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C Antignac

Showing results (1-10 of 103) with videos related to

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La Revue Du Praticien|November 20, 1997
[Contribution of molecular biology to the diagnosis of monogenic hereditary nephropathies]C Antignac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Contribution of molecular biology in the diagnosis of monogenic hereditary nephropathy]C Antignac
Kidney International. Supplement|June 1, 1995
Molecular genetics of basement membranes: the paradigm of Alport syndromeC Antignac
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|July 30, 2005
Molecular basis of steroid-resistant nephrotic syndromeC Antignac
Contributions to Nephrology|January 1, 1996
Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosisC Antignac, L Heidet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Update on nephrotic syndrome]P Niaudet, C Antignac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Current data on hereditary nephropathies]M C Gubler, C Antignac
Advances in Nephrology From the Necker Hospital|January 1, 1995
Toward the identification of a gene for familial juvenile nephronophthisis (autosomal recessive medullary cystic kidney disease)C Antignac, C Kleinknecht, R Habib
The Journal of Biological Chemistry|January 21, 2001
The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motifS Cherqui, V Kalatzis, G Trugnan, et al.
The EMBO Journal|November 2, 2001
Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporterV Kalatzis, S Cherqui, C Antignac, et al.
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
La Revue Du Praticien|November 20, 1997
[Contribution of molecular biology to the diagnosis of monogenic hereditary nephropathies]C Antignac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Contribution of molecular biology in the diagnosis of monogenic hereditary nephropathy]C Antignac
Kidney International. Supplement|June 1, 1995
Molecular genetics of basement membranes: the paradigm of Alport syndromeC Antignac
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|July 30, 2005
Molecular basis of steroid-resistant nephrotic syndromeC Antignac
Contributions to Nephrology|January 1, 1996
Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosisC Antignac, L Heidet
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Update on nephrotic syndrome]P Niaudet, C Antignac
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Current data on hereditary nephropathies]M C Gubler, C Antignac
Advances in Nephrology From the Necker Hospital|January 1, 1995
Toward the identification of a gene for familial juvenile nephronophthisis (autosomal recessive medullary cystic kidney disease)C Antignac, C Kleinknecht, R Habib
The Journal of Biological Chemistry|January 21, 2001
The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motifS Cherqui, V Kalatzis, G Trugnan, et al.
The EMBO Journal|November 2, 2001
Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporterV Kalatzis, S Cherqui, C Antignac, et al.
Pageof 11