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Sacherschließung
Mutation/genetics [MeSH]
(28)
Humans [MeSH]
(26)
Male [MeSH]
(9)
Female [MeSH]
(7)
Young Adult [MeSH]
(5)
Animals [MeSH]
(5)
Adult [MeSH]
(5)
Research
(3)
Article
(3)
Adolescent [MeSH]
(3)
Publikationstyp
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Erscheinungsjahr
2024
(5)
2021
(10)
2020
(13)
Institution
Leibniz-Institut für Zoo- und Wildtierforschung (Berlin)
(2)
Römisch-Germanisches Zentralmuseum
(1)
Leibniz-Institut für Alternsforschung
(1)
28 Treffer
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Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
2020 .
Rheinbay, Esther
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Nielsen, Morten Muhlig
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Abascal, Federico
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Wala, Jeremiah A.
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Shapira, Ofer
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Tiao, Grace
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Hornshøj, Henrik
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Hess, Julian M.
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Juul, Randi Istrup
|
Lin, Ziao
|
Feuerbach, Lars
|
Sabarinathan, Radhakrishnan
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Madsen, Tobias
|
Kim, Jaegil
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Mularoni, Loris
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Shuai, Shimin
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Lanzós, Andres
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Herrmann, Carl
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Maruvka, Yosef E.
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Shen, Ciyue
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Amin, Samirkumar B.
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Bandopadhayay, Pratiti
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Bertl, Johanna
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Boroevich, Keith A.
|
.
PCAWG Drivers and Functional Interpretation Working Group
|
PCAWG Structural Variation Working Group
|
PCAWG Consortium
2020
http://purl.org/ontology/bibo/Article
Emerging Targeted Therapeutics for Genetic Subtypes of Parkinsonism
2020 .
Schneider, Susanne A.
|
Hizli, Baccara
|
Alcalay, Roy N.
2020
http://purl.org/ontology/bibo/Article
Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis
2020 .
Suwala, Abigail K.
|
Stichel, Damian
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Schrimpf, Daniel
|
Kloor, Matthias
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Wefers, Annika K.
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Reinhardt, Annekathrin
|
Maas, Sybren L. N.
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Kratz, Christian P.
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Schweizer, Leonille
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Hasselblatt, Martin
|
Snuderl, Matija
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Abedalthagafi, Malak Sameer J.
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Abdullaev, Zied
|
Monoranu, Camelia M.
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Bergmann, Markus
|
Pekrun, Arnulf
|
Freyschlag, Christian
|
Aronica, Eleonora
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Kramm, Christof M.
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Hinz, Felix
|
Sievers, Philipp
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Korshunov, Andrey
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Kool, Marcel
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Pfister, Stefan M.
|
Sturm, Dominik
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Jones, David T. W.
|
Wick, Wolfgang
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Unterberg, Andreas
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Hartmann, Christian
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Dodgshun, Andrew
|
Tabori, Uri
|
Wesseling, Pieter
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Sahm, Felix
|
von Deimling, Andreas
|
Reuß, David
2020
http://purl.org/ontology/bibo/Article
Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
2020 .
Bork, Konrad
|
Machnig, Thomas
|
Wulff, Karin
|
Witzke, Guenther
|
Prusty, Subhransu
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Hardt, Jochen
2020
http://purl.org/ontology/bibo/Article
Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1
2020 .
Sievers, Philipp
|
Sill, Martin
|
Blume, Christina
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Tauziede-Espariat, Arnault
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Schrimpf, Daniel
|
Stichel, Damian
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Reuss, David E.
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Dogan, Helin
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Hartmann, Christian
|
Mawrin, Christian
|
Hasselblatt, Martin
|
Stummer, Walter
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Schick, Uta
|
Hench, Jürgen
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Frank, Stephan
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Ketter, Ralf
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Schweizer, Leonille
|
Schittenhelm, Jens
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Puget, Stéphanie
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Brandner, Sebastian
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Jaunmuktane, Zane
|
Küsters, Benno
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Abdullaev, Zied
|
Pekmezci, Melike
|
Snuderl, Matija
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Ratliff, Miriam
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Herold-Mende, Christel
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Unterberg, Andreas
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Aldape, Kenneth
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Ellison, David W.
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Wesseling, Pieter
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Reifenberger, Guido
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Wick, Wolfgang
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Perry, Arie
|
Varlet, Pascale
|
Pfister, Stefan M.
|
Jones, David T. W.
|
von Deimling, Andreas
|
Sahm, Felix
2020
http://purl.org/ontology/bibo/Article
Cav2.3 R-type calcium channels: from its discovery to pathogenic de novo CACNA1E variants: a historical perspective
2020 .
Schneider, Toni
|
Neumaier, F.
|
Hescheler, J.
|
Alpdogan, S.
2020
http://purl.org/ontology/bibo/Article
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases
2020 .
Holdhof, Dörthe
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Johann, Pascal D.
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Spohn, Michael
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Bockmayr, Michael
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Safaei, Sepehr
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Joshi, Piyush
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Masliah-Planchon, Julien
|
Ho, Ben
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Andrianteranagna, Mamy
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Bourdeaut, Franck
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Huang, Annie
|
Kool, Marcel
|
Upadhyaya, Santhosh A.
|
Bendel, Anne E.
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Indenbirken, Daniela
|
Foulkes, William D.
|
Bush, Jonathan W.
|
Creytens, David
|
Kordes, Uwe
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Frühwald, Michael C.
|
Hasselblatt, Martin
|
Schüller, Ulrich
2020
http://purl.org/ontology/bibo/Article
Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder
2020 .
Niesler, Beate
|
Rappold, Gudrun A.
2020
http://purl.org/ontology/bibo/Article
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