Telleria D - Search Results

1

A novel frameshift mutation (2436insT) produces an immediate stop codon in the autosomal dominant polycystic kidney disease 2 (PKD2) gene.

Iglesias DM, Telleria D, Viribay M, Herrera M, Bernath VA, Kornblihtt AR, Martin RS, Millán JL. Iglesias DM, et al. Among authors: telleria d. Nephrol Dial Transplant. 2000 Apr;15(4):477-80. doi: 10.1093/ndt/15.4.477. Nephrol Dial Transplant. 2000. PMID: 10727541

2

Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene.

Viribay M, Hayashi T, Tellería D, Mochizuki T, Reynolds DM, Alonso R, Lens XM, Moreno F, Harris PC, Somlo S, San Millán JL. Viribay M, et al. Among authors: telleria d. Hum Genet. 1997 Dec;101(2):229-34. doi: 10.1007/s004390050621. Hum Genet. 1997. PMID: 9402976

3

Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease.

Torra R, Viribay M, Tellería D, Badenas C, Watson M, Harris P, Darnell A, San Millán JL. Torra R, et al. Among authors: telleria d. Kidney Int. 1999 Jul;56(1):28-33. doi: 10.1046/j.1523-1755.1999.00534.x. Kidney Int. 1999. PMID: 10411676 Free article.

4

Dinucleotide repeat polymorphism at the D4S2458 locus close to the PKD2 locus on human chromosome 4q.

Viribay M, Tellería D, Velasco E, Moreno F, San Millán JL. Viribay M, et al. Among authors: telleria d. Hum Genet. 1995 May;95(5):601-2. doi: 10.1007/BF00223883. Hum Genet. 1995. PMID: 7759091

5

[Mutational analysis of the PKD1 and PKD2 (type 1 and 2 dominant autosomal polycystic kidney) genes].

Torra R, Badenas C, Pérez-Oller L, San Millán JL, Tellería D, Estivill X, Darnell A. Torra R, et al. Among authors: telleria d. Nefrologia. 2000 Jan-Feb;20(1):39-46. Nefrologia. 2000. PMID: 10822721 Free article. Spanish.

6

Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.

Peces R, Mena R, Martín Y, Hernández C, Peces C, Tellería D, Cuesta E, Selgas R, Lapunzina P, Nevado J. Peces R, et al. Among authors: telleria d. Mol Genet Genomic Med. 2020 Aug;8(8):e1321. doi: 10.1002/mgg3.1321. Epub 2020 Jun 13. Mol Genet Genomic Med. 2020. PMID: 32533764 Free PMC article.

7

Angiotensin-converting enzyme gene polymorphism and antiproteinuric response to renoprotective therapy.

Gonzalo A, Telleria D, San Millan JL, Ortuño J. Gonzalo A, et al. Among authors: telleria d. Nephrol Dial Transplant. 1998 Apr;13(4):1050-1. doi: 10.1093/oxfordjournals.ndt.a027882. Nephrol Dial Transplant. 1998. PMID: 9580535 No abstract available.

8

The EUROGEM map of human chromosome 5.

Villamar M, Gomendio B, Perera E, Telleria D, Fizames C, San Millan JL, Weissenbach J, Schott JJ, Dixon M, Hollyoake M, et al. Villamar M, et al. Among authors: telleria d. Eur J Hum Genet. 1994;2(3):212-3. Eur J Hum Genet. 1994. PMID: 7834285 No abstract available.

9

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

del Castillo I, Villamar M, Moreno-Pelayo MA, del Castillo FJ, Alvarez A, Tellería D, Menéndez I, Moreno F. del Castillo I, et al. Among authors: telleria d. N Engl J Med. 2002 Jan 24;346(4):243-9. doi: 10.1056/NEJMoa012052. N Engl J Med. 2002. PMID: 11807148 Free article.

10

Insulin gene variable number of tandem repeats regulatory polymorphism is not associated with hyperandrogenism in Spanish women.

Calvo RM, Tellería D, Sancho J, San Millán JL, Escobar-Morreale HF. Calvo RM, et al. Among authors: telleria d. Fertil Steril. 2002 Apr;77(4):666-8. doi: 10.1016/s0015-0282(01)03238-1. Fertil Steril. 2002. PMID: 11937112 Free article.

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