Pentapeptide sharing betweenCorynebacterium diphtheriatoxin and the human neural protein network
出版年份 2010 全文链接
标题
Pentapeptide sharing betweenCorynebacterium diphtheriatoxin and the human neural protein network
作者
关键词
-
出版物
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
Volume 33, Issue 2, Pages 360-372
出版商
Informa UK Limited
发表日期
2010-09-29
DOI
10.3109/08923973.2010.518618
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Identification of Uncommon Recurrent Potocki-Lupski Syndrome-Associated Duplications and the Distribution of Rearrangement Types and Mechanisms in PTLS
- (2010) Feng Zhang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genetic Heterogeneity in Human Disease
- (2010) Jon McClellan et al. CELL
- Tuberous sclerosis complex: a brave new world?
- (2010) Kevin C Ess CURRENT OPINION IN NEUROLOGY
- Peptidomics Coming of Age: A Review of Contributions from a Bioinformatics Angle
- (2010) Gerben Menschaert et al. JOURNAL OF PROTEOME RESEARCH
- Protein information content resides in rare peptide segments
- (2010) Darja Kanduc PEPTIDES
- Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome
- (2010) N. A. Zaghloul et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly
- (2010) S. Seo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR ) in the etiology of autistic disorders on high-functioning level
- (2009) Anne-Kathrin Wermter et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL PSYCHIATRY
- Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome
- (2009) B. Chakrabarti et al. Autism Research
- Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
- (2009) Simon G Gregory et al. BMC Medicine
- “Self-Nonself” Peptides in the Design of Vaccines
- (2009) Darja Kanduc CURRENT PHARMACEUTICAL DESIGN
- Clinical spectrum ofSCN1Amutations
- (2009) Antonio Gambardella et al. EPILEPSIA
- A Substitution Involving the NLGN4 Gene Associated with Autistic Behavior in the Greek Population
- (2009) Andreas Pampanos et al. Genetic Testing and Molecular Biomarkers
- International External Quality Assurance for Laboratory Diagnosis of Diphtheria
- (2009) S. E. Neal et al. JOURNAL OF CLINICAL MICROBIOLOGY
- Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions
- (2009) Helen L. May-Simera et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay
- (2009) S. R. Williams et al. JOURNAL OF MEDICAL GENETICS
- Fragile X syndrome: from molecular genetics to therapy
- (2009) C D'Hulst et al. JOURNAL OF MEDICAL GENETICS
- A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
- (2009) C. Zhang et al. JOURNAL OF NEUROSCIENCE
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
- (2009) Kai Wang et al. NATURE
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Association of Autistic Spectrum Disorders With Dystrophinopathies
- (2009) Veronica J. Hinton et al. PEDIATRIC NEUROLOGY
- Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism
- (2009) Bert van der Zwaag et al. PLoS One
- Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation
- (2009) Vincent Marion et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Possible association between the androgen receptor gene and autism spectrum disorder
- (2009) Susanne Henningsson et al. PSYCHONEUROENDOCRINOLOGY
- Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes
- (2009) Maja Bucan et al. PLoS Genetics
- Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
- (2008) Vincent Cantagrel et al. AMERICAN JOURNAL OF HUMAN GENETICS
- No evidence for involvement of genetic variants in the X-linked neuroligin genesNLGN3andNLGN4Xin probands with autism spectrum disorder on high functioning level
- (2008) Anne-Kathrin Wermter et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Genes Controlling Affiliative Behavior as Candidate Genes for Autism
- (2008) Carolyn M. Yrigollen et al. BIOLOGICAL PSYCHIATRY
- HTR1B and HTR2C in autism spectrum disorders in Brazilian families
- (2008) G.M. Orabona et al. BRAIN RESEARCH
- Familial deletion within NLGN4 associated with autism and Tourette syndrome
- (2008) Amy Lawson-Yuen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Tuberous sclerosis complex proteins control axon formation
- (2008) Y.-J. Choi et al. GENES & DEVELOPMENT
- Neuropsychiatric Disorders in Males With Duchenne Muscular Dystrophy: Frequency Rate of Attention-Deficit Hyperactivity Disorder (ADHD), Autism Spectrum Disorder, and Obsessive—Compulsive Disorder
- (2008) Joseph G. M. Hendriksen et al. JOURNAL OF CHILD NEUROLOGY
- Post-vaccination encephalomyelitis: Literature review and illustrative case
- (2008) William Huynh et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Disruption of contactin 4 in three subjects with autism spectrum disorder
- (2008) J Roohi et al. JOURNAL OF MEDICAL GENETICS
- Massive peptide sharing between viral and human proteomes
- (2008) Darja Kanduc et al. PEPTIDES
- The Timothy syndrome mutation differentially affects voltage- and calcium-dependent inactivation of CaV1.2 L-type calcium channels
- (2008) C. F. Barrett et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Duplication of 17(p11.2p11.2) in a male child with autism and severe language delay
- (2007) Alisa Nakamine et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population
- (2007) Hui Li et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started