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Leena Peltonen

Veröffentlichungen von Leena Peltonen zu Peltonen, Leena ->
weitere Veröffentlichungen von Leena Peltonen:
Alterations in copper and collagen metabolism in Menkes' syndrome and a new subtype of Ehlers-Danlos syndrome (1983)
All out for chromosome six (1995)
From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene (1997)
From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene (1997)
Effects of aging and life-long physical training on collagen in slow and fast skeletal muscle in rats (1987)
BglII RFLPs in the COL1A2 gene in the Finnish population (1988)
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4 (1990)
Elicitor-induced changes of phenylalanine ammonia-lyase activity in barley cell suspension cultures (1997)
Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome (1994)
From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene (1997)
An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21 (1994)
Three-dimensional structure of human lysosomal aspartylglucosaminidase (1995)
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24 (1995)
Large-scale purification and preliminary X-ray diffraction studies of human aspartylglucosaminidase (1996)
DNA-polymorphism of type I collagen gene detected with Bgl II in the genetically isolated finnish population (1987)
Veröffentlichungen zu Peltonen, Leena
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1
Peltonen, Leena. Alterations in copper and collagen metabolism in Menkes' syndrome and a new subtype of Ehlers-Danlos syndrome
In: Biochemistry. - Columbus, Ohio : American Chemical Society, ISSN 1520-4995, Vol. 22, No. 26 (1983), p. 6156-6163
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1983
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2
Peltonen, Leena All out for chromosome six
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 378, No. 6558 (1995), p. 665-666
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1995
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3
Hellsten, Elina. From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 28, No. 01 (2. 1997), p. 9-11
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1997
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4
Hellsten, Elina. From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 28, No. 01 (2. 1997), p. 9-11
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1997
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5
Kovanen, Vuokko, Suominen, Harri, ... Effects of aging and life-long physical training on collagen in slow and fast skeletal muscle in rats
in: Cell & tissue research , ISSN 1432-0878, Vol. 248 (2. 1987), p. 247-255
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1987
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6
Ahti, Hannele, Palotie, Aarno, ... BglII RFLPs in the COL1A2 gene in the Finnish population
in: Human genetics , ISSN 1432-1203, Vol. 80 (1. 1988), p. 110-110
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1988
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7
Grön, Kristiina, Aula, Pertti, ... Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4
in: Human genetics , ISSN 1432-1203, Vol. 85 (2. 1990), p. 233-236
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1990
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8
Peltonen, Sari, Mannonen, Leena, ... Elicitor-induced changes of phenylalanine ammonia-lyase activity in barley cell suspension cultures
in: Plant cell, tissue and organ culture , ISSN 1573-5044, Vol. 50 (3. 1997), p. 185-193
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1997
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9
Kainulainen, Katariina, Karttunen, Leena, ... Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 6, No. 1 (1994), p. 64-69
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1994
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10
Hellsten, Elina., Vesa, Jouni., ... From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 28, No. 01 (1997), p. 9-11
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1997
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11
Aaltonen, Johanna, Björses, Petra, ... An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 8, No. 1 (1994), p. 83-87
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1994
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12
Oinonen, Carita, Tikkanen, Ritva, ... Three-dimensional structure of human lysosomal aspartylglucosaminidase
in: Nature structural biology . - New York, NY : Nature America, ISSN 1072-8368, Vol. 2, No. 12 (1995), p. 1102-1108
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1995
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13
Paavola, Paulina, Salonen, Riitta, ... The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 11, No. 2 (1995), p. 213-215
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1995
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14
Tikkanen, Ritva., Rouvinen, Juha., ... Large-scale purification and preliminary X-ray diffraction studies of human aspartylglucosaminidase
in: Proteins: Structure, Function, and Genetics, in: Proteins: Structure, Function, and Genetics . - New York, NY : Wiley-Liss, ISSN 0887-3585, ZDB-ID 1475032-6 Vol. 24 (2. 1996), p. 253-258
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1996
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15
Ahti, Hannele, Palotie, Aarno, ... DNA-polymorphism of type I collagen gene detected with Bgl II in the genetically isolated finnish population
in: Human genetics , ISSN 1432-1203, Vol. 75 (1. 1987), p. 79-80
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1987
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16
Helminen, Päivi, Johnsson, Vivian, ... Proving paternity of children with deceased fathers
in: Human genetics , ISSN 1432-1203, Vol. 87 (6. 1991), p. 657-660
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1991
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17
Helminen, Päivi, Johnsson, Vivian, ... Proving paternity of children with deceased fathers
in: Human genetics , ISSN 1432-1203, Vol. 90 (1/2. 1992), p. 193-193
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1992
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18
Ikonen, Elina, Ignatius, Jaakko, ... Huntington disease in Finland: a molecular and genealogical study
in: Human genetics , ISSN 1432-1203, Vol. 89 (3. 1992), p. 275-280
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1992
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19
Nieminen, Pekka, Arte, Sirpa, ... Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes
in: Human genetics , ISSN 1432-1203, Vol. 96 (3. 1995), p. 305-308
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1995
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20
Schleutker, Johanna, Haataja, Leena, ... Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease
in: Human genetics , ISSN 1432-1203, Vol. 88 (1. 1991), p. 95-97
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1991