日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Expanding the Prenatal Phenotypic Spectrum of TRPV6 Variants With Ocular Anomalies

扩大TRPV6变异体与眼部异常相关的产前表型谱

Leyne, Edouard; Martinovic, Jelena; Kamenický, Peter; Linglart, Agnès; Saada, Julien; Benachi, Alexandra; Vivanti, Alexandre J; Bouligand, Jérôme

21 Trainee Abstract Award: Long-term effects of reduced docosahexaenoic acid placental transfer on offspring neurobehavioral outcomes in mice

21 实习生摘要奖:减少二十二碳六烯酸胎盘转运对小鼠后代神经行为结果的长期影响

Horackova, Hana; Zhao, Qiuying; Faulkner, Shakeela; Alvarez, Jennifer; Akiz, Cenk; Liu, Yilin; Crosthwait, Josephine; Dai, Weiye; Santoyo, Danielle; Pham-Chang, Duke; Bhinderwala, Nabeel; Tagliaferro, Thea; Wallace, W Dean; Walia, Saloni; Martinovic, Jelena; Baldauf, Claire; Montagne, Axel; Bonnin, Alexandre; Hernandez, Marta Hita; Barentsen, Kenneth; Bidne, Katie; Henry, Jamie; Dietz, Robert; Jansson, Thomas; Powell, Theresa L

Orchestration of human multi-lineage hematopoietic cell development by humanized in vivo bone marrow models.

利用人源化体内骨髓模型调控人类多系造血细胞发育

Renou Laurent, Sun Wenjie, Friedrich Chloe, Galant Klaudia, Conrad Cecile, Consalus Anne, Plantier Evelia, Schallmoser Katharina, Krisch Linda, Barroca Vilma, Devanand Saryami, Dechamps Nathalie, Reinisch Andreas, Martinovic Jelena, Magnani Alessandra, Faivre Lionel, Lewandowski Daniel, Calvo Julien, Perie Leila, Kosmider Olivier, Pflumio Françoise

Histologic and molecular features shared between antibody-mediated rejection of kidney allografts and chronic histiocytic intervillositis support common pathogenesis.

抗体介导的肾移植排斥反应与慢性组织细胞性绒毛间炎在组织学和分子特征上存在共同之处,这支持了二者共同的发病机制

Albersammer Léonie, Leon Juliette, Martinovic Jelena, Dagobert Jessy, Lebraud Emilie, Bessières Bettina, Loeuillet Laurence, Eloudzeri Maëva, Vivanti Alexandre J, Dumery Grégoire, Marchaudon Valérie, Antal Cristina, Korganow Anne-Sophie, Quibel Thibaud, Costedoat-Chalumeau Nathalie, Tsatsaris Vassilis, Benachi Alexandra, Zuber Julien, Rabant Marion

Chronic Oral D-Galactose Induces Oxidative Stress but Not Overt Organ Dysfunction in Male Wistar Rats

长期口服D-半乳糖可诱导雄性Wistar大鼠产生氧化应激,但不会引起明显的器官功能障碍。

Martinovic, Jelena; Gusevac Stojanovic, Ivana; Nesic, Sladjan; Todorovic, Ana; Bobic, Katarina; Stankovic, Sanja; Drakulic, Dunja

Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla

编码 Crumbs 细胞极性复合物组分 2 的 CRB2 基因的双等位基因变异会导致非交通性脑积水,这是由于中脑导水管和延髓中央管闭锁所致。

Tessier, Aude; Roux, Nathalie; Boutaud, Lucile; Lunel, Elodie; Hakkakian, Leila; Parisot, Mélanie; Garfa-Traoré, Meriem; Ichkou, Amale; Elkhartoufi, Nadia; Bole, Christine; Nitschke, Patrick; Amiel, Jeanne; Martinovic, Jelena; Encha-Razavi, Férechté; Attié-Bitach, Tania; Thomas, Sophie

Prolonged Zaleplon Treatment Increases the Expression of Proteins Involved in GABAergic and Glutamatergic Signaling in the Rat Hippocampus.

