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

Candida albicans releases a peptide from the Rbt1 protein to promote its invasion into the gut epithelium

白色念珠菌会从 Rbt1 蛋白中释放一种肽,以促进其侵入肠道上皮细胞。

Bègue, Hervé; Ducreux, Amandine; Paradis, Tracy; Loiselet, Alicia; Mourer, Thierry; Lucchi, Géraldine; Kieffer-Jaquinod, Sylvie; Coute, Yohann; Hube, Bernhard; Theodorou, Ilias; Thenet, Sophie; Gillet, Benjamin; Hughes, Sandrine; Lapaquette, Pierre; Basmaciyan, Louise; Bachellier-Bassi, Sophie; d'Enfert, Christophe; Bon, Fabienne; Dalle, Frédéric

Severe Respiratory and Swallowing Disorders in Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease Type 1: Two Cases

婴儿期起病的多系统神经、内分泌和胰腺疾病1型伴严重呼吸和吞咽障碍:两例报告

Berling, Edouard; Latour, Philippe; Loiselet, Klervie; Guémy, Clément; Vidoni, Léo; Romero, Norma B; Lacene, Emmanuelle; Evangelista, Teresinha; Stojkovic, Tanya

NON-CREDIBLE ADOLESCENT SURVEY RESPONSES AND LATER-IN-LIFE ALZHEIMER’S DISEASE AND RELATED DISORDERS

不可信的青少年调查回复与成年后阿尔茨海默病及相关疾病的关系

Verrelli, Brian C; McDonald, John H; Argyropoulos, George; Destro-Bisol, Giovanni; Froment, Alain; Drousiotou, Anthi; Lefranc, Gerard; Helal, Ahmed N; Loiselet, Jacques; Tishkoff, Sarah A; Strombotne, K; Horner, E; Walters, E; Lapham, S J

Towards high-resolution laser ionization spectroscopy of the heaviest elements in supersonic gas jet expansion

迈向超音速气体射流膨胀中最重元素的高分辨率激光电离光谱研究

Ferrer, R; Barzakh, A; Bastin, B; Beerwerth, R; Block, M; Creemers, P; Grawe, H; de Groote, R; Delahaye, P; Fléchard, X; Franchoo, S; Fritzsche, S; Gaffney, L P; Ghys, L; Gins, W; Granados, C; Heinke, R; Hijazi, L; Huyse, M; Kron, T; Kudryavtsev, Yu; Laatiaoui, M; Lecesne, N; Loiselet, M; Lutton, F; Moore, I D; Martínez, Y; Mogilevskiy, E; Naubereit, P; Piot, J; Raeder, S; Rothe, S; Savajols, H; Sels, S; Sonnenschein, V; Thomas, J-C; Traykov, E; Van Beveren, C; Van den Bergh, P; Van Duppen, P; Wendt, K; Zadvornaya, A

Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects

家族性地中海热患者的淀粉样变性:与MEFV基因型、SAA1和MICA多态性效应的相关性

Medlej-Hashim, Myrna; Delague, Valérie; Chouery, Eliane; Salem, Nabiha; Rawashdeh, Mohammed; Lefranc, Gérard; Loiselet, Jacques; Mégarbané, André

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22

耳蜗蛋白(Otoancorin)是一种内耳蛋白,仅存在于感觉上皮顶端表面与其上覆无细胞凝胶之间的界面处。常染色体隐性遗传性耳聋 DFNB22 中,耳蜗蛋白存在缺陷。

Zwaenepoel, Ingrid; Mustapha, Mirna; Leibovici, Michel; Verpy, Elisabeth; Goodyear, Richard; Liu, Xue Zhong; Nouaille, Sylvie; Nance, Walter E; Kanaan, Moien; Avraham, Karen B; Tekaia, Fredj; Loiselet, Jacques; Lathrop, Marc; Richardson, Guy; Petit, Christine

Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene

黎巴嫩人群中常染色体隐性非综合征性听力损失:30delG突变的患病率以及连接蛋白26 (GJB2)基因中两个新突变的报告

Mustapha, M; Salem, N; Delague, V; Chouery, E; Ghassibeh, M; Rai, M; Loiselet, J; Petit, C; Mégarbané, A

Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene

在一个黎巴嫩近亲结婚的大家族中,将常染色体隐性遗传性脱髓鞘性夏科-马里-图斯病的新基因位点定位到19q13.1-13.3:排除MAG作为候选基因

Delague, V; Bareil, C; Tuffery, S; Bouvagnet, P; Chouery, E; Koussa, S; Maisonobe, T; Loiselet, J; Mégarbané, A; Claustres, M

Further refinement of Pendred syndrome locus by homozygosity analysis to a 0.8 cM interval flanked by D7S496 and D7S2425

通过纯合性分析进一步将Pendred综合征基因位点精确定位到D7S496和D7S2425之间的0.8 cM区间。

Mustapha, M; Azar, S T; Moglabey, Y B; Saouda, M; Zeitoun, G; Loiselet, J; Slim, R