Showing 301 - 320 results of 759 for search '"recession"', query time: 0.08s Refine Results
  1. 301

    Surface prereacted glass-ionomer particles incorporated into resin composites promote biocompatibility for restoration of subgingival dental defects by Yueyi Yang, Jing Huang, Xuchen Hu, Meiling Jing, Yujie Zhang, Chenci Xu, Wenduo Tan, Xiaoyu Liu, Chenguang Niu, Zhengwei Huang

    Published 2025-04-01
    “…These defects commonly accompany lesions involving marginal alveolar bone loss and gingival recession, and their clinical management is challenging. …”
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    Article
  2. 302
  3. 303

    Designing an entrepreneurial model in the banking network with a digital technology approach by Afshin Nobakht, majid nasiri, parviz Saeedi

    Published 2024-12-01
    “…The entrepreneurship of banks in the context of digital technologies, which is associated with information transparency, can remove the economy from recession by eliminating the problem of unemployment at the same time. …”
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    Article
  4. 304

    Analytical and Comparative Analysis of Copper Industry Development Programs in Iran by Adel Rouhi Jouybari, Seyed Mohammad Esmaiel Jalali

    Published 2024-10-01
    “…In the conditions of the domestic market recession, most mineral and mining products have experienced a decline in exports, and among the country's economic activists, it is known as self-sanctioning. …”
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    Article
  5. 305

    Changes on Sugar and Starch Contents during Seed Development of Synergistic Sweet Corn and Implication on Seed Quality by Bhornchai Harakotr, Warisa Sutthiluk, Panumart Rithichai

    Published 2022-01-01
    “…The optimal time to harvest seeds was genotype-dependent, which were 38 DAP for triple-recessive gene (btbtsh2sh2wxwx) and single-recessive genes (BtBtsh2sh2WxWx and Sh2Sh2susuWxWx) and 42 DAP for double-recessive genes (BtBtsh2sh2wxwx). …”
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    Article
  6. 306

    Protein C Deficiency Caused by a Novel Mutation in the PROC Gene in an Infant with Delayed Onset Purpura Fulminans by Mariam S. Al Harbi, Ayman W. El-Hattab

    Published 2017-01-01
    “…Therefore, early recognition is critical in preventing morbidity and mortality associated with autosomal recessive PCD.…”
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    Article
  7. 307

    Association between vitamin D receptor gene polymorphism and essential hypertension: An updated systematic review, meta-analysis, and meta-regression. by Iwan Dakota, Muhamad Fajri Adda'i, Rido Maulana, Ignatius Ivan, Renan Sukmawan, Bambang Widyantoro

    Published 2024-01-01
    “…Twenty-two studies from thirteen countries were analyzed. The recessive model suggested lower EH risk in individuals with the recessive allele (bb) of BsmI (OR: 0.81; 95%CI, 0.69 to 0.94, p = 0.007; I2 = 35%, p = 0.13). …”
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  8. 308

    Polymorphic Single‐Nucleotide Variants in miRNA Genes and the Susceptibility to Colorectal Cancer: Combined Evaluation by Pairwise and Network Meta‐Analysis, Thakkinstian's Algorit... by Qing Liu, Ivan Archilla, Sandra Lopez‐Prades, Ferran Torres, Jordi Camps, Miriam Cuatrecasas

    Published 2025-01-01
    “…Additionally, the miR‐196a2 (rs11614913), miR‐143/145 (rs41291957), and miR‐34b/c (rs4938723), with the dominant, recessive, and recessive models identified as the optimal, might confer protective effects against CRC among Asians.…”
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    Article
  9. 309

    Optimization of Identification and Zoning Method for Landscape Characters of Urban Historic Districts by Hong YUN, Zixuan HU, Zehao HU

    Published 2025-01-01
    “…By this way, recessive genes, which do not have spatial attribution, can be mapped into space. …”
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    Article
  10. 310

    GJB6-D13S1830 and GJB6-D13S1854 Deletions in Patients with non-Syndromic Prelingual Deafness by Mercedes Arceo Álvarez, Estela Morales Peralta, Yuledmi Perdomo Chacón, Teresa Collazo Mesa

    Published 2024-08-01
    “…<strong>Foundation:</strong> GJB6-D13S1830 and GJB6-D13S1854 deletions are pathogenic variants of the GJB6 gene, which has been shown to be the second cause of autosomal recessive non-syndromic deafness in Spain, where some of our ancestors come from. …”
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    Article
  11. 311

