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                             60 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of polymorphic markers located in the HEXA gene region associated with Tay-Sachs disease Vahhab, Nasrin

26 C p.
artikel
2 An introduction to EpiPol (Epigenetic affecting Polymorphism) concept with an in silico identification of CpG-affecting SNPs in the upstream regulatory sequences of human AHR gene Aftabi, Younes

26 C p.
artikel
3 A novel homozygous variant in the TRAPPC9 gene causing intellectual disability and autism Spectrum disorder Ashaat, Engy A.

26 C p.
artikel
4 Association between dietary inflammatory index and lipid profiles with consideration of Apo B Ins/ Del SNP in type 2 diabetic patients Mohamadinarab, Maryam

26 C p.
artikel
5 Association between the rs2234671 polymorphism and the risk of recurrent urinary tract infections in Iraqi women Abbas, Hussein Mahmood

26 C p.
artikel
6 Association of estrogen receptor 1 (ESR1) gene (rs2234693) polymorphism, ESR1 promoter methylation status, and serum heavy metals concentration, with breast cancer: A study on Iranian women population Mirzaeyan, Pardis

26 C p.
artikel
7 Association of rs7041 and rs4588 polymorphisms of vitamin D binding protein gene in pulmonary tuberculosis Harishankar, Murugesan

26 C p.
artikel
8 Association of rs3735025 and rs9656169 variants with autism, and schizophrenia: A GWAS-replication study in an Iranian population Darvish, Hossein

26 C p.
artikel
9 Association of SPOCK1 gene locus with rheumatoid arthritis in Caucasians Zamanpoor, Mansour

26 C p.
artikel
10 Astrocyte elevated gene-1: A potential molecular non-invasive marker for prognosis of esophageal cancer patients AlMourgi, Majed

26 C p.
artikel
11 Biochemical and molecular study of long non-coding RNAs (HOTTIP, ZEB-AS1 and MEG-3) in hepatocellular carcinoma Soliman, Shimaa E.

26 C p.
artikel
12 CDKAL1 (rs10946398) and TCF7L2 (rs7903146) gene polymorphisms and their association with risk of type-2 diabetes mellitus in population of Uttarakhand, India Verma, Amit Kumar

26 C p.
artikel
13 Deletion allele of IFNAR1 gene polymorphism (rs17875871) is associated with a lower risk of breast cancer: A preliminary report Sarabandi, Sahel

26 C p.
artikel
14 Distribution of Indian population-specific transporter SNPs among Asians and their physiological consequences Srivastava, Shivani

26 C p.
artikel
15 Distribution of Lactobacillus species in Iranian women with both human papillomavirus (HPV) infection and bacterial vaginosis (BV) Ghaniabadi, Roghayeh

26 C p.
artikel
16 D190Y mutation in C-terminal tail region of TNNI3 gene causing severe form of restrictive cardiomyopathy with mild hypertrophy in an Indian patient Kapoor, Mitali

26 C p.
artikel
17 Effect of coated carbon nanotubes with chitosan and cover of flaxseed in the induction of MDA-MB-231 apoptosis by analyzing the expression of Bax and Bcl-2 Kavousi, Mahsa

26 C p.
artikel
18 Effect of gilbert's syndrome associated polymorphic alleles (rs8175347 and rs4148323) of UDP-glucuronyl transferase on serum bilirubin level Aliarab, Azadeh

26 C p.
artikel
19 Epigenetic silencing of the DAPK1 gene in Egyptian patients with chronic myeloid Leukemia Elsayed, Fatma M.

26 C p.
artikel
20 Estimation of variance components and genetic parameters for lactation persistency indices in crossbred cattle using Bayesian and REML methods Mandal, Ajoy

26 C p.
artikel
21 Evaluation of genetic susceptibility of six type II diabetes Genome-Wide association tudies loci for obesity Ashour, Esmat

26 C p.
artikel
22 Fatty acid synthesis and cancer: Aberrant expression of the ACACA and ACACB genes increases the risk for cancer Bhattacharjee, Kasturi

26 C p.
artikel
23 Folate metabolism: Impact of involved genetic variants on homocycteine and folate levels in type 2 diabetic patients with coronary artery disease Gharib, Amal F.

