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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 3 4 5 Hits 1 – 20 of 94 1 Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy. Korb, Manisha; Peck, Allison; Alfano, Lindsay N... In: Orphanet journal of rare diseases, vol 17, iss 1 (2022) BASE Show details 2 Secondary Structures of Proteins Follow Menzerath–Altmann Law Vladimír Matlach; Daniel Dostál; Marian Novotný In: International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1569 (2022) BASE Show details 3 Le léopard et la tortue Klade, Anne-Marie; Karabenta, Haaji; Kaka Traoré, Youssouf. - 2021 BASE Show details 4 Waranikala ni korokara Balo ɲuman ; Le leopard and the tortoise ; Healthy diet ; Le léopard et la tortue ; La bonne nourriture Klade, Anne-Marie; Korenzo, Modibo. - 2021 BASE Show details 5 Investigating the Concept and Origin of Viruses Nasir, Arshan; Romero-Severson, Ethan; Claverie, Jean-Michel 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) BASE Show details 6 Hubness in the protein sequence universe Feldbauer, Roman Vinzenz. - 2020 BASE Show details 7 Children's biobehavioral reactivity to challenge predicts DNA methylation in adolescence and emerging adulthood. Goodman, Sarah J; Roubinov, Danielle S; Bush, Nicole R... In: Developmental science, vol 22, iss 2 (2019) BASE Show details 8 Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies. Fountain, Michael D; Oleson, David S; Rech, Megan E... In: Genetics in medicine : official journal of the American College of Medical Genetics, vol 21, iss 8 (2019) BASE Show details 9 STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics. ... O'Brien, Sinéad; Ng-Cordell, Elise; DDD Study. - : Apollo - University of Cambridge Repository, 2019 BASE Show details 10 Cap-Independent mRNA Translation in Germ Cells Brett D. Keiper In: International Journal of Molecular Sciences ; Volume 20 ; Issue 1 (2019) BASE Show details 11 Cap-Independent mRNA Translation in Germ Cells Keiper, Brett D.. - 2019 BASE Show details 12 Trans-acting translational regulatory RNA binding proteins. Harvey, RF; Smith, TS; Mulroney, T. - : Wiley, 2019 BASE Show details 13 Partial remission and early stages of pediatric type 1 diabetes display immunoregulatory changes. A pilot study Villalba Felipe, Adrián; Fonolleda, Mireia; Murillo-Vallés, Marta. - 2019 BASE Show details 14 The Plasmodium falciparum cytoplasmic translation apparatus: a promising therapeutic target not yet exploited by clinically approved anti-malarials. Sheridan, Christine Moore; Garcia, Valentina E; Ahyong, Vida... In: Malaria journal, vol 17, iss 1 (2018) BASE Show details 15 Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder. Berg, Elizabeth L; Copping, Nycole A; Rivera, Josef K... In: Autism research : official journal of the International Society for Autism Research, vol 11, iss 4 (2018) BASE Show details 16 The helicase Ded1p controls use of near-cognate translation initiation codons in 5' UTRs. Guenther, Ulf-Peter; Weinberg, David E; Zubradt, Meghan M... In: Nature, vol 559, iss 7712 (2018) BASE Show details 17 mTOR-4EBP1/2-Independent Translational Regulation of mRNAs Encoding Ribosomal Proteins Li, Ben Bicen. - 2018 BASE Show details 18 Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. Ansar, M.; Riazuddin, S.; Sarwar, M.T.... In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018) BASE Show details 19 Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features Zhang, Jing; Gambin, Tomasz; Yuan, Bo... 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) BASE Show details 20 Evaluation of chemical and gene/protein entity recognition systems at BioCreative V.5: the CEMP and GPRO patents tracks Pérez-Pérez, Martin; Rabal, Obdulia; Pérez-Rodríguez, Gael. - 2017 BASE Show details Page: 1 2 3 4 5

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