Estivill X - Search Results

1

Mapping of the human Zn-alpha 2-glycoprotein gene (AZGP1) to chromosome 7q22 by in situ hybridization.

Pendás AM, Matilla T, Uría JA, Freije JP, Fueyo A, Estivill X, López-Otín C. Pendás AM, et al. Among authors: estivill x. Cytogenet Cell Genet. 1994;66(4):263-6. doi: 10.1159/000133708. Cytogenet Cell Genet. 1994. PMID: 8162703

2

The human collagenase-3 (CLG3) gene is located on chromosome 11q22.3 clustered to other members of the matrix metalloproteinase gene family.

Pendás AM, Matilla T, Estivill X, López-Otín C. Pendás AM, et al. Among authors: estivill x. Genomics. 1995 Apr 10;26(3):615-8. doi: 10.1016/0888-7543(95)80186-p. Genomics. 1995. PMID: 7607691

3

Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1).

Castellví-Bel S, Matilla T, Banchs MI, Kruyer H, Corral J, Milà M, Estivill X. Castellví-Bel S, et al. Among authors: estivill x. J Med Genet. 1994 Aug;31(8):654-5. doi: 10.1136/jmg.31.8.654. J Med Genet. 1994. PMID: 7815428 Free PMC article.

4

Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2.

Guimera J, Pritchard M, Nadal M, Estivill X. Guimera J, et al. Among authors: estivill x. Cytogenet Cell Genet. 1997;77(3-4):182-4. doi: 10.1159/000134571. Cytogenet Cell Genet. 1997. PMID: 9284911

5

The human HERC3 gene maps to chromosome 4q21 by fluorescence in situ hybridization.

Cruz C, Nadal M, Ventura F, Bartrons R, Estivill X, Rosa JL. Cruz C, et al. Among authors: estivill x. Cytogenet Cell Genet. 1999;87(3-4):263-4. doi: 10.1159/000015442. Cytogenet Cell Genet. 1999. PMID: 10702688 No abstract available.

6

Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.

Matilla T, Volpini V, Genís D, Rosell J, Corral J, Dávalos A, Molins A, Estivill X. Matilla T, et al. Among authors: estivill x. Hum Mol Genet. 1993 Dec;2(12):2123-8. doi: 10.1093/hmg/2.12.2123. Hum Mol Genet. 1993. PMID: 8111382

7

Molecular cloning, expression, and chromosomal localization of a ubiquitously expressed human 6-phosphofructo-2-kinase/ fructose-2, 6-bisphosphatase gene (PFKFB3).

Manzano A, Rosa JL, Ventura F, Pérez JX, Nadal M, Estivill X, Ambrosio S, Gil J, Bartrons R. Manzano A, et al. Among authors: estivill x. Cytogenet Cell Genet. 1998;83(3-4):214-7. doi: 10.1159/000015181. Cytogenet Cell Genet. 1998. PMID: 10072580

8

Prenatal diagnosis of Werdnig-Hoffmann disease: DNA analysis of a mummified umbilical cord using closely linked microsatellite markers.

Matilla T, Corral J, Miranda M, Troyano J, Morrison K, Volpini V, Estivill X. Matilla T, et al. Among authors: estivill x. Prenat Diagn. 1994 Mar;14(3):219-22. doi: 10.1002/pd.1970140314. Prenat Diagn. 1994. PMID: 8052572

9

Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms.

Genis D, Matilla T, Volpini V, Rosell J, Dávalos A, Ferrer I, Molins A, Estivill X. Genis D, et al. Among authors: estivill x. Neurology. 1995 Jan;45(1):24-30. doi: 10.1212/wnl.45.1.24. Neurology. 1995. PMID: 7824128 Free article.

10

Cloning, expression, and mapping of PDCD9, the human homolog of Gallus gallus pro-apoptotic protein p52.

Carim L, Sumoy L, Nadal M, Estivill X, Escarceller M. Carim L, et al. Among authors: estivill x. Cytogenet Cell Genet. 1999;87(1-2):85-8. doi: 10.1159/000015397. Cytogenet Cell Genet. 1999. PMID: 10640817

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