Sortiert nach
Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
2016
Link zum Volltext
Cell, 2014-04, Vol.157 (3), p.651-663
- Schaffer, Ashleigh E.
- Eggens, Veerle R.C.
- Caglayan, Ahmet Okay
- Reuter, Miriam S.
- Scott, Eric
- Coufal, Nicole G.
- Silhavy, Jennifer L.
- Xue, Yuanchao
- Kayserili, Hulya
- Yasuno, Katsuhito
- Rosti, Rasim Ozgur
- Abdellateef, Mostafa
- Caglar, Caner
- Kasher, Paul R.
- Cazemier, J. Leonie
- Weterman, Marian A.
- Cantagrel, Vincent
- Cai, Na
- Zweier, Christiane
- Altunoglu, Umut
- Satkin, N. Bilge
- Aktar, Fesih
- Tuysuz, Beyhan
- Yalcinkaya, Cengiz
- Caksen, Huseyin
- Bilguvar, Kaya
- Fu, Xiang-Dong
- Trotta, Christopher R.
- Gabriel, Stacey
- Reis, André
- Gunel, Murat
- Baas, Frank
- Gleeson, Joseph G.
2014
Link zum Volltext
Scientific reports, 2020-01, Vol.10 (1), p.1204-1204, Article 1204
2020
Link zum Volltext
Disease models & mechanisms, 2019-05, Vol.12 (5)
2019
Link zum Volltext
Scientific reports, 2020-11, Vol.10 (1), p.19030-19030, Article 19030
2020
Link zum Volltext
Scientific reports, 2024-02, Vol.14 (1), p.2975-2975, Article 2975
2024
Link zum Volltext
Journal of medical genetics, 2019-10, Vol.56 (10), p.701
- Jønch, Aia Elise
- Douard, Elise
- Moreau, Clara
- Van Dijck, Anke
- Passeggeri, Marzia
- Kooy, Frank
- Puechberty, Jacques
- Campbell, Carolyn
- Sanlaville, Damien
- Lefroy, Henrietta
- Richetin, Sonia
- Pain, Aurelie
- Geneviève, David
- Kini, Usha
- Le Caignec, Cédric
- Lespinasse, James
- Skytte, Anne-Bine
- Isidor, Bertrand
- Zweier, Christiane
- Caberg, Jean-Hubert
- Delrue, Marie-Ange
- Møller, Rikke Steensbjerre
- Bojesen, Anders
- Hjalgrim, Helle
- Brasch-Andersen, Charlotte
- Lemyre, Emmanuelle
- Ousager, Lilian Bomme
- Jacquemont, Sébastien
2019
Link zum Volltext
Clinical genetics, 2019-04, Vol.95 (4), p.462-478
- Zollino, Marcella
- Zweier, Christiane
- Van Balkom, Ingrid D.
- Sweetser, David A.
- Alaimo, Joseph
- Bijlsma, Emilia K.
- Cody, Jannine
- Elsea, Sarah H.
- Giurgea, Irina
- Macchiaiolo, Marina
- Smigiel, Robert
- Thibert, Ronald L.
- Benoist, Ingrid
- Clayton‐Smith, Jill
- De Winter, Channa F.
- Deckers, Stijn
- Gandhi, Anusha
- Huisman, Sylvia
- Kempink, Dagmar
- Kruisinga, Frea
- Lamacchia, Vittoria
- Marangi, Giuseppe
- Menke, Leonie
- Mulder, Paul
- Nordgren, Ann
- Renieri, Alessandra
- Routledge, Sue
- Saunders, Carol J.
- Stembalska, Agnieszka
- Van Balkom, Hans
- Whalen, Sandra
- Hennekam, Raoul C.
