Kola Peninsula Neolithic by Evgeniy M. Kolpakov, Alevtina M. Kiseleva, Anton I. Murashkin, Vladimir Ya. Shumkin

“…Structurally complicated dwellings, recessed up to 1 m deep, became common. Most of the finds, made of bone, horn and stone, belong to this culture. …”
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A Framework for Developing Biodiversity Conservation Networks Based on Morphological Spatial Pattern Analysis and the Maximum Entropy Model: A Case Study of the Jianghan Plain, Chi... by Xiaohua Guo, Chang Liu, Shibo Bi, Xuewen Zhang

“…Our findings indicated the following: (1) The Jianghan Plain hosts 21 major ecological sources, primarily natural water bodies at the plain’s edge, which can be classified into five primary and 16 secondary sources based on biodiversity grades. (2) The recessive corridors, comprising 10 primary and 95 secondary ones, are mainly concentrated in the central Jianghan Plain, with primary corridors located centrally and westward, characterized by a large overall span. (3) Changhu Lake and Honghu Lake, two critical water bodies with high-quality habitats and significant biodiversity, were identified as key ecological nodes from the ecological sources, bridging and guiding the central and southern corridors. (4) Based on the ecological network distribution and key nodes and corridors, a “three zones, three belts, and two points” strategy was proposed for optimizing the Jianghan Plain’s ecological network. …”
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Identification and development of source material for breeding early bushy and short-vined cultivars of <i>Cucurbita moschata</i> Duch. ex Poir. by A. G. Elatskova

“…Bushiness is inherited monogenetically and controlled by the recessive bu (bush) gene. Identified for breeding were early (93–95 days) bushy lines (KL) with a stem length of 0.8–1.2 m: KL 648, KL 652 and KL 656. …”
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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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Aggressively scaled T-Gated GaN-on-silicon RF power HEMT featuring step graded SRL-AlGaN buffer for next generation broad band power amplifiers by A Akshaykranth, J Ajayan, Sandip Bhattacharya, D Nirmal, Santhosh Paramasivam, Gianluca Gatto, Amit Kumar

“…The effect of gate length (LG), gate recess (GR), work function, gate-to-source (LGS) length scaling, and gate-to-drain (LGD) length scaling was studied. …”
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Interpreting Variants of Uncertain Significance in PCD: Abnormal Splicing Caused by a Missense Variant of DNAAF3 by Haixia Zheng, Chongsheng Cheng, Miao He, Wangji Zhou, Yixuan Li, Jinrong Dai, Ting Zhang, Kai‐Feng Xu, Xue Zhang, Xinlun Tian, Yaping Liu

“…ABSTRACT Background Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disorder characterized by dysfunction of motile cilia. …”
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Round Window Accessibility Prediction in Cochlear Implant Surgery by Salah-eddine Youbi, Omar Oulghoul, Youssef Lakhdar, Atmane Zaroual, Mohamed Chehbouni, Othmane Benhoummad, Youssef Rochdi, Abdelaziz Raji

“…Background: Clear identification of the round window (RW) through the facial recess is a key surgical step for successful cochlear implantation (CI) surgery, which may be very challenging in some cases. …”
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Genotypic Spectrum in a Cohort of Sri Lankan Patients With Homocystinuria by Hewa Warawitage Dilanthi, Kandana Liyanage Subhashinie Jayasena, Nambage Dona Priyani Dhammika, Neluwa Liyanage Ruwan Indika, Matara Mahavidanage Nishani De Silva, Imalke Kankananarachchi, Pushpa Malkanthi Gardiye Punchihewa, Dharma Irugalbandara, Sabine Schroeder, Kosala Karunaratne, Eresha Jasinge

“…ABSTRACT Homocystinuria due to cystathionine beta‐synthase (CBS) deficiency is a rare metabolic disorder inherited as an autosomal recessive trait. Spectrum of genetic variants in CBS gene and their correlation with the phenotypes of homocystinuria in Sri Lankan patients have not been reported to date. …”
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Variations in the Obesity Gene “LEPR” Contribute to Risk of Type 2 Diabetes Mellitus: Evidence from a Meta-Analysis by Ming Ming Yang, Jun Wang, Jiao Jie Fan, Tsz Kin Ng, Dian Jun Sun, Xin Guo, Yan Teng, Yan-Bo Li

“…Meta-analysis showed that rs1137101 (p.R223Q) was significantly associated with T2DM in all genetic models: allele model (OR = 1.27, 95% confidence interval (CI) = 1.13–1.42), dominant model (OR = 1.19, 95% CI = 1.05–1.35), homozygote model (OR = 1.82, 95% CI = 1.38–2.39), and recessive model (OR = 1.75, 95% CI = 1.35–2.28), with minimal heterogeneity and no indication of publication bias. …”
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SEMI–DWARF PRODUCTIVE BARLEY LINES by B. A. Batasheva, V. I. Ibisheva, R. A. Abdullaev, O. N. Kovaleva, I. A. Zveinek, E. E. Radchenko

“…The short stem of these cultivars is controlled by recessive alleles of genes. We selected productive lines that significantly exceeded their parental forms in grain weight per area unit and resistance to frit fly: L 15/4 (F6 Sonet × Camincent) and L 16/12 (F6 Sonet × Pyramid). …”
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Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a Pakistani Cohort by Yasir Ali, Suleman Khan, Yangchao Chen, Nadia Farooqi, Zia-Ul Islam, Mehran Akhtar, Aamir, Aisha Aman, Aftab Ali Shah, Muhsin Jamal, Fazal Jalil

