I‐Chun Tsai

发表

Essential Functional Modules for Pathogenic and Defensive Mechanisms in Candida albicans Infections

Yu-Chao Wang, Bor-Sen Chen, Y. Chuang, 2014, BioMed research international.

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.

N. Katsanis, T. Pippucci, M. Tartaglia, 2014, Human molecular genetics.

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome.

N. Katsanis, K. Nakayama, N. Matsumoto, 2019, American journal of human genetics.

Disease‐associated casein kinase I δ mutation may promote adenomatous polyps formation via a Wnt/β‐catenin independent mechanism

H. Yost, D. Virshup, D. Neklason, 2006 .

Regulation of Casein Kinase Iϵ Activity by Wnt Signaling*

H. Yost, D. Virshup, L. Klimowski, 2004, Journal of Biological Chemistry.

Genome-wide suppressor screen identifies USP35/USP38 as therapeutic candidates for ciliopathies.

Kevin MacG. Adams, N. Katsanis, P. L. Tan, 2019, JCI insight.

RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome.

T. Meitinger, T. Strom, A. F. Stewart, 2015, The Journal of clinical investigation.

Clinical findings in patients with RAP 1 A / RAP 1 B mutations Symptom Frequency in KSA RAP 1 A patient RAP 1

T. Meitinger, T. Strom, A. F. Stewart, 2015 .

A Wnt-CKIε-Rap1 Pathway Regulates Gastrulation by Modulating SIPA1L1, a Rap GTPase Activating Protein

H. Yost, V. Band, D. Virshup, 2007 .

Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome.

J. Lupski, R. Gibbs, D. Muzny, 2014, American journal of human genetics.

NP-184[2-(5-methyl-2-furyl) benzimidazole], a novel orally active antithrombotic agent with dual antiplatelet and anticoagulant activities

S. Kuo, C. Chung, Chien-Hsin Chang, 2010, Naunyn-Schmiedeberg's Archives of Pharmacology.

Small molecule inhibition of RAS/MAPK signaling ameliorates developmental pathologies of Kabuki Syndrome

D. J. Price, N. Katsanis, P. L. Tan, 2018, Scientific Reports.

A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features

N. Katsanis, M. Natowicz, Kamal Khan, 2018, Human Genomics.

In vivo modeling of the morbid human genome using Danio rerio.

N. Katsanis, Edwin C. T. Oh, C. Golzio, 2013, Journal of visualized experiments : JoVE.

Cloning and expression of pathogenesis-related protein 4 from jelly fig (Ficus awkeotsang Makino) achenes associated with ribonuclease, chitinase and anti-fungal activities.

J. Tzen, I-Chun Tsai, T. Chung, 2012, Plant physiology and biochemistry : PPB.

Disease-associated casein kinase I delta mutation may promote adenomatous polyps formation via a Wnt/beta-catenin independent mechanism.

H. Yost, D. Virshup, D. Neklason, 2007, International journal of cancer.

Degradation of human thymidine kinase is dependent on serine-13 phosphorylation: involvement of the SCF-mediated pathway.

Z. Chang, I-Chun Tsai, Po-Yuan Ke, 2003, The Biochemical journal.

Pipoxolan inhibits proliferation of HL‐60 human leukaemia cancer cells by arresting the cell cycle at the G0/G1 phase

Chieh-Hsi Wu, H. Tsai, Hsu-Chen Cheng, 2010, Clinical and experimental pharmacology & physiology.

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators.

David S. Parker, N. Katsanis, C. C. Leitch, 2014, The Journal of clinical investigation.

A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features

N. Katsanis, S. Baig, P. Ruggieri, 2018, Human Genomics.

A Wnt-CKIvarepsilon-Rap1 pathway regulates gastrulation by modulating SIPA1L1, a Rap GTPase activating protein.

H. Yost, V. Band, D. Virshup, 2007, Developmental cell.

Renal cystic disease: from mechanisms to drug development

N. Katsanis, I-Chun Tsai, I‐Chun Tsai, 2013 .

Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model

Paul M. Jenkins, Colin A. Johnson, R. Gibbs, 2012, Nature Medicine.

Small molecule inhibition of RAS/MAPK signaling ameliorates developmental pathologies of Kabuki Syndrome

N. Katsanis, P. L. Tan, C. Golzio, 2018, Scientific Reports.

Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome.

J. Lupski, R. Gibbs, A. Sabo, 2014, American journal of human genetics.

Degradation of human thymidine kinase is dependent on serine-13 phosphorylation: involvement of the SCF-mediated pathway.

Z. Chang, Po-Yuan Ke, Che-Chuan Yang, 2003, The Biochemical journal.