Nadal M - Search Results

1

Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons.

Pujana MA, Nadal M, Guitart M, Armengol L, Gratacòs M, Estivill X. Pujana MA, et al. Among authors: nadal m. Eur J Hum Genet. 2002 Jan;10(1):26-35. doi: 10.1038/sj.ejhg.5200760. Eur J Hum Genet. 2002. PMID: 11896453

2

Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.

Pujana MA, Nadal M, Gratacòs M, Peral B, Csiszar K, González-Sarmiento R, Sumoy L, Estivill X. Pujana MA, et al. Among authors: nadal m. Genome Res. 2001 Jan;11(1):98-111. doi: 10.1101/gr.155601. Genome Res. 2001. PMID: 11156619 Free PMC article.

3

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: nadal m. Cytogenet Cell Genet. 1997;77(3-4):182-4. doi: 10.1159/000134571. Cytogenet Cell Genet. 1997. PMID: 9284911

4

Cloning of the human phospholipase A2 activating protein (hPLAP) gene on the chromosome 9p21 melanoma deleted region.

Ruiz A, Nadal M, Puig S, Estivill X. Ruiz A, et al. Among authors: nadal m. Gene. 1999 Oct 18;239(1):155-61. doi: 10.1016/s0378-1119(99)00354-6. Gene. 1999. PMID: 10571045

5

HMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expression.

Sumoy L, Carim L, Escarceller M, Nadal M, Gratacòs M, Pujana MA, Estivill X, Peral B. Sumoy L, et al. Among authors: nadal m. Cytogenet Cell Genet. 2000;88(1-2):62-7. doi: 10.1159/000015486. Cytogenet Cell Genet. 2000. PMID: 10773667

6

A polymorphic genomic duplication on human chromosome 15 is a susceptibility factor for panic and phobic disorders.

Gratacòs M, Nadal M, Martín-Santos R, Pujana MA, Gago J, Peral B, Armengol L, Ponsa I, Miró R, Bulbena A, Estivill X. Gratacòs M, et al. Among authors: nadal m. Cell. 2001 Aug 10;106(3):367-79. doi: 10.1016/s0092-8674(01)00447-0. Cell. 2001. PMID: 11509185 Free article.

7

Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor.

Pujana MA, Ruiz A, Badenas C, Puig-Butille JA, Nadal M, Stark M, Gómez L, Valls J, Solé X, Hernández P, Cerrato C, Madrigal I, de Cid R, Aguilar H, Capellá G, Cal S, James MR, Walker GJ, Malvehy J, Milà M, Hayward NK, Estivill X, Puig S. Pujana MA, et al. Among authors: nadal m. Genes Chromosomes Cancer. 2007 Feb;46(2):155-62. doi: 10.1002/gcc.20396. Genes Chromosomes Cancer. 2007. PMID: 17099875

8

YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.

Nadal M, Milà M, Pritchard M, Mur A, Pujals J, Blouin JL, Antonarakis SE, Ballesta F, Estivill X. Nadal M, et al. Hum Genet. 1996 Oct;98(4):460-6. doi: 10.1007/s004390050240. Hum Genet. 1996. PMID: 8792823

9

Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.

Nadal M, Moreno S, Pritchard M, Preciado MA, Estivill X, Ramos-Arroyo MA. Nadal M, et al. J Med Genet. 1997 Jan;34(1):50-4. doi: 10.1136/jmg.34.1.50. J Med Genet. 1997. PMID: 9032650 Free PMC 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: nadal m. Cytogenet Cell Genet. 1999;87(1-2):85-8. doi: 10.1159/000015397. Cytogenet Cell Genet. 1999. PMID: 10640817

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