Sirchia SM - Search Results

1

Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.

Sironi E, Cerri A, Tomasini D, Sirchia SM, Porta G, Rossella F, Grati FR, Simoni G. Sironi E, et al. Among authors: sirchia sm. J Cutan Pathol. 2004 Apr;31(4):318-22. doi: 10.1111/j.0303-6987.2004.0187.x. J Cutan Pathol. 2004. PMID: 15005689

2

Confined placental mosaicism.

Simoni G, Sirchia SM. Simoni G, et al. Among authors: sirchia sm. Prenat Diagn. 1994 Dec;14(13):1185-9. doi: 10.1002/pd.1970141304. Prenat Diagn. 1994. PMID: 7617565 Review. No abstract available.

3

Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype.

Sirchia SM, De Andreis C, Pariani S, Grimoldi MG, Molinari A, Buscaglia M, Simoni G. Sirchia SM, et al. Hum Genet. 1994 Oct;94(4):355-8. doi: 10.1007/BF00201592. Hum Genet. 1994. PMID: 7927328

4

Aneuploid correction and confined placental mosaicism.

Simoni G, Sirchia SM, Fraccaro M. Simoni G, et al. Among authors: sirchia sm. Acta Genet Med Gemellol (Roma). 1996;45(1-2):153-61. doi: 10.1017/s0001566000001240. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872025 Review. No abstract available.

5

Cytogenetic abnormalities and microsatellite instability in endometrial adenocarcinoma.

Sirchia SM, Pariani S, Rossella F, Garagiola I, De Andreis C, Bulfamante G, Zannoni E, Radaelli U, Simoni G. Sirchia SM, et al. Cancer Genet Cytogenet. 1997 Apr;94(2):113-9. doi: 10.1016/s0165-4608(96)00211-7. Cancer Genet Cytogenet. 1997. PMID: 9109939

6

Highly sensitive chemiluminescent method for the detection of cell contamination.

Sirchia SM, Garagiola I, De Andreis C, Pedranzini L, Poli F, Grati FR, Diomelli B, Simoni G. Sirchia SM, et al. J Biolumin Chemilumin. 1998 Sep-Oct;13(5):303-5. doi: 10.1002/(SICI)1099-1271(1998090)13:5<303::AID-BIO492>3.0.CO;2-A. J Biolumin Chemilumin. 1998. PMID: 9839195

7

Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic study.

Aguglia U, Le Piane E, Gambardella A, Messina D, Russo C, Sirchia SM, Porta G, Quattrone A. Aguglia U, et al. Among authors: sirchia sm. Epilepsia. 1999 Sep;40(9):1316-9. doi: 10.1111/j.1528-1157.1999.tb00865.x. Epilepsia. 1999. PMID: 10487199 Free article.

8

Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas.

Grati FR, Sirchia SM, Garagiola I, Sironi E, Galioto S, Rossella F, Serafini P, Dulcetti F, Bozzetti A, Brusati R, Simoni G. Grati FR, et al. Among authors: sirchia sm. Cancer Genet Cytogenet. 2000 Apr 1;118(1):57-61. doi: 10.1016/s0165-4608(99)00199-5. Cancer Genet Cytogenet. 2000. PMID: 10731592

9

Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta2 promoter in breast cancer cells.

Sirchia SM, Ferguson AT, Sironi E, Subramanyan S, Orlandi R, Sukumar S, Sacchi N. Sirchia SM, et al. Oncogene. 2000 Mar 16;19(12):1556-63. doi: 10.1038/sj.onc.1203456. Oncogene. 2000. PMID: 10734315 Free article.

10

Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters.

Sirchia SM, Sironi E, Grati FR, Serafini P, Garagiola I, Rossella F, Dulcetti F, Pardi G, Garsia S, Simoni G. Sirchia SM, et al. Cancer Genet Cytogenet. 2000 Sep;121(2):156-62. doi: 10.1016/s0165-4608(00)00240-5. Cancer Genet Cytogenet. 2000. PMID: 11063800

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

71 results

Search Page