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C N Hahn

Showing results (31-40 of 47) with videos related to

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The Journal of Biological Chemistry|November 22, 1996
Transcriptional synergism between vitamin D-responsive elements in the rat 25-hydroxyvitamin D3 24-hydroxylase (CYP24) promoterD M Kerry, P P Dwivedi, C N Hahn, et al.
Human Molecular Genetics|February 1, 1997
Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid beta-galactosidaseC N Hahn, M del Pilar Martin, M Schröder, et al.
Human Molecular Genetics|September 16, 1998
Lack of PPCA expression only partially coincides with lysosomal storage in galactosialidosis mice: indirect evidence for spatial requirement of the catalytic rather than the protective function of PPCAR J Rottier, C N Hahn, L W Mann, et al.
Equine Veterinary Journal|January 1, 1996
A possible case of Lyme borreliosis in a horse in the UKC N Hahn, I G Mayhew, K E Whitwell, et al.
Equine Veterinary Journal|December 25, 2015
Bodyweight change aids prediction of survival in chronic equine grass sicknessR C Jago, I Handel, C N Hahn, et al.
Equine Veterinary Journal|January 18, 2006
Horses on pasture may be affected by equine motor neuron diseaseB C McGorum, I G Mayhew, H Amory, et al.
Leukemia|February 14, 2015
Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopeniaC N Hahn, P J Brautigan, C-E Chong, et al.
Equine Veterinary Journal|October 7, 2009
A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breedsR L Stanley, M E McCue, S J Valberg, et al.
Journal of Human Hypertension|October 13, 2017
ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II)S M C De Sousa, M Stowasser, J Feng, et al.
Leukemia|October 28, 2015
Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion geneD M Ross, H K Altamura, C N Hahn, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
The Journal of Biological Chemistry|November 22, 1996
Transcriptional synergism between vitamin D-responsive elements in the rat 25-hydroxyvitamin D3 24-hydroxylase (CYP24) promoterD M Kerry, P P Dwivedi, C N Hahn, et al.
Human Molecular Genetics|February 1, 1997
Generalized CNS disease and massive GM1-ganglioside accumulation in mice defective in lysosomal acid beta-galactosidaseC N Hahn, M del Pilar Martin, M Schröder, et al.
Human Molecular Genetics|September 16, 1998
Lack of PPCA expression only partially coincides with lysosomal storage in galactosialidosis mice: indirect evidence for spatial requirement of the catalytic rather than the protective function of PPCAR J Rottier, C N Hahn, L W Mann, et al.
Equine Veterinary Journal|January 1, 1996
A possible case of Lyme borreliosis in a horse in the UKC N Hahn, I G Mayhew, K E Whitwell, et al.
Equine Veterinary Journal|December 25, 2015
Bodyweight change aids prediction of survival in chronic equine grass sicknessR C Jago, I Handel, C N Hahn, et al.
Equine Veterinary Journal|January 18, 2006
Horses on pasture may be affected by equine motor neuron diseaseB C McGorum, I G Mayhew, H Amory, et al.
Leukemia|February 14, 2015
Characterisation of a compound in-cis GATA2 germline mutation in a pedigree presenting with myelodysplastic syndrome/acute myeloid leukemia with concurrent thrombocytopeniaC N Hahn, P J Brautigan, C-E Chong, et al.
Equine Veterinary Journal|October 7, 2009
A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breedsR L Stanley, M E McCue, S J Valberg, et al.
Journal of Human Hypertension|October 13, 2017
ARMC5 is not implicated in familial hyperaldosteronism type II (FH-II)S M C De Sousa, M Stowasser, J Feng, et al.
Leukemia|October 28, 2015
Delayed diagnosis leading to accelerated-phase chronic eosinophilic leukemia due to a cytogenetically cryptic, imatinib-responsive TNIP1-PDFGRB fusion geneD M Ross, H K Altamura, C N Hahn, et al.
Pageof 5