Nájera C - Search Results

1

Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments.

Aller E, Nájera C, Millán JM, Oltra JS, Pérez-Garrigues H, Vilela C, Navea A, Beneyto M. Aller E, et al. Among authors: najera c. Eur J Hum Genet. 2004 May;12(5):407-10. doi: 10.1038/sj.ejhg.5201138. Eur J Hum Genet. 2004. PMID: 14970843

2

Metal-Catalyzed Enantioconvergent Transformations.

Yus M, Nájera C, Foubelo F, Sansano JM. Yus M, et al. Among authors: najera c. Chem Rev. 2023 Oct 25;123(20):11817-11893. doi: 10.1021/acs.chemrev.3c00059. Epub 2023 Oct 4. Chem Rev. 2023. PMID: 37793021 Free PMC article. Review.

3

Pseudo-multicomponent 1,3-dipolar cycloaddition involving metal-free generation of unactivated azomethine ylides.

Belabbes A, Retamosa MG, Foubelo F, Sirvent A, Nájera C, Yus M, Sansano JM. Belabbes A, et al. Among authors: najera c. Org Biomol Chem. 2023 Mar 1;21(9):1927-1936. doi: 10.1039/d3ob00023k. Org Biomol Chem. 2023. PMID: 36752549

4

Gold and palladium supported on an ionic liquid modified Fe-based metal-organic framework (MOF) as highly efficient catalysts for the reduction of nitrophenols, dyes and Sonogashira-Hagihara reactions.

Karimi S, Gholinejad M, Khezri R, Sansano JM, Nájera C, Yus M. Karimi S, et al. Among authors: najera c. RSC Adv. 2023 Mar 10;13(12):8101-8113. doi: 10.1039/d3ra00283g. eCollection 2023 Mar 8. RSC Adv. 2023. PMID: 36909743 Free PMC article.

5

An autosomal dominant retinitis pigmentosa family with close linkage to D7S480 on 7q.

Millán JM, Martínez F, Vilela C, Beneyto M, Prieto F, Nájera C. Millán JM, et al. Among authors: najera c. Hum Genet. 1995 Aug;96(2):216-8. doi: 10.1007/BF00207382. Hum Genet. 1995. PMID: 7635473

6

Epidemiology of retinitis pigmentosa in the Valencian community (Spain).

Nájera C, Millán JM, Beneyto M, Prieto F. Nájera C, et al. Genet Epidemiol. 1995;12(1):37-46. doi: 10.1002/gepi.1370120105. Genet Epidemiol. 1995. PMID: 7713399 Review.

7

Gly114Asp mutation of rhodopsin in autosomal dominant retinitis pigmentosa.

Millán JM, Fuchs S, Paricio N, Wedemann H, Gal A, Nájera C, Prieto F. Millán JM, et al. Among authors: najera c. Mol Cell Probes. 1995 Feb;9(1):67-9. doi: 10.1016/s0890-8508(95)91052-2. Mol Cell Probes. 1995. PMID: 7760863

8

[Molecular genetics of pigmentary retinopathy].

Millán JM, Nájera C, Beneyto M. Millán JM, et al. Among authors: najera c. Med Clin (Barc). 1994 Jan 15;102(1):30-2. Med Clin (Barc). 1994. PMID: 8133683 Review. Spanish. No abstract available.

9

Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.

Ayuso C, Garcia-Sandoval B, Najera C, Valverde D, Carballo M, Antiñolo G. Ayuso C, et al. Among authors: najera c. Clin Genet. 1995 Sep;48(3):120-2. Clin Genet. 1995. PMID: 8556816

10

Clinical and genetic aspects of two Spanish families with autosomal dominant retinitis pigmentosa (ADRP).

Vilela C, Beneyto M, Bosch R, Millan JM, Marco M, Vallet M, Alonso L, Tormos I, Najera C, Valls B, Paricio N, Prieto F. Vilela C, et al. Among authors: najera c. Ophthalmic Genet. 1996 Mar;17(1):29-33. doi: 10.3109/13816819609057866. Ophthalmic Genet. 1996. PMID: 8740695

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