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Articles by Céline André
A single base pair duplication in the SLC33A1 gene is associated with fetal losses and neonatal lethality in Manech Tête Rousse dairy sheep
INTRODUCTION Most individuals carry roughly 100 loss-of-function alleles in their genome, and among them one to five are predicted to be deleterious (Georges et al., 2019; MacArthur et al., 2012). These variants can cause severe defects, leading to lethality (from the embryonic stage to adulthood) or morphological disorders in the homozygous state. Therefore, the identification of the causal variants is essential for managing these defects.
HER2-Low Luminal Breast Carcinoma Is Not a Homogenous Clinicopathological and Molecular Entity
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Homozygous haplotype deficiency in Manech Tête Rousse dairy sheep revealed a nonsense variant in MMUT gene affecting newborn lamb viability
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A single base pair duplication in SLC33A1 gene causes fetal losses and neonatal lethality in Manech Tete Rousse dairy sheep
Thank you for your interest in spreading the word about bioRxiv. NOTE: Your email address is requested solely to identify you as the sender of this article. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. Message Subject (Your Name) has forwarded a page to you from bioRxiv Message Body (Your Name) thought you would like to see this page from the bioRxiv website.
Homozygous haplotype deficiency in Manech Tête Rousse dairy sheep revealed a nonsense variant in MMUT gene affecting newborn lamb viability
Thank you for your interest in spreading the word about bioRxiv. NOTE: Your email address is requested solely to identify you as the sender of this article. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. Message Subject (Your Name) has forwarded a page to you from bioRxiv Message Body (Your Name) thought you would like to see this page from the bioRxiv website.
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