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

Antisense Oligonucleotide- and CRISPR-Cas9-Mediated Rescue of mRNA Splicing for a Deep Intronic CLRN1 Mutation

反义寡核苷酸和 CRISPR-Cas9 介导的深度内含子 CLRN1 突变的 mRNA 剪接挽救

Anna-Lena Panagiotopoulos, Nina Karguth, Marina Pavlou, Sybille Böhm, Gilles Gasparoni, Jörn Walter, Alexander Graf, Helmut Blum, Martin Biel, Lisa Maria Riedmayr, Elvir Becirovic

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1.

以非洲爪蟾为模型研究 Joubert 综合征:PIBF1 复合杂合变异的人类患者病例

Ott Tim, Kaufmann Lilian, Granzow Martin, Hinderhofer Katrin, Bartram Claus R, Theiß Susanne, Seitz Angelika, Paramasivam Nagarajan, Schulz Angela, Moog Ute, Blum Martin, Evers Christina M

Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver

生长激素受体缺陷的猪与人类拉伦综合征的病理生理相似,并揭示了肝脏信号级联激活的改变

Arne Hinrichs, Barbara Kessler, Mayuko Kurome, Andreas Blutke, Elisabeth Kemter, Maren Bernau, Armin M Scholz, Birgit Rathkolb, Simone Renner, Sebastian Bultmann, Heinrich Leonhardt, Martin Hrabĕ de Angelis, Hiroshi Nagashima, Andreas Hoeflich, Werner F Blum, Martin Bidlingmaier, Rüdiger Wanke, Maik

An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus

多囊蛋白-2在非洲爪蟾左右组织者诱导中的早期功能

Vick, Philipp; Kreis, Jennifer; Schneider, Isabelle; Tingler, Melanie; Getwan, Maike; Thumberger, Thomas; Beyer, Tina; Schweickert, Axel; Blum, Martin

A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity.

Joubert 综合征患者中一种新的纯合 ARL13B 变异会损害其鸟嘌呤核苷酸交换因子活性

Rafiullah Rafiullah, Long Alyssa B, Ivanova Anna A, Ali Hazrat, Berkel Simone, Mustafa Ghulam, Paramasivam Nagarajan, Schlesner Matthias, Wiemann Stefan, Wade Rebecca C, Bolthauser Eugen, Blum Martin, Kahn Richard A, Caspary Tamara, Rappold Gudrun A

Vertebrate Left-Right Asymmetry: What Can Nodal Cascade Gene Expression Patterns Tell Us?

脊椎动物左右不对称性:节点级联基因表达模式能告诉我们什么?

Schweickert, Axel; Ott, Tim; Kurz, Sabrina; Tingler, Melanie; Maerker, Markus; Fuhl, Franziska; Blum, Martin

Cilia are required for asymmetric nodal induction in the sea urchin embryo.

纤毛是海胆胚胎不对称结节诱导所必需的

Tisler Matthias, Wetzel Franziska, Mantino Sabrina, Kremnyov Stanislav, Thumberger Thomas, Schweickert Axel, Blum Martin, Vick Philipp

ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia.

ATP4a 是非洲爪蟾粘膜纤毛表皮发育和功能所必需的——非洲爪蟾粘膜纤毛表皮是研究质子泵抑制剂相关性肺炎的潜在模型

Walentek Peter, Beyer Tina, Hagenlocher Cathrin, Müller Christina, Feistel Kerstin, Schweickert Axel, Harland Richard M, Blum Martin

ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles.

非洲爪蟾胚胎和蝌蚪神经外胚层和内胚层中的 ATP4 和纤毛形成

Walentek Peter, Hagenlocher Cathrin, Beyer Tina, Müller Christina, Feistel Kerstin, Schweickert Axel, Harland Richard M, Blum Martin

Symmetry breakage in the vertebrate embryo: when does it happen and how does it work?

脊椎动物胚胎的对称性破缺:何时发生以及如何发生?

Blum, Martin; Schweickert, Axel; Vick, Philipp; Wright, Christopher V E; Danilchik, Michael V