Found: 58
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Biologic characterization of ABCA3 variants in lung tissue from infants and children with ABCA3 deficiency.
- Published in:
- Pediatric Pulmonology, 2022, v. 57, n. 5, p. 1325, doi. 10.1002/ppul.25862
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- Publication type:
- Article
Comparison of algorithms for contrast enhancement based on triangle orientation discrimination assessments by convolutional neural networks.
- Published in:
- Optical Engineering, 2023, v. 62, n. 4, p. 48103, doi. 10.1117/1.OE.62.4.048103
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- Publication type:
- Article
Detecting vibration features from remote objects based on high-speed imagery.
- Published in:
- Optical Engineering, 2021, v. 60, n. 1, p. 13102, doi. 10.1117/1.OE.60.1.013102
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- Publication type:
- Article
INNUENDO AND DAMAGE TO REPUTATIONS.
- Published in:
- Advances in Consumer Research, 1984, v. 11, n. 1, p. 694
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- Publication type:
- Article
Developmental and Genetic Regulation of Human Surfactant Protein B in vivo.
- Published in:
- Neonatology (16617800), 2008, v. 95, n. 2, p. 117, doi. 10.1159/000153095
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- Publication type:
- Article
Dimensions of Moral Emotions.
- Published in:
- Emotion Review, 2011, v. 3, n. 3, p. 258, doi. 10.1177/1754073911402388
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- Publication type:
- Article
Scanning-Tunneling-Spectroscopy-Directed Design of Tailored Deep-Blue Emitters.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 3, p. 786, doi. 10.1002/anie.201407439
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- Publication type:
- Article
Frontispiece: Scanning-Tunneling-Spectroscopy-Directed Design of Tailored Deep-Blue Emitters.
- Published in:
- 2015
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- Publication type:
- Other
Biallelic ASCC1 variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (SMABF2).
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 7, p. 2190, doi. 10.1002/ajmg.a.62219
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- Publication type:
- Article
Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 544, doi. 10.1002/ajmg.a.61962
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- Publication type:
- Article
Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 5, p. 1053, doi. 10.1002/ajmg.a.61518
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- Publication type:
- Article
The neural substrates of action identification.
- Published in:
- Social Cognitive & Affective Neuroscience, 2010, v. 5, n. 4, p. 392, doi. 10.1093/scan/nsq004
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- Publication type:
- Article
Quantification of rare allelic variants from pooled genomic DNA.
- Published in:
- Nature Methods, 2009, v. 6, n. 4, p. 263, doi. 10.1038/nmeth.1307
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- Publication type:
- Article
The Premature Demise of the Solo Experiment.
- Published in:
- Personality & Social Psychology Bulletin, 1992, v. 18, n. 4, p. 504, doi. 10.1177/0146167292184017
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- Publication type:
- Article
Attribute Generality and the Inference Process in Impression Formation.
- Published in:
- Personality & Social Psychology Bulletin, 1976, v. 3, n. 1, p. 91, doi. 10.1177/014616727600300115
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- Publication type:
- Article
Rastertunnelspektroskopisch gesteuertes Design maßgeschneiderter tiefblauer Triplettemitter.
- Published in:
- Angewandte Chemie, 2015, v. 127, n. 3, p. 798, doi. 10.1002/ange.201407439
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- Publication type:
- Article
Frontispiz: Rastertunnelspektroskopisch gesteuertes Design maßgeschneiderter tiefblauer Triplettemitter.
- Published in:
- 2015
- By:
- Publication type:
- Other
Recombination as a mechanism for sporadic mutation in the surfactant protein-C gene.
- Published in:
- Pediatric Pulmonology, 2008, v. 43, n. 5, p. 443, doi. 10.1002/ppul.20782
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- Publication type:
- Article
Robots with Display Screens: A Robot with a More Humanlike Face Display Is Perceived To Have More Mind and a Better Personality.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072589
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- Publication type:
- Article
The Mind's Self-Portrait.
- Published in:
- Annals of the New York Academy of Sciences, 2003, v. 1001, n. 1, p. 212, doi. 10.1196/annals.1279.011
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- Publication type:
- Article
Digenic Variants in the FGF21 Signaling Pathway Associated with Severe Insulin Resistance and Pseudoacromegaly.
- Published in:
- Journal of the Endocrine Society, 2020, v. 4, n. 12, p. 1, doi. 10.1210/jendso/bvaa138
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- Publication type:
- Article
Lethal neonatal respiratory failure due to biallelic variants in BBS1 and monoallelic variant in TTC21B.
- Published in:
- Pediatric Nephrology, 2023, v. 38, n. 2, p. 605, doi. 10.1007/s00467-022-05616-z
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- Publication type:
- Article
Does the Robot Have a Mind? Mind Perception and Attitudes Towards Robots Predict Use of an Eldercare Robot.
- Published in:
- International Journal of Social Robotics, 2014, v. 6, n. 1, p. 17, doi. 10.1007/s12369-013-0186-y
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- Publication type:
- Article
Homozygous, Intragenic Tandem Duplication of SFTPB Causes Neonatal Respiratory Failure.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2024, v. 70, n. 1, p. 78, doi. 10.1165/rcmb.2023-0156le
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- Publication type:
- Article
Functional Genomics of ABCA3 Variants.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2020, v. 63, n. 4, p. 436, doi. 10.1165/rcmb.2020-0034MA
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- Publication type:
- Article
Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2016, v. 55, n. 5, p. 716, doi. 10.1165/rcmb.2016-0008OC
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- Publication type:
- Article
The United States of Repression.
