Castric, Vincent Batista, Rita Carré, Amélie Mousavi, Soraya Mazoyer, Clément Godé, Cécile Gallina, Sophie Ponitzki, Chloé Theron, Anthony Bellec, Arnaud
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In flowering plants, outcrossing is commonly ensured by self -incompatibility (SI) systems. These can be homomorphic (typically with many different allelic specificities) or can accompany flower heteromorphism (mostly with just two specificities and corresponding floral types). The SI system of the Oleaceae family is unusual, with the long-term mai...
Litite, P. Lebughe; Westhovens, R.; 8450; Nkodila, A.; Malemba, J.J.; de Vlam, K.; 58508;
OBJECTIVE: To develop and validate a screening tool to identify patients with a high likelihood for Spondyloarthritis (SpA) in the Democratic Republic of the Congo (DR Congo). METHODS: The development of the SpA Screening questionnaire in Sub Saharian Africa (SpASSS) questionnaire followed 3 steps: The item generation was carried out by a systemati...
Vanden Abeele, Samuel; Matvijev, Katarina; Hardy, Olivier J.; Assumani, Dieu-Merci; Ilondea, Bhely Angoboy; Beeckman, Hans; Bouka, Gael U.D.; Boupoya, Clay Archange; Deklerck, Victor; Flot, Jean-Francois;
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status: published
Zhang, Qian Pizzorno, Andrés Miorin, Lisa Bastard, Paul Gervais, Adrian Le Voyer, Tom Bizien, Lucy Manry, Jeremy Rosain, Jérémie Philippot, Quentin
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Published in
The Journal of experimental medicine
Autoantibodies neutralizing type I interferons (IFNs) can underlie critical COVID-19 pneumonia and yellow fever vaccine disease. We report here on 13 patients harboring autoantibodies neutralizing IFN-α2 alone (five patients) or with IFN-ω (eight patients) from a cohort of 279 patients (4.7%) aged 6-73 yr with critical influenza pneumonia. Nine and...
Ni, Meng; Yi, Xiaofang; Wang, Qin; Wang, Juan; Wang, Shuang; Liu, Liwang; 83644; Xu, Liang; Wang, Yan;
Radish is a typical self-incompatible crop. The rapid and accurate identification of S haplotypes can circumvent the blindness of the hybrid combination process, which is critical in radish heterosis utilization and the breeding of new varieties. In this study, based on the gene sequence which encodes the S-locus receptor kinase (SRK) of radish, an...
Cornelis, Stéphanie S Runhart, Esmee H Bauwens, Miriam Corradi, Zelia De Baere, Elfride Roosing, Susanne Haer-Wigman, Lonneke Dhaenens, Claire-Marie Vulto-van Silfhout, Anneke T Cremers, Frans P M
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Published in
American journal of human genetics
Recurrence risk calculations in autosomal recessive diseases are complicated when the effect of genetic variants and their population frequencies and penetrances are unknown. An example of this is Stargardt disease (STGD1), a frequent recessive retinal disease caused by bi-allelic pathogenic variants in ABCA4. In this cross-sectional study, 1,619 A...
Ghodsi, Maryam Keshtkar, Abbas Ali Razi, Farideh Mohammad Amoli, Mahsa Nasli-Esfahani, Ensieh Zarrabi, Fariba Khashayar, Patricia Khajavi, Alireza Larijani, Bagher Mohajeri-Tehrani, Mohamad Reza
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Published in
Journal of diabetes and metabolic disorders
This study aims to analyze the association between VDR gene polymorphism and the occurrence of "low bone density (LBD)/osteopenia/osteoporosis" or LBDOO in type 2 diabetes (T2D) patients among a clustered population in northwest of Iran. The studied VDR gene polymorphism included ApaI (rs7975232), BsmI (rs1544410), FokI (rs2228570), EcoRV (rs451603...
Liu, Timing Wang, Furene S Cheah, Felicia SH Gu, Yanghong Shaw, Marie Law, Hai-Yang Tay, Stacey KH Lee, Caroline G Nelson, David L Gecz, Jozef
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10.1016/j.jmoldx.2021.04.015 / JOURNAL OF MOLECULAR DIAGNOSTICS / 23 / 8 / 941-951
An, J Do, AR Kang, HY Kim, WJ Lee, S Lee, J-H Song, W-J Kwon, H-S Cho, YS Moon, H-B
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Purpose Although genome-wide association studies (GWASs) represent the most powerful approach for identifying genes that influence asthma, to date, no studies have established genetic susceptibility to asthma in the Korean population. This study aimed to identify genetic variants associated with adult Korean asthmatics and compare them with the sig...
Andrieu, Nadine Noguès, Catherine
Published in
Genetics in Medicine
PurposeWe assessed the associations between population-based polygenic risk scores (PRS) for breast (BC) or epithelial ovarian cancer (EOC) with cancer risks for BRCA1 and BRCA2 pathogenic variant carriers.MethodsRetrospective cohort data on 18,935 BRCA1 and 12,339 BRCA2 female pathogenic variant carriers of European ancestry were available. Three ...