Výsledky vyhledávání - "J. F. Gibrat"

The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2006, 103 (24), pp.9274-9279. ⟨10.1073/pnas.0603024103⟩
Proceedings of the National Academy of Sciences of the United States of America 24 (103), 9274-9279. (2006)

Lactobacillus delbrueckii ssp. bulgaricus ( L. bulgaricus ) is a representative of the group of lactic acid-producing bacteria, mainly known for its worldwide application in yogurt production. The genome sequence of this bacterium has been determined

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae48ba4a5114037dac9ab27705eeb13d
https://doi.org/10.1073/pnas.0603024103

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Normal mode analysis of human lysozyme : study of the relative motion of the two domains and characterization of the harmonic motion

Autor: Nobuhiro Go, J. F. Gibrat

Publikováno v: Journal de Chimie Physique. 88:2581-2585

A normal mode analysis of human lysozyme has been carried out at room temperature. Human lysozyme is an enzyme constituted of two domains separated by an active site cleft, the motion of which is thought to be relevant for biological function. This m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5858e0e0fa6306697cb632ff090fd4a9
https://doi.org/10.1051/jcp/1991882581

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Annotation and databases : status and prospects

Autor: J.-F. Gibrat, Ph. Bessières, M. Hoebeke, J. Garnier, Hélène Chiapello

Publikováno v: Database annotation in molecular biology : principles and practice
Database annotation in molecular biology : principles and practice, Wiley, 2004, 978-0-470-85681-9
HAL
Database Annotation in Molecular Biology

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9fbbbc26f3d9367625ccfbd71511c2c
https://hal.inrae.fr/hal-02832226

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From GeneWeaver to Agmial

Autor: Bryson, K., Michael Luck, Joy, M., Jones, D., Nicholas, P., Bessieres, P., J-F, Gibrat

Publikováno v: Network Tools and Applications in Biology Workshop on Agents in Bioinformatics (NETTAB 2002)
King's College London

We report on our experiences of developing two multi-agent systems for bioinformatics called GeneWeaver and Agmial. The concepts behind these systems are described and the results of experimenting with different agent communities are given. \ud \ud T

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6ca016eae2fd7625cad66b00c91c9199
http://wrap.warwick.ac.uk/61211/7/bryson_luck_joy_nettab02.pdf

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A molecular approach to dominance in hypophosphatasia

Autor: B. Robin, Eric Bieth, Peter Freisinger, M. Mouchard, H. P. Krohn, Mark E Nunes, J. F. Gibrat, Anne-Sophie Lia-Baldini, Arthur S. Aylsworth, F. Muller, Etienne Mornet, B. Simon-Bouy, J.L. Serre, S. Delanote, J. C.C. Hu, Agnès Taillandier

Publikováno v: Human genetics. 109(1)

Hypophosphatasia is an inherited disorder characterized by defective bone mineralization and a deficiency of tissue-nonspecific alkaline phosphatase (TNSALP) activity. The disease is highly variable in its clinical expression, because of various muta

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ce291e6d4dd54ab8d5f9e78e65ffdbc
https://pubmed.ncbi.nlm.nih.gov/11479741

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A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutations

Autor: E. Mornet, J.-F. Gibrat

Publikováno v: Human Genetics
Human Genetics, Springer Verlag, 2000, 106, pp.330-339

In order to better understand the disease-causing role of missense mutations found in the CYP21 gene from patients affected with congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase deficiency, we built two three-dimensional (3D) models

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec54240c003644709b36c43edf552d74
https://hal.inrae.fr/hal-02699191

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Correlations of genotype and phenotype in hypophosphatasia

Autor: Etienne Mornet, J. F. Gibrat, L. Serre, Agnès Taillandier, F. Muller, B. Simon-Bouy, L. Zurutuza

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 1999, 8 (6), pp.1039-1046

Hypophosphatasia, a rare inherited disorder characterized by defective bone mineralization, is highly variable in its clinical expression. The disease is due to various mutations in the tissue-non-specific alkaline phosphatase ( TNSALP ) gene. We rep

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aee4bfb068b713f4b323333cd5b23dc
https://pubmed.ncbi.nlm.nih.gov/10332035

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In unison: regularization of protein secondary structure predictions that makes use of multiple sequence alignments

Autor: J F Gibrat, K Zimmermann

Publikováno v: Protein engineering. 11(10)

We present a method whose purpose is to post-process thefuzzy results of secondary structure prediction methodsthat use multiple sequence alignments, in order to obtain‘realistic’ secondary structures, i.e., secondary structureelements whose leng

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a456e117fee739cc8a0c60b03e7b06
https://pubmed.ncbi.nlm.nih.gov/9862204

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