Messages from an isolate: lessons from the Finnish gene pool (Q41386249)

30 September 2017

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title

Messages from an isolate: lessons from the Finnish gene pool (English)

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30 September 2017

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Peltonen L

1

1 reference

PubMed ID

9072044

30 September 2017

Pekkarinen P

series ordinal

2

1 reference

PubMed ID

9072044

30 September 2017

Aaltonen J

series ordinal

3

1 reference

30 September 2017

1 December 1995

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Biological chemistry Hoppe-Seyler

30 September 2017

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30 September 2017

376

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30 September 2017

697-704

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30 September 2017

12

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Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

30 September 2017

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Refined localization of the gene causing X-linked juvenile retinoschisis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Disease gene mapping in isolated human populations: the example of Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Genetic dissection of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Mutation in gelsolin gene in Finnish hereditary amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The Finnish population structure A genetic and genealogical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Aberrant splicing of the CHM gene is a significant cause of choroideremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

A biometrical genome search in rats reveals the multigenic basis of blood pressure variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Hypertension in Dahl salt-sensitive rats: biochemical and immunohistochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Recent developments in the understanding of bradykinin receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Molecular cloning and sequence analysis of the mouse kallikrein-binding protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Molecular cloning, sequence analysis, and chromosomal localization of the human protease inhibitor 4 (kallistatin) gene (PI4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Identification of a new tissue-kallikrein-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Molecular cloning and primary structure of rat alpha 1-antitrypsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Differential interactions of human kallikrein-binding protein and alpha 1-antitrypsin with human tissue kallikrein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Chromosomal mapping of human kininogen gene (KNG) to 3q26→qter

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The glandular kallikrein family of enzymes: tissue-specific expression and hormonal regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Urinary kallikrein and salt sensitivity in essential hypertensive males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

The human kininogen gene (KNG) mapped to chromosome 3q26-qter by analysis of somatic cell hybrids using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Accelerated evolution in the reactive centre regions of serine protease inhibitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Salt and hypertension: water-sodium handling in essential hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Intramuscular delivery of rat kallikrein-binding protein gene reverses hypotension in transgenic mice expressing human tissue kallikrein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Structure and chromosomal localization of the gene (BDKRB2) encoding human bradykinin B2 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Molecular biology of tissue kallikrein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Receptor antagonists of bradykinin: a new tool to study the cardiovascular effects of endogenous kinins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Theodore Cooper Memorial Lecture. Kallikreins and kinins. Some unanswered questions about system characteristics and roles in human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Expression cloning of a rat B2 bradykinin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Primary structure and assignment to chromosome 6 of three related rat genes encoding liver serine protease inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Human bradykinin B2 receptor: nucleotide sequence analysis and assignment to chromosome 14

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Human plasma proteinase inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Direct gene delivery of human tissue kallikrein reduces blood pressure in spontaneously hypertensive rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Specific identification of tissue kallikrein in exocrine tissues and in cell-free translation products with monoclonal antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

Muscle delivery of human kallikrein gene reduces blood pressure in hypertensive rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBCHM3.1995.376.12.697

10.1515/BCHM3.1995.376.12.697

21 January 2018

Identifiers

DOI

1 reference

30 September 2017

1 reference

PubMed ID

9072044