“…Interestingly, besides the homozygous recessive model (G/G vs. A/G + A/A) (OR = 1.693(1.06–2.648); P = 0.025), all other models, which included the codominant (χ2 = 5.169; P = 0.075), homozygous dominant (A/A vs. …”
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Association Study between Folate Pathway Gene Single Nucleotide Polymorphisms and Gastric Cancer in Koreans by Jae-Young Yoo, Sook-Young Kim, Jung-Ah Hwang, Seung-Hyun Hong, Aesun Shin, Il Ju Choi, Yeon-Su Lee

“…Especially, in the obese group (body mass index ≥ 25 kg/m2), the codominant (OR, 9.08; 95% CI, 1.01 to 94.59) and recessive model (OR, 3.72; 95% CI, 0.92 to 16.59) showed dramatically increased risk (p < 0.05). …”
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Impact of mealtime social experiences on student consumption of meals at school: a qualitative analysis of caregiver perspectives by Leah Elizabeth Chapman, Wendi Gosliner, Deborah A. Olarte, Monica Daniela Zuercher, Lorrene D. Ritchie, Dania Orta-Aleman, Marlene B. Schwartz, Michele Polacsek, Christina E. Hecht, Kenneth Hecht, Anisha I. Patel, Punam Ohri-Vachaspati, Margaret Read, Juliana FW Cohen

“…Policies such as increasing lunch period lengths and holding recess before lunch have been found to promote school meal consumption and could reinforce the positive social aspects of mealtime for students. …”
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Understanding the Spectrum of Mild Clinical Outcomes and Novel Findings in Arterial Tortuosity Syndrome Among Qatari Patients: Implications of SLC2A10 Mutation by Muhammed Riyas K. Rahmath, Haytham Ibrahim, Muhammad Faiyaz-Ul-Haque, Zafar Nawaz, Ahmad Zitoun, Ahmed Hussein, Ahmed Sadek, Ayman El-Menyar, Reema Kamal, Hassan Al-Thani, Gulab Sher

“…<b>Background</b>/<b>Objectives</b>: Arterial Tortuosity Syndrome (ATS) is a rare, autosomal recessive connective tissue disorder characterized by arterial twists, abnormal bulges, constriction, and tears. …”
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Association of Methylenetetrahydrofolate Reductase C677T Gene Polymorphisms with Mild Cognitive Impairment Susceptibility: A Systematic Review and Meta-Analysis by Jiahui Sun, Xuefan Jiang, Ming Zhao, Lina Ma, Hui Pei, Nanyang Liu, Hao Li

“…There was no significant association between MTHFR C677T (rs1801133) gene variants and MCI susceptibility under the allelic (OR, 1.318; 95% CI, 0.964–1.801; p=0.084), dominant (OR, 1.296; 95% CI, 0.925–1.817; p=0.132), recessive (OR, 1.397; 95% CI, 0.845–2.312; p=0.193), heterozygous (OR, 1.031; 95% CI, 0.855–1.243; p=0.749), or homozygous (OR, 1.506; 95% CI, 0.850–2.667; p=0.160) models. …”
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Al‐Rich AlGaN Transistors with Regrown p‐AlGaN Gate Layers and Ohmic Contacts by Brianna Klein, Andrew Allerman, Andrew Armstrong, Mary Rosprim, Colin Tyznik, Yinxuan Zhu, Chandan Joishi, Chris Chae, Siddharth Rajan

“…Utilizing a deep gate recess etch into the channel and an epitaxial regrown p‐AlGaN gate structure, an Al0.85Ga0.15N barrier/Al0.50Ga0.50N channel HEMT with a large positive threshold voltage (VTH = +3.5 V) and negligible gate leakage is demonstrated. …”
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Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency by Katja Dumic, Tony Yuen, Zorana Grubic, Vesna Kusec, Ingeborg Barisic, Maria I. New

“…Mutations in the CYP11B1 gene, which encodes steroid 11β-hydroxylase, are responsible for this autosomal recessive disorder. Here, we describe the molecular genetics of two previously reported male siblings in whom diagnosis of 11β-OHD has been established based on their hormonal profiles displaying high levels of 11-deoxycortisol and hyperandrogenism. …”
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Screening of local barley accessions for sensitivity to photoperiod by I. A. Zveynek, O. N. Kovaleva

“…The Near East and Central Asian centers of barley diversity were notable for the occurrence of local accessions with the recessive allele of the Eam8 gene. Accessions with the eam8eam8 genotype and heterogeneous forms can serve as sources of earliness in regions with short-light days. …”
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Data on hydrodynamic flow and aspiration mechanisms in a patient-specific pharyngolaryngeal model with variable epiglottis anglesMendeley Data by Amr Seifelnasr, Chen Sun, Peng Ding, Xiuhua April Si, Jinxiang Xi

“…Additionally, the dataset includes photos of the pharyngolaryngeal model setup, photos of the epiglottis models used, and STL files for both the pharyngolaryngeal model and the epiglottis 3D models.The videos document the distinct flow patterns and frequent aspiration sites identified during the experiments, including the interarytenoid notch, the cuneiform tubercular recess, and the vallecula. These data are valuable for researchers aiming to understand the etiology of dysphagia and can be reused to validate computational models, guide future experimental designs, and inform clinical diagnostics and treatment strategies. …”
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Biomorphological and useful agronomic traits of the hexaploid winter triticale cultivar ‘Bilinda’ approved for cultivation in the Northwestern Region of the Russian Federation by L. P. Bekish, V. A. Uspenskaja, T. I. Peneva, N. N. Chikida

“…‘Bilinda’ was developed using individual and mass selection of genotypes with recessive control of the ear’s morphological characters, which resulted in producing a homogeneous population with high yield potential and large plump grains. …”
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