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Various pathogenic factors can lead to oogenesis failure and seriously affect both female reproductive health and fertility. Genetic factors play an important role in folliculogenesis and oocyte maturation but still need to be clarified. Oocyte maturation is a well-organized complex process, regulated by a large number of genes. Pathogenic variants in these genes as well as aneuploidy, defects in mitochondrial genome, and other genetic and epigenetic factors can result in unexplained infertility, early pregnancy loss, and recurrent failures of IVF/ICSI programs due to poor ovarian response to stimulation, oocyte maturation arrest, poor gamete quality, fertilization failure, or early embryonic developmental arrest. In this paper, we review the main genes, as well as provide a description of the defects in the mitochondrial genome, associated with female infertility. [ABSTRACT FROM AUTHOR]

A male factor, commonly associated with poor semen quality, is revealed in about 50% of infertile couples. CFTR gene (Cystic Fibrosis Transmembrane Conduction Regulator) variants are one of the common genetic causes of azoospermia-related male infertility. Notably, the spectrum and frequency of pathogenic CFTR variants vary between populations and geographical regions. In this work, we made an attempt to evaluate the allele frequency (AF) of 12 common CFTR variants in infertile Russian men and healthy individuals from different districts of Russia. Because of the limited number of population-based studies on Russian individuals, we characterized the population AFs based on data from the Registry of Russian cystic fibrosis (CF) patients. In addition to the CF patient registry, we estimated the local frequencies of the same set of variants based on the results of genotyping of CF patients in local biocollections (from St. Petersburg and Yugra regions). AFs of common CFTR variants calculated based on registry and biocollection data showed good concordance with directly measured population AFs. The estimated region-specific frequencies of CFTR variants allowed us to uncover statistically significant regional differences in the frequencies of the F508del (c.1521_1523del; p.Phe508del) and CFTRdele2,3(21kb) (c.54-5940_273+10250del21kb; p.Ser18ArgfsX) variants. The data from population-based studies confirmed previous observations that F508del, CFTRdele2,3(21kb), and L138ins (c.413_415dup; p.Leu138dup)variants are the most abundant among infertile patients, and their frequencies are significantly lower in healthy individuals and should be taken into account during genetic monitoring of the reproductive health of Russian individuals. [ABSTRACT FROM AUTHOR]

Pathogenic CFTR variants cause cystic fibrosis (CF), and CF-related disorders (CF-RD), including bilateral aplasia of the vas deferens (CBAVD). The spectrum of clinical manifestations depends on the CFTR genotype. The frequency and spectrum of the CFTR variants vary between populations and clinical groups. CFTR variants and genotypes were analyzed in Russian men with CF (n = 546) and CBAVD syndrome (n = 125). Pathogenic variants were detected in 93.95% and 39.2% of the CF and CBAVD alleles, respectively. The most frequent c.1521_1523del (F508del; p.Phe508del) variant was found in 541 (49.5%) CF alleles. A total of 162 CFTR genotypes were revealed in CF patients, including 152 homozygous and 394 compound-heterozygous. The most common CF-genotype was F508del/F508del (24.9%). Other frequent CF-genotypes were F508del/3849+10kbC>T, F508del/CFTRdele2,3, and F508del/E92K. CF-causing variants and/or 5T allele were found in 88% of CBAVD patients: 5T/CFTRmut (48.0%), CFTRmut/N (17.6%), CFTRmut/CFTRmut (6.4%), 5T/5T (10.4%), 5T/N (5.6%) and N/N (12.0%), with the most common CBAVD-genotype being F508del/5T (29.6%). The allele frequencies of F508del, CFTRdele2,3 394delTT, and 3849+10kbC>T were significantly higher in CF patients. L138ins/L138ins, 2184insA/E92K, and L138ins/N genotypes were found in CBAVD, but not in CF patients. The results indicate certain differences in the frequency of some CFTR variants and genotypes in Russian CF and CBAVD patients. [ABSTRACT FROM AUTHOR]

Abstract: This paper explores insights and understandings of multilingual dynamics within European-based migrant contexts where Portuguese plays a role. The intermediate position of Portuguese migration in Europe (simultaneously host and sending country) gives Portuguese a bipolar sociolinguistic status at the European scale, both as a ‘dominant’ and ‘non-dominant’ language, useful to use as an analytical springboard. Drawing on linguistic ethnographic work developed in two sites – Portuguese migrant women in London and Eastern European migrant children in Portugal – this paper discusses the tools used to (a) describe the informal emerging and creative multilingual use happening in local configurations of speakers, linguistic ideologies, artifacts, histories and institutions, and (b) explain how this creativity is re-scaled into dominant discourses situated in momentary yet simultaneously long-term historical sociolinguistic configurations, differently narrated by the multiple actors involved. A combined focus on personal trajectories and ‘history in person’, discursive dynamics of recontextualisation and re-scaling and an understanding of the power dynamics in intersubjective spaces helps develop the idea of polycentric speaking positions, affected by local creativities and constraints happening in conflicting historically configured hybrid spaces of verbal interaction. [Copyright &y& Elsevier]

