Transcription factor TCF4: structure, function, and associated diseases by R. R. Savchenko, N. A. Skryabin

“…This further emphasizes the importance of investigating gene functions and molecular pathogenetic pathways associated with single-gene inherited diseases. This review focuses on the TCF4 gene that encodes a transcription factor crucial for nervous system development and functioning. …”
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Development of a patient-reported outcomes tool to monitor changes in joint health and wellbeing for young people with haemophilia B by Bladen Melanie, McDonagh Janet, McLaughlin Paul, Gooding Richard, Holder Kerry-Ann, Thind Sharon, Klooster Brittany, Shields Alan, Turner-Bowker Diane M., Chatterton Kaitlin, Leso Allison, Volpi Connor, Sivasubramaniyam Sujan, Abulizi Jiawula, Khan Nisa

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Distribution and Characteristics of Bacteria Isolated from Cystic Fibrosis Patients with Pulmonary Exacerbation by Soroor Erfanimanesh, Mohammad Emaneini, Mohammad Reza Modaresi, Mohammad Mehdi Feizabadi, Shahnaz Halimi, Reza Beigverdi, Vajiheh Sadat Nikbin, Fereshteh Jabalameli

“…Cystic fibrosis (CF) is an inherited recessive disorder characterized by recurrent and persistent pulmonary infections, resulting in lung function deterioration and early mortality. …”
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Characterization of Patients with Cystic Fibrosis in Multidisciplinary Consultation by Caridad Llull Tombo, Mercedes Fonseca Hernández, Ileana García Rodríguez, Juan Carlos Yanes Macías, Daymí Tió González, Yoandra León Rayas

“…<strong>Foundation:</strong> cystic fibrosis is a multisystemic inherited disorder in children and adults, characterized by obstruction and infection in the respiratory tract and by symptoms and signs of the digestive system with its consequences. …”
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THE SOCIAL PROTEST «WITH CHINESE PARTICULARITY»: THE SHIFTING VECTOR by V. A. Korsun

“…Contemporary partocracy regime of PRC inherited all the negative characteristics of soviet «nomenclature» such as hierarchy career based on loyalty, bureaucracy privileges, special rations and advantages, nepotism, corruption and so on, but has created specific Chinese system of «soft» succession of power from generation to generation. …”
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Fundoscopic Changes in Maroteaux-Lamy Syndrome by Augusto Magalhães, Jorge Meira, Ana Maria Cunha, Raul Jorge Moreira, Elisa Leão-Teles, Manuel Falcão, Jorge Breda, Fernando Falcão-Reis

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The impact of age on genetic risk for common diseases. by Xilin Jiang, Chris Holmes, Gil McVean

“…Inherited genetic variation contributes to individual risk for many complex diseases and is increasingly being used for predictive patient stratification. …”
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USE OF INTERSPECIFIC HYBRIDIZATION IN THE BREEDING OF ADAPTIVE HYBRIDS AND SORTS OF GARDEN CHRYSANTHEMUM (Chrysanthemum morifolium Ramat.) by A. I. Nedoluzhko

“…., which have formed and fixed during evolution, were inherited and manifested in offspring of the multicomponent hybrids and the closely related crosses. …”
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The Importance of Natural Indigo Dye and Its Revitalization and Ethiopian Potential for Indigo Growing by Abera Kechi Kabish, Molla Tadesse Abate, Zelalem Adane Alemar, Solomon Girmay

“…In this regard, natural indigo dye from the indigo plant is getting attention, and thus, it is preferred as good as synthetic indigo dye, owing to its inherited dyeing property. With natural indigo dye, it can be achieved eco-friendly dyeing without the application of mordant attaining commercially acceptable fastness properties. …”
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Organoleptic Quality Attributes and Their Association with Morphological Traits in Arabica Coffee (Coffea arabica L.) Genotypes by Wakuma Merga Sakata, Wosene Gebreselassie Abtew, Weyessa Garedew

