Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Antignac

Showing results (51-60 of 103) with videos related to

Pageof 11
Sort By:
Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, et al.
Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.
Science (New York, N.Y.)|August 27, 1993
Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumorsJ Zhou, T Mochizuki, H Smeets, et al.
Archives Francaises De Pediatrie|August 1, 1985
[Pharmacokinetics of prednisone after oral administration in children with renal grafts. Changes induced by phenobarbital and renal insufficiency]F Perignon, M A Pecquinot, C Ged, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Prenatal diagnosis of autosomal recessive polycystic kidney disease]M F Gagnadoux, T Attié, J Amiel, et al.
Genomics|March 1, 1993
Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3E Austruy, C Jeanpierre, C Antignac, et al.
American Journal of Human Genetics|July 27, 1999
Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assayL Forestier, G Jean, M Attard, et al.
Reproductive Biomedicine Online|February 7, 2008
Preimplantation genetic diagnosis for autosomal recessive polycystic kidney diseaseN Gigarel, N Frydman, P Burlet, et al.
Advances in Nephrology From the Necker Hospital|January 1, 1993
Genetic, clinical, and morphologic heterogeneity in Alport's syndromeM C Gubler, C Antignac, G Deschênes, et al.
Cancer Research|June 15, 1993
Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approachE Austruy, M Cohen-Salmon, C Antignac, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, et al.
Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.
Science (New York, N.Y.)|August 27, 1993
Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumorsJ Zhou, T Mochizuki, H Smeets, et al.
Archives Francaises De Pediatrie|August 1, 1985
[Pharmacokinetics of prednisone after oral administration in children with renal grafts. Changes induced by phenobarbital and renal insufficiency]F Perignon, M A Pecquinot, C Ged, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Prenatal diagnosis of autosomal recessive polycystic kidney disease]M F Gagnadoux, T Attié, J Amiel, et al.
Genomics|March 1, 1993
Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3E Austruy, C Jeanpierre, C Antignac, et al.
American Journal of Human Genetics|July 27, 1999
Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assayL Forestier, G Jean, M Attard, et al.
Reproductive Biomedicine Online|February 7, 2008
Preimplantation genetic diagnosis for autosomal recessive polycystic kidney diseaseN Gigarel, N Frydman, P Burlet, et al.
Advances in Nephrology From the Necker Hospital|January 1, 1993
Genetic, clinical, and morphologic heterogeneity in Alport's syndromeM C Gubler, C Antignac, G Deschênes, et al.
Cancer Research|June 15, 1993
Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approachE Austruy, M Cohen-Salmon, C Antignac, et al.
Pageof 11