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La Revue Du Praticien
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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 syndrome
C Antignac
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
July 30, 2005
Molecular basis of steroid-resistant nephrotic syndrome
C Antignac
Contributions to Nephrology
|
January 1, 1996
Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis
C 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 motif
S 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 transporter
V Kalatzis, S Cherqui, C Antignac, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 103) with videos related to
Sort By:
Page
of 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 syndrome
C Antignac
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
July 30, 2005
Molecular basis of steroid-resistant nephrotic syndrome
C Antignac
Contributions to Nephrology
|
January 1, 1996
Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis
C 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 motif
S 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 transporter
V Kalatzis, S Cherqui, C Antignac, et al.
Page
of 11