Interruption of mitochondrial symbiosis is associated with the development of osteoporosis by Haoling Zhang, Haoling Zhang, Haoling Zhang, Rui Zhao, Xuemei Wang, Yaqian Qi, Doblin Sandai, Wei Wang, Zhijing Song, Zhijing Song, Qiudong Liang

“…In this paper, we reviewed the mechanism of mitochondrial intersymbiosis interruption in OP, discussed the relationship between mitochondrial intersymbiosis interruption and bone marrow mesenchymal stem cells, osteoblasts and osteoclasts, as well as the inheritance and adaptation in the evolutionary process, and prospected the future research direction to provide new ideas for clinical treatment.…”
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A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity by Paal Skytt Andersen, Paula Louise Hedley, Stephen P. Page, Petros Syrris, Johanna Catharina Moolman-Smook, William John McKenna, Perry Mark Elliott, Michael Christiansen

“…Both recessive and dominant patterns of inheritance have been suggested. We studied a large family with a 38-year-old asymptomatic HCM-affected male referred because of a murmur. …”
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Pangenome mining of the Streptomyces genus redefines species’ biosynthetic potential by Omkar S. Mohite, Tue S. Jørgensen, Thomas J. Booth, Pep Charusanti, Patrick V. Phaneuf, Tilmann Weber, Bernhard O. Palsson

“…This synteny suggests that vertical inheritance is a major factor in the diversification of BGCs. …”
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Development of large-fruited bird cherry cultivars on the basis of wild species for northern and eastern regions of Russia by V. S. Simagin, A. V. Lokteva

“…It can be explained by the polygenic nature of fruit weight inheritance. The samples with the largest fruits had an average fruit weight of 1.4–1.5 g and maximum weight of 1.8–1.9 g. …”
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Study of Phenotypic and Molecular Approaches of Potyvirus plumpoxi Resistance Evaluation in New Czech Apricot Hybrids by Eliška Zezulová, Tomáš Kiss, Kateřina Baránková, Tomáš Nečas

“…However, discrepancies in hybrid resistance evaluation highlight the complexity of inheritance and the potential errors in genotyping. …”
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A Case of Rafiq Syndrome (MAN1B1-CDG) in a Palestinian Child, With Brief Literature Review of 44 Cases by Reema Iskafi MD, Bahaa AbuRahmeh MD, Roa’a Aljuneidi MD, Hidaya AlShweiki MD, Siraj Abdelnabi MD, Anas Abukhalaf MBBS, Bara’ Maraqa PBoS

“…The disorder follows an autosomal recessive pattern of inheritance and typically presents with specific facial dysmorphism, intellectual disability, developmental delay, obesity, and hypotonia. …”
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Autism spectrum disorder: definition, global epidemiology, prevalence in Poland and worldwide, and heredity by Martyna Zakrocka, Marta Gruszka, Paulina Polańska, Maria Kubicka

“…We selected the articles according to keywords such as “ASD”, “autism”, “history of autism”, “epidemiology”, “inheritance”, “genetic”. The articles we used were published from 1943, mainly 2019-2024. …”
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The Paradox of Indonesia Cyberspace Policy and Cooperation: Neoclassical Realism Perspective by Muhammad Abdurrohim, Indah Kumalasari, Fathur Rosy

“…The Indonesian government still faced instability at the domestic level to identify the category of threats toward the regime due to the inheritance of the authoritarian regime government model it experienced before. …”
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Recessive transition of rural residential land use from the perspective of value co-creation: A case study of Yiwu City, Zhejiang by ZHANG Cong, LONG Hualou, FENG Dedong

“…[Results] (1) Value co-creation of ural residential land follows the process model of “value consensus-value execution-value win-win” and the operational paradigm of “subject interaction - capacity embedding - benefit sharing”, driving the “element integration - structure reorganization - function optimization” of rural residential land use system, resulting in the dynamic evolution of diverse values such as residential security, economic property, production and operation, ecological protection, and cultural inheritance, and achieving the recessive rural residential land use transition. (2) Yiwu’s practice path of guiding multiple stakeholders to interact collaboratively, constructing “value consensus” for rural residential land, driving with multiple forces, and implementing “value execution” for rural residential land through multi-dimensional rule interaction is a successful model for realizing the recessive rural residential land use transformation through value co-creation. (3) Through the practice of value co-creation, Yiwu has achieved a transformation of the functional value of rural residential land from residential security orientation to economic property orientation, and then to a comprehensive and coordinated approach that encompasses residential security, production and operation, economic assets, and ecological protection, etc. …”
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Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family by Y. N. Khan, M. Imad A.M. Mahmud, N. Othman, H. M. Radzuan, S. Basit

“…Family pedigree shows an autosomal recessive mode of inheritance. DNA was extracted from the blood samples of six members of the family. …”
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Genetics of Primary Adrenal Insufficiency Beyond CAH in Saudi Arabian Population by Mohamed H. Al‐Hamed, Alya Qari, Lamya Alrayes, Mohammed Alotaibi, Zainab Al Masseri, Afaf Alotaibi, Abdullah AlAshwal, Zuhair N. AlHassnan, Afaf Alsagheir

