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Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 10, 2011
The functional muscle-bone unit in obese children - altered bone structure leads to normal strength strain index
S Ehehalt, G Binder, N Schurr, et al.
Applied and Environmental Microbiology
|
October 1, 1993
Isolation and characterization of a pseudomonas strain producing glutaryl-7-aminocephalosporanic Acid acylase
R G Binder, K Numata, D A Lowe, et al.
European Journal of Pediatrics
|
May 14, 1998
De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
G G Massa, G Binder, W Oostdijk, et al.
Hormone Research
|
March 22, 2000
Influence of IGF-I and cell density on MDR1 expression in the T-lymphoblastoid cell line CCRF-CEM
C P Schwarze, S Neu, J Beck, et al.
Journal of Neuroendocrinology
|
October 12, 2007
Mutant and misfolded human growth hormone is rapidly degraded through the proteasomal degradation pathway in a cellular model for isolated growth hormone deficiency type II
K Kannenberg, N E Wittekindt, S Tippmann, et al.
Annales De Genetique
|
August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely
K Eggermann, H A Wollmann, G Binder, et al.
Scientific Reports
|
April 17, 2022
Accuracy and self-validation of automated bone age determination
D D Martin, A D Calder, M B Ranke, et al.
Clinical Endocrinology
|
August 10, 2000
X-linked congenital adrenal hypoplasia: new mutations and long-term follow-up in three patients
G Binder, H Wollmann, C P Schwarze, et al.
Journal of Chemical Ecology
|
November 19, 2013
Attraction of female mediterranean fruit flies to the five major components of male-produced pheromone in a laboratory flight tunnel
E B Jang, D M Light, R G Binder, et al.
Clinical Genetics
|
December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome
T Eggermann, N Schönherr, K Eggermann, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 90) with videos related to
Sort By:
Page
of 9
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association
|
May 10, 2011
The functional muscle-bone unit in obese children - altered bone structure leads to normal strength strain index
S Ehehalt, G Binder, N Schurr, et al.
Applied and Environmental Microbiology
|
October 1, 1993
Isolation and characterization of a pseudomonas strain producing glutaryl-7-aminocephalosporanic Acid acylase
R G Binder, K Numata, D A Lowe, et al.
European Journal of Pediatrics
|
May 14, 1998
De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
G G Massa, G Binder, W Oostdijk, et al.
Hormone Research
|
March 22, 2000
Influence of IGF-I and cell density on MDR1 expression in the T-lymphoblastoid cell line CCRF-CEM
C P Schwarze, S Neu, J Beck, et al.
Journal of Neuroendocrinology
|
October 12, 2007
Mutant and misfolded human growth hormone is rapidly degraded through the proteasomal degradation pathway in a cellular model for isolated growth hormone deficiency type II
K Kannenberg, N E Wittekindt, S Tippmann, et al.
Annales De Genetique
|
August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely
K Eggermann, H A Wollmann, G Binder, et al.
Scientific Reports
|
April 17, 2022
Accuracy and self-validation of automated bone age determination
D D Martin, A D Calder, M B Ranke, et al.
Clinical Endocrinology
|
August 10, 2000
X-linked congenital adrenal hypoplasia: new mutations and long-term follow-up in three patients
G Binder, H Wollmann, C P Schwarze, et al.
Journal of Chemical Ecology
|
November 19, 2013
Attraction of female mediterranean fruit flies to the five major components of male-produced pheromone in a laboratory flight tunnel
E B Jang, D M Light, R G Binder, et al.
Clinical Genetics
|
December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome
T Eggermann, N Schönherr, K Eggermann, et al.
Page
of 9