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Results: 26-50/52
Authors:
Kere, J
Hoglund, P
Citation: J. Kere et P. Hoglund, Inherited disorders of ion transport in the intestine, CUR OP GEN, 10(3), 2000, pp. 306-309
Authors:
Haila, S
Saarialho-Kere, U
Karjalainen-Lindsberg, ML
Lohi, H
Airola, K
Holmberg, C
Hastbacka, J
Kere, J
Hoglund, P
Citation: S. Haila et al., The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells, HISTOCHEM C, 113(4), 2000, pp. 279-286
Authors:
Lohi, H
Kujala, M
Kerkela, E
Saarialho-Kere, U
Kestila, M
Kere, J
Citation: H. Lohi et al., Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger, GENOMICS, 70(1), 2000, pp. 102-112
Authors:
Niemela, M
Lemeta, S
Sainio, M
Rauma, S
Pukkala, E
Kere, J
Bohling, T
Laatikainen, L
Jaaskelainen, J
Summanen, P
Citation: M. Niemela et al., Hemangioblastomas of the retina: impact of von Hippel-Lindau disease, INV OPHTH V, 41(7), 2000, pp. 1909-1915
Authors:
Nopola-Hemmi, J
Taipale, M
Haltia, T
Lehesjoki, AE
Voutilainen, A
Kere, J
Citation: J. Nopola-hemmi et al., Two translocations of chromosome 15q associated with dyslexia, J MED GENET, 37(10), 2000, pp. 771-775
Authors:
Rechardt, O
Elomaa, O
Vaalamo, M
Paakkonen, K
Jahkola, T
Hook-Nikanne, J
Hembry, RM
Hakkinen, L
Kere, J
Saarialho-Kere, U
Citation: O. Rechardt et al., Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines, J INVES DER, 115(5), 2000, pp. 778-787
Authors:
Huopio, H
Reimann, F
Ashfield, R
Komulainen, J
Lenko, HL
Rahier, J
Vauhkonen, I
Kere, J
Laakso, M
Ashcroft, F
Otonkoski, T
Citation: H. Huopio et al., Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1, J CLIN INV, 106(7), 2000, pp. 897-906
Authors:
Cambiaghi, S
Restano, L
Paakkonen, K
Caputo, R
Kere, J
Citation: S. Cambiaghi et al., Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia, ARCH DERMAT, 136(2), 2000, pp. 217-224
Authors:
Toivonen, HTT
Onkamo, P
Vasko, K
Ollikainen, V
Sevon, P
Mannila, H
Herr, M
Kere, J
Citation: Htt. Toivonen et al., Data mining applied to linkage disequilibrium mapping, AM J HU GEN, 67(1), 2000, pp. 133-145
Authors:
Virolainen, E
Wessman, M
Hovatta, I
Niemi, KM
Ignatius, J
Kere, J
Peltonen, L
Palotie, A
Citation: E. Virolainen et al., Assignment of a novel locus for autosomal recessive congenital ichthyosis chromosome 19p13.1-p13.2, AM J HU GEN, 66(3), 2000, pp. 1132-1137
Authors:
Kaksonen, R
Pyykko, I
Kere, J
Starck, J
Toppila, E
Citation: R. Kaksonen et al., Hereditary hearing loss - the role of environmental factors, ACT OTO-LAR, 2000, pp. 70-72
Authors:
Jorde, LB
Watkins, WS
Kere, J
Nyman, D
Eriksson, AW
Citation: Lb. Jorde et al., Gene mapping in isolated populations: New roles for old friends?, HUMAN HERED, 50(1), 2000, pp. 57-65
Authors:
Kere, J
Citation: J. Kere, Kidney kinetics and chloride ion pumps, NAT GENET, 21(1), 1999, pp. 67-68
Authors:
Laiho, E
Niemi, KM
Ignatius, J
Kere, J
Palotie, A
Saarialho-Kere, U
Citation: E. Laiho et al., Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis, EUR J HUM G, 7(6), 1999, pp. 625-632
Authors:
Salmikangas, P
Mykkanen, OM
Gronholm, M
Heiska, L
Kere, J
Carpen, O
Citation: P. Salmikangas et al., Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy, HUM MOL GEN, 8(7), 1999, pp. 1329-1336
Authors:
Ezer, S
Bayes, M
Elomaa, O
Schlessinger, D
Kere, J
Citation: S. Ezer et al., Ectodysplasin 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 cells, HUM MOL GEN, 8(11), 1999, pp. 2079-2086
Authors:
Mikkola, ML
Pispa, J
Pekkanen, M
Paulin, L
Nieminen, P
Kere, J
Thesleff, I
Citation: Ml. Mikkola et al., Ectodysplasin, a protein required for epithelial morphogenesis, is a novelTNF homologue and promotes cell-matrix adhesion, MECH DEVEL, 88(2), 1999, pp. 133-146
Authors:
Swan, H
Piippo, K
Viitasalo, M
Heikkila, P
Paavonen, T
Kainulainen, K
Kere, J
Keto, P
Kontula, I
Toivonen, L
Citation: H. Swan et al., Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts, J AM COL C, 34(7), 1999, pp. 2035-2042
Authors:
Kere, J
Lohi, H
Hoglund, P
Citation: J. Kere et al., Genetic disorders of membrane transport - III. Congenital chloride diarrhea, AM J P-GAST, 39(1), 1999, pp. G7-G13
Authors:
Moseley, RH
Hoglund, P
Wu, GD
Silberg, DG
Haila, S
De la Chapelle, A
Holmberg, C
Kere, J
Citation: Rh. Moseley et al., Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea, AM J P-GAST, 39(1), 1999, pp. G185-G192
Authors:
Pengue, G
Srivastava, AK
Kere, J
Schlessinger, D
Durmowicz, MC
Citation: G. Pengue et al., Functional characterization of the promoter of the X-linked ectodermal dysplasia gene, J BIOL CHEM, 274(37), 1999, pp. 26477-26484
Authors:
Otonkoski, T
Ammala, C
Huopio, H
Cote, GJ
Chapman, J
Cosgrove, K
Ashfield, R
Huang, E
Komulainen, J
Ashcroft, FM
Dunne, MJ
Kere, J
Thomas, PM
Citation: T. Otonkoski et al., A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland, DIABETES, 48(2), 1999, pp. 408-415
Authors:
Pispa, J
Jung, HS
Jernvall, J
Kettunen, P
Mustonen, T
Tabata, MJ
Kere, J
Thesleff, I
Citation: J. Pispa et al., Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF, DEVELOP BIO, 216(2), 1999, pp. 521-534
Authors:
Bjorkqvist, AM
Wolf, M
Nordling, S
Tammilehto, L
Knuuttila, A
Kere, J
Mattson, K
Knuutila, S
Citation: Am. Bjorkqvist et al., Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis, BR J CANC, 81(7), 1999, pp. 1111-1115
Authors:
Watowich, SS
Xie, XL
Klingmuller, U
Kere, J
Lindlof, M
Berglund, S
de la Chapelle, A
Citation: Ss. Watowich et al., Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state, BLOOD, 94(7), 1999, pp. 2530-2532