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Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy.
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In: Orphanet journal of rare diseases, vol 17, iss 1 (2022)
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Secondary Structures of Proteins Follow Menzerath–Altmann Law
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In: International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1569 (2022)
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Waranikala ni korokara Balo ɲuman ; Le leopard and the tortoise ; Healthy diet ; Le léopard et la tortue ; La bonne nourriture
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Investigating the Concept and Origin of Viruses
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In: ISSN: 0966-842X ; Trends in Microbiology ; https://hal-amu.archives-ouvertes.fr/hal-03141377 ; Trends in Microbiology, Elsevier, 2020, 28 (12), pp.959-967. ⟨10.1016/j.tim.2020.08.003⟩ (2020)
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Children's biobehavioral reactivity to challenge predicts DNA methylation in adolescence and emerging adulthood.
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In: Developmental science, vol 22, iss 2 (2019)
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Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
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In: Genetics in medicine : official journal of the American College of Medical Genetics, vol 21, iss 8 (2019)
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STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics. ...
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Cap-Independent mRNA Translation in Germ Cells
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In: International Journal of Molecular Sciences ; Volume 20 ; Issue 1 (2019)
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Trans-acting translational regulatory RNA binding proteins.
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Partial remission and early stages of pediatric type 1 diabetes display immunoregulatory changes. A pilot study
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The Plasmodium falciparum cytoplasmic translation apparatus: a promising therapeutic target not yet exploited by clinically approved anti-malarials.
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In: Malaria journal, vol 17, iss 1 (2018)
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Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder.
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In: Autism research : official journal of the International Society for Autism Research, vol 11, iss 4 (2018)
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The helicase Ded1p controls use of near-cognate translation initiation codons in 5' UTRs.
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In: Nature, vol 559, iss 7712 (2018)
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mTOR-4EBP1/2-Independent Translational Regulation of mRNAs Encoding Ribosomal Proteins
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Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
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In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018)
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Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features
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In: ISSN: 1432-1203 ; Hum Genet ; https://hal.archives-ouvertes.fr/hal-02104155 ; Hum Genet, 2017, 136, pp.377-386. ⟨10.1007/s00439-017-1763-1⟩ ; https://link.springer.com/article/10.1007/s00439-017-1763-1 (2017)
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Evaluation of chemical and gene/protein entity recognition systems at BioCreative V.5: the CEMP and GPRO patents tracks
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