Zobrazeno 1 - 7
of 7
pro vyhledávání: '"MESH: Homeodomain Proteins / genetics"'
Autor:
Caroline Michot, Julie Plaisancié, Marta Corton, Edouard Cottereau, Julian Delanne, Nicolas Chassaing, Nicola K. Ragge, Jacmine Pechmeja, Celia Zazo Seco, P Calvas, Tatiana Lupasco, Carmen Ayuso
Publikováno v:
Ophthalmic Genetics
Ophthalmic Genetics, Taylor & Francis, 2018, 39 (3), pp.314-320. ⟨10.1080/13816810.2018.1430243⟩
Ophthalmic Genetics, 2018, 39 (3), pp.314-320. ⟨10.1080/13816810.2018.1430243⟩
Ophthalmic Genetics, Taylor & Francis, 2018, 39 (3), pp.314-320. ⟨10.1080/13816810.2018.1430243⟩
Ophthalmic Genetics, 2018, 39 (3), pp.314-320. ⟨10.1080/13816810.2018.1430243⟩
Background: Congenital cataract displays large phenotypic (syndromic and isolated cataracts) and genetic heterogeneity. Mutations in several transcription factors involved in eye development, like PITX3, have been associated with congenital cataracts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3b2f8c95d544a4df8f885a3915e4edb
Autor:
P Calvas, S. El Hout, Nicolas Chassaing, C. Zazo Seco, Adeline Vigouroux, Laurence Bouneau, P. Vande Perre, O. Patat, D. Bourgeois
Publikováno v:
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2018, 61 (2), pp.72-78. ⟨10.1016/j.ejmg.2017.10.018⟩
European Journal of Medical Genetics, Elsevier, 2018, 61 (2), pp.72-78. ⟨10.1016/j.ejmg.2017.10.018⟩
International audience; Axenfeld-Rieger syndrome (ARS) is a heterogeneous clinical entity transmitted in an autosomal dominant manner. The main feature, Axenfeld-Rieger Anomaly (ARA), is a malformation of the anterior segment of the eye that can lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f330969446e0c068008632ceb1de024
https://doi.org/10.1016/j.ejmg.2017.10.018
https://doi.org/10.1016/j.ejmg.2017.10.018
Autor:
Elsa Kress, Mathias Heikenwalder, Gerard Lina, David Bauché, Saskia Lippens, Claire Macari, Marie-Cécile Michallet, Mathias Chamaillard, Sophia Djebali, Emilie Plantamura, Lyvia Moudombi, Jacqueline Marvel, Christophe Caux, Julien C. Marie, Annabelle Cesaro, Lilia Boucinha, Amiran Dzutsev, Jean-Philippe Rasigade, Ulrike Rothermel, Giorgio Trinchieri, Azzak Bentaher-Belaaouaj, Oana Dumitrescu, Morgan Grau, Michelina Plateroti, Clovis Bondu
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, 2018, 115 (41), pp.10404-10409. ⟨10.1073/pnas.1722372115⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2018, 115 (41), pp.10404-10409. ⟨10.1073/pnas.1722372115⟩
Proceedings of the National Academy of Sciences of the United States of America, 2018, 115 (41), pp.10404-10409. ⟨10.1073/pnas.1722372115⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2018, 115 (41), pp.10404-10409. ⟨10.1073/pnas.1722372115⟩
International audience; Prominent changes in the gut microbiota (referred to as "dysbiosis") play a key role in the development of allergic disorders, but the underlying mechanisms remain unknown. Study of the delayed-type hypersensitivity (DTH) resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f72c638beb7102ea94a7542c3c80f63
https://hal.science/hal-02398995
https://hal.science/hal-02398995
Autor:
Chassaing, N., Causse, A., Vigouroux, A., Delahayes, A., Alessandri, J.-L., Boespflug-Tanguy, O., Boute-Benejean, O., Dollfus, H., Duban-Bedu, B., Gilbert-Dussardier, B., Giuliano, F., Gonzales, M., Holder-Espinasse, M., Isidor, B., Jacquemont, M.-L., Lacombe, D., Martin-Coignard, D., Mathieu-Dramard, M., Odent, S., Picone, O., Pinson, L., Quelin, C., Sigaudy, Sabine, Toutain, A., Thauvin-Robinet, C., Kaplan, Josseline, Calvas, Patrick
Publikováno v:
