T Hagemann
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Explore the profile of T Hagemann including associated specialties, affiliations and a list of published articles.
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Articles
26
Citations
343
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Recent Articles
11.
Hagemann T, Gunawan B, Schulz M, Fuzesi L, Binder C
Eur J Cancer
. 2001 Sep;
37(15):1839-46.
PMID: 11576837
Altered expression of matrix metalloproteases (MMPs) and their inhibitors, the tissue inhibitors of matrix metalloproteases (TIMPs), has been demonstrated in various tumour tissues. mRNA expression patterns of MMP-1, MMP-2, MMP-3,...
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Zhu Q, Zhang M, Rawlings D, Vihinen M, Hagemann T, Saffran D, et al.
J Exp Med
. 1994 Aug;
180(2):461-70.
PMID: 7519238
The gene responsible for X-linked agammaglobulinemia (XLA) has been recently identified to code for a cytoplasmic tyrosine kinase (Bruton's agammaglobulinemia tyrosine kinase, BTK), required for normal B cell development. BTK,...
14.
Kwan S, Walker A, Hagemann T, Gupta S, Vayuvegula B, Ochs H
Prenat Diagn
. 1994 Jun;
14(6):493-6.
PMID: 7937587
X-linked agammaglobulinaemia is an inherited recessive disease in which the primary defect lies in the failure of pre-B cells to develop into mature circulating B cells, due to a defective...
15.
Hagemann T, Surosky R, Monaco A, Lehrach H, Rosen F, Kwan S
Genomics
. 1994 May;
21(1):262-5.
PMID: 8088799
By using yeast artificial chromosome (YAC) clones, we have generated a physical map of the short arm of the human X chromosome at Xp11.23. The region analyzed spans the distal...
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Kwan S, Lehner T, Hagemann T, Lu B, Blaese M, Ochs H, et al.
Genomics
. 1991 May;
10(1):29-33.
PMID: 1675197
The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive genetic disease in which the basic molecular defect is unknown. We previously located the WAS gene between two DNA markers, DXS7 (Xp11.3)...
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