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BMC Biology|April 6, 2004
A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarctionPelayo González, Antonio Díez-Juan, Eliecer Coto, et al.Pediatric Nephrology (Berlin, Germany)|January 12, 2007
Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five childrenHelena Gil, Fernando Santos, Enrique García, et al.BMC Medical Genetics|March 25, 2010
Mutation analysis of the LCE3B/LCE3C genes in PsoriasisEliecer Coto, Jorge Santos-Juanes, Pablo Coto-Segura, et al.The Australasian Journal of Dermatology|May 11, 2012
Psoriasis and type 2 diabetes risk among psoriatic patients in a Spanish populationSusana Armesto, Jorge Santos-Juanes, Cristina Galache-Osuna, et al.Kidney International Supplements|July 15, 2014
NKG2D and its ligands: active factors in the outcome of solid organ transplantation?Beatriz Suárez-Álvarez, Alba Fernández-Sánchez, Antonio López-Vázquez, et al.Lung|April 29, 2015
A Semiconductor Chip-Based Next Generation Sequencing Procedure for the Main Pulmonary Hypertension GenesJuan Gómez, Julian R Reguero, Celso Alvarez, et al.Journal of Human Genetics|April 25, 2014
The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's diseaseLucía F Cardo, Eliecer Coto, René Ribacoba, et al.Gene|January 22, 2014
Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patientsBeatriz Tavira, Juan Gómez, Carmen Díaz-Corte, et al.International Journal of Cardiology|November 30, 2005
ABCA1 polymorphisms and prognosis after myocardial infarction in young patientsMaría Martín, Pelayo González, J J R Reguero, et al.International Journal of Cardiology|July 12, 2005
Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effectMónica García-Castro, Julián R Reguero, Victoria Alvarez, et al.Pageof 23