Giné R[au] - Search Results

Year	Number of Results
1991	1
1992	1
1993	1
1996	1
1998	1
2021	1
2022	1
2024	0

1

HERMES: a molecular-formula-oriented method to target the metabolome.

Giné R, Capellades J, Badia JM, Vughs D, Schwaiger-Haber M, Alexandrov T, Vinaixa M, Brunner AM, Patti GJ, Yanes O. Giné R, et al. Nat Methods. 2021 Nov;18(11):1370-1376. doi: 10.1038/s41592-021-01307-z. Epub 2021 Nov 1. Nat Methods. 2021. PMID: 34725482 Free PMC article.

2

Neighbors' use of water and sanitation facilities can affect children's health: a cohort study in Mozambique using a spatial approach.

Grau-Pujol B, Cano J, Marti-Soler H, Casellas A, Giorgi E, Nhacolo A, Saute F, Giné R, Quintó L, Sacoor C, Muñoz J. Grau-Pujol B, et al. Among authors: gine r. BMC Public Health. 2022 May 16;22(1):983. doi: 10.1186/s12889-022-13373-9. BMC Public Health. 2022. PMID: 35578273 Free PMC article.

3

Clinical and molecular analysis of five inv dup(15) patients.

Robinson WP, Binkert F, Giné R, Vazquez C, Müller W, Rosenkranz W, Schinzel A. Robinson WP, et al. Among authors: gine r. Eur J Hum Genet. 1993;1(1):37-50. doi: 10.1159/000472386. Eur J Hum Genet. 1993. PMID: 8069650

4

Characterization of topoisomerase I and II activities in nuclear extracts during callogenesis in immature embryos of Zea mays.

Carballo M, Giné R, Santos M, Puigdomènech P. Carballo M, et al. Among authors: gine r. Plant Mol Biol. 1991 Jan;16(1):59-70. doi: 10.1007/BF00017917. Plant Mol Biol. 1991. PMID: 1653630

5

A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.

Milà M, Castellví-Bel S, Giné R, Vazquez C, Badenas C, Sánchez A, Estivill X. Milà M, et al. Among authors: gine r. Hum Genet. 1996 Oct;98(4):419-21. doi: 10.1007/s004390050232. Hum Genet. 1996. PMID: 8792815

6

[West's syndrome associated with inversion duplication of chromosome 15].

Cabrera JC, Martí M, Toledo L, Giné R, Vázquez C. Cabrera JC, et al. Among authors: gine r. Rev Neurol. 1998 Jan;26(149):77-9. Rev Neurol. 1998. PMID: 9533212 Spanish.

7

[The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes].

Giné R, Espinás ML, Antich J, Carballo M. Giné R, et al. Med Clin (Barc). 1992 Feb 1;98(4):121-4. Med Clin (Barc). 1992. PMID: 1552760 Spanish.

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