The genetic control of the day- neutral habit in populations of Fragaria vesca (Rosaceae) in Western Siberia by S. O. Baturin

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Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome using MEGA by Vipan Kumar Sohpal

Subjects: “…molecular evolutionary genetic analysis…”
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A Large PROP1 Gene Deletion in a Turkish Pedigree by Suheyla Gorar, Doga Turkkahraman, Kanay Yararbas

“…On pituitary magnetic resonance, partial empty sella was detected with normal bright spot in all siblings. In genetic analysis, we found a gross deletion involving PROP1 coding region. …”
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Genetic Study In a Pakistani Family Reveals Autosomal Recessive Type of Artemis Deficiency by Saddaf Ayub, Abeerah Zainub, Nida Shafi, Zara Khalid Khan, Lubna Siddique, Syed Irfan Raza

“…Immunological investigations including lymphocyte subset analysis, and serum immunoglobulin levels were performed. Genetic analysis was performed on patients and available parents. …”
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Differentiation of <i>Bos grunniens</i> and <i>Bos taurus</i> based on STR locus polymorphism by K. B. Chekirov, Zh. T. Isakova, V. N. Kipen, M. I. Irsaliev, S. B. Mukeeva, K. A. Aitbaev, G. A. Sharshenalieva, S. B. Beyshenalieva, B. U. Kydyralieva

“…Differentiation of closely related biological species using molecular genetic analysis is important for breeding farm animals, creating hybrid lines, maintaining the genetic purity of breeds, lines and layering. …”
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Space and its form by Александр Раппапорт

“… Space as an object of architectural knowledge and thinking does not yet exist, since no one has done the work of introducing it into the historical and genetic analysis. Nevertheless, the category of space has come into professional use, giving rise to many concepts. …”
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Chemical Composition and Antimicrobial Activity of the Essential Oils of Two Aromatic Plants Cultivated in Morocco (Cinnamomum cassia and Origanum compactum) by Asmae Chahbi, Saâdiya Nassik, Hamid El Amri, Ahmed Douaik, El Haj El Maadoudi, Mohamed Boukharta, El Mestafa El Hadrami

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Evaluation of common COL2A1 gene variants in Iranian patients suspected with Stickler syndrome type I by Fatemeh Abolhasani, Hossein Abdali, Mohammad Kazemi, Bijan Movahedian Attar, Fatemeh Derakhshandeh, Majid Hosseinzadeh

“…Genetic analysis is helpful for the diagnosis of this clinically variable and genetically heterogeneous disorder.…”
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Epidemiological monitoring of avian influenza in the Republic of Crimea in 2019–2020 by D. V. Gadzevich, S. I. Danylchenko, N. V. Vorotilova, M. A. Pasunkina, V. A. Uppe, V. N. Irza, M. S. Volkov, N. G. Zinyakov

“…The comparative genetic analysis of 258 bp nucleic acid sequences of the AIV H gene fragment showed that the identified isolate belongs to the Asian genetic lineage of highly pathogenic AIV subtype H5 (clade 2.3.4.4) associated with the epidemic spread in Asia, Europe, the Middle East and Africa in 2016–2020.…”
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La Ville-de-Montereau by Muriel Berthou Crestey

“…The iconographic study will be compared with the historical context and the textual genetic analysis.…”
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ANALYSIS OF A GENETIC COLLECTION OF TOMATO CULTIVARS AND HYBRID FORMS FOR RESISTANCE TO LEAF MOLD USING DNA MARKERS by I. N. Shamshin, M. V. Maslova, Y. V. Gryazneva

“…A strong lesion was noted on the leaves of only one hybrid. The molecular genetic analysis has shown that among all control samples, only this genotype was a recessive homozygote. …”
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Frameshift variation in the HMG-CoA reductase gene and unresponsiveness to cholesterol-lowering drugs in type 2 diabetes mellitus patients by Esmat Khaleqsefat, Khder Hussein Rasul, Ramiar Kamal Kheder, Sonia Baban, Jamil Baban

“…Biochemical tests were conducted, followed by genetic analysis to identify mutations in the HMGCR gene. …”
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A novel TGFBR2 mutation causes Loeys-Dietz syndrome in a Chinese infant: A case report by Xin Liu, Kaiqing Liu, Lifu Hu, Zixiao Liu, Xinhua Liu, Jiantao Wang

“…Conclusions: Our comprehensive genetic analysis suggested that the p.Glu335_Tyr336delinsAsp variant of TGFBR2 caused aberrant TGF-β signaling and contributed to LDS in the patient.…”
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Le Græculus et la Chananéenne : Salammbô, le roman des traductions by Agnès Bouvier

“…The other translating character in the novel, the heroine herself, practices translation like the art of seduction, until Flaubert, in a writing act that genetic analysis of the drafts can trace, casts on this novel and on its character Babel’s curse, more severe than Tanit’s. …”
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Novel variant of FBN2 in a patient with congenital contractual arachnodactyly by Mina Nakama, Yuki Miwa, Sayaka Manabe, Shigeru Shimamoto, Hidenori Ohnishi

“…We report a case of a boy with suspected Marfan syndrome. Genetic analysis revealed c.3207_3217+9del in a heterozygote form of the fibrillin-2 (FBN2) gene. …”
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Fetal and neonatal cardiac tumor diagnosed as Tuberous Sclerosis associated rhabdomyomas resulting from novel pathogenic missense variant detected in TSC2 gene: A case report by Aya Kawasaki, MD, Hidefumi Tonoki, MD, PhD, Osamu Sasaki, MD, PhD, Yoko Matsushita, MD, PhD, Michiko Watari, MD, PhD, Nobuhiro Takahashi, MD, Satoko Fujieda, MD

“…Here we report a case of a patient with a fetal and neonatal cardiac tumor who underwent a genetic analysis for TS after birth. Multiple fetal cardiac tumors were detected on ultrasonography at 24 weeks, gestation with no other manifestation. …”
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Analysis of the activities of the State Films Fund of Russian Federation in the context of digitalisation by M. I. Kosinova, A. A. Gasilina

“…The study used the method of historical and genetic analysis, descriptive analysis of literature and media materials, qualitative content analysis of documents, reports and other materials, comparative analysis, and secondary analysis of statistical data. …”
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Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders by H. Alshaikh, F. Alsaif, S. Aldukhi

“…However, each of these hereditary conditions possesses a unique genetic mutation, and genetic analysis is thus more useful in the diagnosis of these conditions. …”
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Premature Moustache As Presenting Symptom of Nonclassic Congenital Adrenal Hyperplasia due to 2 Uncommon Mutations of the CYP21A2 Gene by Guy Massa, Philippe Gillis, Marianne Schwartz

“…The endocrine evaluation led to the diagnosis of nonclassic congenital adrenal hyperplasia. Genetic analysis revealed 2 rare mutations of the CYP21A2 gene, the gene encoding for the 21-hydroxylase enzyme: a recently reported R132C mutation in exon 3 and a R339H mutation in exon 8, both reported in the nonclassic CAH. …”
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Beyond the Common Causes of Palmoplantar Keratoderma: Papillon–Lefevre Syndrome with a Unique Mutation by Sanjanaa Srinivasa, Sumedha Ballal, Preetha Tilak, Savitha Murali, Madhukara Jithendriya

“…Here, we report the case of a 45-year-old male, born to a third-degree consanguineous marriage, presenting with hyperkeratotic lesions on palms, soles, and knees from 1 year of age, followed by attrition of teeth from 7 years of age and loss of all teeth by the age of 18 years. Genetic analysis revealed a rare mutation in the cathepsin C gene.…”
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