2019
Link zum Volltext
Scientific reports, 2017-09, Vol.7 (1), p.12225-6, Article 12225
- Hauer, Nadine N
- Sticht, Heinrich
- Boppudi, Sangamitra
- Büttner, Christian
- Kraus, Cornelia
- Trautmann, Udo
- Zenker, Martin
- Zweier, Christiane
- Wiesener, Antje
- Jamra, Rami Abou
- Wieczorek, Dagmar
- Kelkel, Jaqueline
- Jung, Anna-Maria
- Uebe, Steffen
- Ekici, Arif B
- Rohrer, Tilman
- Reis, André
- Dörr, Helmuth-Günther
- Thiel, Christian T
2017
Link zum Volltext
Science (American Association for the Advancement of Science), 2008-02, Vol.319 (5864), p.816-819
- Rauch, Anita
- Thiel, Christian T
- Schindler, Detlev
- Wick, Ursula
- Crow, Yanick J
- Ekici, Arif B
- van Essen, Anthonie J
- Goecke, Timm O
- Al-Gazali, Lihadh
- Chrzanowska, Krystyna H
- Zweier, Christiane
- Brunner, Han G
- Becker, Kristin
- Curry, Cynthia J
- Dallapiccola, Bruno
- Devriendt, Koenraad
- Dörfler, Arnd
- Kinning, Esther
- Megarbane, André
- Meinecke, Peter
- Semple, Robert K
- Spranger, Stephanie
- Toutain, Annick
- Trembath, Richard C
- Voss, Egbert
- Wilson, Louise
- Hennekam, Raoul
- de Zegher, Francis
- Dörr, Helmuth-Günther
- Reis, André
2008
Link zum Volltext
Clinical genetics, 2021-01, Vol.99 (1), p.199-207
2021
Link zum Volltext
American journal of medical genetics. Part A, 2020-11, Vol.182 (11), p.2761-2764
2020
Link zum Volltext
Genetics in medicine, 2020-04, Vol.22 (4), p.797-802
- Nabais Sá, Maria J.
- Venselaar, Hanka
- Wiel, Laurens
- Trimouille, Aurélien
- Lasseaux, Eulalie
- Naudion, Sophie
- Lacombe, Didier
- Piton, Amélie
- Vincent-Delorme, Catherine
- Zweier, Christiane
- Reis, André
- Trollmann, Regina
- Ruiz, Anna
- Gabau, Elisabeth
- Vetro, Annalisa
- Guerrini, Renzo
- Bakhtiari, Somayeh
- Kruer, Michael C.
- Amor, David J.
- Cooper, Monica S.
- Bijlsma, Emilia K.
- Barakat, Tahsin Stefan
- van Dooren, Marieke F.
- van Slegtenhorst, Marjon
- Pfundt, Rolph
- Gilissen, Christian
- Willemsen, Michèl A.
- de Vries, Bert B.A.
- de Brouwer, Arjan P.M.
- Koolen, David A.
2020
Link zum Volltext
Genetics in medicine, 2021-07, Vol.23 (7), p.1234-1245
- Chowdhury, Fuad
- Wang, Lei
- Al-Raqad, Mohammed
- Amor, David J.
- Baxová, Alice
- Bendová, Šárka
- Biamino, Elisa
- Brusco, Alfredo
- Caluseriu, Oana
- Cox, Nancy J.
- Froukh, Tawfiq
- Gunay-Aygun, Meral
- Hančárová, Miroslava
- Haynes, Devon
- Heide, Solveig
- Hoganson, George
- Kaname, Tadashi
- Keren, Boris
- Kosaki, Kenjiro
- Kubota, Kazuo
- Lemons, Jennifer M.
- Magriña, Maria A.
- Mark, Paul R.
- McDonald, Marie T.
- Montgomery, Sarah
- Morley, Gina M.
- Ohnishi, Hidenori
- Okamoto, Nobuhiko
- Rodriguez-Buritica, David
- Rump, Patrick
- Sedláček, Zdeněk
- Schatz, Krista
- Streff, Haley
- Uehara, Tomoko
- Walia, Jagdeep S.
- Wheeler, Patricia G.
- Wiesener, Antje
- Zweier, Christiane
- Kawakami, Koichi
- Wentzensen, Ingrid M.
- Lalani, Seema R.
- Siu, Victoria M.
- Bi, Weimin
- Balci, Tugce B.
