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1دورية أكاديمية
المؤلفون: A. Kleiber, J. Roy, V. Brunet, E. Baranek, J.M. Le-Calvez, T. Kerneis, A. Batard, S. Calvez, L. Pineau, S. Milla, V. Guesdon, L. Calandreau, V. Colson
المصدر: Animal, Vol 18, Iss 3, Pp 101081- (2024)
مصطلحات موضوعية: Aquaculture, Brain markers, Classical conditioning, Occupational enrichment, Signalled predictability, Animal culture, SF1-1100
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: D. Żarski, J. Król, Y. Ledoré, B. Sarosiek, K. Dryl, P. Gomułka, K. Palińska-Żarska, L. Toomey, P. Fontaine, S. Milla
المصدر: Animal, Vol 15, Iss 9, Pp 100340- (2021)
مصطلحات موضوعية: Controlled reproduction, Eurasian perch, Hormonal stimulation, Ovulation, Stress, Animal culture, SF1-1100
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: A. Khendek, A. Chakraborty, J. Roche, Y. Ledoré, A. Personne, T. Policar, D. Żarski, R. Mandiki, P. Kestemont, S. Milla, P. Fontaine
المصدر: Animal, Vol 12, Iss 11, Pp 2335-2346 (2018)
مصطلحات موضوعية: domestication, reproduction, oogenesis, Sander lucioperca, gonadotropic axis, Animal culture, SF1-1100
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: J. Roche, D. Żarski, A. Khendek, I. Ben Ammar, C. Broquard, A. Depp, Y. Ledoré, T. Policar, P. Fontaine, S. Milla
المصدر: Animal, Vol 12, Iss 12, Pp 2587-2597 (2018)
مصطلحات موضوعية: pikeperch, ovulation, dopamine, antagonist, sex steroid, Animal culture, SF1-1100
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Carmona, Pablo S. Milla, Lazo, Darío G., Soto, Ignacio M.
المصدر: Paleobiology, 2018 Jan 01. 44(1), 101-117.
URL الوصول: https://www.jstor.org/stable/48574117
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المؤلفون: Erin M. Dillon, Emma M. Dunne, Tom M. Womack, Miranta Kouvari, Ekaterina Larina, Jordan Ray Claytor, Angelina Ivkić, Mark Juhn, Pablo S. Milla Carmona, Selina Viktor Robson, Anwesha Saha, Jaime A. Villafaña, Michelle E. Zill
المصدر: Paleobiology. :1-17
مصطلحات موضوعية: Ecology, Paleontology, General Agricultural and Biological Sciences, Ecology, Evolution, Behavior and Systematics
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المؤلفون: Sébastien Küry, Jinwei Zhang, Thomas Besnard, Alfonso Caro-Llopis, Xue Zeng, Stephanie M. Robert, Sunday S. Josiah, Emre Kiziltug, Anne-Sophie Denommé-Pichon, Benjamin Cogné, Adam J. Kundishora, Le T. Hao, Hong Li, Roger E. Stevenson, Raymond J. Louie, Wallid Deb, Erin Torti, Virginie Vignard, Kirsty McWalter, F. Lucy Raymond, Farrah Rajabi, Emmanuelle Ranza, Detelina Grozeva, Stephanie A. Coury, Xavier Blanc, Elise Brischoux-Boucher, Boris Keren, Katrin Õunap, Karit Reinson, Pilvi Ilves, Ingrid M. Wentzensen, Eileen E. Barr, Solveig Heide Guihard, Perrine Charles, Eleanor G. Seaby, Kristin G. Monaghan, Marlène Rio, Yolande van Bever, Marjon van Slegtenhorst, Wendy K. Chung, Ashley Wilson, Delphine Quinquis, Flora Bréhéret, Kyle Retterer, Pierre Lindenbaum, Emmanuel Scalais, Lindsay Rhodes, Katrien Stouffs, Elaine M. Pereira, Sara M. Berger, Sarah S. Milla, Ankita B. Jaykumar, Melanie H. Cobb, Shreyas Panchagnula, Phan Q. Duy, Marie Vincent, Sandra Mercier, Brigitte Gilbert-Dussardier, Xavier Le Guillou, Séverine Audebert-Bellanger, Sylvie Odent, Sébastien Schmitt, Pierre Boisseau, Dominique Bonneau, Annick Toutain, Estelle Colin, Laurent Pasquier, Richard Redon, Arjan Bouman, Jill. A. Rosenfeld, Michael J. Friez, Helena Pérez-Peña, Syed Raza Akhtar Rizvi, Shozeb Haider, Stylianos E. Antonarakis, Charles E. Schwartz, Francisco Martínez, Stéphane Bézieau, Kristopher T. Kahle, Bertrand Isidor
