Grønskov K - Search Results

1

The insulin-like growth factor-I receptor. Structure, ligand-binding mechanism and signal transduction.

De Meyts P, Wallach B, Christoffersen CT, Ursø B, Grønskov K, Latus LJ, Yakushiji F, Ilondo MM, Shymko RM. De Meyts P, et al. Among authors: gronskov k. Horm Res. 1994;42(4-5):152-69. doi: 10.1159/000184188. Horm Res. 1994. PMID: 7868068 Review.

2

Role of the time factor in signaling specificity: application to mitogenic and metabolic signaling by the insulin and insulin-like growth factor-I receptor tyrosine kinases.

De Meyts P, Christoffersen CT, Ursø B, Wallach B, Grønskov K, Yakushiji F, Shymko RM. De Meyts P, et al. Among authors: gronskov k. Metabolism. 1995 Oct;44(10 Suppl 4):2-11. doi: 10.1016/0026-0495(95)90214-7. Metabolism. 1995. PMID: 7476307 Review.

3

Mutation of arginine 86 to proline in the insulin receptor alpha subunit causes lack of transport of the receptor to the plasma membrane, loss of binding affinity and a constitutively activated tyrosine kinase in transfected cells.

Grønskov K, Vissing H, Shymko RM, Tornqvist H, De Meyts P. Grønskov K, et al. Biochem Biophys Res Commun. 1993 Apr 30;192(2):905-11. doi: 10.1006/bbrc.1993.1501. Biochem Biophys Res Commun. 1993. PMID: 8484793

4

Expression of insulin receptor spliced variants and their functional correlates in muscle from patients with non-insulin-dependent diabetes mellitus.

Hansen T, Bjørbaek C, Vestergaard H, Grønskov K, Bak JF, Pedersen O. Hansen T, et al. Among authors: gronskov k. J Clin Endocrinol Metab. 1993 Dec;77(6):1500-5. doi: 10.1210/jcem.77.6.8263133. J Clin Endocrinol Metab. 1993. PMID: 8263133

5

Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes.

Stoltze UK, Hansen TVO, Brok JS, Grønskov K, Tumer Z, Ahlborn LB, Schmiegelow K, Wadt KAW. Stoltze UK, et al. Among authors: gronskov k. J Med Genet. 2023 Feb;60(2):128-130. doi: 10.1136/jmedgenet-2021-108335. Epub 2022 Jun 30. J Med Genet. 2023. PMID: 35772845 Free PMC article. No abstract available.

6

Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.

Wadt KA, Aoude LG, Krogh L, Sunde L, Bojesen A, Grønskov K, Wartacz N, Ek J, Tolstrup-Andersen M, Klarskov-Andersen M, Borg Å, Heegaard S, Kiilgaard JF, Hansen TV, Klein K, Jönsson G, Drzewiecki KT, Dunø M, Hayward NK, Gerdes AM. Wadt KA, et al. Among authors: gronskov k. PLoS One. 2015 Mar 24;10(3):e0122662. doi: 10.1371/journal.pone.0122662. eCollection 2015. PLoS One. 2015. PMID: 25803691 Free PMC article.

7

A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome.

Dahl C, Grønskov K, Larsen LA, Guldberg P, Brøndum-Nielsen K. Dahl C, et al. Among authors: gronskov k. Clin Chem. 2007 Apr;53(4):790-3. doi: 10.1373/clinchem.2006.080762. Epub 2007 Jan 26. Clin Chem. 2007. PMID: 17259243

8

High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis.

Larsen LA, Grønskov K, Nørgaard-Pedersen B, Brøndum-Nielsen K, Hasholt L, Vuust J. Larsen LA, et al. Among authors: gronskov k. Hum Genet. 1997 Oct;100(5-6):564-8. doi: 10.1007/s004390050552. Hum Genet. 1997. PMID: 9341871

9

Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. Wakeling EL, et al. Among authors: gronskov k. Nat Rev Endocrinol. 2017 Feb;13(2):105-124. doi: 10.1038/nrendo.2016.138. Epub 2016 Sep 2. Nat Rev Endocrinol. 2017. PMID: 27585961

10

Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia.

Grønskov K, Olsen JH, Sand A, Pedersen W, Carlsen N, Bak Jylling AM, Lyngbye T, Brøndum-Nielsen K, Rosenberg T. Grønskov K, et al. Hum Genet. 2001 Jul;109(1):11-8. doi: 10.1007/s004390100529. Hum Genet. 2001. PMID: 11479730

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