Antignac C - Search Results

1

Endoplasmic reticulum stress drives proteinuria-induced kidney lesions via Lipocalin 2.

El Karoui K, Viau A, Dellis O, Bagattin A, Nguyen C, Baron W, Burtin M, Broueilh M, Heidet L, Mollet G, Druilhe A, Antignac C, Knebelmann B, Friedlander G, Bienaimé F, Gallazzini M, Terzi F. El Karoui K, et al. Among authors: antignac c. Nat Commun. 2016 Jan 20;7:10330. doi: 10.1038/ncomms10330. Nat Commun. 2016. PMID: 26787103 Free PMC article.

2

Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragments.

Knebelmann B, Deschenes G, Gros F, Hors MC, Grünfeld JP, Zhou J, Tryggvason K, Gubler MC, Antignac C. Knebelmann B, et al. Among authors: antignac c. Am J Hum Genet. 1992 Jul;51(1):135-42. Am J Hum Genet. 1992. PMID: 1376965 Free PMC article.

3

Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.

Gubler MC, Knebelmann B, Beziau A, Broyer M, Pirson Y, Haddoum F, Kleppel MM, Antignac C. Gubler MC, et al. Among authors: antignac c. Kidney Int. 1995 Apr;47(4):1142-7. doi: 10.1038/ki.1995.163. Kidney Int. 1995. PMID: 7783412 Free article.

4

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.

Gubler MC, Antignac C, Deschênes G, Knebelmann B, Hors-Cayla MC, Grünfeld JP, Broyer M, Habib R. Gubler MC, et al. Among authors: antignac c. Adv Nephrol Necker Hosp. 1993;22:15-35. Adv Nephrol Necker Hosp. 1993. PMID: 8427057 Review. No abstract available.

5

Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.

Antignac C, Heidet L. Antignac C, et al. Contrib Nephrol. 1996;117:172-82. doi: 10.1159/000424813. Contrib Nephrol. 1996. PMID: 8801045 Review. No abstract available.

6

Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis.

Konrad M, Saunier S, Heidet L, Silbermann F, Benessy F, Calado J, Le Paslier D, Broyer M, Gubler MC, Antignac C. Konrad M, et al. Among authors: antignac c. Hum Mol Genet. 1996 Mar;5(3):367-71. doi: 10.1093/hmg/5.3.367. Hum Mol Genet. 1996. PMID: 8852662

7

Somatic deletion of the 5' ends of both the COL4A5 and COL4A6 genes in a sporadic leiomyoma of the esophagus.

Heidet L, Boye E, Cai Y, Sado Y, Zhang X, Fléjou JF, Fékété F, Ninomiya Y, Gubler MC, Antignac C. Heidet L, et al. Among authors: antignac c. Am J Pathol. 1998 Mar;152(3):673-8. Am J Pathol. 1998. PMID: 9502408 Free PMC article.

8

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

Boye E, Mollet G, Forestier L, Cohen-Solal L, Heidet L, Cochat P, Grünfeld JP, Palcoux JB, Gubler MC, Antignac C. Boye E, et al. Among authors: antignac c. Am J Hum Genet. 1998 Nov;63(5):1329-40. doi: 10.1086/302106. Am J Hum Genet. 1998. PMID: 9792860 Free PMC article.

9

Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys.

Heidet L, Cai Y, Guicharnaud L, Antignac C, Gubler MC. Heidet L, et al. Among authors: antignac c. Am J Pathol. 2000 Jun;156(6):1901-10. doi: 10.1016/S0002-9440(10)65063-8. Am J Pathol. 2000. PMID: 10854213 Free PMC article.

10

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

Heidet L, Arrondel C, Forestier L, Cohen-Solal L, Mollet G, Gutierrez B, Stavrou C, Gubler MC, Antignac C. Heidet L, et al. Among authors: antignac c. J Am Soc Nephrol. 2001 Jan;12(1):97-106. doi: 10.1681/ASN.V12197. J Am Soc Nephrol. 2001. PMID: 11134255

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