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The Journal of Biological Chemistry
|
August 17, 2018
The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
Sylvia Hoff, Daniel Epting, Nathalie Falk, et al.
Orphanet Journal of Rare Diseases
|
November 17, 2023
An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia
Alena Welters, Sarah M Leiter, Nadine Bachmann, et al.
Cellular and Molecular Life Sciences : CMLS
|
October 25, 2023
PATJ inhibits histone deacetylase 7 to control tight junction formation and cell polarity
Julia Fiedler, Thomas Moennig, Johanna H Hinrichs, et al.
Brain : a Journal of Neurology
|
February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy
Jan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2021
Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation
Eva Schrezenmeier, Elisa Kremerskothen, Fabian Halleck, et al.
Kidney International
|
April 28, 2019
Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease
Isabel Ottlewski, Johannes Münch, Timo Wagner, et al.
Scientific Reports
|
April 17, 2025
Non-invasive screening for liver fibrosis by acoustic radiation force impulse in patients with ciliopathies
Johanna Bresch, Jens König, Martin Konrad, et al.
Plos One
|
September 30, 2017
Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease
Stéphanie De Rechter, Jonathan Kringen, Peter Janssens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 13, 2021
The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation
Eva Schrezenmeier, Elisa Kremerskothen, Fabian Halleck, et al.
The Journal of Investigative Dermatology
|
June 15, 2012
Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing
Jutta Busch, Valeska Frank, Nadine Bachmann, et al.
Page
of 23
Search research articles
Search
Showing results (111-120 of 228) with videos related to
Sort By:
Page
of 23
The Journal of Biological Chemistry
|
August 17, 2018
The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
Sylvia Hoff, Daniel Epting, Nathalie Falk, et al.
Orphanet Journal of Rare Diseases
|
November 17, 2023
An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia
Alena Welters, Sarah M Leiter, Nadine Bachmann, et al.
Cellular and Molecular Life Sciences : CMLS
|
October 25, 2023
PATJ inhibits histone deacetylase 7 to control tight junction formation and cell polarity
Julia Fiedler, Thomas Moennig, Johanna H Hinrichs, et al.
Brain : a Journal of Neurology
|
February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy
Jan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2021
Correction to: The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation
Eva Schrezenmeier, Elisa Kremerskothen, Fabian Halleck, et al.
Kidney International
|
April 28, 2019
Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease
Isabel Ottlewski, Johannes Münch, Timo Wagner, et al.
Scientific Reports
|
April 17, 2025
Non-invasive screening for liver fibrosis by acoustic radiation force impulse in patients with ciliopathies
Johanna Bresch, Jens König, Martin Konrad, et al.
Plos One
|
September 30, 2017
Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease
Stéphanie De Rechter, Jonathan Kringen, Peter Janssens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 13, 2021
The underestimated burden of monogenic kidney disease in adults waitlisted for kidney transplantation
Eva Schrezenmeier, Elisa Kremerskothen, Fabian Halleck, et al.
The Journal of Investigative Dermatology
|
June 15, 2012
Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing
Jutta Busch, Valeska Frank, Nadine Bachmann, et al.
Page
of 23