Hasil Pencarian - Thomas Haaf
- Menampilkan 1 - 20 hasil dari 31
- Ke Halaman Berikutnya
-
1
High-Resolution Analysis of DNA Replication in Released Chromatin Fibers Containing 5-Bromodeoxyuridine oleh Thomas Haaf
Diterbitkan 1996-12-01
Artikel -
2
DNA Nicks and Increased Sensitivity of DNA to Fluorescence In Situ End Labeling during Functional Spermiogenesis oleh Avril Smith, Thomas Haaf
Diterbitkan 1998-09-01
Artikel -
3
Genetics of Tinnitus: Still in its Infancy oleh Barbara Vona, Indrajit Nanda, Wafaa Shehata-Dieler, Thomas Haaf
Diterbitkan 2017-05-01
Artikel -
4
Male obesity effects on sperm and next-generation cord blood DNA methylation. oleh Ramya Potabattula, Marcus Dittrich, Martin Schorsch, Thomas Hahn, Thomas Haaf, Nady El Hajj
Diterbitkan 2019-01-01
Artikel -
5
-
6
Epigenetic signatures of gestational diabetes mellitus on cord blood methylation oleh Larissa Haertle, Nady El Hajj, Marcus Dittrich, Tobias Müller, Indrajit Nanda, Harald Lehnen, Thomas Haaf
Diterbitkan 2017-03-01
Artikel -
7
Hereditary hearing loss SNP-microarray pilot study oleh Barbara Vona, Michaela A. H. Hofrichter, Jörg Schröder, Wafaa Shehata-Dieler, Indrajit Nanda, Thomas Haaf
Diterbitkan 2018-06-01
Artikel -
8
-
9
D4Z4 Hypomethylation in Human Germ Cells oleh Ramya Potabattula, Jana Durackova, Sarah Kießling, Alina Michler, Thomas Hahn, Martin Schorsch, Tom Trapphoff, Stefan Dieterle, Thomas Haaf
Diterbitkan 2024-09-01
Artikel -
10
-
11
A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family oleh Julia Doll, Michaela A. H. Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, Barbara Vona
Diterbitkan 2020-08-01
Artikel -
12
-
13
Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals. oleh Larissa Haertle, Anna Maierhofer, Julia Böck, Harald Lehnen, Yvonne Böttcher, Matthias Blüher, Martin Schorsch, Ramya Potabattula, Nady El Hajj, Silke Appenzeller, Thomas Haaf
Diterbitkan 2017-01-01
Artikel -
14
Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication oleh Indrajit Nanda, Claus Steinlein, Thomas Haaf, Eva M. Buhl, Domink G. Grimm, Scott L. Friedman, Steffen K. Meurer, Sarah K. Schröder, Ralf Weiskirchen
Diterbitkan 2022-05-01
Artikel -
15
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report oleh Caroline Lekszas, Indrajit Nanda, Barbara Vona, Julia Böck, Farah Ashrafzadeh, Nahid Donyadideh, Farnoosh Ebrahimzadeh, Najmeh Ahangari, Reza Maroofian, Ehsan Ghayoor Karimiani, Thomas Haaf
Diterbitkan 2019-06-01
Artikel -
16
Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion oleh Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, Eva-Maria König, Indrajit Nanda, Barbara Vona, Peter De Coster, Rita Cauwels, Vivek Malhotra, Thomas Haaf
Diterbitkan 2020-02-01
Artikel -
17
Species-Specific Paternal Age Effects and Sperm Methylation Levels of Developmentally Important Genes oleh Andreas Prell, Mustafa Orkun Sen, Ramya Potabattula, Laura Bernhardt, Marcus Dittrich, Thomas Hahn, Martin Schorsch, Federica Zacchini, Grazyna Ewa Ptak, Heiner Niemann, Thomas Haaf
Diterbitkan 2022-02-01
Artikel -
18
A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesity oleh Laura Bernhardt, Marcus Dittrich, Rabih El-Merahbi, Antoine-Emmanuel Saliba, Tobias Müller, Grzegorz Sumara, Jörg Vogel, Stefanie Nichols-Burns, Megan Mitchell, Thomas Haaf, Nady El Hajj
Diterbitkan 2021-01-01
Artikel -
19
A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation oleh Ignacio Rodriguez-Polo, Sophie Mißbach, Stoyan Petkov, Felix Mattern, Anna Maierhofer, Iga Grządzielewska, Yuliia Tereshchenko, Daniel Urrutia-Cabrera, Thomas Haaf, Ralf Dressel, Iris Bartels, Rüdiger Behr
Diterbitkan 2021-07-01
Artikel -
20
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family oleh Michaela A. H. Hofrichter, Majid Mojarad, Julia Doll, Clemens Grimm, Atiye Eslahi, Neda Sadat Hosseini, Mohsen Rajati, Tobias Müller, Marcus Dittrich, Reza Maroofian, Thomas Haaf, Barbara Vona
Diterbitkan 2018-05-01
Artikel