Literature DB >> 17397250

MEN1 935-1G>C splicing mutation in an Indian patient with multiple endocrine neoplasia type 1.

Rani Raghavan1, Sudeep Shah, Altaf A Kondkar, Alpa J Dherai, Devendra Desai, Phulrenu Chauhan, Murad Lala, Tester F Ashavaid.   

Abstract

BACKGROUND AND
OBJECTIVE: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome characterized mainly by multiple tumors involving parathyroid, pancreatic, and pituitary glands. To date, there have been no genetic studies reported on MEN1 in the Indian population. In order to begin to establish molecular diagnosis to improve the management of MEN1 in India, we performed a molecular analysis of the MEN1 gene in a patient of Indian origin.
METHODS: Molecular analysis of the MEN1 gene was performed to identify mutations in an Indian patient previously diagnosed with sporadic MEN1. All the 10 exons of the MEN1 gene were amplified using the polymerase chain reaction and screened by direct DNA sequencing.
RESULTS: The DNA sequencing results revealed the presence of an intronic, heterozygous, splicing mutation 935-1G>C in intron 5 of the MEN1 gene.
CONCLUSION: This study provides the first data on genetic analysis of MEN1 in Indian patients.

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Year:  2007        PMID: 17397250     DOI: 10.1007/BF03256233

Source DB:  PubMed          Journal:  Mol Diagn Ther        ISSN: 1177-1062            Impact factor:   4.074


  11 in total

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Authors:  M R Toliat; W Berger; H H Ropers; P Neuhaus; B Wiedenmann
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3.  Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group.

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4.  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

5.  Positional cloning of the gene for multiple endocrine neoplasia-type 1.

Authors:  S C Chandrasekharappa; S C Guru; P Manickam; S E Olufemi; F S Collins; M R Emmert-Buck; L V Debelenko; Z Zhuang; I A Lubensky; L A Liotta; J S Crabtree; Y Wang; B A Roe; J Weisemann; M S Boguski; S K Agarwal; M B Kester; Y S Kim; C Heppner; Q Dong; A M Spiegel; A L Burns; S J Marx
Journal:  Science       Date:  1997-04-18       Impact factor: 47.728

6.  Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis.

Authors:  A A Pannett; R V Thakker
Journal:  J Clin Endocrinol Metab       Date:  2001-09       Impact factor: 5.958

7.  Genotype-phenotype analysis in multiple endocrine neoplasia type 1.

Authors:  Maria A Kouvaraki; Jeffrey E Lee; Suzanne E Shapiro; Robert F Gagel; Steven I Sherman; Rena V Sellin; Gilbert J Cote; Douglas B Evans
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8.  Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.

Authors:  N Hai; N Aoki; A Shimatsu; T Mori; S Kosugi
Journal:  Clin Endocrinol (Oxf)       Date:  2000-04       Impact factor: 3.478

9.  Multiple endocrine neoplasia type 1 (MEN1) in two Asian families.

Authors:  B T Teh; S I Hii; R David; V Parameswaran; S Grimmond; M K Walters; T T Tan; D J Nancarrow; S P Chan; J Mennon
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Review 10.  Multiple endocrine neoplasia type 1.

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2.  Long-term follow-up and novel splice donor mutation in MEN1 in a Chinese family.

Authors:  Minghao Li; Qianqian Liu; Peihua Liu; Xiaoping Yi; Xiao Guan; Anze Yu; Longfei Liu; Feizhou Zhu
Journal:  Oncotarget       Date:  2017-12-07
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