Literature DB >> 1303246

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease.

R S Kandt1, J L Haines, M Smith, H Northrup, R J Gardner, M P Short, K Dumars, E S Roach, S Steingold, S Wall.   

Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects numerous body systems including skin, brain and kidneys. Some TSC has been linked to chromosome 9, additional TSC genes on chromosomes 11 and 12 have been proposed, but the majority of TSC families remain unlinked. Using TSC families in which data had excluded linkage to chromosome 9, we failed to detect linkage with loci on chromosomes 11, 12 and others. One marker examined was D16S283, the closest locus on the proximal side of the polycystic kidney disease type 1 (PKD1) gene. Linkage between TSC and D16S283 demonstrated a lod score of 9.50 at theta = 0.02 with one family independently presenting a lod score of 4.44 at theta = 0.05. These data reveal an important TSC locus near the region of PKD1 on chromosome 16p13.

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Year:  1992        PMID: 1303246     DOI: 10.1038/ng0992-37

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  73 in total

1.  Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.

Authors:  M van Slegtenhorst; S Verhoef; A Tempelaars; L Bakker; Q Wang; M Wessels; R Bakker; M Nellist; D Lindhout; D Halley; A van den Ouweland
Journal:  J Med Genet       Date:  1999-04       Impact factor: 6.318

Review 2.  Ras and Rap signaling in synaptic plasticity and mental disorders.

Authors:  Ruth L Stornetta; J Julius Zhu
Journal:  Neuroscientist       Date:  2010-04-29       Impact factor: 7.519

Review 3.  Amino acid management in cancer.

Authors:  Zhi-Yang Tsun; Richard Possemato
Journal:  Semin Cell Dev Biol       Date:  2015-08-12       Impact factor: 7.727

4.  The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.

Authors:  H C Tsou; D H Teng; X L Ping; V Brancolini; T Davis; R Hu; X X Xie; A C Gruener; C A Schrager; A M Christiano; C Eng; P Steck; J Ott; S V Tavtigian; M Peacocke
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 5.  Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature.

Authors:  Elisabeth B Winterkorn; Ghaleb H Daouk; Sudha Anupindi; Elizabeth A Thiele
Journal:  Pediatr Nephrol       Date:  2006-06-22       Impact factor: 3.714

6.  Resting and task-modulated high-frequency brain rhythms measured by scalp encephalography in infants with tuberous sclerosis complex.

Authors:  Catherine Stamoulis; Vanessa Vogel-Farley; Geneva Degregorio; Shafali S Jeste; Charles A Nelson
Journal:  J Autism Dev Disord       Date:  2015-02

Review 7.  Roles for neuronal and glial autophagy in synaptic pruning during development.

Authors:  Ori J Lieberman; Avery F McGuirt; Guomei Tang; David Sulzer
Journal:  Neurobiol Dis       Date:  2018-04-28       Impact factor: 5.996

Review 8.  Neurological manifestations of tuberous sclerosis complex.

Authors:  P Curatolo
Journal:  Childs Nerv Syst       Date:  1996-09       Impact factor: 1.475

9.  Autism in tuberous sclerosis complex.

Authors:  G C Gutierrez; S L Smalley; P E Tanguay
Journal:  J Autism Dev Disord       Date:  1998-04

10.  Autism and tuberous sclerosis complex: prevalence and clinical features.

Authors:  P Baker; J Piven; Y Sato
Journal:  J Autism Dev Disord       Date:  1998-08
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