Showing 1 - 20 results of 160 for search '"growth deficiency"', query time: 0.44s Refine Results
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    4PBA reduces growth deficiency in osteogenesis imperfecta by enhancing transition of hypertrophic chondrocytes to osteoblasts by Amanda L. Scheiber, Kevin J. Wilkinson, Akiko Suzuki, Motomi Enomoto-Iwamoto, Takashi Kaito, Kathryn S.E. Cheah, Masahiro Iwamoto, Sergey Leikin, Satoru Otsuru

    Published 2022-02-01
    “…These results highlight the importance of targeting HCs to treat growth deficiency in OI. Our findings demonstrate that HC dysfunction induced by ER disruption plays a critical role in the pathogenesis of OI growth deficiency, which lays the foundation for developing new therapies for OI.…”
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    SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. by Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M Solomon, Sally A Camper, Pinchas Cohen, Uta Francke

    Published 2008-03-01
    “…They have early-onset postnatal growth deficiency, but normal fertility and lifespan. While pituitary structure and somatotrophs are normal, liver Igf1 mRNA is decreased. …”
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    Mandibular Vertical Growth Deficiency After Botulinum-Induced Hypotrophy of Masticatory Closing Muscles in Juvenile Nonhuman Primates by Hak-Jin Kim, Hye-Jin Tak, Joo-Won Moon, Sang-Hoon Kang, Seong Taek Kim, Jinquan He, Zhenguo Piao, Sang-Hwy Lee

    Published 2019-04-01
    “…After unilateral hypotrophy of masticatory muscles in group II, vertical growth deficiency was prominent on the BTX side, with compensatory overgrowth on the control side. …”
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    Growth Deficiency of a Xanthomonas oryzae pv. oryzae fur Mutant in Rice Leaves Is Rescued by Ascorbic Acid Supplementation by Sujatha Subramoni, Ramesh V. Sonti

    Published 2005-07-01
    “…Exogenous supplementation with ascorbic acid (an antioxidant) rescues the growth deficiency of the fur mutant in rice leaves. The virulence deficiency of the X. oryzae pv. oryzae fur mutant is proposed to be due, at least in part, to an impaired ability to cope with the oxidative stress conditions that are encountered during infection.…”
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    Severe insulin resistance and intrauterine growth deficiency associated with haploinsufficiency for INSR and CHN2: new insights into synergistic pathways involved in growth and metabolism. by Suliman, S, Stanik, J, McCulloch, L, Wilson, N, Edghill, E, Misovicova, N, Gasperikova, D, Sandrikova, V, Elliott, K, Barak, L, Ellard, S, Volpi, E, Klimes, I, Gloyn, A

    Published 2009
    “…CONCLUSIONS: We present a likely digenic cause of insulin resistance and growth deficiency resulting from the combined heterozygous disruption of INSR and CHN2, implicating CHN2 for the first time as a key element of proximal insulin signaling in vivo.…”
    Journal article
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    Genetic and functional studies implicate synaptic overgrowth and ring gland cAMP/PKA signaling defects in the Drosophila melanogaster neurofibromatosis-1 growth deficiency. by James A Walker, Jean Y Gouzi, Jennifer B Long, Sidong Huang, Robert C Maher, Hongjing Xia, Kheyal Khalil, Arjun Ray, David Van Vactor, René Bernards, André Bernards

    Published 2013-11-01
    “…Novel modifiers that implicate synaptic defects in the dNf1 growth deficiency include the intersectin-related synaptic scaffold protein Dap160 and the cholecystokinin receptor-related CCKLR-17D1 drosulfakinin receptor. …”
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    Directed Evolution of RecA Variants with Enhanced Capacity for Conjugational Recombination. by Taejin Kim, Sindhu Chitteni-Pattu, Benjamin L Cox, Elizabeth A Wood, Steven J Sandler, Michael M Cox

    Published 2015-06-01
    “…The growth deficiency is alleviated by expression of the functionally robust RecX protein from Neisseria gonorrhoeae. …”
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    Combination of Klinefelter syndrome and celiac disease: A case report by Ahmed Ramiz Baykan

    Published 2017-09-01
    “…We present a case of a 20-year-old patient who applied to our clinic because of growth deficiency and was concurrently diagnosed with Klinefelter syndrome and celiac disease.…”
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    Wiedemann‐Steiner syndrome: A case report by Lorna Hirst, Robert Evans

    Published 2021-03-01
    “…Clinical features include dysmorphic facial and skeletal features, growth deficiency, developmental delay, hypertrichosis cubiti and various dental features. …”
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    An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions. by Bum Jun Kim, Hitisha P Zaveri, Oleg A Shchelochkov, Zhiyin Yu, Andrés Hernández-García, Michelle L Seymour, John S Oghalai, Fred A Pereira, David W Stockton, Monica J Justice, Brendan Lee, Daryl A Scott

    Published 2013-01-01
    “…Individuals with terminal and interstitial deletions of chromosome 1p36 have a spectrum of defects that includes eye anomalies, postnatal growth deficiency, structural brain anomalies, seizures, cognitive impairment, delayed motor development, behavior problems, hearing loss, cardiovascular malformations, cardiomyopathy, and renal anomalies. …”
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    Circumscribed Storiform Collagenoma Associated with Rubinstein-Taybi Syndrome in a Young Adolescent by Nick Zavras, Rosario Mennonna, Spyros Maris, George Vaos

    Published 2016-03-01
    “…Rubinstein-Taybi syndrome is a rare congenital neurodevelopmental disorder characterized by dysmorphic features, skeletal abnormalities, growth deficiency, and mental retardation. Circumscribed storiform collagenoma is a distinct benign fibromatous tumor that presents either as solitary tumor or in association with other syndromes. …”
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    Special features of generative reproduction of Aglaonema commutatum Schott (Araceae Juss.) under introduction by B.O. Ivanytska, A.I. Zhila

    Published 2010-09-01
    “…The special feature of A. commutatum seed germination is emergence of 3–6 leaves (cataphyll) before additional root growth. Deficiency of embryonic root seedlings of A. commutatum would be considered as extreme ephemeral feature in monocotyledonous.…”
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    Chronic growth faltering amongst a birth cohort of Indian children begins prior to weaning and is highly prevalent at three years of age by Jaffar Shabbar, Muliyil Jayaprakash, Verghese Valsan P, Gladstone Beryl P, Rehman Andrea M, Kang Gagandeep

    Published 2009-09-01
    “…In total 224/331 (68%) children at three years had at least one growth deficiency (were stunted and/or underweight and/or wasted); even as early as one month of age 186/377 (49%) children had at least one growth deficiency. …”
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