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321
Physical Activity Behavior in Swiss Secondary School Students: A Segmented Analysis
Published 2025-01-01“…During school hours, the proportion of time allocated to MVPA varies significantly across segments (PE = 31.2%, recess = 18.46%, classroom time = 5.45%; p < 0.001), falling well below the recommended targets for PE (50% MVPA) and recess (40% MVPA). …”
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322
Symbiotic nitrogen fixation in legumes as a genetic and selection trait
Published 2015-07-01“…From the large set, supernodulating (proved to be recessive) and dominant hypernodulating types of symbiotic mutants were chosen for breeding programs. …”
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323
Investigation of the Low-Temperature Behavior of FD-SOI MOSFETs in the Saturation Regime Using Y and Z Functions
Published 2014-01-01“…Ultrathin body (UTB) and gate recessed channel (GRC) devices were fabricated simultaneously on the same silicon wafer through a selective “gate recessed” process. …”
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324
Alpha II Antiplasmin Deficiency Complicating Pregnancy: A Case Report
Published 2011-01-01“…It is inherited in an autosomal recessive fashion. Case. 30-year-old Gravida 1, Para 0, presented for prenatal care with her first and subsequently her second pregnancy. …”
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325
Quantifying the Robustness of Countries’ Competitiveness by Network-Based Methods
Published 2018-01-01“…The robustness characterizes the stability of countries’ competitiveness against economic recessions. The experiments in the international trade networks show that FCM could characterize the robustness better than MR. …”
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326
GENETIC CONTROL OF FERTILITY RESTORATION IN CMS LINES OF FLAX (<i>LINUM USITATISSIMUM</i>)
Published 2018-06-01“…Other recessive (alternative) alleles of pollen fertility restoration genes rfo6, rfo6-2, rfo6-3, rfo7 do not affect the corolla’s shape.…”
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327
Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family
Published 2024-05-01“…Frank–Ter Haar syndrome (FTHS) is a rare genetic hereditary autosomal recessive disorder characterized by defective malformation of cardiovascular, craniofacial, and skeletal system. …”
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328
The Associations between VEGF Gene Polymorphisms and Diabetic Retinopathy Susceptibility: A Meta-Analysis of 11 Case-Control Studies
Published 2014-01-01“…A significant relationship between VEGF+936C/T (rs3025039) polymorphism and DR was found in a recessive model (OR = 3.19, 95% CI = 1.20–8.41, and P(z)=0.01) in Asian and overall populations, while a significant association was also found between –460T/C (rs833061) polymorphism and DR risk under a recessive model (OR = 2.12, 95% CI = 1.12–4.01, and P(z)=0.02). …”
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329
Association of the Interleukin-10-592C/A Polymorphism and Cervical Cancer Risk: A Meta-Analysis
Published 2022-01-01“…Regarding ethnicity, a significant association of the -592C/A polymorphism of the IL-10 gene was linked to an elevated risk of cervical cancer for all genetic models (recessive, dominant, and additive) in the Asian populations and for the recessive and additive models in Caucasians with P<0.05. …”
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330
Feasibility and Safety of the C1 “Zero Angle” Screw: A Novel “In–Out–In” Technique for Atlantoaxial Dislocation
Published 2025-02-01“…Radiographic measurements included (A) the distance from the recess to the transverse foramen (RTF); (B) the tricortical screw zone (TSZ); (C) the lateral mass height along the C1ZAS trajectory (LMH); (D) the screw length of C1ZAS (ZSL); (E) the screw length of C1 PS (PSL); (F) the distances from the recess to the dura (RD); (G) the distance from the recess to the spinal cord (RSC); (H) the distance from the inner of lateral mass to the spinal cord (ILMSC). …”
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331
Hepatocellular Adenoma in a Patient with Ornithine Transcarbamylase Deficiency
Published 2019-01-01“…Ornithine transcarbamylase (OTC) deficiency is an X-linked recessive disorder that leads to hyperammonemia and liver damage. …”
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332
Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation.
Published 2013-01-01“…The use of autozygosity as a mapping tool in the search for autosomal recessive disease genes is well established. We hypothesized that autozygosity not only unmasks the recessiveness of disease causing variants, but can also reveal natural knockouts of genes with less obvious phenotypic consequences. …”
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333
Primary Amenorrhea in a 15‐Year‐Old Girl Leading to the Diagnosis of Bardet‐Biedl Syndrome: A Case Report
Published 2025-01-01“…ABSTRACT This case report highlights the clinical complexity of Bardet‐Biedl syndrome, a rare autosomal recessive disorder, emphasizing reproductive anomalies to aid in diagnosis and management. …”
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334
Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum
Published 2018-01-01“…Lysosomal acid lipase (LAL) deficiency is an autosomal recessive lysosomal storage disorder caused by mutations in the LIPA gene that leads to premature organ damage and mortality. …”
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335
Thermoacoustic Stability Boundaries in the Model Combustion Chamber with a Gas-Centered Swirl Coaxial Injector
Published 2019-01-01“…First, flame shapes induced by the injector are analyzed for various recess lengths from experimental results. The spreading angle and flame size are reduced as the recess length increases. …”
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336
Associations between Vascular Endothelial Growth Factor Gene Polymorphisms and Different Types of Diabetic Retinopathy Susceptibility: A Systematic Review and Meta-Analysis
Published 2021-01-01“…There were significant associations between rs2010963 and NPDR in Asian (dominant model: OR=1.29, 95%CI=1.04−1.60); and rs2010963 is associated with PDR in total population (dominant model: OR=1.20, 95%CI=1.03−1.41), either Asian (recessive model: OR=1.57, 95%CI=1.04−2.35) or Caucasian (recessive model: OR=1.83, 95%CI=1.28−2.63). …”
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337
Smith-Lemli-Opitz Syndrome: A Case with Annular Pancreas
Published 2014-01-01“…Smith-Lemli-Opitz syndrome is an autosomal recessive disease of cholesterol metabolism. It is a multiple malformation syndrome with typical dysmorphic features such as bitemporal narrowing, ptosis, epicanthus, microcephaly, micrognathia, and cardiovascular, skeletal, urogenital, and gastrointestinal anomalies. …”
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338
Digital Etching of Molybdenum Interconnects Using Plasma Oxidation
Published 2025-01-01“…These two steps are repeated in cycles until the intended metal recess is achieved. High uniformity of plasma oxidation defines the etching uniformity, and small metal recess per cycle (typically 1–2 nm) provides precise control over the etching depth. …”
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339
Phenotype and genetic spectrum of six Indian patients with bestrophinopathy
Published 2024-12-01“…Sporadic autosomal dominant and recessive inheritance was observed in these families. …”
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340
INFLUENCE OF THE TIME OF DISINHIBITION TO TRANSIENTS AND WEAR OF THE FRICTION LININGS IN AN ASYNCHRONOUS MOTOR
Published 2016-09-01“…Time and the stopping distance of the electric drive with frequent starting-and-braking modes that contain embedded asynchronous motor with a recessed combined braking device depend on the moment of an electromagnet disinhibition. …”
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