Pragliola A - Search Results

1

A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28.

Levin ML, Chatterjee A, Pragliola A, Worley KC, Wehnert M, Zhuchenko O, Smith RF, Lee CC, Herman GE. Levin ML, et al. Among authors: pragliola a. Genome Res. 1996 Jun;6(6):465-77. doi: 10.1101/gr.6.6.465. Genome Res. 1996. PMID: 8828036 Free article.

2

A YAC clone map spanning 7.5 megabases of human chromosome band Xq28.

Rogner UC, Kioschis P, Wilke K, Gong W, Pick E, Dietrich A, Zechner U, Hameister H, Pragliola A, Herman GE, et al. Rogner UC, et al. Among authors: pragliola a. Hum Mol Genet. 1994 Dec;3(12):2137-46. doi: 10.1093/hmg/3.12.2137. Hum Mol Genet. 1994. PMID: 7881410

3

Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes.

Incerti B, Guioli S, Pragliola A, Zanaria E, Borsani G, Tonlorenzi R, Bardoni B, Franco B, Wheeler D, Ballabio A, et al. Incerti B, et al. Among authors: pragliola a. Nat Genet. 1992 Dec;2(4):311-4. doi: 10.1038/ng1292-311. Nat Genet. 1992. PMID: 1303285

4

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tonlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, Brown CJ, Willard HF, Lawrence C, Graziella Persico M, Camerino G, Ballabio A. Franco B, et al. Among authors: pragliola a. Nature. 1991 Oct 10;353(6344):529-36. doi: 10.1038/353529a0. Nature. 1991. PMID: 1922361

5

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome.

Bick D, Franco B, Sherins RJ, Heye B, Pike L, Crawford J, Maddalena A, Incerti B, Pragliola A, Meitinger T, Ballabio A. Bick D, et al. Among authors: pragliola a. N Engl J Med. 1992 Jun 25;326(26):1752-5. doi: 10.1056/NEJM199206253262606. N Engl J Med. 1992. PMID: 1594017 Free article. No abstract available.

6

Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.

Pragliola A, Jurecic V, Chau CK, Philip N, Baldini A. Pragliola A, et al. Am J Hum Genet. 1997 Dec;61(6):1456-9. doi: 10.1086/301652. Am J Hum Genet. 1997. PMID: 9399910 Free PMC article. No abstract available.

7

Chromosomal Microarray Analysis Identifies a Novel SALL1 Deletion, Supporting the Association of Haploinsufficiency with a Mild Phenotype of Townes-Brocks Syndrome.

Innoceta AM, Olivucci G, Parmeggiani G, Scarano E, Pragliola A, Graziano C. Innoceta AM, et al. Among authors: pragliola a. Genes (Basel). 2023 Jan 19;14(2):258. doi: 10.3390/genes14020258. Genes (Basel). 2023. PMID: 36833185 Free PMC article. Review.

8

Hyperinsulinemic Hypoglycaemia in a Turner Syndrome with Ring (X).

Cappella M, Graziani V, Pragliola A, Sensi A, Hussain K, Muratori C, Marchetti F. Cappella M, et al. Among authors: pragliola a. Case Rep Pediatr. 2015;2015:561974. doi: 10.1155/2015/561974. Epub 2015 Apr 29. Case Rep Pediatr. 2015. PMID: 26064751 Free PMC article.

9

Heterogeneous phenotype of human glioblastoma: in vitro study.

Denysenko T, Gennero L, Juenemann C, Morra I, Masperi P, Ceroni V, Pragliola A, Ponzetto A, Melcarne A. Denysenko T, et al. Among authors: pragliola a. Cell Biochem Funct. 2014 Mar;32(2):164-76. doi: 10.1002/cbf.2988. Epub 2013 Jul 8. Cell Biochem Funct. 2014. PMID: 23836332

10

Acquisition of i(8q) as an early event in malignant triton tumors.

Magrini E, Pragliola A, Fantasia D, Calabrese G, Gaiba A, Farnedi A, Collina G, Pession A. Magrini E, et al. Among authors: pragliola a. Cancer Genet Cytogenet. 2004 Oct 15;154(2):150-5. doi: 10.1016/j.cancergencyto.2004.02.007. Cancer Genet Cytogenet. 2004. PMID: 15474151

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