Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gerda Neubert"'
Autor:
Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, Ethiraj Ravindran, Shyamala Mani, Olaf Ninnemann, Angela M Kaindl
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136684 (2015)
Autosomal recessive primary microcephaly (MCPH) is a rare neurodevelopmental disorder characterized by a pronounced reduction of brain volume and intellectual disability. A current model for the microcephaly phenotype invokes a stem cell proliferatio
Externí odkaz:
https://doaj.org/article/77601ca3df8b415280757c17314ab930
Publikováno v:
Neurological Research. 34:664-668
Gene expression analysis via quantitative real-time PCR (qPCR) is a key approach in biological and medical research. Here, variations between runs and samples are compensated for by in-parallel analysis of reference genes, which require a most stable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afb7d2ddc895fcdb13091ac76a7ab359
https://doi.org/10.1179/1743132812y.0000000060
https://doi.org/10.1179/1743132812y.0000000060
Autor:
Sami Zaqout, Ralph Gräf, Olaf Ninnemann, Angela M. Kaindl, Detlev Schindler, Ethiraj Ravindran, Nadine Kraemer, Andrea Seiler, Gerda Neubert
Biallelic mutations in the gene encoding centrosomal CDK5RAP2 lead to autosomal recessive primary microcephaly (MCPH), a disorder characterized by pronounced reduction in volume of otherwise architectonical normal brains and intellectual deficit. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceedbdc6a39c442f2092276e1a736c5f
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/38766
https://publishup.uni-potsdam.de/frontdoor/index/index/docId/38766
Autor:
Gerda Neubert, Ethiraj Ravindran, Shyamala Mani, Lina Issa-Jahns, Olaf Ninnemann, Angela M. Kaindl, Nadine Kraemer
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136684 (2015)
PLoS ONE
PLoS ONE
Autosomal recessive primary microcephaly (MCPH) is a rare neurodevelopmental disorder characterized by a pronounced reduction of brain volume and intellectual disability. A current model for the microcephaly phenotype invokes a stem cell proliferatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164e65e294d7cd4f0d49eb47c9bed7c5
http://eprints.iisc.ernet.in/52442/
http://eprints.iisc.ernet.in/52442/
Autor:
Olaf Ninnemann, Gerda Neubert, Lina Issa, Andrea Seiler, Deborah J. Morris-Rosendahl, Angela M. Kaindl, Nadine Krämer
Publikováno v:
Neuropediatrics. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f5c2351fad1164b629acd04fa9bd312
https://doi.org/10.1055/s-0033-1337810
https://doi.org/10.1055/s-0033-1337810
Autor:
Gerda Neubert, Angela M. Kaindl, Andreas Tzschach, Katrin Drossel, Renate Nickel, Katja von Au, Denise Horn
Publikováno v:
Gene. 512(2)
Angelman syndrome is a neurodevelopmental disorder characterized by mental retardation, severe speech disorder, facial dysmorphism, secondary microcephaly, ataxia, seizures, and abnormal behaviors such as easily provoked laughter. It is most frequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a88ac5c38a44324bd0147074bc2e69ef
https://pubmed.ncbi.nlm.nih.gov/23124039
https://pubmed.ncbi.nlm.nih.gov/23124039
Publikováno v:
Neuropediatrics. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5acc5508d4af5207fee7f71b10271754
https://doi.org/10.1055/s-0032-1307168
https://doi.org/10.1055/s-0032-1307168