    Le multiplicateur budgétaire endogène au cycle dans un modèle macroéconomique post-keynésien by Sébastien Charles

    Published 2020-01-01
    “…We perform some simulations showing that the multiplier increases during recessions which logically does not advocate a reduction in public spending when the economy is in crisis…”
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  12. 312

    GENETIC CONTROL OF ULTRA-EARLINESS IN CHINESE BARLEY LANDRACES by I. A. Zveinek, O. N. Kovaleva

    Published 2018-08-01
    “…Ultra-early maturity of the Chinese barley landraces k-15881 (Hordeum vulgare L. var. coeleste L.) and k-15882 (var. nudipyramidatum Koern.) from VIR’s barley collection is controlled by three identical recessive genes. This homozygous genotype determines the period from shoot emergence to heading =32 days, with two recessives genes =36 days, and with one =40 days. …”
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  13. 313

    Adult Lactose Digestion Status and Effects on Disease by Andrew Szilagyi

    Published 2015-01-01
    “…BACKGROUND: Adult assimilation of lactose divides humans into dominant lactase-persistent and recessive nonpersistent phenotypes.…”
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  14. 314

    Concomitant Extramedullary Plasmacytoma in the Oropharynx and Hypopharyngeal Squamous Cell Carcinoma by Hiroki Sato, Shoko Yoshimasu, Isaku Okamoto, Akira Shimizu, Yasuaki Katsube, Hideki Tanaka, Kiyoaki Tsukahara

    Published 2018-01-01
    “…In addition, a protruding tumor was observed on the mucosal surface in the right piriform recess of the hypopharynx, and computed tomography revealed thickening of the pharyngeal wall at the right tongue base and in the right piriform recess of the hypopharynx. …”
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  15. 315

    De Novo Mutation of the ADAMTS13 Gene with Mesenteric Ischemia in an Infant with Congenital Thrombotic Thrombocytopenic Purpura by Ibrahim Alharbi, Sarah Alqarni, Wed Khayyat, Amirah Almatrafi

    Published 2021-01-01
    “…Congenital thrombotic thrombocytopenic purpura (cTTP) is a rare autosomal recessive disease characterized by ADAMTS13 deficiency or a severe decrease in its activity that is caused by homozygous or combined heterozygous mutations in its encoding gene. …”
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  16. 316

    Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance by Alessandra Zanon, Peter P. Pramstaller, Andrew A. Hicks, Irene Pichler

    Published 2018-01-01
    “…The identification and validation of such modifiers leading to reduced penetrance or increased susceptibility in the case of heterozygous carriers of recessive mutations are relevant for a better understanding of mechanisms contributing to disease onset. …”
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    Article
  17. 317

    A pathogenic COL7A1 variant highlights semi-dominant inheritance in dystrophic epidermolysis bullosa by Saira Sattar, Thashi Bharadwaj, Umm-e- Kalsoom, Anushree Acharya, Saadullah Khan, Suzanne M. Leal, Isabelle Schrauwen

    Published 2025-02-01
    “…Both autosomal dominant and recessive inheritance has been reported with variable phenotype. …”
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  18. 318

    Clinical, genetic aspects and molecular pathogenesis of osteopetrosis by D. D. Nadyrshina, R. I. Khusainova

    Published 2023-07-01
    “…The disease can be autosomal recessive, autosomal dominant, X-linked or sporadic. …”
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  19. 319

    Prediction of Optimal Daily Step Count Achievement from Segmented School Physical Activity by Ryan D. Burns, Timothy A. Brusseau, James C. Hannon

    Published 2015-01-01
    “…The school segment that related in strongest way to a student achieving 6,000 steps during school hours was afternoon recess (OR = 40.03; P<0.001) and for achieving 12,000 steps for the entire day was lunch recess (OR = 5.03; P<0.001). …”
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  20. 320

    Genetic control of scald resistance in barley landraces by O. N. Soboleva, G. S. Konovalova, E. E. Radchenko

    Published 2016-12-01
    “…Accessions k-15868 and k-3481 possess two complementary recessive genes for scald resistance, k-18989 has two recessive genes, and k-3307 carries one recessive gene for pathogen resistance. …”
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    Article