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Journal of the American Society of Nephrology : JASN
|
July 23, 2003
Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations
Laszlo Furu, Luiz F Onuchic, Ali Gharavi, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Cerebral, cerebellar, and colobomatous anomalies in three related males: Sex-linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndrome
Hester Y Kroes, Rutger-Jan A J Nievelstein, Peter G Barth, et al.
Kidney International Reports
|
October 21, 2024
Erratum to "Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition" [<i>Kidney International Reports</i> Volume 9, Issue 4, April 2024, Pages 919-928]
Jessica K Kaufeld, Lucas Kühne, Ulf Schönermarck, et al.
Kidney International Reports
|
July 31, 2024
Challenges and Considerations in Managing Thrombotic Microangiopathy and Disseminated Intravascular Coagulation in Postpartum Hemorrhage
Jessica K Kaufeld, Ulf Schönermarck, Lucas Kühne, et al.
Human Molecular Genetics
|
October 3, 2012
The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZ
Sandra Habbig, Malte P Bartram, Josef G Sägmüller, et al.
Clinical Endocrinology
|
June 14, 2020
Comparative meta-analysis of Kabuki syndrome with and without hyperinsulinaemic hypoglycaemia
Henrike Hoermann, Omar El-Rifai, Martin Schebek, et al.
European Journal of Human Genetics : EJHG
|
July 14, 2018
Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants
Elisa Molinari, Eva Decker, Holly Mabillard, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2015
LRP5 variants may contribute to ADPKD
Wybrich R Cnossen, René H M te Morsche, Alexander Hoischen, et al.
Journal of the American Society of Nephrology : JASN
|
March 11, 2014
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD
Ekim Z Taskiran, Emine Korkmaz, Safak Gucer, et al.
The Journal of Clinical Investigation
|
June 6, 2017
Ubiquitin ligase RNF146 coordinates bone dynamics and energy metabolism
Yoshinori Matsumoto, Jose La Rose, Melissa Lim, et al.
Page
of 23
Search research articles
Search
Showing results (131-140 of 228) with videos related to
Sort By:
Page
of 23
Journal of the American Society of Nephrology : JASN
|
July 23, 2003
Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations
Laszlo Furu, Luiz F Onuchic, Ali Gharavi, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Cerebral, cerebellar, and colobomatous anomalies in three related males: Sex-linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndrome
Hester Y Kroes, Rutger-Jan A J Nievelstein, Peter G Barth, et al.
Kidney International Reports
|
October 21, 2024
Erratum to "Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition" [<i>Kidney International Reports</i> Volume 9, Issue 4, April 2024, Pages 919-928]
Jessica K Kaufeld, Lucas Kühne, Ulf Schönermarck, et al.
Kidney International Reports
|
July 31, 2024
Challenges and Considerations in Managing Thrombotic Microangiopathy and Disseminated Intravascular Coagulation in Postpartum Hemorrhage
Jessica K Kaufeld, Ulf Schönermarck, Lucas Kühne, et al.
Human Molecular Genetics
|
October 3, 2012
The ciliopathy disease protein NPHP9 promotes nuclear delivery and activation of the oncogenic transcriptional regulator TAZ
Sandra Habbig, Malte P Bartram, Josef G Sägmüller, et al.
Clinical Endocrinology
|
June 14, 2020
Comparative meta-analysis of Kabuki syndrome with and without hyperinsulinaemic hypoglycaemia
Henrike Hoermann, Omar El-Rifai, Martin Schebek, et al.
European Journal of Human Genetics : EJHG
|
July 14, 2018
Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants
Elisa Molinari, Eva Decker, Holly Mabillard, et al.
European Journal of Human Genetics : EJHG
|
April 30, 2015
LRP5 variants may contribute to ADPKD
Wybrich R Cnossen, René H M te Morsche, Alexander Hoischen, et al.
Journal of the American Society of Nephrology : JASN
|
March 11, 2014
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD
Ekim Z Taskiran, Emine Korkmaz, Safak Gucer, et al.
The Journal of Clinical Investigation
|
June 6, 2017
Ubiquitin ligase RNF146 coordinates bone dynamics and energy metabolism
Yoshinori Matsumoto, Jose La Rose, Melissa Lim, et al.
Page
of 23