Clinical Genetics
Clinical Genetics, Wiley, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. ⟨10.1111/cge.12275⟩
Clinical Genetics, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. 〈10.1111/cge.12275〉
Clinical Genetics, Wiley, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. ⟨10.1111/cge.12275⟩
Clinical Genetics, 2014, 86 (4), pp.326-334. ⟨10.1111/cge.12275⟩
Clinical Genetics, Wiley, 2014, 86 (4), pp.326--334. 〈10.1111/cge.12275〉
International audience; Anophthalmia and microphthalmia (AM) are the most severe malformations of the eye, corresponding respectively to reduced size or absent ocular globe. Wide genetic heterogeneity has been reported and different genes have been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4aacf8c5d4d2e23e38ea8b0dc8884cb8
https://hal.archives-ouvertes.fr/hal-01064928
https://hal.archives-ouvertes.fr/hal-01064928
Publikováno v:
Plant Journal
Plant Journal, Wiley, 2012, 71, pp.99-107. ⟨10.1111/j.1365-313X.2012.04973.x⟩
Plant Journal, Wiley, 2012, 71, pp.99-107. ⟨10.1111/j.1365-313X.2012.04973.x⟩
International audience; Leaf organogenesis occurs within the peripheral zone of the shoot apical meristem (SAM). The initiation and subsequent development of a leaf requires the stable repression of a highly conserved class of plant genes, namely cla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9fb6e336f08e9fd56d0f7f2b3587edcb
https://pubmed.ncbi.nlm.nih.gov/22380849
https://pubmed.ncbi.nlm.nih.gov/22380849
Autor:
Nicolas Dray, Michel Vervoort, Guillaume Balavoine, Bruno Hudry, Martine Le Gouar, Alexandra Saudemont
Publikováno v:
Developmental Biology
Developmental Biology, Elsevier, 2008, 317 (2), pp.430-443. ⟨10.1016/j.ydbio.2008.02.013⟩
Developmental Biology, Elsevier, 2008, 317 (2), pp.430-443. ⟨10.1016/j.ydbio.2008.02.013⟩
International audience; NK genes are related pan-metazoan homeobox genes. In the fruitfly, NK genes are clustered and involved in patterning various mesodermal derivatives during embryogenesis. It was therefore suggested that the NK cluster emerged i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c8a4fa399ed6be9f63e1c7e71667ad
https://hal.archives-ouvertes.fr/hal-02462532
https://hal.archives-ouvertes.fr/hal-02462532
Autor:
Neven, Benedicte, Perot, Philippe, Bruneau, Julie, Pasquet, Marlene, Ramirez, Marie, Diana, Jean-Sebastien, Luzi, Stephanie, Corre-Catelin, Nicole, Chardot, Christophe, Despina Moshous, Leclerc Mercier, Stephanie, Mahlaoui, Nizar, Aladjidi, Nathalie, Le Bail, Brigitte, Lecuit, Marc, Bodemer, Christine, Molina, Thierry Jo, Blanche, Stephane, Eloit, Marc
Publikováno v:
ResearcherID
Clinical Infectious Diseases
Clinical Infectious Diseases, 2016, 64 (1), pp.83-86. ⟨10.1093/cid/ciw675⟩
Clinical Infectious Diseases, Oxford University Press (OUP), 2016, 64 (1), pp.83-86. ⟨10.1093/cid/ciw675⟩
Clinical Infectious Diseases
Clinical Infectious Diseases, 2016, 64 (1), pp.83-86. ⟨10.1093/cid/ciw675⟩
Clinical Infectious Diseases, Oxford University Press (OUP), 2016, 64 (1), pp.83-86. ⟨10.1093/cid/ciw675⟩
Erratum in : Erratum. [Clin Infect Dis. 2017]; International audience; Persistence of rubella live vaccine has been associated with chronic skin granuloma in 3 children with primary immunode-ficiency. We describe 6 additional children with these find
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ca99ecbfb52840f445add3e48e964ea3
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:27810866&KeyUID=MEDLINE:27810866
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=MEDLINE&KeyUT=MEDLINE:27810866&KeyUID=MEDLINE:27810866