Results 221 to 230 of about 746,762 (326)

Whole-genome paternal uniparental disomy identified through prenatal single-nucleotide polymorphism-based cell-free DNA screening. [PDF]

Ultrasound Obstet Gynecol
Benn P, Hashimoto K, Souter V, Dhamankar R, Xu W, Kijacic D.   +5 more
europepmc   +1 more source

A Common Single Nucleotide Polymorphism in Endoplasmic Reticulum Aminopeptidase 2 Induces a Specificity Switch That Leads to Altered Antigen Processing

Journal of Immunology, 2012
Irini Evnouchidou, J. Birtley, S. Seregin, A. Papakyriakou, E. Zervoudi, M. Samiotaki, G. Panayotou, P. Giastas, Olivia Petrakis, D. Georgiadis, A. Amalfitano, E. Saridakis, I. Mavridis, E. Stratikos   +13 more
semanticscholar   +1 more source

Clinical application of single nucleotide polymorphism array in prenatal diagnosis: Experience with 8753 samples. [PDF]

PLoS One
Wen L, Zhang Y, Zhang W, Mao A, Li X.
europepmc   +1 more source

Association of polycystic ovarian syndrome with inflammatory single nucleotide polymorphism for IL-1 & IL-6 genes: A case-control study. [PDF]

Indian J Med Res
Benjamin JJ, Ramaswamy P, Kuppusamy MK, Vembu R, Rajamani K, Puttaswamy N, Narayanasa MK, Mathews RR, Koshy T.   +8 more
europepmc   +1 more source

Association of ficolin single nucleotide polymorphism with systemic lupus erythematosus in the Chinese Han Population. [PDF]

Rheumatol Immunol Res
Yin F, Gu J, Zhao P, Chen J.
europepmc   +1 more source

Exploring the presence of the GPR126 single nucleotide polymorphism (rs536714306) in periodontal patients of European ancestry. [PDF]

BMC Res Notes
Chatzopoulou E, Fanourakis G, Papanikolaou N, Chatzistamou I, Dereka X, Vastardis H.   +5 more
europepmc   +1 more source

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.

Cancer Research, 2005
Y. Nannya, M. Sanada, K. Nakazaki, N. Hosoya, Lili Wang, A. Hangaishi, M. Kurokawa, S. Chiba, D. Bailey, G. Kennedy, S. Ogawa   +10 more
semanticscholar   +1 more source

review marcatori genetici acquacoltura [PDF]

, 2012
Guarniero, Ilaria
core  

The causal relationship between systemic lupus erythematosus and juvenile myoclonic epilepsy: A Mendelian randomization study and mediation analysis

Ibrain, Volume 11, Issue 1, Page 98-105, Spring 2025.
Mendelian randomization (MR) studies were conducted using the inverse‐variance weighted (IVW) method, MR‐Egger and weighted median on juvenile myoclonic epilepsy (JME), and systemic lupus erythematosus (SLE) data from the Integrative Epidemiology Unit (IEU) Open genome‐wide association study (GWAS) database and the International League Against Epilepsy
Sirui Chen, Ningning Zhang, Ruirui Zhang, Lan Zhang, Dadong Luo, Junqiang Li, Yaqing Liu, Yunan Wang, Xinyue Duan, Xin Tian, Tiancheng Wang   +10 more
wiley   +1 more source

Mitochondrial ATP synthase 8 single-nucleotide polymorphism affects oxidative stress and survival of mice. [PDF]

Pflugers Arch
Reichart G, Mayer J, Tokay T, Kirschstein T, Lange F, Köhling R.   +5 more
europepmc   +1 more source