Kristiansen A - Search Results

1

Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients.

Wilson PJ, Ramesh V, Kristiansen A, Bove C, Jozwiak S, Kwiatkowski DJ, Short MP, Haines JL. Wilson PJ, et al. Among authors: kristiansen a. Hum Mol Genet. 1996 Feb;5(2):249-56. doi: 10.1093/hmg/5.2.249. Hum Mol Genet. 1996. PMID: 8824881

2

Polymerase chain reaction amplification of a measles virus sequence from human temporal bone sections with active otosclerosis.

McKenna MJ, Kristiansen AG, Haines J. McKenna MJ, et al. Among authors: kristiansen ag. Am J Otol. 1996 Nov;17(6):827-30. Am J Otol. 1996. PMID: 8915408

3

Association of COL1A1 and otosclerosis: evidence for a shared genetic etiology with mild osteogenesis imperfecta.

McKenna MJ, Kristiansen AG, Bartley ML, Rogus JJ, Haines JL. McKenna MJ, et al. Among authors: kristiansen ag. Am J Otol. 1998 Sep;19(5):604-10. Am J Otol. 1998. PMID: 9752968

4

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.

Liu XZ, Xia XJ, Adams J, Chen ZY, Welch KO, Tekin M, Ouyang XM, Kristiansen A, Pandya A, Balkany T, Arnos KS, Nance WE. Liu XZ, et al. Among authors: kristiansen a. Hum Mol Genet. 2001 Dec 1;10(25):2945-51. doi: 10.1093/hmg/10.25.2945. Hum Mol Genet. 2001. PMID: 11741837

5

McKenna MJ, Kristiansen AG, Tropitzsch AS. McKenna MJ, et al. Ann Otol Rhinol Laryngol. 2002 Feb;111(2):184-9. doi: 10.1177/000348940211100214. Ann Otol Rhinol Laryngol. 2002. PMID: 11860074

6

Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis.

McKenna MJ, Nguyen-Huynh AT, Kristiansen AG. McKenna MJ, et al. Otol Neurotol. 2004 Jul;25(4):447-50. doi: 10.1097/00129492-200407000-00008. Otol Neurotol. 2004. PMID: 15241219

7

Temporal bone histopathologic and genetic studies in Mohr-Tranebjaerg syndrome (DFN-1).

Merchant SN, McKenna MJ, Nadol JB Jr, Kristiansen AG, Tropitzsch A, Lindal S, Tranebjaeizrg L. Merchant SN, et al. Among authors: kristiansen ag. Otol Neurotol. 2001 Jul;22(4):506-11. doi: 10.1097/00129492-200107000-00017. Otol Neurotol. 2001. PMID: 11449109

8

Deoxyribonucleic acid contamination in archival human temporal bones: a potentially significant problem.

McKenna MJ, Kristiansen AG, Tropitzsch AS, Tranebjaerg L, Merchant SN. McKenna MJ, et al. Otol Neurotol. 2002 Sep;23(5):789-92. doi: 10.1097/00129492-200209000-00030. Otol Neurotol. 2002. PMID: 12218636

9

Molecular biology of otosclerosis.

McKenna MJ, Kristiansen AG. McKenna MJ, et al. Adv Otorhinolaryngol. 2007;65:68-74. doi: 10.1159/000098674. Adv Otorhinolaryngol. 2007. PMID: 17245026 Review.

10

Studies of otic capsule morphology and gene expression in the Mov13 mouse--an animal model of type I osteogenesis imperfecta.

Stankovic KM, Kristiansen AG, Bizaki A, Lister M, Adams JC, McKenna MJ. Stankovic KM, et al. Among authors: kristiansen ag. Audiol Neurootol. 2007;12(5):334-43. doi: 10.1159/000104789. Epub 2007 Jun 26. Audiol Neurootol. 2007. PMID: 17595534

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