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Academic Journal

Gain of oncogenic function of p53 mutants induces invasive phenotypes in human breast cancer cells by silencing CCN5/WISP-2.

  • Authors : Dhar G; Cancer Research Unit, VA Medical Center, Kansas City, Missouri, USA.; Banerjee S

Subjects: RNA Interference*; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*genetics ; Breast Neoplasms/Breast Neoplasms/Breast Neoplasms/*pathology

  • Source: Cancer research [Cancer Res] 2008 Jun 15; Vol. 68 (12), pp. 4580-7.Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 2984705R Publication Model: Print Cited Medium:

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Academic Journal

[Construction of WISP3 gene's mutants in SEDT-PA and their expression in COS-7 cells].

  • Authors : Wang M; Institute of Metablism and Endocrinology, Second Xiangya Hospital, Central South University, Changsha 410011,China.; Peng YQ

Subjects: Mutation* ; Transfection*; Insulin-Like Growth Factor Binding Proteins/Insulin-Like Growth Factor Binding Proteins/Insulin-Like Growth Factor Binding Proteins/*genetics

  • Source: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences [Zhong Nan Da Xue Xue Bao Yi Xue Ban] 2008 Jan; Vol. 33 (1), pp. 8-15.Publisher:

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Academic Journal

Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation.

  • Authors : Zhou HD; Institute of Endocrinology and Metabolism, The Second Xiang-Ya Hospital of Central South University, 139# Mid-RenMin Road, Changsha, Hunan, 410011, China.; Bu YH

Subjects: Mutation*; Cartilage, Articular/Cartilage, Articular/Cartilage, Articular/*metabolism ; Insulin-Like Growth Factor Binding Proteins/Insulin-Like Growth Factor Binding Proteins/Insulin-Like Growth Factor Binding Proteins/*genetics

  • Source: Journal of molecular medicine (Berlin, Germany) [J Mol Med (Berl)] 2007 Sep; Vol. 85 (9), pp. 985-96. Date of Electronic Publication: 2007 May 05.Publisher: Springer International Country of Publication: Germany NLM ID: 9504370 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Mutant WISP3 triggers the phenotype shift of articular chondrocytes by promoting sensitivity to IGF-1 hypothesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA).

  • Authors : Yang Y; Institute of Endocrinology and Metabolism, The Second Xiang-Ya Hospital of Central South University, Changsha 410011, China.; Liao E

Subjects: Models, Biological* ; Mutation*; Cartilage, Articular/Cartilage, Articular/Cartilage, Articular/*metabolism

  • Source: Medical hypotheses [Med Hypotheses] 2007; Vol. 68 (6), pp. 1406-10. Date of Electronic Publication: 2007 Mar 23.Publisher: Eden Press Country of Publication: United States NLM ID: 7505668 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Genetic and epigenetic changes of components affecting the WNT pathway in colorectal carcinomas stratified by microsatellite instability.

  • Authors : Thorstensen L; Department of Genetics, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo, Norway.; Lind GE

Subjects: Chromosomal Instability* ; Microsatellite Repeats* ; Signal Transduction*

  • Source: Neoplasia (New York, N.Y.) [Neoplasia] 2005 Feb; Vol. 7 (2), pp. 99-108.Publisher: Elsevier Country of Publication: United States NLM ID: 100886622 Publication Model: Print Cited Medium: Print ISSN: 1522-8002 (Print)

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Editorial & Opinion

WNT-inducible signaling pathway protein 3, WISP-3, is mutated in microsatellite unstable gastrointestinal carcinomas but not in endometrial carcinomas.

Subjects: Mutation*; Endometrial Neoplasms/Endometrial Neoplasms/Endometrial Neoplasms/*genetics ; Gastrointestinal Neoplasms/Gastrointestinal Neoplasms/Gastrointestinal Neoplasms/*genetics

  • Source: Gastroenterology [Gastroenterology] 2003 Jan; Vol. 124 (1), pp. 270-1.Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print Cited Medium: Print ISSN: 0016-5085

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Academic Journal

N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.

Subjects: Cell Cycle Proteins*; Hereditary Sensory and Motor Neuropathy/Hereditary Sensory and Motor Neuropathy/Hereditary Sensory and Motor Neuropathy/*genetics ; Mutation/Mutation/Mutation/*genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2000 Jul; Vol. 67 (1), pp. 47-58. Date of Electronic Publication: 2000 May 30.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.

  • Authors : Hurvitz JR; Department of Genetics and Center for Human Genetics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, Ohio 44106, USA.; Suwairi WM

Subjects: Immediate-Early Proteins* ; Intercellular Signaling Peptides and Proteins* ; Mutation*

  • Source: Nature genetics [Nat Genet] 1999 Sep; Vol. 23 (1), pp. 94-8.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Print ISSN: 1061-4036

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  • 1-8 of  8 results for ""CCN Intercellular Signaling Proteins""