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pro vyhledávání: '"Melanie Heitmann"'
Autor:
Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, Melanie Heitmann, Katrin Rademacher, Julia Richter, Almuth Caliebe, Reiner Siebert, Bernhard Horsthemke, Karin Buiting
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76953 (2013)
NLRP7 is a maternal effect gene as maternal mutations in this gene cause recurrent hydatidiform moles, spontaneous abortions and stillbirths, whereas live births are very rare. We have studied a patient with multiple anomalies born to a mother with a
Externí odkaz:
https://doaj.org/article/b267fa47602e407cbe702eab9b649df3
Autor:
Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, Melanie Heitmann, Katrin Rademacher, Julia Richter, Almuth Caliebe, Reiner Siebert, Bernhard Horsthemke, Karin Buiting
Publikováno v:
PLoS ONE, Vol 8, Iss 12 (2013)
Externí odkaz:
https://doaj.org/article/9816cf63afe24c779c703cd199537ce4
Autor:
Melanie Heitmann
Bachelorarbeit aus dem Jahr 2019 im Fachbereich Didaktik - Sport, Sportpädagogik, Note: 1,5, Georg-August-Universität Göttingen (Institut für Sportwissenschaften), Sprache: Deutsch, Abstract:'Sport als Integrationsmotor', so heißt es beispielswe
Autor:
Cecilia Anichini, Katrin Rademacher, Flavia Cerrato, Jasmin Beygo, Margherita Silengo, Andrea Riccio, Bernhard Horsthemke, Thorsten Enklaar, Karin Buiting, Angela Sparago, Maria Vittoria Cubellis, Andrea Guala, Dirk Prawitt, Notker Graf, Agostina De Crescenzo, Valentina Citro, Melanie Heitmann
Publikováno v:
Human molecular genetics
22(3) (2013): 544–557. doi:10.1093/hmg/dds465
info:cnr-pdr/source/autori:Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A./titolo:The molecular function and clinical phenotype of partial deletions of the IGF2%2FH19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites/doi:10.1093%2Fhmg%2Fdds465/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:544/pagina_a:557/intervallo_pagine:544–557/volume:22(3)
Human Molecular Genetics
22(3) (2013): 544–557. doi:10.1093/hmg/dds465
info:cnr-pdr/source/autori:Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A./titolo:The molecular function and clinical phenotype of partial deletions of the IGF2%2FH19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites/doi:10.1093%2Fhmg%2Fdds465/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:544/pagina_a:557/intervallo_pagine:544–557/volume:22(3)
Human Molecular Genetics
At chromosome 11p15.5, the imprinting centre 1 (IC1) controls the parent of origin-specific expression of the IGF2 and H19 genes. The 5 kb IC1 region contains multiple target sites (CTS) for the zinc-finger protein CTCF, whose binding on the maternal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc68c41f6160eb6b91717145212bb5fa
http://hdl.handle.net/11591/187142
http://hdl.handle.net/11591/187142
Autor:
Ole Ammerpohl, Karin Buiting, Bernhard Horsthemke, Reiner Siebert, Julia Richter, Almuth Caliebe, Jasmin Beygo, Katrin Rademacher, Melanie Heitmann, Daniela Gritzan
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 10, p e76953 (2013)
PLoS ONE, Vol 8, Iss 10, p e76953 (2013)
NLRP7 is a maternal effect gene as maternal mutations in this gene cause recurrent hydatidiform moles, spontaneous abortions and stillbirths, whereas live births are very rare. We have studied a patient with multiple anomalies born to a mother with a