Tiina Marttila
Overview
Explore the profile of Tiina Marttila including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
160
Followers
0
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Recent Articles
1.
Kulkarni A, Ferreira T, Bretscher C, Grewenig A, El-Andaloussi N, Bonifati S, et al.
Nat Commun
. 2021 Jun;
12(1):3834.
PMID: 34158478
H-1 parvovirus (H-1PV) is a promising anticancer therapy. However, in-depth understanding of its life cycle, including the host cell factors needed for infectivity and oncolysis, is lacking. This understanding may...
2.
Hristov G, Marttila T, Durand C, Niesler B, Rappold G, Marchini A
Hum Mol Genet
. 2013 Nov;
23(6):1619-30.
PMID: 24186869
The SHOX gene encodes for a transcription factor important for normal bone development. Mutations in the gene are associated with idiopathic short stature and are responsible for the growth failure...
3.
Li J, Bonifati S, Hristov G, Marttila T, Valmary-Degano S, Stanzel S, et al.
EMBO Mol Med
. 2013 Oct;
5(10):1537-55.
PMID: 24092664
The rat parvovirus H-1PV has oncolytic and tumour-suppressive properties potentially exploitable in cancer therapy. This possibility is being explored and results are encouraging, but it is necessary to improve the...
4.
Allaume X, El-Andaloussi N, Leuchs B, Bonifati S, Kulkarni A, Marttila T, et al.
J Virol
. 2012 Jan;
86(7):3452-65.
PMID: 22258256
The rat parvovirus H-1PV is a promising anticancer agent given its oncosuppressive properties and the absence of known side effects in humans. H-1PV replicates preferentially in transformed cells, but the...
5.
Marchini A, Hacker B, Marttila T, Hesse V, Emons J, Weiss B, et al.
Hum Mol Genet
. 2007 Sep;
16(24):3081-7.
PMID: 17881654
Short stature due to SHOX deficiency represents a common congenital form of growth failure and is involved in the aetiology of 'idiopathic' short stature and the growth deficits and skeletal...
6.
Marchini A, Daeffler L, Marttila T, Schneider K, Blaschke R, Schnolzer M, et al.
J Mol Biol
. 2005 Dec;
355(3):590-603.
PMID: 16325853
Mutations within the homeobox SHOX gene have been associated with short stature and the skeletal deformities found in Léri-Weill, Turner and Langer syndromes implying an involvement of SHOX in growth...
7.
Schneider K, Marchini A, Sabherwal N, Roth R, Niesler B, Marttila T, et al.
Hum Mutat
. 2005 Jun;
26(1):44-52.
PMID: 15931687
Haploinsufficiency of the short stature homeobox gene SHOX has been found in patients with idiopathic short stature (ISS) and Leri-Weill dyschondrosteosis (LWD). In addition to complete gene deletions and nonsense...
8.
Marchini A, Marttila T, Winter A, Caldeira S, Malanchi I, Blaschke R, et al.
J Biol Chem
. 2004 May;
279(35):37103-14.
PMID: 15145945
Mutations in the homeobox gene SHOX cause growth retardation and the skeletal abnormalities associated with Léri-Weill, Langer, and Turner syndromes. Little is known about the mechanism underlying these SHOX-related inherited...