Literature DB >> 9412851

Searching for migraine genes: exclusion of 290 cM out of the whole human genome.

L Monari1, M Mochi, M L Valentino, C Arnaldi, P Cortelli, A De Monte, G Pierangeli, G Prologo, C Scapoli, S Soriani, P Montagna.   

Abstract

A linkage and association analysis was made on 14 Italian families with recurrent migraine. We analyzed five chromosomal regions surrounding the candidate genes 5HT1D (1p36.3-34.3), 5HT1B (6q13), 5HT2A (13q14-21), 5HT transporter (17q11.2-12), CACNLB1 (17q11.2-22) and FHM (19p13), using 29 DNA polymorphic markers. All two-point lod scores were negative, and the chi 2 sib-pair analyses were not significant, thus indicating the probable exclusion of these regions as sites of migraine genes in our population.

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Year:  1997        PMID： 9412851     DOI： 10.1007/bf02083304

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN： 0392-0461


  15 in total

1.  Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene.

Authors:  P A Powers; S Liu; K Hogan; R G Gregg
Journal:  J Biol Chem       Date:  1992-11-15       Impact factor: 5.157

2.  The 1993-94 Généthon human genetic linkage map.

Authors:  G Gyapay; J Morissette; A Vignal; C Dib; C Fizames; P Millasseau; S Marc; G Bernardi; M Lathrop; J Weissenbach
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

3.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

4.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

5.  Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Authors:  R A Ophoff; G M Terwindt; M N Vergouwe; R van Eijk; P J Oefner; S M Hoffman; J E Lamerdin; H W Mohrenweiser; D E Bulman; M Ferrari; J Haan; D Lindhout; G J van Ommen; M H Hofker; M D Ferrari; R R Frants
Journal:  Cell       Date:  1996-11-01       Impact factor: 41.582

6.  Testing models for genetic determination in migraine.

Authors:  M Mochi; S Sangiorgi; P Cortelli; V Carelli; C Scapoli; M Crisci; L Monari; G Pierangeli; P Montagna
Journal:  Cephalalgia       Date:  1993-12       Impact factor: 6.292

7.  Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility.

Authors:  D E Iles; B Segers; R C Sengers; K Monsieurs; L Heytens; P J Halsall; P M Hopkins; F R Ellis; J L Hall-Curran; A D Stewart
Journal:  Hum Mol Genet       Date:  1993-07       Impact factor: 6.150

8.  A gene for familial hemiplegic migraine maps to chromosome 19.

Authors:  A Joutel; M G Bousser; V Biousse; P Labauge; H Chabriat; A Nibbio; J Maciazek; B Meyer; M A Bach; J Weissenbach
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

9.  Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.

Authors:  A May; R A Ophoff; G M Terwindt; C Urban; R van Eijk; J Haan; H C Diener; D Lindhout; R R Frants; L A Sandkuijl
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

10.  Genetic heterogeneity of familial hemiplegic migraine.

Authors:  R A Ophoff; R van Eijk; L A Sandkuijl; G M Terwindt; C P Grubben; J Haan; D Lindhout; M D Ferrari; R R Frants
Journal:  Genomics       Date:  1994-07-01       Impact factor: 5.736
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  6 in total

Review 1.  STin2 VNTR polymorphism in the serotonin transporter gene and migraine: pooled and meta-analyses.

Authors:  Markus Schürks; Pamela M Rist; Tobias Kurth
Journal:  J Headache Pain       Date:  2010-06-29       Impact factor: 7.277

Review 2.  5-HTTLPR polymorphism in the serotonin transporter gene and migraine: a systematic review and meta-analysis.

Authors:  Markus Schürks; Pamela M Rist; Tobias Kurth
Journal:  Cephalalgia       Date:  2010-03-26       Impact factor: 6.292

3.  Lack of association between five serotonin metabolism-related genes and medication overuse headache.

Authors:  Sabina Cevoli; Nadia Marzocchi; Sabina Capellari; Chiara Scapoli; Giulia Pierangeli; Daniela Grimaldi; Federica Naldi; L Alberto Pini; Pasquale Montagna; Pietro Cortelli
Journal:  J Headache Pain       Date:  2010-02       Impact factor: 7.277

Review 4.  Migraine as a sex-conditioned inherited disorder: evidences from China and the world.

Authors:  Xiao-Ping Wang; Hong-Liu Ding; Chang-Ming Geng; Yu-Mei Jiang
Journal:  Neurosci Bull       Date:  2008-04       Impact factor: 5.203

5.  The primary headaches: genetics, epigenetics and a behavioural genetic model.

Authors:  Pasquale Montagna
Journal:  J Headache Pain       Date:  2008-03-15       Impact factor: 7.277

6.  Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures.

Authors:  Rokhsareh Meamar; Maryam Ostadsharif; Mohammad Saadatnia; Abbas Ghorbani; Nayereh Nouri; Leila Dehghani; Mansoor Salehi
Journal:  J Res Med Sci       Date:  2013-03       Impact factor: 1.852
  6 in total

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