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1 . Academic Journal
Ablation of collagen XII disturbs joint extracellular matrix organization and causes patellar subluxation
저자
by
Zhu, Mengjie
;
Metzen, Fabian
;
Hopkinson, Mark
;
Betz, Janina
;
Heilig, Juliane
, et al.
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iScience
21 July 2023 26(7)
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7 . Academic Journal
Oncogenic role and target properties of the lysine-specific demethylase KDM1A in chronic lymphocytic leukemia
저자
by
Jiang, Qu
;
Stachelscheid, Johanna
;
Bloehdorn, Johannes
;
Pacholewska, Alicja
;
Aszyk, Christoph
, et al.
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Blood
6 July 2023 142(1):44-61
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7 . Academic Journal
Epigenetic regulation of plastin 3 expression by the macrosatellite DXZ4 and the transcriptional regulator CHD4
저자
by
Strathmann, Eike A.
;
Hölker, Irmgard
;
Tschernoster, Nikolai
;
Hosseinibarkooie, Seyyedmohsen
;
Come, Julien
, et al.
소스
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The American Journal of Human Genetics
2 March 2023 110(3):442-459
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7 . Academic Journal
NIK/MAP3K14 in hepatocytes orchestrates NASH to hepatocellular carcinoma progression via JAK2/STAT5 inhibition
저자
by
Vesting, Anna Juliane
;
Jais, Alexander
;
Klemm, Paul
;
Steuernagel, Lukas
;
Wienand, Peter
, et al.
소스
In
Molecular Metabolism
December 2022 66
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7 . Academic Journal
Modeling of ACTN4-Based Podocytopathy Using Drosophila Nephrocytes
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by
Odenthal, Johanna
;
Dittrich, Sebastian
;
Ludwig, Vivian
;
Merz, Tim
;
Reitmeier, Katrin
, et al.
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Kidney International Reports
October 2022
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7 . Academic Journal
In-depth cell-free DNA sequencing reveals genomic landscape of Hodgkin’s lymphoma and facilitates ultrasensitive residual disease detection
저자
by
Sobesky, Sophia
;
Mammadova, Laman
;
Cirillo, Melita
;
Drees, Esther E.E.
;
Mattlener, Julia
, et al.
소스
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Med
8 October 2021 2(10):1171-1193
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7 . Academic Journal
MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease
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by
Khuller, Katharina
;
Yigit, Gökhan
;
Martínez Grijalva, Carolina
;
Altmüller, Janine
;
Thiele, Holger
, et al.
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European Journal of Medical Genetics
October 2021 64(10)
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7 . Academic Journal
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
저자
by
May, Patrick
;
Girard, Simon
;
Harrer, Merle
;
Bobbili, Dheeraj R
;
Schubert, Julian
, et al.
소스
In
The Lancet Neurology
August 2018 17(8):699-708
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7 . Academic Journal
Complex karyotypes and KRAS and POT1 mutations impact outcome in CLL after chlorambucil-based chemotherapy or chemoimmunotherapy
저자
by
Herling, Carmen Diana
;
Klaumünzer, Marion
;
Rocha, Cristiano Krings
;
Altmüller, Janine
;
Thiele, Holger
, et al.
소스
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Blood
21 July 2016 128(3):395-404
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7 . Academic Journal
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome
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by
Ammann, Sandra
;
Schulz, Ansgar
;
Krägeloh-Mann, Ingeborg
;
Dieckmann, Nele M.G.
;
Niethammer, Klaus
, et al.
소스
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25 February 2016 127(8):997-1006
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