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J Horst

Showing results (101-110 of 278) with videos related to

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Acta Endocrinologica|July 1, 1977
Sex hormone binding globulin binding capacity, testosterone, 5alpha-dihydrotestosterone, oestradiol and prolactin in plasma of patients with prostatic carcinoma under various types of hormonal treatmentW Bartsch, H J Horst, H Becker, et al.
Deutsche Medizinische Wochenschrift (1946)|October 21, 1994
[The Kallmann syndrome. Its pathophysiology and clinical picture]D Meschede, H M Behre, E Nieschlag, et al.
Human Genetics|January 1, 1984
Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German familiesJ Horst, E U Griese, E Kleihauer, et al.
Blood|June 1, 1989
Beta-thalassemia gene analysis in a Turkish family reveals a 7 BP deletion in the coding regionJ Schnee, E U Griese, A Eigel, et al.
JDR Clinical and Translational Research|April 2, 2019
Letter to the Editor: "Preventing Caries in American Indian Children: Lost Battle or New Hope?"J Tanzer, P Milgrom, C E Huebner, et al.
Klinische Wochenschrift|December 17, 1990
Circadian rhythm of interleukin-1 production of monocytes and the influence of endogenous and exogenous glucocorticoids in manP Zabel, H J Horst, C Kreiker, et al.
The Journal of Cell Biology|December 1, 1987
Cytoskeletal-membrane interactions: a stable interaction between cell surface glycoconjugates and doublet microtubules of the photoreceptor connecting ciliumC J Horst, D M Forestner, J C Besharse
Blood|May 1, 1989
A beta-thalassemia gene caused by a 290-base pair deletion: analysis by direct sequencing of enzymatically amplified DNAR Spiegelberg, C Aulehla-Scholz, H Erlich, et al.
Human Reproduction (Oxford, England)|November 1, 1995
Genetic risk in micromanipulative assisted reproductionD Meschede, C De Geyter, E Nieschlag, et al.
Human Mutation|January 1, 1993
Phenylalanine hydroxylase gene: a novel splice mutation in intron 2 in two German and Polish families with severe phenylketonuriaM Zygulska, A Eigel, J J Pietrzyk, et al.
Pageof 28

Showing results (101-110 of 278) with videos related to

Sort By:
Pageof 28
Acta Endocrinologica|July 1, 1977
Sex hormone binding globulin binding capacity, testosterone, 5alpha-dihydrotestosterone, oestradiol and prolactin in plasma of patients with prostatic carcinoma under various types of hormonal treatmentW Bartsch, H J Horst, H Becker, et al.
Deutsche Medizinische Wochenschrift (1946)|October 21, 1994
[The Kallmann syndrome. Its pathophysiology and clinical picture]D Meschede, H M Behre, E Nieschlag, et al.
Human Genetics|January 1, 1984
Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German familiesJ Horst, E U Griese, E Kleihauer, et al.
Blood|June 1, 1989
Beta-thalassemia gene analysis in a Turkish family reveals a 7 BP deletion in the coding regionJ Schnee, E U Griese, A Eigel, et al.
JDR Clinical and Translational Research|April 2, 2019
Letter to the Editor: "Preventing Caries in American Indian Children: Lost Battle or New Hope?"J Tanzer, P Milgrom, C E Huebner, et al.
Klinische Wochenschrift|December 17, 1990
Circadian rhythm of interleukin-1 production of monocytes and the influence of endogenous and exogenous glucocorticoids in manP Zabel, H J Horst, C Kreiker, et al.
The Journal of Cell Biology|December 1, 1987
Cytoskeletal-membrane interactions: a stable interaction between cell surface glycoconjugates and doublet microtubules of the photoreceptor connecting ciliumC J Horst, D M Forestner, J C Besharse
Blood|May 1, 1989
A beta-thalassemia gene caused by a 290-base pair deletion: analysis by direct sequencing of enzymatically amplified DNAR Spiegelberg, C Aulehla-Scholz, H Erlich, et al.
Human Reproduction (Oxford, England)|November 1, 1995
Genetic risk in micromanipulative assisted reproductionD Meschede, C De Geyter, E Nieschlag, et al.
Human Mutation|January 1, 1993
Phenylalanine hydroxylase gene: a novel splice mutation in intron 2 in two German and Polish families with severe phenylketonuriaM Zygulska, A Eigel, J J Pietrzyk, et al.
Pageof 28