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Yohei Katoh

kyoto university

H指数:32

被引数:3,179

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β-Arrestin mediates the export of ciliary GPR161 but not Smoothened together with the BBSome and intraflagellar transport machinery

β-Arrestin与BBSome和内含纤毛转运机制共同介导GPR161的纤毛外运，但不介导Smoothened的外运。

JOURNAL OF CELL SCIENCE

IF3.6

2025-10-010

PRE

Skeletal ciliopathy variants of the dynein-2 DYNC2LI1 subunit impair osteogenic differentiation of mesenchymal stem cells

动力蛋白2的DYNC2LI1亚基骨骼纤毛病变变异会损害间充质干细胞的成骨分化

JOURNAL OF CELL SCIENCE

IF3.6

2025-10-011

PRE

Lipid flippases ATP9A and ATP9B form a complex and contribute to the exocytic pathway from the Golgi

LIFE SCIENCE ALLIANCE

IF2.9

2025-04-150

OAAI

TXNDC15, an ER-localized thioredoxin-like transmembrane protein, contributes to ciliary transition zone integrity

JOURNAL OF CELL SCIENCE

IF3.6

2024-12-160

PRE

Positive regulation of Hedgehog signaling via phosphorylation of GLI2/GLI3 by DYRK2 kinase

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2024-07-050

PRE

Defects in diffusion barrier function of ciliary transition zone caused by ciliopathy variations of TMEM218

HUMAN MOLECULAR GENETICS

IF3.2

2024-05-150

PRE

Mirror-Image Single-Domain Antibody for a Novel Nonimmunogenic Drug Scaffold

BIOCONJUGATE CHEMISTRY

IF3.9

2023-10-265

PRE

Compound heterozygous IFT81 variations in a skeletal ciliopathy patient cause Bardet-Biedl syndrome-like ciliary defects

HUMAN MOLECULAR GENETICS

IF3.2

2023-07-102

PRE

Multiple interactions of the dynein-2 complex with the IFT-B complex are required for effective intraflagellar transport

有效的鞭毛内运输需要dynein-2复合物与if-b复合物的多种相互作用

JOURNAL OF CELL SCIENCE

IF3.6

2023-02-0710

OAAI

Disease-associated mutations in WDR34 lead to diverse impacts on the assembly and function of dynein-2

WDR34中与疾病相关的突变导致对dynein-2的组装和功能的不同影响

JOURNAL OF CELL SCIENCE

IF3.6

2022-11-074

OAAI

CEP19-RABL2-IFT-B axis controls BBSome-mediated ciliary GPCR export

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2022-11-016

OAAI

BROMI/TBC1D32 together with CCRK/CDK20 and FAM149B1/JBTS36 contributes to intraflagellar transport turnaround involving ICK/CILK1

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2022-08-017

OAAI

Molecular basis underlying the ciliary defects caused by IFT52 variations found in skeletal ciliopathies

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2022-08-017

OAAI

Combinations of deletion and missense variations of the dynein-2 DYNC2LI1 subunit found in skeletal ciliopathies cause ciliary defects

SCIENTIFIC REPORTS

IF3.9

2022-01-079

OAAI

Impaired cooperation between IFT74/BBS22-IFT81 and IFT25-IFT27/BBS19 causes Bardet-Biedl syndrome

HUMAN MOLECULAR GENETICS

IF3.2

2021-12-0921

PRE

Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia

HUMAN MOLECULAR GENETICS

IF3.2

2021-01-3019

PREAI

Cooperation of the IFT-A complex with the IFT-B complex is required for ciliary retrograde protein trafficking and GPCR import

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2021-01-0143

OAAI

Formation of the B9-domain protein complex MKS1-B9D2-B9D1 is essential as a diffusion barrier for ciliary membrane proteins

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2020-09-1519

OAAI

Practical method for superresolution imaging of primary cilia and centrioles by expansion microscopy using an amplibody for fluorescence signal amplification

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2020-09-1521

OAAI

Anterograde trafficking of ciliary MAP kinase-like ICK/CILK1 by the intraflagellar transport machinery is required for intraciliary retrograde protein trafficking

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2020-09-0123

OAAI