Wengler GS - Search Results

1

High prevalence of nonsense, frame shift, and splice-site mutations in 16 patients with full-blown Wiskott-Aldrich syndrome.

Wengler GS, Notarangelo LD, Berardelli S, Pollonni G, Mella P, Fasth A, Ugazio AG, Parolini O. Wengler GS, et al. Blood. 1995 Nov 15;86(10):3648-54. Blood. 1995. PMID: 7579329 Free article.

2

Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1).

Wengler GS, Giliani S, Fiorini M, Mella P, Mantuano E, Zanola A, Pollonini G, Eibl MM, Ugazio AG, Notarangelo LD, Parolini O. Wengler GS, et al. Br J Haematol. 1998 Jun;101(3):586-91. doi: 10.1046/j.1365-2141.1998.00721.x. Br J Haematol. 1998. PMID: 9633906 Free article.

3

Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis.

Giliani S, Fiorini M, Mella P, Candotti F, Schumacher RF, Wengler GS, Lalatta F, Fasth A, Badolato R, Ugazio AG, Albertini A, Notarangelo LD. Giliani S, et al. Among authors: wengler gs. Prenat Diagn. 1999 Jan;19(1):36-40. Prenat Diagn. 1999. PMID: 10073904

4

Mutation analysis in Wiskott Aldrich syndrome on chorionic villus DNA.

Wengler GS, Notarangelo LD, Giliani S, Pirastru MG, Ugazio AG, Parolini O. Wengler GS, et al. Lancet. 1995 Sep 2;346(8975):641-2. doi: 10.1016/s0140-6736(95)91477-3. Lancet. 1995. PMID: 7651032 No abstract available.

5

A PCR-based non-radioactive X-chromosome inactivation assay for genetic counseling in X-linked primary immunodeficiencies.

Wengler GS, Parolini O, Fiorini M, Mella P, Smith H, Ugazio AG, Notarangelo LD. Wengler GS, et al. Life Sci. 1997;61(14):1405-11. doi: 10.1016/s0024-3205(97)00686-3. Life Sci. 1997. PMID: 9335230

6

In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI).

Wengler GS, Lanfranchi A, Frusca T, Verardi R, Neva A, Brugnoni D, Giliani S, Fiorini M, Mella P, Guandalini F, Mazzolari E, Pecorelli S, Notarangelo LD, Porta F, Ugazio AG. Wengler GS, et al. Lancet. 1996 Nov 30;348(9040):1484-7. doi: 10.1016/s0140-6736(96)09392-0. Lancet. 1996. PMID: 8942778

7

Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency.

Wengler GS, Allen RC, Parolini O, Smith H, Conley ME. Wengler GS, et al. J Immunol. 1993 Jan 15;150(2):700-4. J Immunol. 1993. PMID: 8093460

8

Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome.

Wengler G, Gorlin JB, Williamson JM, Rosen FS, Bing DH. Wengler G, et al. Blood. 1995 May 1;85(9):2471-7. Blood. 1995. PMID: 7537115 Free article.

9

Molecular signature detection of circulating tumor cells using a panel of selected genes.

Gervasoni A, Monasterio Muñoz RM, Wengler GS, Rizzi A, Zaniboni A, Parolini O. Gervasoni A, et al. Among authors: wengler gs. Cancer Lett. 2008 May 18;263(2):267-79. doi: 10.1016/j.canlet.2008.01.003. Epub 2008 Feb 8. Cancer Lett. 2008. PMID: 18262345

10

Use of highly sensitive mitochondrial probes to detect microchimerism in xenotransplantation models.

Soncini M, Signoroni PB, Bailo M, Zatti D, Gregori A, Lombardi G, Albertini A, Wengler GS, Parolini O. Soncini M, et al. Among authors: wengler gs. Xenotransplantation. 2006 Jan;13(1):80-5. doi: 10.1111/j.1399-3089.2005.00256.x. Xenotransplantation. 2006. PMID: 16497216

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