Publications by authors named "RB Chadwick"

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A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome.
Taraneh Esmailpour, Hamidreza Riazifar, Linan Liu, Sandra Donkervoort, Vincent H Huang, Robert B Chadwick

J Med Genet· March 2014

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Prepubertal OVX increases IGF-I expression and bone accretion in C57BL/6J mice.
Kristen E Govoni, Jon E Wergedal, Robert B Chadwick, Apurva K Srivastava, Subburaman Mohan

Am J Physiol Endocrinol Metab· November 2008

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Chemical mutagenesis induced two high bone density mouse mutants map to a concordant distal chromosome 4 locus.
S Mohan, V Chest, R B Chadwick, J E Wergedal, A K Srivastava

Bone· November 2007

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Tumor necrosis factor-alpha augments matrix metalloproteinase-9 production in skeletal muscle cells through the activation of transforming growth factor-beta-activated kinase 1 (TAK1)-dependent signaling pathway.
Apurva K Srivastava, Xuezhong Qin, Nia Wedhas, Marc Arnush, Thomas A Linkhart, Robert B Chadwick

J Biol Chem· November 2007

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Digit tip regrowth and differential gene expression in MRL/Mpj, DBA/2, and C57BL/6 mice.
Robert B Chadwick, Liming Bu, Hongrun Yu, Yan Hu, Jon E Wergedal

Wound Repair Regen· June 2007

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Whole genome microarray analysis of growth hormone-induced gene expression in bone: T-box3, a novel transcription factor, regulates osteoblast proliferation.
Kristen E Govoni, Seong Keun Lee, Robert B Chadwick, Hongrun Yu, Yuji Kasukawa

Am J Physiol Endocrinol Metab· July 2006

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Microarray analysis of gene expression during the inflammation and endochondral bone formation stages of rat femur fracture repair.
Charles H Rundle, Hali Wang, Hongrun Yu, Robert B Chadwick, Emile I Davis

Bone· April 2006

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Global gene expression analysis in the bones reveals involvement of several novel genes and pathways in mediating an anabolic response of mechanical loading in mice.
Weirong Xing, David Baylink, Chandrasekhar Kesavan, Yan Hu, Susanna Kapoor, Robert B Chadwick

J Cell Biochem· December 2005

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Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.
Subburaman Mohan, Anil Kapoor, Anny Singgih, Zhang Zhang, Tim Taylor, Robert B Chadwick

J Bone Miner Res· September 2005

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EGFR and EGFRvIII expression in primary breast cancer and cell lines.
James M Rae, Joshua O Scheys, Kim M Clark, Robert B Chadwick, Michael C Kiefer

Breast Cancer Res Treat· September 2004

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Single-nucleotide polymorphisms (SNPs) in human beta-defensin 1: high-throughput SNP assays and association with Candida carriage in type I diabetics and nondiabetic controls.
Richard J Jurevic, Mai Bai, Robert B Chadwick, Theodore C White, Beverly A Dale

J Clin Microbiol· January 2003

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A polymorphism in the CYP17 gene and risk of prostate cancer.
Janet L Stanford, Elizabeth A Noonan, Lori Iwasaki, Suzanne Kolb, Robert B Chadwick

Cancer Epidemiol Biomarkers Prev· March 2002

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Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily.
G Steele-Perkins, W Fang, X H Yang, M Van Gele, T Carling, R B Chadwick

Genes Dev· September 2001

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Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.
R B Chadwick, R E Pyatt, T H Niemann, S K Richards, C K Johnson

J Med Genet· July 2001

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MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer.
J Huang, S A Kuismanen, T Liu, R B Chadwick, C K Johnson

Cancer Res· February 2001

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Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosome.
M D Mailman, T Hemingway, R L Darsey, C E Glasure, Y Huang, R B Chadwick

Hum Genet· February 2001

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Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer.
H Nakagawa, R B Chadwick, P Peltomaki, C Plass, Y Nakamura

Proc Natl Acad Sci U S A· January 2001

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Polymorphisms in a pseudogene highly homologous to PMS2.
R B Chadwick, J E Meek, T W Prior, P Peltomaki, A de La Chapelle

Hum Mutat· December 2000

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Recurrent germline mutation in MSH2 arises frequently de novo.
D C Desai, J C Lockman, R B Chadwick, X Gao, A Percesepe

J Med Genet· September 2000

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Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis.
R B Chadwick, G L Jiang, G A Bennington, B Yuan, C K Johnson

Proc Natl Acad Sci U S A· March 2000

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Case report on hereditary non-polyposis colon cancer (HNPCC) in Nigeria.
C A Adebamowo, O Adeyi, R Pyatt, T W Prior, R B Chadwick

Afr J Med Med Sci· March 2000

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Conversion of diploidy to haploidy.
H Yan, N Papadopoulos, G Marra, C Perrera, J Jiricny, R B Chadwick

Nature· February 2000

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Polymorphic variation at the BAT-25 and BAT-26 loci in individuals of African origin. Implications for microsatellite instability testing.
R Pyatt, R B Chadwick, C K Johnson, C Adebamowo, A de la Chapelle

Am J Pathol· August 1999

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Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.
M Aminoff, J E Carter, R B Chadwick, C Johnson, R Gräsbeck

Nat Genet· March 1999

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The I1307K polymorphism of the APC gene in colorectal cancer.
T W Prior, R B Chadwick, A C Papp, A N Arcot, A M Isa

Gastroenterology· January 1999

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