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Results 1 to 25 of 147807

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Identification of HNF1A-MODY and HNF4A-MODY in Irish families: Phenotypic characteristics and therapeutic implicationsKYITHAR, M. P; BACON, S; PANNU, K. K et al.Diabetes & metabolism. 2011, Vol 37, Num 6, pp 512-519, issn 1262-3636, 8 p.Article

New leptin receptor mutations in mice: Leprdb-rtnd, Leprdb-dmpg and leprdb-rlpyJUNG HAN KIM; TAYLOR, Paul N; YOUNG, Dawn et al.The Journal of nutrition. 2003, Vol 133, Num 5, pp 1265-1271, issn 0022-3166, 7 p.Article

Rapid LightCycler assay for identification of the Perforin codon 374 Trp → stop mutation in patients and families with hemophagocytic lymphohistiocytosis (HLH)STADT, Udo Zur; KABISCH, Hartmut; JANKA, Gritta et al.Medical and pediatric oncology. 2003, Vol 41, Num 1, pp 26-29, issn 0098-1532, 4 p.Article

The independence of phonology and morphology : The Celtic mutationsGREEN, Antony D.Lingua (Haarlem. Print). 2006, Vol 116, Num 11, pp 1946-1985, issn 0024-3841, 40 p.Conference Paper

Modernité tardive, religion et mutation du public et du privé (à partir de l'exemple français)BAUBEROT, Jean.Social compass. 2006, Vol 53, Num 2, pp 155-168, issn 0037-7686, 14 p.Conference Paper

CEBPα mutations in childhood acute myeloid leukemiaLIANG, D.-C; SHIH, L.-Y; HUANG, C.-F et al.Leukemia. 2005, Vol 19, Num 3, pp 410-414, issn 0887-6924, 5 p.Article

Pathogenic mitochondrial dna mutations in protein-coding genesWONG, Lee-Jun C.Muscle & nerve. 2007, Vol 36, Num 3, pp 279-293, issn 0148-639X, 15 p.Article

La contextualisation de la théologie protestante comme lieu de changement du christianisme en Océanie = The contextualisation of protestant theology in Oceania as a Sign of a Changing ChristianityVIDAL, Gilles.Archives de sciences sociales des religions. 2012, Vol 157, pp 157-177, issn 0335-5985, 21 p.Article

Mbd1, MBD2 and CGBP genes at chromosome 18q21 are infrequently mutated in human colon and lung cancersBADER, Scott; WALKER, Marion; MCQUEEN, Heather A et al.Oncogene (Basingstoke). 2003, Vol 22, Num 22, pp 3506-3510, issn 0950-9232, 5 p.Article

Molecular analysis of the androgen receptor in ten prostate cancer specimens obtained before and after androgen ablationLAMB, Dolores J; PUXEDDU, Efisio; MALIK, Nusrat et al.Journal of andrology. 2003, Vol 24, Num 2, pp 215-225, issn 0196-3635, 11 p.Article

OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484YAMADA, Tetsuya; HAYASAKA, Seiji; KANAI, Atsushi et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 4, pp 409-411, issn 0021-5155, 3 p.Article

Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasiansVEIGA-DA-CUNHA, M; DELPLANQUE, J; GILLAIN, A et al.Diabetologia (Berlin). 2003, Vol 46, Num 5, pp 704-711, issn 0012-186X, 8 p.Article

Plastid transformation in Lesquerella fendleri, an oilseed BrassicaceaSKARJINSKAIA, Marina; SVAB, Zora; MALIGA, Pal et al.Transgenic research. 2003, Vol 12, Num 1, pp 115-122, issn 0962-8819, 8 p.Article

Evaluation of Accuracy and Applicability of Protein Models: Retrospective Analysis of Biological and Biomedical PredictionsKHAN, Sofia; VIHINEN, Mauno.In silico biology (Gedrukt). 2009, Vol 9, Num 5-6, pp 307-331, issn 1386-6338, 25 p.Article

SGCZ MUTATIONS ARE UNLIKELY TO BE ASSOCIATED WITH MYOCLONUS DYSTONIAPEALL, K. J; RITZ, K; WAITE, A. J et al.Neuroscience. 2014, Vol 272, pp 88-91, issn 0306-4522, 4 p.Article

Studies on thiabendazole resistance of Penicillium expansum of pears: pathogenic fitness and genetic characterizationBARALDI, E; MARI, M; CHIERICI, E et al.Plant pathology. 2003, Vol 52, Num 3, pp 362-370, issn 0032-0862, 9 p.Article

Higher order chromatin degradation: Implications for neurodegenerationKONAT, Gregory W.Neurochemical research. 2002, Vol 27, Num 11, pp 1447-1451, issn 0364-3190, 5 p.Article

Anticorps polyréactifs: étude structurale et génétique d'une IgG2b polyréactive = Polyrective antibodies: structural and genetic characterization of a polyreactive IG2bSequeira-Le Grand, Anabelle; Avrameas, Stratis.1991, 193 p.Thesis

Severe congenital neutropenia : inheritance and pathophysiologySKOKOWA, Julia; GERMESHAUSEN, Manuela; ZEIDLER, Cornelia et al.Current opinion in hematology. 2007, Vol 14, Num 1, pp 22-28, issn 1065-6251, 7 p.Article

Catastrophe and what to do about it if you are a bacterium: The importance of frameshift mutantsKOCH, Arthur L.Critical reviews in microbiology. 2004, Vol 30, Num 1, pp 1-6, issn 1040-841X, 6 p.Article

What Is a Mutation? Identifying Heritable Change in the Offspring of Survivors at Hiroshima and NagasakiLINDEE, M. S.Journal of the history of biology. 1992, Vol 25, Num 2, pp 231-255, issn 0022-5010Article

From Culture as Organism to Organism as Cell : Historical Origins of Bacterial GeneticsSUMMERS, W. C.Journal of the history of biology. 1991, Vol 24, Num 2, pp 171-190, issn 0022-5010Article

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermiaCOUTTON, Charles; ZOUARI, Raoudha; SERMONDADE, Nathalie et al.Human reproduction (Oxford. Print). 2012, Vol 27, Num 8, pp 2549-2558, issn 0268-1161, 10 p.Article

Mutation Analysis of the Inwardly Rectifying K+ Channel KCNJ3 (GIRK1) in a Tunisian Family with Juvenile Myocionic EpilepsyLAYOUNI, Samia; CHOUCHANE, Lotfi; DOGUI, Mohamed et al.MHA (Sousse). 2009, Vol 21, Num 61, pp 36-39, issn 0330-8030, 4 p.Article

High susceptibility of p53 knockout mice to esophageal and urinary bladder carcinogenesis induced by N, N-dibutylnitrosamineNISHIKAWA, Takayuki; SALIM, Elsayed I; MORIMURA, Keiichirou et al.Cancer letters. 2003, Vol 194, Num 1, pp 45-54, issn 0304-3835, 10 p.Article

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