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Toll-like receptor 7 is not necessary for retroviral neuropathogenesis but does contribute to virus-induced neuroinflammation.
- Published in:
- Journal of NeuroVirology, 2008, v. 14, n. 6, p. 492, doi. 10.1080/13550280802345723
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- Publication type:
- Article
Use of Mobile Technology Paired with Heart Rate Monitor to Remotely Quantify Behavioral Health Markers among Military Reservists and First Responders.
- Published in:
- 2021
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- Publication type:
- journal article
A new acro-osteolysis syndrome caused by duplications including PTHLH.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 9, p. 484, doi. 10.1038/jhg.2014.58
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- Publication type:
- Article
Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survival.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 10, p. 1, doi. 10.1002/ajmg.a.63779
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- Publication type:
- Article
Exon skip‐inducing variants in FLNA in an attenuated form of frontometaphyseal dysplasia.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 12, p. 3675, doi. 10.1002/ajmg.a.62424
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- Publication type:
- Article
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 7, p. 1739, doi. 10.1002/ajmg.a.38267
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- Publication type:
- Article
Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 10, p. 2706, doi. 10.1002/ajmg.a.37804
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- Publication type:
- Article
Recurrence of frontometaphyseal dysplasia in two sisters with a mutation in FLNA and an atypical paternal phenotype: Insights into genotype-phenotype correlation.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 5, p. 1161, doi. 10.1002/ajmg.a.36981
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- Publication type:
- Article
Isotope-specific Resonance Ionization Mass Spectrometry Using Continuous-wave Diode and Pulsed Dye Lasers for Trace Detection and Enrichment of Elements of Environmental and Medical Importance, Exemplified for Strontium (Sr)-Part I: Theoretical Modelling.
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- Rapid Communications in Mass Spectrometry: RCM, 1996, v. 10, n. 14, p. 1725, doi. 10.1002/(SICI)1097-0231(199611)10:14<1725::AID-RCM720>3.0.CO;2-X
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- Publication type:
- Article
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1300, doi. 10.1038/ng.2765
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- Publication type:
- Article
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 95, doi. 10.1038/ng.270
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- Publication type:
- Article
Meetings Committee.
- Published in:
- Aquatic Veterinarian, 2018, v. 12, n. 3, p. 12
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- Publication type:
- Article
COMMITTEE REPORTS.
- Published in:
- Aquatic Veterinarian, 2017, v. 11, n. 4, p. 8
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- Publication type:
- Article
THE AQUATIC VETERINARIAN COMMITTEE REPORTS.
- Published in:
- Aquatic Veterinarian, 2017, v. 11, n. 1, p. 8
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- Publication type:
- Article
PRIVILEGES & BENEFITS OF WAVMA MEMBERSHIP.
- Published in:
- Aquatic Veterinarian, 2016, v. 10, n. 4, p. 10
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- Publication type:
- Article
PRIVILEGES & BENEFITS OF WAVMA MEMBERSHIP.
- Published in:
- Aquatic Veterinarian, 2016, v. 10, n. 3, p. 10
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- Publication type:
- Article
Credentialing Committee.
- Published in:
- Aquatic Veterinarian, 2016, v. 10, n. 2, p. 12
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- Publication type:
- Article
Evaluating 21-day Doxycycline and Azithromycin Treatments for Experimental Chlamydophila paittaci infection in Cockatiels (Nymphicus hollandicus).
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- Journal of Avian Medicine & Surgery, 2010, v. 24, n. 1, p. 35, doi. 10.1647/2009-009R.1
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- Publication type:
- Article
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.
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- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 494, doi. 10.1038/ejhg.2012.209
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- Publication type:
- Article
Solving the Wickedest Problem: Reconciling Differing Worldviews.
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- Journal of Futures Studies, 2020, v. 24, n. 4, p. 83, doi. 10.6531/JFS.202006_24(4).0008
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- Publication type:
- Article
Biofeedback-Assisted Resilience Training for Traumatic and Operational Stress: Preliminary Analysis of a Self-Delivered Digital Health Methodology.
- Published in:
- Journal of Medical Internet Research, 2019, v. 21, n. 9, p. N.PAG, doi. 10.2196/12590
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- Publication type:
- Article
How does the optometry profession move up a gear to tackle the problem of climate change?
- Published in:
- Ophthalmic & Physiological Optics, 2022, v. 42, n. 1, p. 4, doi. 10.1111/opo.12920
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- Publication type:
- Article
Clinical Implications of Hepatic Steatosis in Patients with Chronic Hepatitis C: A Multicenter Study of U.S. Veterans.
- Published in:
- Digestive Diseases & Sciences, 2007, v. 52, n. 2, p. 570
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- Publication type:
- Article
Segmentation and quantification of intra-ventricular/cerebral hemorrhage in CT scans by modified distance regularized level set evolution technique.
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- International Journal of Computer Assisted Radiology & Surgery, 2012, v. 7, n. 5, p. 785, doi. 10.1007/s11548-012-0670-0
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- Publication type:
- Article
Basin‐scale fluvial correlation and response to the Tethyan marine transgression: An example from the Triassic of central Spain.
- Published in:
- Basin Research, 2021, v. 33, n. 1, p. 1, doi. 10.1111/bre.12451
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- Publication type:
- Article
The male phenotype in osteopathia striata congenita with cranial sclerosis.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 10, p. 2397, doi. 10.1002/ajmg.a.34178
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- Publication type:
- Article
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ<sup>1</sup>-pyrroline-5-carboxylate synthase (P5CS).
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 1848, doi. 10.1002/ajmg.a.34057
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- Publication type:
- Article
Differential regulation of two FLNA transcripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies.
- Published in:
- Human Mutation, 2018, v. 39, n. 1, p. 103, doi. 10.1002/humu.23355
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- Publication type:
- Article
Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic mosaicism cases.
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- Human Mutation, 2017, v. 38, n. 10, p. 1360, doi. 10.1002/humu.23281
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- Publication type:
- Article
Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity.
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- Human Mutation, 2012, v. 33, n. 4, p. 665, doi. 10.1002/humu.22012
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- Publication type:
- Article
Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.
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- Journal of Molecular Medicine, 2015, v. 93, n. 7, p. 773, doi. 10.1007/s00109-015-1261-7
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- Publication type:
- Article
Intragenic Deletions in FLNB Are Part of the Mutational Spectrum Causing Spondylocarpotarsal Synostosis Syndrome.
- Published in:
- Genes, 2021, v. 12, n. 4, p. 528, doi. 10.3390/genes12040528
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- Publication type:
- Article
Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis.
- Published in:
- Genes, 2020, v. 11, n. 12, p. 1439, doi. 10.3390/genes11121439
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- Publication type:
- Article
Commentary on 'Designing phase II studies in cancer with time-to-event endpoints.'.
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- Clinical Trials, 2008, v. 5, n. 3, p. 222, doi. 10.1177/1740774508092145
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- Publication type:
- Article