Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Jürgen Horst"'
Autor:
Anita Kloss-Brandstätter, Monika Summerer, David Horst, Basil Horst, Gertraud Streiter, Julia Raschenberger, Florian Kronenberg, Torpong Sanguansermsri, Jürgen Horst, Hansi Weissensteiner
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Cambodia harbours a variety of human aboriginal populations that have scarcely been studied in terms of genetic diversity of entire mitochondrial genomes. Here we present the matrilineal gene pool of 299 Cambodian refugees from three differe
Externí odkaz:
https://doaj.org/article/8c959a9f0f054139a72eaecab9bc4e55
Autor:
David Horst, Anita Kloss-Brandstätter, Florian Kronenberg, Jürgen Horst, Torpong Sanguansermsri, Basil A. Horst, Gertraud Streiter, Hansi Weissensteiner, Monika Summerer, Julia Raschenberger
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Cambodia harbours a variety of human aboriginal populations that have scarcely been studied in terms of genetic diversity of entire mitochondrial genomes. Here we present the matrilineal gene pool of 299 Cambodian refugees from three different ethnic
Autor:
Jürgen Horst, D. Meschede
Publikováno v:
In Vitro Fertilisation in the 1990s ISBN: 9780429453441
In Vitro Fertilisation in the 1990s
In Vitro Fertilisation in the 1990s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05dec255479b5ab8e42320d7ee13ff66
https://doi.org/10.4324/9780429453441-13
https://doi.org/10.4324/9780429453441-13
Publikováno v:
Ion Exchange and Solvent Extraction ISBN: 9780203749753
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36099a20adb730def03ca4be38bfe10e
https://doi.org/10.1201/9780203749753-3
https://doi.org/10.1201/9780203749753-3
Autor:
Manfred W. Baumstark, Jürgen Horst, Christine Schaeffer, H. Wieland, Sabine Preisler-Adams, Thomas Epting, Emmanuel Bissé, Agnès Hovasse, Alain Van Dorsselaer
Publikováno v:
Journal of Chromatography B. 871:55-59
A new δ-chain variant, δ143 (H21) His → Tyr or Hb Noah Mehmet Oeztuerk, was discovered during the investigation of the cause of hemolytic anaemia in a 6-month-old infant of Turkish descent. It was detected by Cation exchange high-performance liqu
Publikováno v:
Clinical Genetics. 38:270-273
Analyzing a panel of 94 phenylketonuria (PKU) alleles for mutations within the phenylalanine hydroxylase (PAH) gene, we identified a G to A transition in exon 7 corresponding to nucleotide 957 in the cDNA sequence. This nucleotide substitution genera
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 118:661-664
A 28-year-old man and his 27-year-old wife were investigated for infertility of 3 1/2 years' duration. There was azoospermia caused by bilateral aplasia of the vas deferens, and therefore it was planned to aspirate spermatozoa from the epididymis for
Autor:
Jürgen Horst, Hartmut Pollmann, Roswith Eisert, Albena Todorova, Marcin Chlystun, Nadja Bogdanova, C. Wermes, Arseni Markoff, Ulrike Nowak-Göttl
Publikováno v:
Human Mutation. 28:54-60
The amount of residual F8 (FVIII:C) determines the clinical severity of hemophilia A. Recently, we showed that the mutation detection rate in severely affected male patients (FVIII:C1% of normal) is virtually 100% when testing for the common intron 2
Autor:
Bert van den Heuvel, Brigitte Welling, Gert Vriend, Eric A. Shoubridge, Orly Elpeleg, Jürgen Horst, Heleen Diepstra, Hana Antonicka, Florin Sasarman, Avraham Shaag, Jasmine Jacob-Hirsch, Paul Smits, Ann Saada, Gideon Rechavi, Richard J. Rodenburg, Jan A.M. Smeitink
Publikováno v:
American Journal of Human Genetics, 79, 5, pp. 869-77
American Journal of Human Genetics, 79, 869-77
American Journal of Human Genetics, 79, 869-77
Contains fulltext : 35941.pdf (Publisher’s version ) (Closed access) The 13 polypeptides encoded in mitochondrial DNA (mtDNA) are synthesized in the mitochondrial matrix on a dedicated protein-translation apparatus that resembles that found in prok
Autor:
Thomas Epting, Alain Van Dorsselaer, Heinrich Wieland, Nathalie Zorn, Stéphanie Boussert, Jürgen Horst, Manfred W. Baumstark, Emmanuel Bissé
Publikováno v:
Journal of Chromatography A
Journal of Chromatography A, Elsevier, 2006, 1115 (1-2), pp.118-124. ⟨10.1016/j.chroma.2006.02.082⟩
Journal of Chromatography A, Elsevier, 2006, 1115 (1-2), pp.118-124. ⟨10.1016/j.chroma.2006.02.082⟩
The first hemoglobin (Hb) variant carrying a mutation at s4 was identified as s4(A1)Thr → Asn or Hb Wurzburg and constituted 38% of the total hemoglobin. It showed a slightly elevated oxygen affinity and a slightly decreased cooperativity index (n5