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1.
Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α.
BMC Cancer
; 12: 450, 2012 Oct 04.
Article
in English
| MEDLINE | ID: mdl-23033967
2.
Maternal aerobic exercise during pregnancy can increase spatial learning by affecting leptin expression on offspring's early and late period in life depending on gender.
ScientificWorldJournal
; 2012: 429803, 2012.
Article
in English
| MEDLINE | ID: mdl-23028249
3.
Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.
Eur J Med Genet
; 65(6): 104497, 2022 Jun.
Article
in English
| MEDLINE | ID: mdl-35430327
4.
Functional divergence of the two Elongator subcomplexes during neurodevelopment.
EMBO Mol Med
; 14(7): e15608, 2022 07 07.
Article
in English
| MEDLINE | ID: mdl-35698786
5.
Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects.
Am J Med Genet A
; 155A(1): 203-6, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-21204233
6.
OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development.
Epileptic Disord
; 23(6): 843-853, 2021 Dec 01.
Article
in English
| MEDLINE | ID: mdl-34704946
7.
TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement.
Rheumatol Int
; 30(5): 667-70, 2010 Mar.
Article
in English
| MEDLINE | ID: mdl-19597734
8.
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
Turk J Pediatr
; 60(3): 229-237, 2018.
Article
in English
| MEDLINE | ID: mdl-30511534
9.
Exercise increases leptin levels correlated with IGF-1 in hippocampus and prefrontal cortex of adolescent male and female rats.
J Chem Neuroanat
; 81: 27-33, 2017 04.
Article
in English
| MEDLINE | ID: mdl-28179125
10.
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.
BMC Med Genet
; 6: 21, 2005 May 17.
Article
in English
| MEDLINE | ID: mdl-15904506
11.
An excess of chromosome 1 breakpoints in male infertility.
Eur J Hum Genet
; 12(12): 993-1000, 2004 Dec.
Article
in English
| MEDLINE | ID: mdl-15367911
12.
A novel subtype of distal symphalangism affecting only the 4th finger.
Am J Med Genet A
; 149A(7): 1571-3, 2009 Jul.
Article
in English
| MEDLINE | ID: mdl-19533773
13.
DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors.
Cancer Genet Cytogenet
; 145(2): 108-14, 2003 Sep.
Article
in English
| MEDLINE | ID: mdl-12935921
14.
Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.
Genet Test Mol Biomarkers
; 18(4): 261-8, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24571861
15.
The effect of the alternative solutions to formaldehyde and xylene on tissue processing.
Indian J Pathol Microbiol
; 56(3): 221-30, 2013.
Article
in English
| MEDLINE | ID: mdl-24152498
16.
TLR polymorphisms in FMF: association of TLR-2 (Arg753Gln) and TLR-4 (Asp299Gly, Thre399Ile) polymorphisms and myeloid cell TLR-2 and TLR-4 expression with the development of secondary amyloidosis in FMF.
Inflammation
; 34(5): 379-87, 2011 Oct.
Article
in English
| MEDLINE | ID: mdl-20714796
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