2021
Link zum Volltext
Molecular autism, 2018-03, Vol.9 (1), p.20-20, Article 20
2018
Link zum Volltext
BMC cancer, 2019-05, Vol.19 (1), p.435-435, Article 435
2019
Link zum Volltext
Orphanet journal of rare diseases, 2021-03, Vol.16 (1), p.136-136, Article 136
- Hüffmeier, Ulrike
- Kraus, Cornelia
- Reuter, Miriam S
- Uebe, Steffen
- Abbott, Mary-Alice
- Ahmed, Syed A
- Rawson, Kristyn L
- Barr, Eileen
- Li, Hong
- Bruel, Ange-Line
- Faivre, Laurence
- Tran Mau-Them, Frédéric
- Botti, Christina
- Brooks, Susan
- Burns, Kaitlyn
- Ward, D Isum
- Dutra-Clarke, Marina
- Martinez-Agosto, Julian A
- Lee, Hane
- Nelson, Stanley F
- Zacher, Pia
- Abou Jamra, Rami
- Klöckner, Chiara
- McGaughran, Julie
- Kohlhase, Jürgen
- Schuhmann, Sarah
- Moran, Ellen
- Pappas, John
- Raas-Rothschild, Annick
- Sacoto, Maria J Guillen
- Henderson, Lindsay B
- Palculict, Timothy Blake
- Mullegama, Sureni V
- Zghal Elloumi, Houda
- Reich, Adi
- Schrier Vergano, Samantha A
- Wahl, Erica
- Reis, André
- Zweier, Christiane
2021
Link zum Volltext
Journal of vascular anomalies (Philadelphia, Pa.), 2023-12, Vol.4 (4), p.e076
2023
Link zum Volltext
Frontiers in cardiovascular medicine, 2022-07, Vol.9, p.916036-916036
2022
Link zum Volltext
PLoS genetics, 2013-10, Vol.9 (10), p.e1003911-e1003911
- Oortveld, Merel A W
- Keerthikumar, Shivakumar
- Oti, Martin
- Nijhof, Bonnie
- Fernandes, Ana Clara
- Kochinke, Korinna
- Castells-Nobau, Anna
- van Engelen, Eva
- Ellenkamp, Thijs
- Eshuis, Lilian
- Galy, Anne
- van Bokhoven, Hans
- Habermann, Bianca
- Brunner, Han G
- Zweier, Christiane
- Verstreken, Patrik
- Huynen, Martijn A
- Schenck, Annette
- Flint, Jonathan
2013
Link zum Volltext
Medizinische Genetik, 2015-12, Vol.27 (4), p.362-368
2015
Link zum Volltext
Medizinische Genetik, 2018-11, Vol.30 (3), p.334-341
2018
Link zum Volltext
Annals of clinical and translational neurology, 2019-07, Vol.6 (7), p.1263-1272
- Cameron, Jillian M.
- Maljevic, Snezana
- Nair, Umesh
- Aung, Ye Htet
- Cogné, Benjamin
- Bézieau, Stéphane
- Blair, Edward
- Isidor, Bertrand
- Zweier, Christiane
- Reis, André
- Koenig, Mary Kay
- Maarup, Timothy
- Sarco, Dean
- Afenjar, Alexandra
- Huq, A. H. M. Mahbubul
- Kukolich, Mary
- Billette de Villemeur, Thierry
- Nava, Caroline
- Héron, Bénédicte
- Petrou, Steven
- Berkovic, Samuel F.
2019
Link zum Volltext
Medizinische Genetik, 2018, Vol.30 (3), p.305-305
2018
Link zum Volltext
American journal of human genetics, 2016-01, Vol.98 (1), p.149-164
2016
Link zum Volltext
Aktive Filter
Suchergebnisse filtern
Filter anzeigenNur zeigen
Erscheinungsjahr
n.n
n.n
Thema
- Science & Technology
- Life Sciences & Biomedicine
- Humans
- Genetics & Heredity
- Mutation
- Intellectual Disability - Genetics
- Male
- Female
- Intellectual Disabilities
- Phenotype
- Neurodevelopmental Disorders
- Genetics
- Phenotypes
- Animals
- Intellectual Disability
- Biological And Medical Sciences
- Medical Sciences
- Life Sciences
- Medical Genetics
- Epilepsy
Kollektion
- EZB Electronic Journals Library
- MEDLINE
- Journals@Ovid Full Text
- Ingenta
- Wiley-Blackwell Journals
- Wiley Online Library
- Elsevier ScienceDirect Journals Complete
- SpringerLink
- Nature Publishing Group website
- IngentaConnect Journals
- Publisher or Other Site
- SpringerLINK Contemporary (Konsortium Baden-Württemberg)
- BMJ Publishing
- BMJ Journals Archiv - DFG Nationallizenzen
- Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
- De Gruyter journals
- Kohlhammer eLibrary Gesamt
- Ebook Central Perpetual and DDA
- Nexis Uni
- Cambridge Journals Online (DEFF)
Zeitschrift / Serie
Neu hinzugefügt