E-LIB Suche - Ergebnisse für: Ochoa‐Garay, Gorka

1

Two novel variants that disrupt the RHCE start codon with v..:

Vege, Sunitha ; Floch, Aline ; Burgos, Anna...
Transfusion. 63 (2023) 4 - p. , 2023

Link: https://doi.org/10.1111/..

2

Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles:

Lomas‐Francis, Christine ; Vege, Sunitha ; Fuertes, June...
Transfusion. 63 (2023) 12 - p. , 2023

Link: https://doi.org/10.1111/..

3

Four novelABO*AWalleles associated with weak antigen expres..:

Tahiri, Toufik ; Vege, Sunitha ; Floch, Aline...
Transfusion. 62 (2022) 12 - p. , 2022

Link: https://doi.org/10.1111/..

4

Novel KEL*02N allele in Saudi Arabia encoding a Kell null (..:

Albasri, Jasem ; Alsuhaibani, Omar ; Almarry, Noorah...
Transfusion. 61 (2021) 7 - p. , 2021

Link: https://doi.org/10.1111/..

5

An intron c.149‐2632T>A change in RHD is associated with ab..:

Floch, Aline ; Vege, Sunitha ; Berardi, Philip...
Transfusion. 62 (2021) 2 - p. , 2021

Link: https://doi.org/10.1111/..

6

RH genotyping by nonspecific quantitative next‐generation s..:

Stef, Marianne ; Fennell, Katie ; Apraiz, Izaskun...
Transfusion. 60 (2020) 11 - p. 2691-2701 , 2020

Link: https://doi.org/10.1111/..

7

Two newRHDalleles with deletions spanning multiple exons:

Matteocci, Antonella ; Monge‐Ruiz, Jorge ; Stef, Marianne...
Transfusion. 61 (2020) 3 - p. 682-686 , 2020

Link: https://doi.org/10.1111/..

8

A GYPB variant encoding an altered leader peptide leads to ..:

Cote, Jacqueline ; Cen, Selena ; Fennell, Katie...
Transfusion. 59 (2019) 7 - p. 2461-2462 , 2019

Link: https://doi.org/10.1111/..

9

Genotyping by sequencing defines independent novel RHD vari..:

Lopez, Genghis H. ; McGowan, Eunike C. ; Condon, Jennifer A....
Transfusion. 57 (2017) 9 - p. 2281-2283 , 2017

Link: https://doi.org/10.1111/..

10

Effect on gene expression of three allelic variants in GATA..:

Fennell, Katie ; Hoffman, Roser ; Yoshida, Ken...
Transfusion. 57 (2017) 11 - p. 2804-2808 , 2017

Link: https://doi.org/10.1111/..

11

Three new alleles encoding an apparent Kellnull phenotype:

Puente, Fernando ; Cemborain‐Garcia, Arantxa ; Rodriguez‐Wilhelmi, Pablo...
Transfusion. 57 (2016) 1 - p. 221-222 , 2016

Link: https://doi.org/10.1111/..

12

Identification of new KLF1 and LU alleles during the resolu..:

Garcia‐Sanchez, Felix ; Pardi, Cecilia ; Kupatawintu, Pawinee...
Transfusion. 56 (2016) 6 - p. 1413-1418 , 2016

Link: https://doi.org/10.1111/..

13

FYA silencing by the GATA‐motif variant FYA(−69C) in a Ca..:

Písačka, Martin ; Marinov, Iuri ; Králová, Miroslava...
Transfusion. 55 (2015) 11 - p. 2616-2619 , 2015

Link: https://doi.org/10.1111/..

14

Identification of six new RHCE variant alleles in individua..:

Goldman, Mindy ; Cemborain, Arantxa ; Cote, Jacqueline...
Transfusion. 56 (2015) 1 - p. 244-248 , 2015

Link: https://doi.org/10.1111/..

15

Rh‐null phenotype caused by a complete RHAG deletion:

Gómez‐Torreiro, Eduardo ; Eiras‐Martínez, Adolfo ; Rodríguez‐Calvo, María Inmaculada...
Transfusion. 55 (2014) 1 - p. 197-198 , 2014

Link: https://doi.org/10.1111/..