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Results 1 to 25 of 49

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Generation of transgenic mice for conditional overexpression of Sox9KIM, Youngwoo; MURAO, Hiroki; YAMAMOTO, Koji et al.Journal of bone and mineral metabolism (English ed.). 2011, Vol 29, Num 1, pp 123-129, issn 0914-8779, 7 p.Article

Downregulation of miR-29 contributes to cisplatin resistance of ovarian cancer cellsYU, Pei-Ning; YAN, Ming-De; LAI, Hung-Cheng et al.International journal of cancer (Print). 2014, Vol 134, Num 3, pp 542-551, issn 0020-7136, 10 p.Article

RNAi-mediated inhibition of COL1A1 and COL3A1 in human skin fibroblastsQIONG WANG; ZHENHUI PENG; SHENGXIANG XIAO et al.Experimental dermatology. 2007, Vol 16, Num 7, pp 611-617, issn 0906-6705, 7 p.Article

Dermatofibrosarcoma protuberans with COL1a1 (exon 18): PDGFB (exon 2) fusion transcriptSAEKI, H; OHMATSU, H; HOASHI, T et al.British journal of dermatology (1951). 2003, Vol 148, Num 5, pp 1028-1031, issn 0007-0963, 4 p.Article

COL1A1 Mutation in an Indian Child with Caffey DiseaseRANGANATH, Prajnya; LAINE, Christine M; GUPTA, Divya et al.Indian journal of pediatrics. 2011, Vol 78, Num 7, pp 877-879, issn 0019-5456, 3 p.Article

A novel fusion gene of collagen type I alpha 1 (exon 31) and platelet-derived growth factor B-chain (exon 2) in dermatofibrosarcoma protuberansNAKANISHI, Gen; LIN, Song-Nan; ASAGOE, Kenji et al.EJD. European journal of dermatology. 2007, Vol 17, Num 3, pp 217-219, issn 1167-1122, 3 p.Article

COL1A1 Association and Otosclerosis: A Meta-AnalysisSCHRAUWEN, Isabelle; KHALFALLAH, Ayda; EALY, Megan et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 5, pp 1066-1070, issn 1552-4825, 5 p.Article

A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defectVENTURI, Giacomo; MONTI, Elena; DALLE CARBONARE, Luca et al.Bone (New York, NY). 2012, Vol 50, Num 1, pp 343-349, issn 8756-3282, 7 p.Article

Heterozygous C-Propeptide Mutations in COL1A1: Osteogenesis Imperfecta Type IIC and Dense Bone VariantTAKAGI, Masaki; HORI, Naoaki; HASEGAWA, Tomonobu et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2269-2273, issn 1552-4825, 5 p.Article

Studies of otic capsule morphology and gene expression in the Mov13 mouse - : An animal model of type I osteogenesis imperfectaSTANKOVIC, Konstantina M; KRISTIANSEN, Arthur G; BIZAKI, Argyro et al.Audiology & neuro-otology. 2007, Vol 12, Num 5, pp 334-343, issn 1420-3030, 10 p.Article

Gene mutation analysis in five cases of dermatofibrosarcoma protuberans using formalin-fixed, paraffin-embedded tissuesSAEKI, Hidehisa; TSUNEMI, Yuichiro; OHTSUKI, Mamitaro et al.Acta dermato-venereologica. 2005, Vol 85, Num 3, pp 221-224, issn 0001-5555, 4 p.Article

Polymorphisms in the 5' flank of COL1A1 gene and osteoporosis: meta-analysis of published studiesJIN, H; EVANGELOU, E; IOANNIDIS, J. P. A et al.Osteoporosis international. 2011, Vol 22, Num 3, pp 911-921, issn 0937-941X, 11 p.Article

A Rare Haplotype in the Upstream Regulatory Region of COL1A1 Is Associated With Reduced Bone Quality and Hip FractureHUILIN JIN; STEWART, Tracy L; VAN'T HOF, Rob et al.Journal of bone and mineral research (Print). 2009, Vol 24, Num 3, pp 448-454, issn 0884-0431, 7 p.Article

