日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins.

人类血管类器官的高通量分化揭示了脑海绵状血管畸形蛋白的重叠和独特功能

Skowronek Dariush, Pilz Robin A, Saenko Valeriia V, Mellinger Lara, Singer Debora, Ribback Silvia, Weise Anja, Claaßen Kevin, Büttner Christian, Brockmann Emily M, Hübner Christian A, Aung Thiha, Haerteis Silke, Bekeschus Sander, Ekici Arif B, Felbor Ute, Rath Matthias

Inhibition of ceramide synthesis improves the outcome of ischemia/reperfusion injury in cardiomyocytes derived from human induced pluripotent stem cell.

抑制神经酰胺合成可改善人类诱导多能干细胞来源的心肌细胞缺血/再灌注损伤的结果

Haxhikadrija Pellumb, Wu Jasmine M F, Hübner Sascha, Grün Katja, Kretzschmar Tom, Müller Tina, Gräler Markus H, Backsch Claudia, Weise Anja, Klein Elisabeth, Schulze P Christian, Bekhite Mohamed M

Satellite DNA Amplification in Advanced Prostate Cancer Is Largely Independent From Euchromatic and Oncogene Amplicons

晚期前列腺癌中的卫星DNA扩增在很大程度上独立于常染色质和癌基因扩增子。

Weise, Anja; Ornellas, Antonio Augusto; Alves, Gilda; Pentzold, Constanze; Holler, Jenny; Wolter, Melanie; Jamali, Elena; Theis, Bernhard; Liehr, Thomas

De novo AHDC1 Deletions Identified by Genome Sequencing in Two Individuals with Xia-Gibbs Syndrome

通过基因组测序在两名患有夏吉布斯综合征的个体中鉴定出新生AHDC1缺失

Bertrand, Miriam; Shah, Gulalai; Pedersen, Brent S; Schulz, Alexander; Weise, Anja; Liehr, Thomas; Huppke, Peter; DiTroia, Stephanie; Quinlan, Aaron R; Haack, Tobias B; Husain, Ralf A

Small supernumerary marker chromosomes derived from human chromosome 11

源自人类11号染色体的小型超数标记染色体

Liehr, Thomas; Ziegler, Monika; Person, Luisa; Kankel, Stefanie; Padutsch, Niklas; Weise, Anja; Weimer, Jörg Paul; Williams, Heather; Ferreira, Susana; Melo, Joana B; Carreira, Isabel M

Non-Invasive Prenatal Testing in Germany

德国无创产前检测

Liehr, Thomas; Harutyunyan, Tigran; Williams, Heather; Weise, Anja

First Comprehensive Characterization of Phayre's Leaf-Monkey (Trachypithecus phayrei) Karyotype

首次对费氏叶猴(Trachypithecus phayrei)核型进行全面表征

Fan, Xiaobo; Pinthong, Krit; de Oliveira, Edivaldo H C; Tanomtong, Alongklod; Chen, Hongwei; Weise, Anja; Liehr, Thomas

Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report

Phelan-McDermid 综合征和 22q13 重复综合征的分子细胞遗传学和表型特征:病例报告

Khalifa, Yousif; Hassan, Hisham Y; Weise, Anja; Liehr, Thomas; Alkhayyat, Haya

Sites of chromosomal instability in the context of nuclear architecture and function

染色体不稳定位点在核结构和功能中的作用

Pentzold, Constanze; Kokal, Miriam; Pentzold, Stefan; Weise, Anja

Association of Lymphatic Abnormalities with Early Complications after Fontan Operation

淋巴系统异常与Fontan手术后早期并发症的相关性

Dittrich, Sven; Weise, Anja; Cesnjevar, Robert; Rompel, Oliver; Rüffer, André; Schöber, Martin; Moosmann, Julia; Glöckler, Martin