Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tessa Kasia"'
Autor:
Jack Barton, Katherine Pacey, Neha Jain, Tessa Kasia, Darren Edwards, Christine Thevanesan, Karin Straathof, Giuseppe Barone, John Anderson
Publikováno v:
F1000Research, Vol 8 (2019)
Background: Primary cell culture using serum free media supplemented with growth factors has been used in a number of cancers to propagate primary cells with stem like properties, which form as spherical cellular aggregates. Methods: We systematicall
Externí odkaz:
https://doaj.org/article/d5704da54a7846139c1435a460cecb63
Autor:
Mehul T. Dattani, Louise C. Gregory, Evelien F. Gevers, Frédéric Bilan, Mark J. McCabe, María Caimari, Tessa Kasia, Kling Chong, Joanne Baker, Dragana Josifova
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Introduction: CHARGE syndrome is a multisystem disorder that, in addition to Kallmann syndrome/isolated hypogonadotrophic hypogonadism, has been associated with anterior pituitary hypoplasia (APH). However, structural abnormalities such as an ectopic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b9cd2697a45afa705b5ab2f879c2ab
https://doi.org/10.1210/jc.2012-3467
https://doi.org/10.1210/jc.2012-3467
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49482492d194470b54fb130f1fc63061
https://doi.org/10.1530/endoabs.36.p76
https://doi.org/10.1530/endoabs.36.p76
Autor:
Chiara Bacchelli, Fowzan S. Alkuraya, Muhammad Talal Alrifai, Biljana Lukovic, Cynthia L. Andoniadou, Seyedeh Neda Mousavy-Gharavy, Mark J. McCabe, Francesco Lescai, Jane C. Sowden, Emma A Webb, Juan Pedro Martinez-Barbera, Abdul Banyan, Al Alsawaid, Mohammed A L Balwi, W. Kling Chong, Robert Kleta, Mohammed A. Alahmesh, Angham Almutair, Dorothy A. Thompson, Daniel Kelberman, Tessa Kasia, Derek Burke, Elia Stupka, Estelle Chanudet, Philip L. Beales, Mehul T. Dattani
Publikováno v:
Europe PubMed Central
Webb, E A, AlMutair, A, Kelberman, D, Bacchelli, C, Chanudet, E, Lescai, F, Andoniadou, C L, Banyan, A, Alsawaid, A, Alrifai, M T, Alahmesh, M A, Balwi, M, Mousavy-Gharavy, S N, Lukovic, B, Burke, D, McCabe, M J, Kasia, T, Kleta, R, Stupka, E, Beales, P L, Thompson, D A, Chong, W K, Alkuraya, F S, Martinez-Barbera, J-P, Sowden, J C & Dattani, M T 2013, ' ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies ', Brain, vol. 136, no. Pt 10, pp. 3096-105 . https://doi.org/10.1093/brain/awt218
Webb, E A, AlMutair, A, Kelberman, D, Bacchelli, C, Chanudet, E, Lescai, F, Andoniadou, C L, Banyan, A, Alsawaid, A, Alrifai, M T, Alahmesh, M A, Balwi, M, Mousavy-Gharavy, S N, Lukovic, B, Burke, D, McCabe, M J, Kasia, T, Kleta, R, Stupka, E, Beales, P L, Thompson, D A, Chong, W K, Alkuraya, F S, Martinez-Barbera, J-P, Sowden, J C & Dattani, M T 2013, ' ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies ', Brain, vol. 136, no. Pt 10, pp. 3096-105 . https://doi.org/10.1093/brain/awt218
We describe a previously unreported syndrome characterized by secondary (post-natal) microcephaly with fronto-temporal lobe hypoplasia, multiple pituitary hormone deficiency, seizures, severe visual impairment and abnormalities of the kidneys and uri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::676f478a3e24049042ed945d41d92b75
https://europepmc.org/articles/PMC3784281/
https://europepmc.org/articles/PMC3784281/
