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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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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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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Inverse Modeling of Nonlinear Artificial Muscle Using Polynomial Parameterization and Particle Swarm Optimization by Mohd Azuwan Mat Dzahir, Shin-ichiroh Yamamoto

“…Apart from this, it also inherits frictional presliding behavior with nonlocal memory effect. …”
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Compatible bedfellows: Enriching grammar pedagogical tasks with cognitive linguistics to teach present simple vs. progressive by Mojtaba Maghsoudi, Abolfazl Khodamoradi

“…The cognitive group (N = 18) received cognitive linguistic explanations followed by examples indicating inherited epistemic contingency in English present progressive tense (including, current ongoingness, historical present progressive, future present progressive, temporary validity, duration, iteration, repetition, and modality) and structural construal indicated by present simple. …”
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Bilge Kağan Hazinesinin Gün Yüzüne Çıkarılması: Bilge Kağan Anıt Alanı Kazı Çalışmaları by Kürşat KOÇAK, L. Gürkan GÖKÇEK

“…The Göktürk goverment declared independence in 682 in the leadership of Kutlug and Tonyukuk after 40 years captivity following the collapse in 634 because Bilge Kağan and Kül Tigin were at small ages Kapgan Kağan’s ascended the throne after Kutlug Kağan’s death. Later İnel Kağan inherited the throne. Bilge Kağan and Kül Tigin came to power by staging a coup in 716. …”
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Assessment of Developmental Prosopagnosia in an Individual with Tourette Syndrome and Attention Deficit Hyperactivity Disorder: A Case Report by Petter Espeseth Emhjellen, Randi Starrfelt, Rune Raudeberg, Bjørnar Hassel

“…This suggests that, in this case, the conditions were likely inherited through different genetic pathways. Conclusions: Proper assessment of face recognition problems, which includes a broad spectrum of clinical assessment tools, could help patients develop awareness and acceptance of themselves and their difficulties, and could serve as a basis for the development of clinical interventions. …”
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A Lexicon-Based Framework for Mining and Analysis of Arabic Comparative Sentences by Alaa Hamed, Arabi Keshk, Anas Youssef

“…Mining and analyzing Arabic text have been a big challenge due to many complications inherited in Arabic language. Although, many research studies have already investigated the Arabic text sentiment analysis problem, this paper investigates the specific research topic that addresses Arabic comparative opinion mining. …”
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An Assessment on Balkan Historiography by Abdulkadir Macit

“…In addition to their own originality in historiography, Muslims inherited the accumulation of ancient civilizational basins such as Hijaz, Bilad al-Sham, Egypt, Maghreb, Andalusia, Iraq, Iran, Sindh and Mawara' al-Nahr. …”
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Surfing with the tide: Real estate as a hedge against inflation by Malović Marko, Roganović Miloš

“…Also, the aim of the paper is to compare the real estate protective potential against inflation with the performance of stocks, bonds and gold in conserving inherited purchasing power.…”
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Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome by Thi Kim Lien Nguyen, Van Dem Pham, Thu Huong Nguyen, Trung Kien Pham, Thi Quynh Huong Nguyen, Huy Hoang Nguyen

“…Congenital nephrotic syndrome, a rare and severe disease, is inherited as an autosomal recessive trait. The disease manifests shortly after birth and occurs predominantly in families of Finnish origin but has now been observed in all countries and races. …”
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Recurrence of Thrombotic Thrombocytopenic Purpura after mRNA-1273 COVID-19 Vaccine Administered Shortly after COVID-19 by Korin Karabulut, Ana Andronikashvili, Ahmet Hakki Kapici

“…It is characterized by microangiopathic hemolytic anemia and thrombocytopenia with the development of microthrombi caused by inherited or acquired deficiency of the von Willebrand factor-cleaving protease ADAMTS13 and resulting end-organ damage. …”
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Prediction of the Sex-Associated Genomic Region in Tunas (Thunnus Fishes) by Yoji Nakamura, Kentaro Higuchi, Kazunori Kumon, Motoshige Yasuike, Toshinori Takashi, Koichiro Gen, Atushi Fujiwara

“…The genome-wide mapping of previously resequenced data indicated that, among the functionally annotated genes, only this gene, named sult1st6y, was paternally inherited in the males of Pacific bluefin tuna. We reviewed the RNA-seq data of southern bluefin tuna (T. maccoyii) in the public database and found that sult1st6y of southern bluefin tuna was expressed in all male testes, but absent or suppressed in the female ovary. …”
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Study on early inflorescence development in bread wheat (T. aestivum L.) lines with non-standard SCR-morphotype by O. B. Dobrovolskaya, A. A. Krasnikov, K. I. Popova, P. Martinek, N. Watanabe

“…It was shown that SCR is inherited as a dominant monogenic trait; its expression can be modified by genotypic background. …”
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Quality of Life in Wilson’s Disease: A Systematic Literature Review by Chakrapani Balijepalli, Kevin Yan, Lakshmi Gullapalli, Stephane Barakat, Helene Chevrou-Severac, Eric Druyts

“…**Background:** Wilson’s disease (WD) is a rare inherited genetic disorder characterized by the progressive accumulation of copper in the brain, liver, and other major organ systems. …”
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Case Study: Analyzing CFTR Mutations and SNPs in Pulmonary Fibrosis Patients with Unclear Symptoms by Sahar Yousaf, null Sumaira, Iqbal Bano, Atia Rehman, Samra Kousar, Muhammad Usman Ghani, Mariam Shahid

“…Cystic fibrosis (CF) is a genetic monogenic disorder inherited in an autosomal recessive manner, marked by persistent airway infections in the endobronchial region. …”
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