Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yvonne Merki"'
Autor:
Morgan Gueuning, Gian Andri Thun, Nadine Trost, Linda Schneider, Sonja Sigurdardottir, Charlotte Engström, Naemi Larbes, Yvonne Merki, Beat M. Frey, Christoph Gassner, Stefan Meyer, Maja P. Mattle-Greminger
Publikováno v:
Biomedicines, Vol 12, Iss 1, p 225 (2024)
Due to substantial improvements in read accuracy, third-generation long-read sequencing holds great potential in blood group diagnostics, particularly in cases where traditional genotyping or sequencing techniques, primarily targeting exons, fail to
Externí odkaz:
https://doaj.org/article/8cd38d3c754c48a6a585818cdf159813
Autor:
Morgan Gueuning, Gian Andri Thun, Michael Wittig, Anna-Lena Galati, Stefan Meyer, Nadine Trost, Elise Gourri, Janina Fuss, Sonja Sigurdardottir, Yvonne Merki, Kathrin Neuenschwander, Yannik Busch, Peter Trojok, Marco Schäfer, Jochen Gottschalk, Andre Franke, Christoph Gassner, Wolfgang Peter, Beat M. Frey, Maja P. Mattle-Greminger
Publikováno v:
Blood Advances. 7:878-892
In the era of blood group genomics, reference collections of complete and fully resolved blood group gene alleles have gained high importance. For most blood groups, however, such collections are currently lacking, as resolving full-length gene seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd4cd21d4586f352144042ba5c118236
https://doi.org/10.1182/bloodadvances.2022007133
https://doi.org/10.1182/bloodadvances.2022007133
Autor:
Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, Eduardo Meyer, Elise Gourri, Linda Schneider, Yvonne Merki, Nadine Trost, Kathrin Neuenschwander, Charlotte Engström, Beat M. Frey, Stefan Meyer, Maja P. Mattle-Greminger
Background and ObjectivesMixed-field agglutination in ABO phenotyping (A3, B3) has been linked to genetically different blood cell populations like in chimerism, or to rare variants in eitherABOexon 7 or regulatory regions. Clarification of such case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a11727171c87c08bbaf30ee65c1cf44
https://doi.org/10.1101/2023.05.04.539366
https://doi.org/10.1101/2023.05.04.539366
Autor:
Sonja Sigurdardottir, Eduardo Meyer, Beat M. Frey, Hans H. Jung, Christoph Gassner, Charlotte Engström, Yvonne Merki, Chantal Brönnimann, John D. O'Sullivan, Maja Patricia Mattle-Greminger
Publikováno v:
Transfusion. 57:2125-2135
BACKGROUND McLeod syndrome (MLS) is hematologically defined by the absence of the red blood cell (RBC) antigen Kx on the transmembrane RBC protein, XK, representing a highly specific diagnostic marker. Direct molecular assessment of XK therefore repr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0deb0a2fe0bf0acca9b9094786665f25
https://doi.org/10.1111/trf.14172
https://doi.org/10.1111/trf.14172
Autor:
Laura Infanti, Daniel Bessero, Nadine Trost, Claudia Portmann, Beat M. Frey, Amira Sarraj, Jörg Sigle, Jochen Gottschalk, Caroline Tinguely, Michael Krawczak, Sophie Waldvogel-Abramovski, Stefan Meyer, Jutta Thierbach, Charlotte Engström, Andre Franke, Kathrin Neuenschwander, Yvonne Merki, Emmanuel Rigal, Christoph Gassner, Andreas Buser, Damiano Castelli, Frauke Degenhardt, Monica C. Braisch, Thomas Schulzki, Jean-Daniel Tissot, Caren Vollmert, Tina Weingand, Simon M. Mauvais, Sonja Sigurdardottir, Antigoni Zorbas, Sonja Heer, Michele Stalder, Soraya Amar el Dusouqui
Background: High-frequency blood group antigens (HFA) are present in >90% of the human population, according to some reports even in >99% of individuals. Therefore, patients lacking HFA may become challenging for transfusion support because compatibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca73da7223109244000a0ef42d43a19
https://europepmc.org/articles/PMC6158591/
https://europepmc.org/articles/PMC6158591/
Autor:
Yvonne Merki, Cédric Vrignaud, Beat M. Frey, T. Peyrard, Christoph Gassner, Elise Gourri, Gregory A. Denomme, Erwin A. Scharberg
Publikováno v:
British journal of haematology. 177(4)
The GYPC gene encodes the glycophorins C and D. The two moieties express 12 known antigens of the Gerbich blood group system and functionally stabilize red blood cell membranes through their intracellular interaction with protein 4.1 and p55. Three G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b645e7c01a03f5b5ec46dcbda691f51
https://pubmed.ncbi.nlm.nih.gov/28272739
https://pubmed.ncbi.nlm.nih.gov/28272739
Autor:
Christoph, Gassner, Chantal, Brönnimann, Yvonne, Merki, Maja P, Mattle-Greminger, Sonja, Sigurdardottir, Eduardo, Meyer, Charlotte, Engström, John D, O'Sullivan, Hans H, Jung, Beat M, Frey
Publikováno v:
Transfusion. 57(9)
McLeod syndrome (MLS) is hematologically defined by the absence of the red blood cell (RBC) antigen Kx on the transmembrane RBC protein, XK, representing a highly specific diagnostic marker. Direct molecular assessment of XK therefore represents a de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d03c3d0053e2da6fbee756a19529c68
https://pubmed.ncbi.nlm.nih.gov/28555782
https://pubmed.ncbi.nlm.nih.gov/28555782