Mergenthaler S[au] - Search Results

Year	Number of Results
1998	1
2000	5
2001	8
2002	1
2003	2
2005	5
2009	1
2024	0

1

Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literature.

Mergenthaler S, Wollmann HA, Burger B, Eggermann K, Kaiser P, Ranke MB, Schwanitz G, Eggermann T. Mergenthaler S, et al. Ann Genet. 2000 Jan-Mar;43(1):15-21. doi: 10.1016/s0003-3995(00)00010-1. Ann Genet. 2000. PMID: 10818216 Review.

2

Origin of uniparental disomy 6: presentation of a new case and review on the literature.

Eggermann T, Marg W, Mergenthaler S, Eggermann K, Schemmel V, Stoffers U, Zerres K, Spranger S. Eggermann T, et al. Among authors: mergenthaler s. Ann Genet. 2001 Jan-Mar;44(1):41-5. doi: 10.1016/s0003-3995(01)01035-8. Ann Genet. 2001. PMID: 11334617 Review.

3

Evaluation of a soybean lectin-based method for the enrichment of erythroblasts.

Babochkina T, Mergenthaler S, Lapaire O, Kiefer V, Yura H, Koike K, Holzgreve W, Hahn S. Babochkina T, et al. Among authors: mergenthaler s. J Histochem Cytochem. 2005 Mar;53(3):329-30. doi: 10.1369/jhc.4B6408.2005. J Histochem Cytochem. 2005. PMID: 15750012

4

Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profiles.

Schoch C, Kohlmann A, Schnittger S, Brors B, Dugas M, Mergenthaler S, Kern W, Hiddemann W, Eils R, Haferlach T. Schoch C, et al. Among authors: mergenthaler s. Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):10008-13. doi: 10.1073/pnas.142103599. Epub 2002 Jul 8. Proc Natl Acad Sci U S A. 2002. PMID: 12105272 Free PMC article.

5

Tenascin-C is a novel RBPJkappa-induced target gene for Notch signaling in gliomas.

Sivasankaran B, Degen M, Ghaffari A, Hegi ME, Hamou MF, Ionescu MC, Zweifel C, Tolnay M, Wasner M, Mergenthaler S, Miserez AR, Kiss R, Lino MM, Merlo A, Chiquet-Ehrismann R, Boulay JL. Sivasankaran B, et al. Among authors: mergenthaler s. Cancer Res. 2009 Jan 15;69(2):458-65. doi: 10.1158/0008-5472.CAN-08-2610. Cancer Res. 2009. PMID: 19147558

6

Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status.

Mergenthaler S, Eggermann K, Tomiuk J, Ranke MB, Wollmann HA, Eggermann T. Mergenthaler S, et al. J Med Genet. 2000 Dec;37(12):E44. doi: 10.1136/jmg.37.12.e44. J Med Genet. 2000. PMID: 11106362 Free PMC article. No abstract available.

7

Nucleic acid based biosensors: the desires of the user.

Hahn S, Mergenthaler S, Zimmermann B, Holzgreve W. Hahn S, et al. Among authors: mergenthaler s. Bioelectrochemistry. 2005 Oct;67(2):151-4. doi: 10.1016/j.bioelechem.2004.07.006. Bioelectrochemistry. 2005. PMID: 16019267 Review.

8

Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients.

Mergenthaler S, Blagitko-Dorfs N, Wollmann HA, Ranke MB, Ropers HH, Kalscheuer VM, Eggermann T. Mergenthaler S, et al. Hum Mutat. 2000 Jul;16(1):96. doi: 10.1002/1098-1004(200007)16:1<96::AID-HUMU32>3.0.CO;2-V. Hum Mutat. 2000. PMID: 10874328 No abstract available.

9

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

Mergenthaler S, Hitchins MP, Blagitko-Dorfs N, Monk D, Wollmann HA, Ranke MB, Ropers HH, Apostolidou S, Stanier P, Preece MA, Eggermann T, Kalscheuer VM, Moore GE. Mergenthaler S, et al. Am J Hum Genet. 2001 Feb;68(2):543-5. doi: 10.1086/318192. Am J Hum Genet. 2001. PMID: 11170901 Free PMC article. No abstract available.

10

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.

Eggermann T, Eggermann K, Mergenthaler S, Kuner R, Kaiser P, Ranke MB, Wollmann HA. Eggermann T, et al. Among authors: mergenthaler s. J Med Genet. 1998 Sep;35(9):784-6. doi: 10.1136/jmg.35.9.784. J Med Genet. 1998. PMID: 9733042 Free PMC article.

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