A Novel De Novo 1.1 Mb Duplication of 17q21.33 Associated With Cognitive Impairment and Other AnomaliesZAHIR, Farah R; LANGLOIS, Sylvie; GALL, Kim et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1257-1262, issn 1552-4825, 6 p.Article

Natural variation in four human collagen genes across an ethnically diverse populationCHAN, Ting-Fung; POON, Annie; BASU, Analabha et al.Genomics (San Diego, Calif.). 2008, Vol 91, Num 4, pp 307-314, issn 0888-7543, 8 p.Article

Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisCHEN, W; MEYER, N. C; MCKENNA, M. J et al.Clinical genetics. 2007, Vol 71, Num 5, pp 406-414, issn 0009-9163, 9 p.Article

Conventional gene targeting protocols lead to loss of targeted cells when applied to a silent gene locus in primary fibroblastsMARQUES, Margarita M; THOMSON, Alison J; MCCREATH, Kenneth J et al.Journal of biotechnology. 2006, Vol 125, Num 2, pp 185-193, issn 0168-1656, 9 p.Article

Detection of COL1A1-PDGFB fusion transcripts and platelet-derived growth factor α and β receptors in giant cell fibroblastoma of the postsacrococcygeal regionKASHIMA, A; YAMASHITA, A; MORIGUCHI, S et al.British journal of dermatology (1951). 2006, Vol 154, Num 5, pp 983-987, issn 0007-0963, 5 p.Article

Rapid genotyping of the osteoporosis-associated polymorphic transcription factor Sp1 binding site in the COL1A1 gene by pyrosequencingELLNEBO-SVEDLUND, Katarina; LARSSON, Lasse; JONASSON, Jon et al.Molecular biotechnology. 2004, Vol 26, Num 1, pp 87-90, issn 1073-6085, 4 p.Article

Dermatofibrosarcoma protuberans: clinical, pathological, and genetic (COL1A1-PDGFB) study with therapeutic implicationsLLOMBART, Beatriz; SANMARTIN, Onofre; GUILLEN, Carlos et al.Histopathology. 2009, Vol 54, Num 7, pp 860-872, issn 0309-0167, 13 p.Article

Mutation analysis of coding sequences for type I procollagen in individuals with low bone densitySPOTILA, L. D; COLIGE, A; ATTIE, M et al.Journal of bone and mineral research (Print). 1994, Vol 9, Num 6, pp 923-932, issn 0884-0431Article

ETUDE DES MECANISMES MOLECULAIRES RESPONSABLES DE LA REGULATION DE L'EXPRESSION DU GENE CODANT POUR LA CHAINE ALPHA 1 DU COLLAGENE DE TYPE I = STUDY OF THE MOLECULAR MECHANISMS RESPONSIBLE FOR THE REGULATION OF THE EXPRESSION OF THE GENE CODING FOR THE ALPHA 1 CHAIN OF THE TYPE I COLLAGENDurasnel Terraz, Catherine; Rossert, Jerome.2001, 203 p.Thesis

Positive Regulation of Adult Bone Formation by Osteoblast-Specific Transcription Factor OsterixBAEK, Wook-Young; LEE, Min-A; JI WON JUNG et al.Journal of bone and mineral research (Print). 2009, Vol 24, Num 6, pp 1055-1065, issn 0884-0431, 11 p.Article

COL1A1 Sp1 polymorphism associates with bone density in early pubertySUURINIEMI, Miia; KOVANEN, Vuokko; MAHONEN, Anitta et al.Bone (New York, NY). 2006, Vol 39, Num 3, pp 591-597, issn 8756-3282, 7 p.Article

Substitution of glycine-661 by serine in the α1(I) and α2(I) chains of type I collagen results in different clinical and biochemical phenotypesNUYTINCK, L; DALGLEISH, R; SPOTILA, L et al.Human genetics. 1996, Vol 97, Num 3, pp 324-329, issn 0340-6717Article

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