| scholarly article | Q13442814 |
| P50 | author | David A. Buchner | Q42512672 |
| Andrew Furley | Q42779329 | ||
| P2093 | author name string | Takeshi Sakurai | |
| Michael W Schwartz | |||
| Joseph H Nadeau | |||
| Karl J Kaiyala | |||
| Diana L Kunze | |||
| Colleen M Croniger | |||
| Patricia A Glazebrook | |||
| Michael G Morgan | |||
| Sabrina H Spiezio | |||
| Jon M Geisinger | |||
| P2860 | cites work | Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels | Q22011028 |
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| Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene | Q24305575 | ||
| Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders | Q24305646 | ||
| Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 | Q24312199 | ||
| A functional genetic link between distinct developmental language disorders | Q24312638 | ||
| Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1 | Q24321543 | ||
| Genetic Advances in the Study of Speech and Language Disorders | Q24609855 | ||
| Genome-wide analysis reveals novel molecular features of mouse recombination hotspots | Q24611454 | ||
| The voltage-gated potassium channel Kv1.3 regulates peripheral insulin sensitivity | Q24624806 | ||
| Kv1.3 gene-targeted deletion alters longevity and reduces adiposity by increasing locomotion and metabolism in melanocortin-4 receptor-null mice | Q24642217 | ||
| A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism | Q24643479 | ||
| Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers | Q24675297 | ||
| The voltage-gated potassium channel Kv1.3 regulates energy homeostasis and body weight | Q28209877 | ||
| The neural adhesion molecule TAG-1 modulates responses of sensory axons to diffusible guidance signals | Q28504792 | ||
| Prevalence of obesity among children with chronic conditions | Q43492944 | ||
| Leptin expression in hypothalamic PVN reverses dietary obesity and hyperinsulinemia but stimulates ghrelin | Q44196009 | ||
| A novel, noninvasive method for the measurement of intestinal fat absorption | Q44965228 | ||
| Dissecting the architecture of a quantitative trait locus in yeast | Q46110868 | ||
| Identification of SH2-B as a key regulator of leptin sensitivity, energy balance, and body weight in mice | Q47372073 | ||
| Assignment of the mouse Rbpsuh gene to chromosome 5 and one processed pseudogene Rbpsuh-rs3 to chromosome 6. | Q47858276 | ||
| Evaluation of a quantitative magnetic resonance method for mouse whole body composition analysis | Q48919151 | ||
| Effect of K+ channel modulation on mouse feeding behaviour. | Q51540550 | ||
| A supersized list of obesity genes | Q56968708 | ||
| Effects of parabiosis of obese with diabetes and normal mice | Q69634353 | ||
| Deep congenic analysis identifies many strong, context-dependent QTLs, one of which, Slc35b4, regulates obesity and glucose homeostasis | Q28512493 | ||
| Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes | Q28588262 | ||
| The mystery of missing heritability: Genetic interactions create phantom heritability | Q28732355 | ||
| Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
| Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations | Q29614573 | ||
| Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 | ||
| Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2 | Q29616085 | ||
| Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits | Q29618411 | ||
| Obesity and the regulation of energy balance | Q30080025 | ||
| Computer-based methods for the mouse full-length cDNA encyclopedia: real-time sequence clustering for construction of a nonredundant cDNA library. | Q30649625 | ||
| Novel leptin-regulated genes revealed by transcriptional profiling of the hypothalamic paraventricular nucleus | Q33385599 | ||
| The prevalence of obesity in children with autism: a secondary data analysis using nationally representative data from the National Survey of Children's Health | Q33533625 | ||
| Association of epilepsy and comorbid conditions | Q33574289 | ||
| Analysing complex genetic traits with chromosome substitution strains | Q33853268 | ||
| Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases | Q33855666 | ||
| Analysis of gene-gene interactions | Q33860591 | ||
| A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. | Q33892998 | ||
| Identification of body fat mass as a major determinant of metabolic rate in mice | Q33930234 | ||
| Ancestral paternal genotype controls body weight and food intake for multiple generations | Q34184779 | ||
| Clustered K+ channel complexes in axons | Q34343185 | ||
| Toward a more complete (and less controversial) understanding of energy expenditure and its role in obesity pathogenesis | Q34448641 | ||
| Composition, assembly, and maintenance of excitable membrane domains in myelinated axons. | Q34567677 | ||
| Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes | Q34657208 | ||
| Detecting gene-gene interactions that underlie human diseases | Q34980492 | ||
| Genetic analysis of complex traits in the emerging Collaborative Cross | Q35145475 | ||
| Mammalian recombination hot spots: properties, control and evolution. | Q35311047 | ||
| Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis | Q37018913 | ||
| Diet-induced hepatocellular carcinoma in genetically predisposed mice | Q37272350 | ||
| Comparative recombination rates in the rat, mouse, and human genomes | Q37322300 | ||
| Obesity is a common comorbidity for pediatric patients with untreated, newly diagnosed epilepsy | Q37324686 | ||
| Genetic, molecular and physiological insights into human obesity | Q37851541 | ||
| Using biological networks to search for interacting loci in genome-wide association studies | Q41754041 | ||
| Analyzing complex traits with congenic strains | Q42938759 | ||
| Obesity and obesity-related secondary conditions in adolescents with intellectual/developmental disabilities | Q42970634 | ||
| P433 | issue | 7-8 | |
| P921 | main subject | obesity | Q12174 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 431-442 | |
| P577 | publication date | 2012-07-01 | |
| P1433 | published in | Mammalian Genome | Q1348949 |
| P1476 | title | The juxtaparanodal proteins CNTNAP2 and TAG1 regulate diet-induced obesity | |
| P478 | volume | 23 |
| Q37567595 | Chromosome substitution strains: gene discovery, functional analysis, and systems studies |
| Q48333335 | Contactin-2/TAG-1, active on the front line for three decades |
| Q35664102 | Contrasting genetic architectures in different mouse reference populations used for studying complex traits. |
| Q40416954 | Dissection of Host Susceptibility to Bacterial Infections and Its Toxins |
| Q38308258 | Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue |
| Q34019187 | Fine-mapping QTLs in advanced intercross lines and other outbred populations |
| Q35168433 | First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes |
| Q34322168 | Genetic control of obesity and gut microbiota composition in response to high-fat, high-sucrose diet in mice |
| Q48323438 | Genetics of metabolic syndrome: potential clues from wild-derived inbred mouse strains |
| Q35951589 | Genome-wide association between single nucleotide polymorphisms with beef fatty acid profile in Nellore cattle using the single step procedure. |
| Q59131775 | Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? |
| Q52563148 | Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation. |
| Q27318473 | Maternal nutrition induces pervasive gene expression changes but no detectable DNA methylation differences in the liver of adult offspring |
| Q39398105 | Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and Its Interaction with Contactin 2 (CNTN2). |
| Q45722488 | Moo1 obesity quantitative trait locus in BTBR T+ Itpr3tf/J mice increases food intake |
| Q26782027 | Obesity genetics in mouse and human: back and forth, and back again |
| Q33784367 | PTPRT regulates high-fat diet-induced obesity and insulin resistance |
| Q37266082 | Specific splice variants are associated with Parkinson's disease |
| Q38474337 | Systems genetics of obesity in an F2 pig model by genome-wide association, genetic network, and pathway analyses |
| Q91212051 | The virtuous cycle of human genetics and mouse models in drug discovery |
| Q47267620 | Unexpected phenotypic effects of a transgene integration causing a knockout of the endogenous Contactin-5 gene in mice. |
| Q42705169 | Widespread epistasis regulates glucose homeostasis and gene expression |
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