Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Katarzyna Tilgner"'
Autor:
Katarzyna Tilgner
Publikováno v:
Językoznawstwo, Iss 1/16 (2022)
The aim of the article is to compare the development of some family-related vocabulary from Latin (with PIE backgrounds) to Hispano-Romance with the old and modern Polish terms. The comparative analysis covers the words for ‘uncle’/’aunt’,
Externí odkaz:
https://doaj.org/article/52bef09436794adb8e37b383d268c0b2
Publikováno v:
Cell Reports, Vol 24, Iss 2, Pp 489-502 (2018)
Summary: The genetic basis of naive pluripotency maintenance and loss is a central question in embryonic stem cell biology. Here, we deploy CRISPR-knockout-based screens in mouse embryonic stem cells to interrogate this question through a genome-wide
Externí odkaz:
https://doaj.org/article/aee341e07bbd433b9251e8cbce2f87dc
Autor:
Amanda J. Collier, Adam Bendall, Charlene Fabian, Andrew A. Malcolm, Katarzyna Tilgner, Claudia I. Semprich, Katarzyna Wojdyla, Paola Serena Nisi, Kamal Kishore, Valar Nila Roamio Franklin, Bahar Mirshekar-Syahkal, Clive D’Santos, Kathrin Plath, Kosuke Yusa, Peter J. Rugg-Gunn
Publikováno v:
Science advances, vol 8, iss 12
Uncovering the mechanisms that establish naïve pluripotency in humans is crucial for the future applications of pluripotent stem cells including the production of human blastoids. However, the regulatory pathways that control the establishment of na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d76944bf9fc5e5949191c7b1aa813c1d
https://www.repository.cam.ac.uk/handle/1810/336442
https://www.repository.cam.ac.uk/handle/1810/336442
Autor:
Ludovic Vallier, Pedro Madrigal, Daniele Muraro, Katarzyna Tilgner, Mariya Chhatriwala, Sapna Vyas, Crystal Y. Chia, Evelyn Olszanowski, Ranna El-Khairi, Santiago A. Rodríguez-Seguí
Publikováno v:
Stem Cell Reports
Summary Heterozygous mutations in HNF1B in humans result in a multisystem disorder, including pancreatic hypoplasia and diabetes mellitus. Here we used a well-controlled human induced pluripotent stem cell pancreatic differentiation model to elucidat
Publikováno v:
Cell Reports
Cell Reports, Vol 24, Iss 2, Pp 489-502 (2018)
Cell Reports, Vol 24, Iss 2, Pp 489-502 (2018)
Summary The genetic basis of naive pluripotency maintenance and loss is a central question in embryonic stem cell biology. Here, we deploy CRISPR-knockout-based screens in mouse embryonic stem cells to interrogate this question through a genome-wide,
Autor:
Lyle Armstrong, Inmaculada Moreno-Gimeno, Irina Neganova, Majlinda Lako, Jumana Y. Al-Aama, Stefan Przyborski, Sun Yung, Gabriele Saretzki, Miodrag Stojkovic, Deborah J. Burks, Penny A. Jeggo, Andrew R. Gennery, Katarzyna Tilgner, Chatchawan Singhapol, Vera Gorbunova, Jerry Evans
Publikováno v:
Cell Death & Differentiation. 20:1089-1100
A human iPSC model of Ligase IV deficiency reveals an important role for NHEJ-mediated-DSB repair in the survival and genomic stability of induced pluripotent stem cells and emerging haematopoietic progenitors
Autor:
Sun Yung, Stuart P. Atkinson, Majlinda Lako, Anna Golebiewska, Miodrag Stojkovic, Lyle Armstrong, Katarzyna Tilgner, Rubén Moreno
Publikováno v:
Stem Cells. 28:84-92
The isolation of significant numbers of human primordial germ cells at several developmental stages is important for investigations of the mechanisms by which they are able to undergo epigenetic reprogramming. Only small numbers of these cells can be
Autor:
Lyle Armstrong, Majlinda Lako, Stuart P. Atkinson, Anna Golebiewska, Miodrag Stojkovic, Katarzyna Tilgner
Publikováno v:
Stem Cells. 26:3075-3085
Of all the cell types that can be obtained from the differentiation of embryonic stem cells, primordial germ cells are arguably the most fascinating, as they represent the in vitro completion of the reproductive cycle of the organism from which the e
Autor:
Katarzyna Tilgner, Irena Hausmanowa-Petrusewicz, Frans C. S. Ramaekers, Margareth Dorobek, Christopher J. Hutchison, Georgia Salpingidou, Mark van de Wetering, Juliet A. Ellis, Robert G. Wilson, Nick Barker, W. Matthijs Blankesteijn, Jos L. V. Broers, Ewa Markiewicz, Hans Clevers
Publikováno v:
EMBO Journal, 25, 3275-3285. Nature Publishing Group
Emerin is a type II inner nuclear membrane (INM) protein of unknown function. Emerin function is likely to be important because, when it is mutated, emerin promotes both skeletal muscle and heart defects. Here we show that one function of Emerin is t
Autor:
Majlinda Lako, Bernard Keavney, Rafiqul Hussain, Andrew W. Trafford, Miodrag Stojkovic, Stefan Przyborski, Lyle Armstrong, Lenka Tesarov, Cyril G. Eleftheriou, Joseph Collin, Tomáš Bárta, Graham Kirkwood, Evelyne Sernagor, Yan Jiang, Jumana Y. Al-Aama, Katarzyna Tilgner, Saba Habibollah
Publikováno v:
Stem cells translational medicine, 2014, Vol.3(4), pp.416-423 [Peer Reviewed Journal]
Hypoplastic left heart syndrome (HLHS) is a serious congenital cardiovascular malformation resulting in hypoplasia or atresia of the left ventricle, ascending aorta, and aortic and mitral valves. Diminished flow through the left side of the heart is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::246e2bd6a95538bdfb24dcbe6ef0bfd6