“…Consanguinity can impact the detection of recessively inherited genes. Here, we report families with PAI in a consanguineous population of Saudi Arabia. …”
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Modern classification and molecular-genetic aspects of osteogenesis imperfecta by A. R. Zaripova, R. I. Khusainova

“…Osteogenesis imperfecta occurs in both men and women, the disease is inherited in both autosomal dominant and autosomal recessive types, there are sporadic cases of the disease due to de novomutations, as well as X-linked forms. …”
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Exploration of the molecular mechanism behind a novel natural genic male-sterile mutation of 1205A in Brassica napus by Lijing Xiao, Jinze Zhang, Shaomin Guo, Hairun Jin, Qingjing Ouyang, Xu Long, Zhongbin Yan, Entang Tian

“…Cytological investigations reveal that the mutation occurs at the early microspore stage, resulting in premature degradation of pollen. Through inheritance analysis, linkage mapping, and bulked-segregant analysis sequencing (BSA-Seq), a single gene locus, designated Bna1205ams1, was identified within the QTL region on chrC03 (15.36–18.90 Mb). …”
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An association study of polymorphisms in the P2RX7 gene in an Iranian population with the risk of type 2 diabetes mellitus by Homa Noori, Majid Rajabian, Mahdi Majidpour, Mahboobeh Sabeti Akbar-Abad, Ramin Saravani

“…TT + CC) and Allelic (C vs. T) inheritance models increased T2DM risk by 2.81, 2.94, 1.62, and 2.20 folds, respectively. …”
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Toward the calibration of 2D thermomechanical simulations of magma poor passive continental margins: method, validation and case example by Perron, Paul, Le Pourhiet, Laetitia, Jourdon, Anthony, Cornu, Tristan, Gout, Claude

“…Acknowledging structural inheritance as a form of kinematic forcing in the models, and recognizing the challenge of anticipating and identifying all inherited geological structures present before rifting, a new modeling approach was devised. …”
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Electroencephalographic and Epilepsy Findings in ZNF711 Variants: A Case Series of Two Siblings by Michele Minerva, Lorenzo Perilli, Samanta Carbone, Margherita Maria Rossi, Federica Lotti, Luisa Lonoce, Maria Rosaria Curcio, Salvatore Grosso

“…Both children underwent various genetic testing and counselling, including an extended next-generation sequencing (NGS) panel, revealing a hemizygous c.657C > G pathogenic variant in the ZNF711 gene from maternal inheritance. Conclusions: This case expands the clinical range of ZNF711 variants by highlighting epilepsy as a potential comorbidity and suggesting other possible causal candidates for generalized epilepsy. …”
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Impact of predictive selection of LbCas12a CRISPR RNAs upon on‐ and off‐target editing rates in soybean by Linda Rymarquis, Chenxi Wu, Diane Hohorst, Miguel Vega‐Sanchez, Thomas E. Mullen, Vijetha Vemulapalli, Douglas R. Smith

“…In addition, edits at off‐target sites have lower inheritance rates than on‐target edits, suggesting that they occur later in the plant's lifecycle. …”
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Clinical Epidemiological Look at Patients with Congenital Heart Disease: a Study that has Become a Priority by Jan O´neil González Ramos, Nancy González Vales, Eida María Mena Albernal, Elsy Roxana Geroy Moya, Nicolás Ramón Cruz Pérez, Annia Quintana Marrero

“…The maternal risk factor with the highest incidence was arterial hypertension, the most frequent inheritance and presentation was the murmur. Surgery was the predominant form of resolution, genetic diseases were the most frequent fetal risks. …”
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Monoallelic variants resulting in substitutions of MAB21L1 Arg51 Cause Aniridia and microphthalmia. by Hildegard Nikki Hall, Hemant Bengani, Robert B Hufnagel, Giuseppe Damante, Morad Ansari, Joseph A Marsh, Graeme R Grimes, Alex von Kriegsheim, David Moore, Lisa McKie, Jamalia Rahmat, Catia Mio, Moira Blyth, Wee Teik Keng, Lily Islam, Meriel McEntargart, Marcel M Mannens, Veronica Van Heyningen, Joe Rainger, Brian P Brooks, David R FitzPatrick

“…These mutations occurred de novo in 3/5 families, with the remaining families being compatible with autosomal dominant inheritance. Mice engineered to carry the p.Arg51Leu change showed a highly-penetrant optic disc anomaly in heterozygous animals with severe microphthalmia in homozygotes. …”
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Phytoalexin deficient 4 is associated with the lesion mimic trait in watermelon clalm mutant (Citrullus lanatus) by Jiale Shi, Congji Yang, Yuanyuan Qin, Qingqing Liu, Shengqi Hua, Defeng Wu, Wei Dong

“…In this study, we tested a seven-generation family to determine the inheritance and genetic basis of this trait. As revealed by analysis of the lesion mimic mutant clalm, this trait is controlled by a single dominant gene. …”
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