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Juha Kere

Veröffentlichungen von Juha Kere zu Kere, Juha ->
weitere Veröffentlichungen von Juha Kere:
Kidney kinetics and chloride ion pumps (1999)
HUMAN POPULATION GENETICS: Lessons from Finland (2001)
Cystic fibrosis in Finland: a molecular and genealogical study (1989)
Cystic fibrosis mutation ΔF508 in Finland: other mutations predominate (1990)
A rare reciprocal translocation (12;21) segregating for nine generations (1993)
Genomic structure of the human ezrin gene (1998)
Cystic fibrosis in a low-incidence population: two major mutations in Finland (1994)
Mutations of the Down–regulated in adenoma (DRA) gene cause congenital chloride diarrhoea (1996)
The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells (2000)
X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein (1996)
Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187 (1992)
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28 (2000)
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population (2001)
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction (2005)
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus (2007)
Veröffentlichungen zu Kere, Juha
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1 		Kere, Juha Kidney kinetics and chloride ion pumps
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 21, No. 1 (1999), p. 67-68
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ähnliche Vorschläge 		1999
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2 		Kere, Juha. HUMAN POPULATION GENETICS: Lessons from Finland
in: Annual Review of Genomics and Human Genetics, in: Annual Review of Genomics and Human Genetics. - Palo Alto, Calif., ISSN 1527-8204 Vol. 2 (2001), p. 103-128
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ähnliche Vorschläge 		2001
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3 		Kere, Juha, Norio, Reijo, ... Cystic fibrosis in Finland: a molecular and genealogical study
in: Human genetics , ISSN 1432-1203, Vol. 83 (1. 1989), p. 20-25
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ähnliche Vorschläge 		1989
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4 		Kere, Juha, Savilahti, Erkki, ... Cystic fibrosis mutation ΔF508 in Finland: other mutations predominate
in: Human genetics , ISSN 1432-1203, Vol. 85 (4. 1990), p. 413-415
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ähnliche Vorschläge 		1990
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5 		Koskinen, Sari, Onnelainen, Tuija, ... A rare reciprocal translocation (12;21) segregating for nine generations
in: Human genetics , ISSN 1432-1203, Vol. 92 (5. 1993), p. 509-512
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ähnliche Vorschläge 		1993
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6 		Majander-Nordenswan, P., Sainio, Markku, ... Genomic structure of the human ezrin gene
in: Human genetics , ISSN 1432-1203, Vol. 103 (6. 1998), p. 662-665
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ähnliche Vorschläge 		1998
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7 		Kere, Juha, Estivill, Xavier, ... Cystic fibrosis in a low-incidence population: two major mutations in Finland
in: Human genetics , ISSN 1432-1203, Vol. 93 (2. 1994), p. 162-166
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ähnliche Vorschläge 		1994
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8 		Höglund, Pia, Haila, Siru, ... Mutations of the Down–regulated in adenoma (DRA) gene cause congenital chloride diarrhoea
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 14, No. 3 (1996), p. 316-319
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ähnliche Vorschläge 		1996
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9 		Haila, Siru, Saarialho-Kere, Ulpu, ... The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells
in: Histochemistry and cell biology , ISSN 1432-119X, Vol. 113 (4. 2000), p. 279-286
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ähnliche Vorschläge 		2000
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10 		Kere, Juha, Srivastava, Anand K., ... X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 13, No. 4 (1996), p. 409-416
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ähnliche Vorschläge 		1996
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11 		de la Chapelle, Albert, Tolvanen, Ritva, ... Gelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 2, No. 2 (1992), p. 157-160
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ähnliche Vorschläge 		1992
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12 		Taillon-Miller, Patricia, Bauer-Sardiña, Irma, ... Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 25, No. 3 (2000), p. 324-328
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ähnliche Vorschläge 		2000
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13 		Laitinen, Tarja, Daly, Mark J., ... A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 28, No. 1 (2001), p. 87-91
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ähnliche Vorschläge 		2001
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14 		Swanberg, Maria, Lidman, Olle, ... MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 37, No. 5 (2005), p. 486-494
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ähnliche Vorschläge 		2005
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15 		Lee-Kirsch, Min Ae, Gong, Maolian, ... Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 9 (2007), p. 1065-1067
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ähnliche Vorschläge 		2007
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16 		Erkko, Hannele, Xia, Bing, ... A recurrent mutation in PALB2 in Finnish cancer families
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 446, No. 7133 (2007), p. 316-319
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ähnliche Vorschläge 		2007