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Communications Biology|June 9, 2023
Y chromosome sequence and epigenomic reconstruction across human populationsPaula Esteller-Cucala, Marc Palmada-Flores, Lukas F K Kuderna, et al.
American Journal of Human Genetics|December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosisEva Klopocki, Silke Lohan, Francesco Brancati, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
High-throughput sequencing of microdissected chromosomal regionsAnja Weise, Bernd Timmermann, Manfred Grabherr, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Genes & Development|July 3, 2004
The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutationHanaa Ben Abdelkhalek, Anja Beckers, Karin Schuster-Gossler, et al.
Molecular Plant|September 3, 2023
Improving photosynthetic efficiency toward food security: Strategies, advances, and perspectivesEdward N Smith, Marvin van Aalst, Tiina Tosens, et al.
Science Translational Medicine|January 14, 2021
The intratumoral CXCR3 chemokine system is predictive of chemotherapy response in human bladder cancerTino Vollmer, Stephan Schlickeiser, Leila Amini, et al.
Nature Communications|December 14, 2017
H3K14ac is linked to methylation of H3K9 by the triple Tudor domain of SETDB1Renata Z Jurkowska, Su Qin, Goran Kungulovski, et al.
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