المساهمون: Clinical Genetics, Clinical sciences, Medical Genetics, Reproduction and Genetics, Centre hospitalier universitaire de Nantes (CHU Nantes), unité de recherche de l'institut du thorax UMR1087 UMR6291 (ITX), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Nantes Université - UFR de Médecine et des Techniques Médicales (Nantes Univ - UFR MEDECINE), Nantes Université - pôle Santé, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ)-Nantes Université - pôle Santé, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ), University of Exeter, MitoVasc - Physiopathologie Cardiovasculaire et Mitochondriale (MITOVASC), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), The Greenwood Genetic Center, GeneDx [Gaithersburg, MD, USA], Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Centre hospitalier universitaire de Poitiers (CHU Poitiers), Centre Hospitalier Régional Universitaire de Brest (CHRU Brest), CHU Pontchaillou [Rennes], Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Imagerie et cerveau (iBrain - Inserm U1253 - UNIV Tours ), Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université de Genève = University of Geneva (UNIGE), Yale School of Medicine [New Haven, Connecticut] (YSM), This work was granted by the French network of University Hospitals HUGO ('Hôpitaux Universitaires du Grand Ouest'), the French Ministry of Health, and the Health Regional Agencies from Poitou-Charentes (represented by Frédérique Allaire), Bretagne, Pays de la Loire, and Centre-Val de Loire (HUGODIMS, 2013, RC14_0107). W.K.C. was supported by grants from Simons Foundation Autism Research Initiative, United
المصدر: Genetics in Medicine, 24(9), 1941-1951. Lippincott Williams & Wilkins
GENETICS IN MEDICINE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Genetics in Medicine
Genetics in Medicine, 2022, 24 (9), pp.1941-1951. ⟨10.1016/j.gim.2022.05.009⟩مصطلحات موضوعية: MESH: Symporters, Exome sequencing, Male, KCC2, Mutation, Missense, MESH: Catalytic Domain, Neurodevelopmental disease, Protein Serine-Threonine Kinases, X-linked intellectual disability, MESH: Brain, WNK3, SDG 3 - Good Health and Well-being, Loss of Function Mutation, Catalytic Domain, MESH: Mental Retardation, X-Linked, Humans, Phosphorylation, MESH: Hemizygote, Genetics (clinical), Hemizygote, MESH: Mutation, Missense, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, MESH: Phosphorylation, Symporters, Brain, MESH: Loss of Function Mutation, MESH: Protein Serine-Threonine Kinases, MESH: Male, Mental Retardation, X-Linked, Maternal Inheritance, MESH: Maternal Inheritance
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::711e752a43d1442b0a91b2645fc1747e
https://doi.org/10.1016/j.gim.2022.05.009 -
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المؤلفون: Jennifer H. Li, Sarah S. Milla, Grace Y. Gombolay
المصدر: Neuropediatrics
مصطلحات موضوعية: Anti-N-Methyl-D-Aspartate Receptor Encephalitis, Ovarian Neoplasms, endocrine system, endocrine system diseases, Adolescent, Infant, Newborn, Teratoma, Infant, General Medicine, Receptors, N-Methyl-D-Aspartate, female genital diseases and pregnancy complications, Article, Young Adult, Child, Preschool, Pediatrics, Perinatology and Child Health, Humans, Female, Neurology (clinical), Child, neoplasms, Retrospective Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0513ea3fc66bbf24cbad8a02bbd1114e
https://pubmed.ncbi.nlm.nih.gov/34872133 -
9دورية أكاديمية
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.