Search Results - "Reader RH"

Exome sequencing in severe non-syndromic specific learning and language disorders in a French cohort.

Authors: Viora-Dupont, Eléonore Delanne, Julian Garde, Aurore et al.

Source: Molecular Autism. 10/30/2025, Vol. 16 Issue 1, p1-17. 17p.

Domain antibody-displayed phages as a novel biofilm-targeted therapy for Staphylococcus aureus.

Authors: Khongrin K Aiamsung M Rasri N et al.

Source: International microbiology : the official journal of the Spanish Society for Microbiology [Int Microbiol] 2025 Dec; Vol. 28 (8), pp. 2391-2404. Date of Electronic Publication: 2025 Jul 26.

Publication Type: Journal Article

Journal Info: Publisher: Springer Nature Country of Publication: Switzerland NLM ID: 9816585 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1618-1905 (Electronic) Linking ISSN: 11396709 NLM ISO Abbreviation: Int Microbiol Subsets: MEDLINE

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Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder.

Authors: Bouzid, Amal Belcadhi, Malek Souissi, Amal et al.

Source: Scientific Reports. 1/2/2025, Vol. 15 Issue 1, p1-13. 13p.

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders.

Authors: De Wachter M van der Lei MB Decleve A et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Aug; Vol. 34 (8), pp. 1070-1080. Date of Electronic Publication: 2026 Jul 01.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Prediction of Glioma Grade and IDH Status Using 18 F-FET PET/CT Dynamic and Multiparametric Texture Analysis.

Authors: Hajri, Rami Nicod-Lalonde, Marie Hottinger, Andreas F. et al.

Source: Diagnostics (2075-4418). Aug2023, Vol. 13 Issue 15, p2604. 13p.

Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes.

Authors: Yasmin, Tahira Andres, Erin M. Ashraf, Komal et al.

Source: Annals of Human Biology. Feb2023, Vol. 50 Issue 1, p101-108.

Investigating Sequence Variations in CNTNAP2 and SETBP1 Genes in Language Disorders.

Authors: Turan, Betül Göktaş, Emine Uzun, Necati et al.

Source: Clinical Psychopharmacology & Neuroscience. Feb2025, Vol. 23 Issue 1, p100-109. 10p.

Recent selection of candidate genes for mammal domestication in Europeans and language change in Europe: a hypothesis.

Authors: Benítez-Burraco, Antonio Chekalin, Evgeny Bruskin, Sergey et al.

Source: Annals of Human Biology. Jun2021, Vol. 48 Issue 4, p313-320.

Effects of enzymolysis and fermentation of Chinese herbal medicines on serum component, egg production, and hormone receptor expression in laying hens.

Authors: Mei Hong Jiang Tao Zhang Qing Ming Wang et al.

Source: Animal Bioscience. Jan2024, Vol. 37 Issue 1, p95-104. 10p.

Candidate gene variant effects on language disorders in Robinson Crusoe Island.

Authors: Mountford, Hayley S. Villanueva, Pía Fernández, María Angélica et al.

Source: Annals of Human Biology. Mar2019, Vol. 46 Issue 2, p109-119.

A rapid novel strategy for screening of antibody phage libraries for production, purification, and functional characterization of amber stop codons containing single‐chain antibody fragments.

Authors: Perween, Reshma Ahmed, Shubbir Shrivastava, Tripti et al.

Source: Biotechnology Progress. May2021, Vol. 37 Issue 3, p1-9. 9p.

Deep mixed model for marginal epistasis detection and population stratification correction in genome-wide association studies.

Authors: Wang, Haohan Yue, Tianwei Yang, Jingkang et al.

Source: BMC Bioinformatics. 12/27/2019, Vol. 20 Issue 1, p1-11. 11p. 2 Diagrams, 3 Charts, 2 Graphs.

Cognitive and Behavioral Functioning Among Fraternal Twins with an Unbalanced Translocation of Chromosomes 10q and 12p: A Case Report.

Authors: Badaly, Daryaneh Heinrich, Kimberley P. Davis, Anna et al.

Source: Journal of Developmental & Physical Disabilities. Oct2019, Vol. 31 Issue 5, p635-651. 17p.

Decoding the biology of language and its implications in language acquisition.

Authors: RAHUL, D. R. PONNIAH, R. JOSEPH

Source: Journal of Biosciences. Mar2019, Vol. 44 Issue 1, p1-6. 6p.

TLDc proteins: new players in the oxidative stress response and neurological disease.

Authors: Finelli, Mattéa Oliver, Peter

Source: Mammalian Genome. Oct2017, Vol. 28 Issue 9/10, p395-406. 12p.

Parallel evaluation of cell-based phage display panning strategies: Optimized selection and depletion steps result in AML blast-binding consensus antibodies.

Authors: Weber, Theresa Pscherer, Sibylle Gamerdinger, Ulrike et al.

Source: Molecular Medicine Reports. Nov2021, Vol. 24 Issue 5, pN.PAG-N.PAG. 1p.

Development of bispecific antibodies with enhanced neutralization activity against tested SARS-CoV-2 Omicron subvariants.

Authors: Hsu CH Chang TY Chang YM et al.

Source: Frontiers in immunology [Front Immunol] 2026 Jun 17; Vol. 17, pp. 1793368. Date of Electronic Publication: 2026 Jun 17 (Print Publication: 2026).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE

An antibody uniquely binding short 2'-O-methyl RNA oligonucleotide duplexes: formation and recognition of target duplexes on cell surfaces.

Authors: Dunn IS Lawler MM Fagundes L et al.

Source: Frontiers in immunology [Front Immunol] 2026 Jan 12; Vol. 16, pp. 1699400. Date of Electronic Publication: 2026 Jan 12 (Print Publication: 2025).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

Authors: Pettigrew, Kerry A. Reeves, Emily Leavett, Ruth et al.

Source: PLoS ONE. 8/11/2015, Vol. 10 Issue 8, p1-11. 11p.