- Published in:
- Behavioral & Brain Sciences, 2006, v. 29, n. 5, p. 528, doi. 10.1017/S0140525X06399116
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- Publication type:
- Article
The Godfather of soul.
- Published in:
- Behavioral & Brain Sciences, 2006, v. 29, n. 5, p. 482, doi. 10.1017/S0140525X06449104
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- Publication type:
- Article
Frequently asked questions about conscious will.
- Published in:
- Behavioral & Brain Sciences, 2004, v. 27, n. 5, p. 679, doi. 10.1017/S0140525X04450158
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- Publication type:
- Article
Précis of The illusion of conscious will.
- Published in:
- Behavioral & Brain Sciences, 2004, v. 27, n. 5, p. 649, doi. 10.1017/S0140525X04000159
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- Publication type:
- Article
Learning the Futility of the Thought Suppression Enterprise in Normal Experience and in Obsessive Compulsive Disorder.
- Published in:
- Behavioural & Cognitive Psychotherapy, 2010, v. 38, n. 1, p. 1, doi. 10.1017/S1352465809990439
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- Publication type:
- Article
Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
- Published in:
- 2014
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- Publication type:
- journal article
Genotype-Phenotype Correlations for Infants and Children with ABCA3 Deficiency.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 189, n. 12, p. E1, doi. 10.1164/rccm.201402-0342oc
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- Publication type:
- Article
Genotype--Phenotype Correlations for Infants and Children with ABCA3 Deficiency.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 189, n. 12, p. 1538, doi. 10.1164/rccm.201402-0342oc
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- Publication type:
- Article
The Trouble with Action.
- Published in:
- Social Cognition, 1987, v. 5, n. 3, p. 179, doi. 10.1521/soco.1987.5.3.179
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- Publication type:
- Article
The Presentation of Self Through Action Identification.
- Published in:
- Social Cognition, 1987, v. 5, n. 3, p. 301, doi. 10.1521/soco.1987.5.3.301
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- Publication type:
- Article
Action Identification in the Emergence of Social Behavior.
- Published in:
- Social Cognition, 1986, v. 4, n. 1, p. 18, doi. 10.1521/soco.1986.4.1.18
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- Publication type:
- Article
Social Awareness in Story Comprehension.
- Published in:
- Social Cognition, 1983, v. 2, n. 1, p. 1, doi. 10.1521/soco.1983.2.1.1
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- Publication type:
- Article
Moral Judgment and Distributive Justice.
- Published in:
- Human Development (0018716X), 1977, v. 20, n. 3, p. 160, doi. 10.1159/000271554
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- Publication type:
- Article
Origins of Ruminative Thought: Trauma, Incompleteness, Nondisclosure, and Suppression.
- Published in:
- Journal of Applied Social Psychology, 1995, v. 25, n. 14, p. 1245, doi. 10.1111/j.1559-1816.1995.tb02617.x
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- Publication type:
- Article
A mutation in Site‐1 Protease is associated with a complex phenotype that includes episodic hyperCKemia and focal myoedema.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.733
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- Publication type:
- Article
Spatially resolved electronic and vibronic properties of single diamondoid molecules.
- Published in:
- Nature Materials, 2008, v. 7, n. 1, p. 38, doi. 10.1038/nmat2066
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- Publication type:
- Article
An orbitally derived single-atom magnetic memory.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06337-4
- By:
- Publication type:
- Article
Gene variants of the phosphatidylcholine synthesis pathway do not contribute to RDS in the Chinese population.
- Published in:
- World Journal of Pediatrics, 2018, v. 14, n. 1, p. 52, doi. 10.1007/s12519-017-0109-3
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- Publication type:
- Article
Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.
- Published in:
- World Journal of Pediatrics, 2016, v. 12, n. 2, p. 190, doi. 10.1007/s12519-015-0047-x
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- Publication type:
- Article
Functional characterization of four ATP‐binding cassette transporter A3 gene (ABCA3) variants.
- Published in:
- Human Mutation, 2020, v. 41, n. 7, p. 1298, doi. 10.1002/humu.24014
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- Publication type:
- Article
Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants.
- Published in:
- Human Mutation, 2018, v. 39, n. 12, p. 1875, doi. 10.1002/humu.23627
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- Publication type:
- Article
Survival among children with 'Lethal' congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene ( GLDN).
- Published in:
- Human Mutation, 2017, v. 38, n. 11, p. 1477, doi. 10.1002/humu.23297
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- Publication type:
- Article
Genetic variant characterization in intron 4 of the surfactant protein B gene.
- Published in:
- Human Mutation, 2005, v. 26, n. 5, p. 494, doi. 10.1002/humu.9378
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- Publication type:
- Article
Precise breakpoint detection in a patient with 9p- syndrome.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2020, v. 6, n. 3, p. 1, doi. 10.1101/mcs.a005348
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- Publication type:
- Article