Swedish population substructure revealed by genome-wide single nucleotide polymorphism dataThe axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexiaCentrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organizationPopulation substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPsMyotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophyEctodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cellsMicrosatellite diversity and the demographic history of modern humansMapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchangerFunctional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathiaIdentification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cellsDYX1C1 functions in neuronal migration in developing neocortexCharacterization of GPRA, a novel G protein-coupled receptor related to asthmaIntrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancerIncreased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neuronsX-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinDCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingMutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoeaIsoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domainsFunctional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexiaSplit hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosusGenetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait.Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Direct selection: a method for the isolation of cDNAs encoded by large genomic regionsHuman chromosome 7: DNA sequence and biologyThe human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosusA common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysisAbsence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaA candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brainFine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribedSex specific protective effects of interleukin-9 receptor haplotypes on childhood wheezing and sensitisationTransglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationA missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage diseaseGenomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern EuropeThe anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeatsThe IL9R region contribution in asthma is supported by genetic association in an isolated populationGene mapping in isolated populations: new roles for old friends?SLC26A7: a basolateral Cl-/HCO3- exchanger specific to intercalated cells of the outer medullary collecting duct
P50
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P50
description
Finnish researcher, MD, PhD, p ...... Karolinska Institutet, Sweden)
@en
Fins arts
@nl
dokter asal Finlandia
@id
finnischer Arzt und Professor
@de
suomalainen tutkija, lääkäri, ...... genetiikan professori (Ruotsi)
@fi
طبيب فنلندي
@ar
name
Juha Kere
@ast
Juha Kere
@ca
Juha Kere
@en
Juha Kere
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Juha Kere
@fi
Juha Kere
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Juha Kere
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Juha Kere
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Juha Kere
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Juha Kere
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type
label
Juha Kere
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Juha Kere
@ca
Juha Kere
@en
Juha Kere
@es
Juha Kere
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Juha Kere
@fr
Juha Kere
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Juha Kere
@nl
Juha Kere
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Juha Kere
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altLabel
Kere, Juha Kalervo.
@en
prefLabel
Juha Kere
@ast
Juha Kere
@ca
Juha Kere
@en
Juha Kere
@es
Juha Kere
@fi
Juha Kere
@fr
Juha Kere
@ga
Juha Kere
@nl
Juha Kere
@sl
Juha Kere
@sq
P1015
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P244
P5587
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P1015
P1053
A-9179-2008
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P3829
P4854
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0000-0003-1974-0271
P5587
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