, Almarry, Gorka, Ochoa-Garay, Kathleen M, Bensing, Danielle, Biese, Madeline, Knier, Gregory A, Denomme
Publikováno v:
TransfusionREFERENCES. 61(7)
Publikováno v:
Immunohematology. 36(4)
In recent years, polymerase chain reaction-based genotyping platforms, which provide a predicted phenotype, have increased in both patient and high-throughput donor testing, especially in situations where serologic methods or reagents are limited. Th
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
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
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