About: Jean-Marc Lalouel

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Ph.D. in medicine

Attributes	Values
rdf:type	Item
description	docteur en médecine (fr) Ph.D. in medicine (en)
rdfs:label	Jean-Marc Lalouel (de) Jean-Marc Lalouel (en) Jean-Marc Lalouel (es) Jean-Marc Lalouel (fr) Jean-Marc Lalouel (nl) Jean-Marc Lalouel (ast)
skos:prefLabel	Jean-Marc Lalouel (de) Jean-Marc Lalouel (en) Jean-Marc Lalouel (es) Jean-Marc Lalouel (fr) Jean-Marc Lalouel (nl) Jean-Marc Lalouel (ast)
name	Jean-Marc Lalouel (de) Jean-Marc Lalouel (en) Jean-Marc Lalouel (es) Jean-Marc Lalouel (fr) Jean-Marc Lalouel (nl) Jean-Marc Lalouel (ast)
given name	wds:Q67189879-518187A7-F64E-4D73-ACAF-2102C5C24898
given name	Jean-Marc
instance of	wds:Q67189879-F63DBC64-5BF3-4547-AFAE-500F5F901060
instance of	Homo sapiens
skos:altLabel	J Lalouel (en) J M Lalouel (en) J-M Lalouel (en) J. Lalouel (en) J. M. Lalouel (en) J.-M. Lalouel (en) JM Lalouel (en) Lalouel (en) Lalouel J (en) Lalouel J. (en) Lalouel J. M. (en) Lalouel J.-M. (en) Lalouel JM (en)
sex or gender	wds:Q67189879-d80a32b5-4041-5b16-c599-774ec26960e6
sex or gender	male
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67189879
is author of	The CEPH consortium linkage map of human chromosome 1 Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene Guidelines of the National Heart, Lung, and Blood Institute Working Group on Blood Drawing, Processing, and Storage for Genetic Studies Isolation and mapping of a polymorphic DNA sequence (pMCA1-1) on chromosome 15 [D15S33] Isolation and mapping of a polymorphic DNA sequence (pMCT15) on chromosome 21 [D21S113] Etiological heterogeneity in X-linked spastic paraplegia Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy Easy calculations of lod scores and genetic risks on small computers Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information Isolation and mapping of a polymorphic DNA sequence pEKZ105 on chromosome 2 (D2S55). Twenty loci form a continuous linkage map of markers for human chromosome 2 Report of the Committee on Methods of Linkage Analysis and Reporting Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. Genotyping and sequence analysis of apolipoprotein E isoforms Isolation and mapping of a polymorphic DNA sequence (pRMU7.4) on chromosome 7p [D7S370] Chromosome mapping with DNA markers A mutation of angiotensinogen in a patient with preeclampsia leads to altered kinetics of the renin-angiotensin system. A unified model for complex segregation analysis Exclusion of the Na(+)-H+ antiporter as a candidate gene in human essential hypertension Multilocus linkage analysis in humans: detection of linkage and estimation of recombination Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Molecular basis of human hypertension: role of angiotensinogen A systematic study of HLA class II-beta DNA restriction fragments in insulin-dependent diabetes mellitus Isolation and mapping of a polymorphic DNA sequence pRMU3 on chromosome 17q [D17S24] A mapped set of DNA markers for human chromosome 17. Strategies for multilocus linkage analysis in humans Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44). Linkage studies in spinocerebellar ataxia (SCA) A linkage and physical map of chromosome 22, and some applications to gene mapping Isolation and mapping of a polymorphic DNA sequence (pYNZ32) on chromosome 4p [D4S125] Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57] Construction of human linkage maps: likelihood calculations for multilocus linkage analysis. Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84] Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22). Isolation and mapping of a polymorphic DNA sequence (pHHH157) on chromosome 6p [D6S29] Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro Isolation and mapping of a polymorphic DNA sequence cEFD52 on chromosome 17q [D17S26] Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22 A primary genetic map of markers of human chromosome 10 Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript The carboxyl-terminal domain of lipoprotein lipase binds to the low density lipoprotein receptor-related protein/alpha 2-macroglobulin receptor (LRP) and mediates binding of normal very low density lipoproteins to LRP. Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30). Isolation and mapping of a polymorphic DNA sequence (pEFD64.2) on chromosome 3 [D3S46] Isolation and mapping of a polymorphic DNA sequence (pEFD134.7) on chromosome 3 [D3S45] Isolation and mapping of a polymorphic DNA sequence (cMCOD13) on chromosome 3 [D3S44] Isolation and mapping of a polymorphic DNA sequence (pEFD145) on chromosome 3 [D3S32] Isolation and mapping of a polymorphic DNA sequence (pMCT32.1) on chromosome 3 [D3S31] Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3. Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4] Twelve loci form a continuous linkage map for human chromosome 18 Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome A closely linked genetic marker for cystic fibrosis

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