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Mostrando 81 - 100 Resultados de 653 Para Buscar '"All in the Family"', tiempo de consulta: 0.30s Limitar resultados
  1. 81
    “…Patients/families (n  =  13) reported the new card was a valuable tool enabling them to ask questions, although not all patients or family members expressed the need to use the card. …”
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    Online Artículo Texto
    Empowering Patients With a Shared Communication Tool: A Patient-Oriented Multimethods Pilot Study
  2. 82
    “…Targeted and whole genome analysis of >16,600 samples and >4900 ASD probands revealed that likely recessive, rare, inherited variants in HARs, VEs, and CNEs substantially contribute to ASD risk in probands whose parents share ancestry, which enriches for recessive contributions, but modestly, if at all, in simplex family structures. We identified multiple patient variants in HARs near IL1RAPL1 and in a VE near SIM1 and showed that they change enhancer activity. …”
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    Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk
  3. 83
    “…Further sequence alignment of the core domain of glucosyl hydrolase showed that all GhBAM family genes had the glycosyl hydrolase family 14 domain. …”
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    Genome-Wide Identification and Preliminary Functional Analysis of BAM (β-Amylase) Gene Family in Upland Cotton
  4. 84
    “…Here, we describe the dynamic expression patterns of all known plexin family members in comparison to the neuropilins in the developing chicken spinal cord. …”
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    Expression patterns of plexins and neuropilins are consistent with cooperative and separate functions during neural development
  5. 85
    “…We demonstrate that a short region proximal to the TCF-4 HMG box mediates the interaction and that all Tcf/Lef family members associate with Dazap2. Interestingly, knockdown of Dazap2 not only reduced the activity of Wnt signalling as measured by Tcf/β-catenin reporters but additionally altered the expression of Wnt-signalling target genes. …”
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    Dazap2 modulates transcription driven by the Wnt effector TCF-4
  6. 86
    “…BACKGROUND & OBJECTIVES: A substance dependent person in the family affects almost all aspects of family life. This leads to problems, difficulties or adverse events which impact the lives of family members and causes enormous burden on family caregivers. …”
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    Family burden with substance dependence: a study from India
  7. 87
    “…In this study, we investigated the role of annexin repeats, a conserved structure of all the annexin family, responsible for platinum-resistance as well as the effect of knockdown of ANXA4. …”
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    Annexin A4 induces platinum resistance in a chloride-and calcium-dependent manner
  8. 88
    “…Whole-exome sequencing (WES) was performed on samples from one unaffected and two affected individuals to systematically search for deafness susceptibility genes, and the candidate mutations and the co-segregation of the phenotype were verified by polymerase chain reaction amplification and by Sanger sequencing in all of the family members. Then, we identified a novel EYA4 mutation in exon 8, c.511G>C; p.G171R, which segregated with postlingual and progressive autosomal dominant sensorineural hearing loss (SNHL). …”
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    Online Artículo Texto
    Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss
  9. 89
    “…We identify Notch1 and Notch3, but not Notch2, as novel Pim substrates and demonstrate that for Notch1, the serine residue 2152 is phosphorylated by all three Pim family kinases. This target site is located in the second nuclear localization sequence (NLS) of the Notch1 intracellular domain (N1ICD), and is shown to be important for both nuclear localization and transcriptional activity of N1ICD. …”
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    Phosphorylation of Notch1 by Pim kinases promotes oncogenic signaling in breast and prostate cancer cells
  10. 90
    “…Targeted next generation sequencing identified a novel heterozygous large deletion [exon5-exon16; c.423_8532del] of APC gene, which segregated with the FAP phenotypes in the proband and in all the affected family members. Unaffected family members and normal controls did not carry this deletion. …”
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    A novel pathogenic large germline deletion in adenomatous polyposis coli gene in a Chinese family with familial adenomatous polyposis
  11. 91
    “…In this study, we identified 60 MTs from Arabidopsis thaliana and five Brassica species. All the MT family genes from Brassica are closely related to Arabidopsis MTs, encoding putative proteins that share similar functions within the same clades. …”
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    Genome-Wide Characterization and Analysis of Metallothionein Family Genes That Function in Metal Stress Tolerance in Brassica napus L.
  12. 92
    por Dhar, Poshmaal, McAuley, Julie
    Publicado 2019
    “…The family of cell surface (cs-) mucins are constitutively expressed at the cell surface by nearly all epithelial cells, beneath the gel-mucin layer. All cs-mucin family members have structural features that enable them to act as a releasable decoy barrier to mucosal pathogens, by providing ligands for pathogen binding and the ability to shed the bound extracellular domain. …”
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    The Role of the Cell Surface Mucin MUC1 as a Barrier to Infection and Regulator of Inflammation
  13. 93
    “…Subsequent dose-response kinase assays showed that Ter directly inhibited all three PIM family members, with the highest activities against PIM-3 and -1. …”
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    Leflunomide Synergizes with Gemcitabine in Growth Inhibition of PC Cells and Impairs c-Myc Signaling through PIM Kinase Targeting
  14. 94
    “…The results show that children and parents used mobile devices during all aspects of family time in 2015, but device use was notably concentrated during alone‐together time. …”
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    Changing Times Together? A Time‐Diary Analysis of Family Time in the Digital Age in the United Kingdom
  15. 95
    “…The entire IRF6‐coding region and the exon–intron boundaries including exons 3–8 and part of exon 9 were screened among all the collected family members by Sanger sequencing. RESULTS: We found a novel splice site variant c.175‐6T>A, two novel missense variants (p.Lys66Arg and p.Pro107Thr), in addition with a previously reported missense variant (p.Leu87Phe), which were all located in and nearby exon 4 of IRF6. …”
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    Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome
  16. 96
    “…Historically, it begins with early unreported work by the Tomalia Group (i.e., The Dow Chemical Co.) revealing that all known dendrimer family types may be divided into two major symmetry categories; namely: Category I: symmetrical branch cell dendrimers (e.g., Tomalia, Vögtle, Newkome-type dendrimers) possessing interior hollowness/porosity and Category II: asymmetrical branch cell dendrimers (e.g., Denkewalter-type) possessing no interior void space. …”
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    Online Artículo Texto
    The Role of Branch Cell Symmetry and Other Critical Nanoscale Design Parameters in the Determination of Dendrimer Encapsulation Properties
  17. 97
    “…We screened for all the PIP family reductase transcripts from the RNA-Seq data. …”
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    Sweet Basil Has Distinct Synthases for Eugenol Biosynthesis in Glandular Trichomes and Roots with Different Regulatory Mechanisms
  18. 98
    “…Males and older participants showed a worse performance in all groups. Group family therapy with FDRs of BD might include training in the recognition of nonverbal cues, which might increase the understanding of their familiars with BD, in order to modify communication abilities.…”
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    Social cognition in first-degree relatives of bipolar disorder: Theory of Mind and nonverbal sensitivity
  19. 99
    “…They belong to three genera, all in the family Closteroviridae. For the sake of convenience, these viruses are named as grapevine leafroll-associated viruses (GLRaV-1, -2, -3, -4, -7, and -13). …”
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    Probing into the Effects of Grapevine Leafroll-Associated Viruses on the Physiology, Fruit Quality and Gene Expression of Grapes
  20. 100
    “…More than half of all women had family history of UI in Stress UI and Mixed UI subgroups. …”
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    Association of gene polymorphisms with women urinary incontinence
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