E-LIB Suche - Ergebnisse für: Hildebrandt, F.

1

WCN23-0159 ENPP6 IS A POTENTIAL NOVEL CANDIDATE GENE FOR MO..:

MERTENS, N.D. ; Kano, K. ; Merz, L.M....
Kidney International Reports. 8 (2023) 3 - p. S242 , 2023

Link: https://doi.org/10.1016/..

2

Planet-star interactions with precise transit timing: III. ..:

Maciejewski, G. ; Fernández, M. ; Sota, A....
Astronomy & Astrophysics. 667 (2022) - p. A127 , 2022

Link: https://doi.org/10.1051/..

3

Mutations of IFT81, encoding an IFT-B core protein, as a ra..:

Perrault, I ; Halbritter, J ; Porath, J...
Cilia. 4 (2015) S1 - p. , 2015

Link: https://doi.org/10.1186/..

4

WDR19: An ancient, retrograde, intraflagellar ciliary prote..:

Coussa, R G ; Otto, E A ; Gee, H‐Y...
Clinical Genetics. 84 (2013) 2 - p. 150-159 , 2013

Link: https://doi.org/10.1111/..

5

Weed seed survival following ensiling and mesophilic anaero..:

WESTERMAN, P R ; HILDEBRANDT, F ; GEROWITT, B
Weed Research. 52 (2012) 3 - p. 286-295 , 2012

Link: https://doi.org/10.1111/..

6

Exome resequencing identifies novel NPHP genes, implicating..:

Hildebrandt, F
Cilia. 1 (2012) S1 - p. , 2012

Link: https://doi.org/10.1186/..

7

Co‐occurrence of Joubert syndrome and Jeune asphyxiating th..:

Lehman, A.M. ; Eydoux, P. ; Doherty, D....
American Journal of Medical Genetics Part A. 152A (2010) 6 - p. 1411-1419 , 2010

Link: https://doi.org/10.1002/..

8

Genetic and physical interaction between the NPHP5 and NPHP..:

Schafer, T. ; Putz, M. ; Lienkamp, S....
Human Molecular Genetics. 18 (2009) 21 - p. 4226-4226 , 2009

Link: https://doi.org/10.1093/..

9

HomozygosityMapper--an interactive approach to homozygosity..:

Seelow, D. ; Schuelke, M. ; Hildebrandt, F..
Nucleic Acids Research. 37 (2009) Web Server - p. W593-W599 , 2009

Link: https://doi.org/10.1093/..

10

Mapping of a new locus for congenital anomalies of the kidn..:

Ashraf, S. ; Hoskins, B. E. ; Chaib, H....
Nephrology Dialysis Transplantation. 25 (2009) 5 - p. 1496-1501 , 2009

Link: https://doi.org/10.1093/..

11

Monogene Ursachen des nephrotischen Syndroms:

Heeringa, S.F. ; Hildebrandt, F.
Monatsschrift Kinderheilkunde. 157 (2009) 3 - p. 218-225 , 2009

Link: https://doi.org/10.1007/..

12

Thirteen novel NPHS1 mutations in a large cohort of childre..:

Heeringa, S. F. ; Vlangos, C. N. ; Chernin, G....
Nephrology Dialysis Transplantation. 23 (2008) 11 - p. 3527-3533 , 2008

Link: https://doi.org/10.1093/..

13

Missense mutations in EYA1 and TCF2 are a rare cause of uri..:

Hoskins, B. E. ; Cramer, C. H. ; Tasic, V....
Nephrology Dialysis Transplantation. 23 (2007) 2 - p. 777-779 , 2007

Link: https://doi.org/10.1093/..

14

Mutations in PLCE1 are a major cause of isolated diffuse me..:

Gbadegesin, R. ; Hinkes, B. G. ; Hoskins, B. E....
Nephrology Dialysis Transplantation. 23 (2007) 4 - p. 1291-1297 , 2007

Link: https://doi.org/10.1093/..

15

Nephronophthise: Neueste Erkenntnisse in der molekularen Di..:

Hoefele, J. ; Hildebrandt, F. ; Benz, M.R..
Der Nephrologe. 2 (2007) 5 - p. 372-376 , 2007

Link: https://doi.org/10.1007/..