This article aims to explore the multiple uses and consequences of different technologies and infrastructures in the context of migrations and how such uses and consequences inhabit and transform migrants' rights and subjectivities. It reviews relevant literature at the intersection of citizenship, critical migration studies and science and technology studies (STS), focusing in particular on the current debates underway within critical citizenship studies that examine how technologies and infrastructures shape the ability to acts of citizenship. By mobilizing insights from STS, we focus on how these political subjectivities are shaped by certain sociomaterial and epistemic practices. By introducing the notion of material citizenship politics, the article outlines a way to differentiate three different constitutive forms between technologies, infrastructures and citizenship in migrations. Technologies and infrastructures can (1) constrain acts of citizenship in migration and border regimes; (2) constitute contestation and participation over citizenship; or (3) enable and shape alternative acts of citizenship in migration and border regimes. As it provides a theoretical background to the special issue, the article also serves as the introduction to the issue. [ABSTRACT FROM AUTHOR]

(1) Introduction: Pathogenic variants in the CFTR (Cystic Fibrosis Transmembrane conductance Regulator, OMIM: 602421) gene cause Cystic Fibrosis (CF, OMIM: 219700) and CF-related disorders (CF-RD), often accompanied by obstructive azoospermia due to congenital bilateral aplasia of vas deferens (CBAVD, OMIM: 277180) in male patients. The L138ins (c.413_415dup; p. (Leu138dup)) is a mild variant in the CFTR gene that is relatively common among CF-patients in Slavic populations. The frequency of this variant in Russian infertile men has not been sufficiently studied; (2) Materials and Methods: The sample consisted of 6033 Russian infertile men. The patients were tested for 22 common in Russian populations pathogenic variants of the CFTR gene and the IVS9Tn-polymorphic locus of the intron 9. Molecular-genetic studies were performed using amplified fragment length polymorphism (AFLP-PCR), multiplex ligation-dependent probe amplification (MLPA), and nested PCR (for analysis of the IVS9Tn-polymorphic locus); (3) Results: Pathogenic variants in the CFTR were detected in 3.9% of patients. The most frequent variants were F508del and CFTRdele2.3(21kb), accounted for 61.0% and 7.1% of detected variants, respectively. The L138ins variant was detected in 17 (0.28%) individuals: one of them was homozygous, 10 patients were heterozygous, and 6 patients were compound-heterozygous (F508del/L138ins, n = 4; L138ins/N1303K, n = 1; L138ins/5T, n = 1). Two pathogenic CF-causing variants in the CFTR gene were detected in 8 patients, including 7 compound heterozygous (F508del/L138ins, n = 4; F508del/N1303K, n = 1; 2184insA/E92K, n = 1; 3849+10kbC>T/E92K, n = 1) and one homozygous (L138ins/L138ins). The L138ins variant was found in 7 out of 16 (43.75%) chromosomes in six of these patients. The most common pathogenic variant, F508del, was identified in five out of them, in 5 of 16 (31.25%) chromosomes. The allele frequency (AF) of the L138ins variant in the sample has been found to be 0.0014.; (4) Conclusions: The L138ins variant of the CFTR gene is the third most common variant after F508del and CFTRdele2.3(kb) among Russian infertile men. [ABSTRACT FROM AUTHOR]

Written in collaboration - four hands and three disciplinary gazes - and revisiting "Literatura e emigração: poetas emigrantes nos estados de Massachusetts e Rhode Island" (Capinha, 1993), this article illustrates how a literature of/in e/immigration contributes to understand acts of identification and meaning-making in contemporary societies permeated by mobilities. Writing poetry - and poetic writing - allows us the possibility to study spaces of speaking, writing and biographizing that unveil the essentially political nature of lived migrant experience, both singular and collective, subject to juxtaposed, ever changing, ever more unequal and violent social structures. In this text, complexified by the impact of recent migration in the imagination of centres and peripheries within the modern Portuguese State, we stand against static views of language as monoglossic systems that manipulate and control, and call for political attention to languaging in action (poien), as radically local language doings in movement and situated in history. 'Telling oneself again' forges spaces of breathing, where poets/writers/speakers reinvent themselves in-between places and new metaphors. [ABSTRACT FROM AUTHOR]