(Q24338821)

GOA release 2020-03-11

author name string

Junko Nagano

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Kenichiro Kitamura

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Kristine M Hujer

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Christopher J Ward

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Richard J Bram

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Ulrich Hopfer

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Kimio Tomita

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Chunfa Huang

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R Tyler Miller

Biochemical and Biophysical Research Communications

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language of work or name

English

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publication date

16 December 2005

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published in

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volume

338

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issue

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page(s)

880-9

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cites work

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Calcium-modulating cyclophilin ligand desensitizes hormone-evoked calcium release.

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Polycystins: from mechanosensation to gene regulation

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

CAML is a p56Lck-interacting protein that is required for thymocyte development

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Molecular genetics of autosomal recessive polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

CAML is required for efficient EGF receptor recycling

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Calcium signalling in T cells stimulated by a cyclophilin B-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

A hydrophobic domain of Ca2+-modulating cyclophilin ligand modulates calcium influx signaling in T lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Co-localization of calcium-modulating cyclophilin ligand with intracellular calcium pools

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Parallel activation of phosphatidylinositol 4-kinase and phospholipase C by the extracellular calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Calcium restriction allows cAMP activation of the B-Raf/ERK pathway, switching cells to a cAMP-dependent growth-stimulated phenotype

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Role of the hepatocyte nuclear factor-1beta (HNF-1beta) C-terminal domain in Pkhd1 (ARPKD) gene transcription and renal cystogenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Identification of calcium-modulating cyclophilin ligand (CAML) as transducer of angiotensin II-mediated nuclear factor of activated T cells (NFAT) activation

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

PKHDL1, a homolog of the autosomal recessive polycystic kidney disease gene, encodes a receptor with inducible T lymphocyte expression

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia.

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Molecular basis of polycystic kidney disease: PKD1, PKD2 and PKHD1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

The quest for the gene responsible for medullary cystic kidney disease type 1

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

NF-AT Activation Induced by a CAML-Interacting Member of the Tumor Necrosis Factor Receptor Superfamily

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Kaposi's sarcoma-associated herpesvirus mitochondrial K7 protein targets a cellular calcium-modulating cyclophilin ligand to modulate intracellular calcium concentration and inhibit apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Murine models of polycystic kidney disease: molecular and therapeutic insights

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021

Cystic kidney diseases: all roads lead to the cilium

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2005.10.022

7 January 2021