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Cell Division
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November 21, 2018
Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers
Ramona Jühlen, Dana Landgraf, Angela Huebner, et al.
Biology Open
|
November 2, 2016
Identification of a novel putative interaction partner of the nucleoporin ALADIN
Ramona Jühlen, Dana Landgraf, Angela Huebner, et al.
Contributions to Nephrology
|
December 13, 2016
What Is the Optimal Target Convective Volume in On-Line Hemodiafiltration Therapy?
Bernard Canaud, Katrin Koehler, Sudhir Bowry, et al.
Biochemical and Biophysical Research Communications
|
September 29, 2009
The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope
Barbara Kind, Katrin Koehler, Mike Lorenz, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
August 14, 2010
Intracellular ROS level is increased in fibroblasts of triple A syndrome patients
Barbara Kind, Katrin Koehler, Manuela Krumbholz, et al.
International Ophthalmology
|
June 1, 2011
New ophthalmic features in a family with triple A syndrome
Marilita M Moschos, Ioannis Margetis, Katrin Koehler, et al.
BMC Pediatrics
|
January 17, 2018
"Crying without tears" as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports
Daniel Tibussek, Sujal Ghosh, Angela Huebner, et al.
European Journal of Pediatrics
|
January 4, 2008
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation
Tatjana Milenković, Katrin Koehler, Manuela Krumbholz, et al.
Hormone Research
|
May 28, 2008
Familial glucocorticoid deficiency type 1 due to a novel compound heterozygous MC2R mutation
Artur Mazur, Katrin Koehler, Markus Schuelke, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
July 11, 2008
Triple A syndrome mimicking ALS
Maria Strauss, Katrin Koehler, Manuela Krumbholz, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Cell Division
|
November 21, 2018
Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers
Ramona Jühlen, Dana Landgraf, Angela Huebner, et al.
Biology Open
|
November 2, 2016
Identification of a novel putative interaction partner of the nucleoporin ALADIN
Ramona Jühlen, Dana Landgraf, Angela Huebner, et al.
Contributions to Nephrology
|
December 13, 2016
What Is the Optimal Target Convective Volume in On-Line Hemodiafiltration Therapy?
Bernard Canaud, Katrin Koehler, Sudhir Bowry, et al.
Biochemical and Biophysical Research Communications
|
September 29, 2009
The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope
Barbara Kind, Katrin Koehler, Mike Lorenz, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
August 14, 2010
Intracellular ROS level is increased in fibroblasts of triple A syndrome patients
Barbara Kind, Katrin Koehler, Manuela Krumbholz, et al.
International Ophthalmology
|
June 1, 2011
New ophthalmic features in a family with triple A syndrome
Marilita M Moschos, Ioannis Margetis, Katrin Koehler, et al.
BMC Pediatrics
|
January 17, 2018
"Crying without tears" as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports
Daniel Tibussek, Sujal Ghosh, Angela Huebner, et al.
European Journal of Pediatrics
|
January 4, 2008
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation
Tatjana Milenković, Katrin Koehler, Manuela Krumbholz, et al.
Hormone Research
|
May 28, 2008
Familial glucocorticoid deficiency type 1 due to a novel compound heterozygous MC2R mutation
Artur Mazur, Katrin Koehler, Markus Schuelke, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
July 11, 2008
Triple A syndrome mimicking ALS
Maria Strauss, Katrin Koehler, Manuela Krumbholz, et al.
Page
of 5