Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maja P. Mattle-Greminger"'
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:
Adrian Belosevic, Anna-Elisabeth Minder, Morgan Gueuning, Franziska van Breemen, Gian Andri Thun, Maja P. Mattle-Greminger, Stefan Meyer, Alessandra Baumer, Elisabeth I. Minder, Xiaoye Schneider-Yin, Jasmin Barman-Aksözen
Publikováno v:
Life, Vol 13, Iss 9, p 1889 (2023)
Acute porphyrias are a group of monogenetic inborn errors of heme biosynthesis, characterized by acute and potentially life-threatening neurovisceral attacks upon exposure to certain triggering factors. Biochemical analyses can determine the type of
Externí odkaz:
https://doaj.org/article/1aa2f4fc9c104c9db505d8c902b9f107
Autor:
Maja P. Mattle-Greminger, Tugce Bilgin Sonay, Alexander Nater, Marc Pybus, Tariq Desai, Guillem de Valles, Ferran Casals, Aylwyn Scally, Jaume Bertranpetit, Tomas Marques-Bonet, Carel P. van Schaik, Maria Anisimova, Michael Krützen
Publikováno v:
Genome Biology, Vol 19, Iss 1, Pp 1-13 (2018)
Abstract Background Integrating demography and adaptive evolution is pivotal to understanding the evolutionary history and conservation of great apes. However, little is known about the adaptive evolution of our closest relatives, in particular if an
Externí odkaz:
https://doaj.org/article/46fd2b4542f14eadb2810e6b6086bc5a
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
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:
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