长期使用扎来普隆治疗可增加大鼠海马中参与 GABA 能和谷氨酸能信号传导的蛋白质的表达

Martinovic Jelena, Samardzic Janko, Zaric Kontic Marina, Ivkovic Sanja, Dacic Sanja, Major Tamara, Radosavljevic Milica, Svob Strac Dubravka

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

在胎儿队列研究中发现科芬-西里斯综合征表型谱的新部分

van der Sluijs, Pleuntje J; Joosten, Marieke; Alby, Caroline; Attié-Bitach, Tania; Gilmore, Kelly; Dubourg, Christele; Fradin, Mélanie; Wang, Tianyun; Kurtz-Nelson, Evangeline C; Ahlers, Kaitlyn P; Arts, Peer; Barnett, Christopher P; Ashfaq, Myla; Baban, Anwar; van den Born, Myrthe; Borrie, Sarah; Busa, Tiffany; Byrne, Alicia; Carriero, Miriam; Cesario, Claudia; Chong, Karen; Cueto-González, Anna Maria; Dempsey, Jennifer C; Diderich, Karin E M; Doherty, Dan; Farholt, Stense; Gerkes, Erica H; Gorokhova, Svetlana; Govaerts, Lutgarde C P; Gregersen, Pernille A; Hickey, Scott E; Lefebvre, Mathilde; Mari, Francesca; Martinovic, Jelena; Northrup, Hope; O'Leary, Melanie; Parbhoo, Kareesma; Patrier, Sophie; Popp, Bernt; Santos-Simarro, Fernando; Stoltenburg, Corinna; Thauvin-Robinet, Christel; Thompson, Elisabeth; Vulto-van Silfhout, Anneke T; Zahir, Farah R; Scott, Hamish S; Earl, Rachel K; Eichler, Evan E; Vora, Neeta L; Wilnai, Yael; Giordano, Jessica L; Wapner, Ronald J; Rosenfeld, Jill A; Haak, Monique C; Santen, Gijs W E

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

未确诊先天性多发性关节挛缩症的表型谱和基因组学

Laquerriere, Annie; Jaber, Dana; Abiusi, Emanuela; Maluenda, Jérome; Mejlachowicz, Dan; Vivanti, Alexandre; Dieterich, Klaus; Stoeva, Radka; Quevarec, Loic; Nolent, Flora; Biancalana, Valerie; Latour, Philippe; Sternberg, Damien; Capri, Yline; Verloes, Alain; Bessieres, Bettina; Loeuillet, Laurence; Attie-Bitach, Tania; Martinovic, Jelena; Blesson, Sophie; Petit, Florence; Beneteau, Claire; Whalen, Sandra; Marguet, Florent; Bouligand, Jerome; Héron, Delphine; Viot, Géraldine; Amiel, Jeanne; Amram, Daniel; Bellesme, Céline; Bucourt, Martine; Faivre, Laurence; Jouk, Pierre-Simon; Khung, Suonavy; Sigaudy, Sabine; Delezoide, Anne-Lise; Goldenberg, Alice; Jacquemont, Marie-Line; Lambert, Laetitia; Layet, Valérie; Lyonnet, Stanislas; Munnich, Arnold; Van Maldergem, Lionel; Piard, Juliette; Guimiot, Fabien; Landrieu, Pierre; Letard, Pascaline; Pelluard, Fanny; Perrin, Laurence; Saint-Frison, Marie-Hélène; Topaloglu, Haluk; Trestard, Laetitia; Vincent-Delorme, Catherine; Amthor, Helge; Barnerias, Christine; Benachi, Alexandra; Bieth, Eric; Boucher, Elise; Cormier-Daire, Valerie; Delahaye-Duriez, Andrée; Desguerre, Isabelle; Eymard, Bruno; Francannet, Christine; Grotto, Sarah; Lacombe, Didier; Laffargue, Fanny; Legendre, Marine; Martin-Coignard, Dominique; Mégarbané, André; Mercier, Sandra; Nizon, Mathilde; Rigonnot, Luc; Prieur, Fabienne; Quélin, Chloé; Ranjatoelina-Randrianaivo, Hanitra; Resta, Nicoletta; Toutain, Annick; Verhelst, Helene; Vincent, Marie; Colin, Estelle; Fallet-Bianco, Catherine; Granier, Michèle; Grigorescu, Romulus; Saada, Julien; Gonzales, Marie; Guiochon-Mantel, Anne; Bessereau, Jean-Louis; Tawk, Marcel; Gut, Ivo; Gitiaux, Cyril; Melki, Judith

Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia

对 47 例先天性膈疝胎儿和新生儿进行拷贝数变异分析

Boisson, Marie; Cordier, Anne-Gael; Martinovic, Jelena; Receveur, Aline; Mouka, Aurélie; Diot, Romain; Egoroff, Catherine; Esnault, Geoffroy; Drévillon, Loïc; Benachi, Alexandra; Tachdjian, Gérard; Tosca, Lucie