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pro vyhledávání: '"Kanavakis, E"'
Akademický článek
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Autor:
Sakellariou, P., Kekou, K., Fryssira, H., Sofocleous, C., Manta, P., Panousopoulou, A., Gounaris, K., Kanavakis, E.
Publikováno v:
In Neuromuscular Disorders April 2012 22(4):339-349
Purpose: To investigate whether preimplantation genetic testing for aneuploidy (PGT-A) improves the clinical outcome in patients with advanced maternal age (AMA), recurrent miscarriages (RM), and recurrent implantation failure (RIF). Methods: Retrosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::bbe89082967392576ad4346ed4f013f4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220419
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220419
Background: ITPR1 gene encodes inositol 1,4,5-trisphosphate-receptor-type 1, a Ca2+ channel highly expressed in cerebellar Purkinje cells. ITPR1 gene variants, through a loss-of-function mechanism, have been found to be related with the manifestation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::36d0f3b43485efdc095fe98f9d682110
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2996926
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2996926
Akademický článek
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Autor:
Tsezou, A., Tzetis, M., Gennatas, C., Giannatou, E., Pampanos, A., Malamis, G., Kanavakis, E., Kitsiou, S.
Publikováno v:
In The Breast 2008 17(2):159-166
Coffin-Siris Syndrome 4 is an autosomal dominant congenital malformation syndrome caused by heterozygous mutations in the SMARCA4 gene with its main features being intellectual disability, developmental delay, behavioral abnormalities, and hypoplasti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::4d91aa45c6ad643e2d34ec43c77963e6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078626
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078626
Summary. Introduction. Mesenchymal stromal cells (MSCs) can be derived from a wide range of fetal and adult sources including pluripotent stem cells (PSCs). The properties of PSC-derived MSCs need to be fully characterized, in order to evaluate the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f7361d05acba96a54e0547fd84421862
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3121480
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3121480
Diabetic neuropathy (DN) is a common long-term complication of type 1 (T1D) and type 2 (T2D) diabetes mellitus, with significant morbidity and mortality. DN is defined as impaired function of the autonomic and/or peripheral nervous system, often subc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::7d0178fd5ed7fd565d61eb40673c0d9d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077615
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077615
Acute Lymphoblastic Leukemia (ALL) is a malignancy of the immature lymphoid cells mainly associated with numerical and structural chromosomal aberrations. The current standard for profiling the diverse genetic background comprises a combination of co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3b183d2cc4cd493585ef95b3a52eb380
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078688
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078688