“…Therefore, an experiment was conducted to determine the quality attributes of the genotypes and correlate their inherited quality with morphological traits. The experiment was superimposed on five-year-old plants of 17 coffee genotypes during the 2018 cropping season at Teppi and Gemadro sites. …”
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Hereditary Tyrosinemia Type 1 in Jordan: A Retrospective Study by Noor A. Megdadi, Ahmad K. Almigdad, Mo’men O. Alakil, Shahrazad M. Alqiam, Sumaia G. Rababah, Moshera A. Dwiari

“…Hereditary tyrosinemia type 1 (HT1) is a recessively inherited inborn error of metabolism affecting the final step of tyrosine catabolism. …”
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Modified Weights-of-Evidence Modeling with Example of Missing Geochemical Data by Daojun Zhang, Frits Agterberg

“…As an improved WofE model based on LR, modified weights of evidence (MWofE) inherit the advantages of both LR and WofE, i.e., eliminates bias due to lack of CI and can handle missing data as well. …”
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The implication of leaf anatomical structure for the selective breeding of lilacs by L. M. Pshennikova

“…In S. oblata, this trait is inherited down the maternal line. To establish lilac cultivars resistant to fungal diseases, it is advisable to cross the two species (S. oblata and S. vulgaris) or their cultivars using one of S. oblata subspecies as a maternal plant.…”
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The Sociology of Karl Mannheim’s Knowledge and the Methodological Foundations of the History of Socio-Political Ideas by Alexander A. Chanyshev, Vasilisa A. Kuznetsova

“…This significance is determined, firstly, by the critical attitude inherited by Mannheim from the Marxist tradition. In this case, however, criticism is not aimed at simplistically linear “exposure” of the social orientation of ideas, where the content of the latter is explained as a simple function of the author’s predilections and group interests that determine these predilections - and the desired source of the ideological content of the concept, therefore, can be found in the sphere of the “natural” action of common social causes. …”
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Role of CTCF protein in regulating FMR1 locus transcription. by Stella Lanni, Martina Goracci, Loredana Borrelli, Giorgia Mancano, Pietro Chiurazzi, Umberto Moscato, Fabrizio Ferrè, Manuela Helmer-Citterich, Elisabetta Tabolacci, Giovanni Neri

“…Fragile X syndrome (FXS), the leading cause of inherited intellectual disability, is caused by epigenetic silencing of the FMR1 gene, through expansion and methylation of a CGG triplet repeat (methylated full mutation). …”
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Piotr Stolypin and the National question in the Russian Empire in 1906-1911: new trends in Russian historiography by Ryšard Gaidis

“…The collection of subjects and problems, inherited from the Soviet historiography, is reconsidered and reinterpreted, thereby acquiring the form of opposition to the Soviet historiographical tradition. …”
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Vaccines for cancer interception in familial adenomatous polyposis by David E. Johnson, Mary L. Disis

“…Familial adenomatous polyposis (FAP) is an inherited autosomal dominant disorder caused by germline mutations in the adenomatous polyposis coli (APC) gene. …”
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Ainu Representation in the World of Japanese Comics: Shumari and Golden Kamuy Take on the Ruling Narratives of Hokkaidō History by Zsófia Keller

“…To avoid misinterpretation in the analysis of Japanese comics, it is essential to approach them with what Tessa Morris-Suzuki terms historical truthfulness, recognising them as gateways to a complex web of inherited ideas rather than direct representations of the historical periods that they depict. …”
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Research Progress of Flexible Wearable Devices in Rehabilitation Medicine by Zijun HE, Qing ZENG, Ze GONG, Rong CHEN, Hang QU, Shilin LI, Pengcheng LU, Jihua ZOU, Guozhi HUANG

“…The wearable devices made of flexible materials inherit the advantages of flexible materials so that they might make up for the shortcomings of traditional wearable devices and then be widely applied in the field of rehabilitation medicine. …”
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Harlequin Ichthyosis: Case Series by Huriye Ezveci, Sukran Dogru, Fatih Akkus, Kazim Gezginc

“… Objective: Harlequin ichthyosis (HI) is an autosomal-recessive inherited disorder. The incidence is extremely rare and is reported to range from 1/300 000 to 1/1 000 000. …”
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