26 C p.
artikel
24 Genetic association of GSTM1, GSTT1, and GSTP1 polymorphisms with sickle cell disease complications: A systematic review and meta-analysis Verma, Henu Kumar

26 C p.
artikel
25 Genetic variants of HBS1L-MYB with Hb subtypes level among Filipino β°-deletion carriers co-inherited with −α3.7 deletion thalassaemia Lim, Lay Ngor

26 C p.
artikel
26 Genetic variants of ZNF385B and COMT are associated with autism spectrum disorder in the Bangladeshi children Uddin, Md. Giash

26 C p.
artikel
27 Genomic scanning of the promoter sequence in osmo/halo-tolerance related QTLs in Zygosaccharomyces rouxii Menon, Athira M.

26 C p.
artikel
28 Identification of the potential type 2 diabetes susceptibility genetic elements in South Asian populations Batool, Hina

26 C p.
artikel
29 IL-17 A and IL-17 F single nucleotide polymorphisms and acute myeloid leukemia susceptibility and response to induction therapy in Egypt Zayed, Rania A.

26 C p.
artikel
30 Impact of cytokines levels and interleukin 6 (-634 C>G) polymorphism on clinical outcomes in patients with sepsis de Oliveira Filho, Romério Alencar

26 C p.
artikel
31 Increased homocysteine expression associated with genetic changes in the folate pathway as a key determinant of preeclampsia: A prospective study from lower Assam, India Sultana, Rizwana

26 C p.
artikel
32 Influence of GSTM1 and GSTT1 genetic polymorphisms on petrol-induced toxicities: A systematic review Abubakar, Murtala Bello

26 C p.
artikel
33 Investigating circulatory microRNA expression profiles in Egyptian patients infected with hepatitis C virus mediated hepatic disorders Gibriel, Abdullah Ahmed

26 C p.
artikel
34 Lack of association between Mannose Binding Lectin-2 gene polymorphisms and periodontitis: A meta-analysis da Silva, Felipe Rodolfo Pereira

26 C p.
artikel
35 Methods for making multiple alignment of genomic sequences for severe acute respiratory syndrome coronavirus 2 Suzuki, Yoshiyuki

26 C p.
artikel
36 MiR-155 expression is a potential biomarker of systemic lupus erythematosus diagnosis and disease activity prediction El-Shaer, Osama S.

26 C p.
artikel
37 MMP9 (RS20544) and ADCY2 (RS58502974) as susceptibility factors for schizophrenia in Iranian population Abolghasemi, Mahsa

26 C p.
artikel
38 Molecular characterization, antibiogram and distribution of zntA gene in zinc-resistant Escherichia coli population recovered from anthropogenically-influenced surface water sources in Nigeria Adekanmbi, Abimbola Olumide

26 C p.
artikel
39 Molecular identification of glutaryl CoA dehydrogenase gene variations and clinical course in three glutaric aciduria type I patients Shaik, Muntaj

26 C p.
artikel
40 MTHFR C677T polymorphism not associated with meningiomas: Study of an interethnic Brazilian population, and meta-analysis Bastos, Carlos Eduardo Matos Carvalho

26 C p.
artikel
41 Mutational analysis revealed 97 key cancer metastasis genes from extracellular vesicles associated with patient survival Luo, Mingyu

26 C p.
artikel
42 Novel missense variants in FGFR1 and FGFR3 causes short stature in enrolled families from Pakistan Mustafa, Saima

26 C p.
artikel
43 Paclitaxel resistance resulted in a stem-like state in triple-negative breast cancer: A systems biology approach Ghorbani, Mohammad

26 C p.
artikel
44 Polymorphic evaluation of NFKBIA and SRR with type 2 diabetes mellitus in population of southern Punjab Raza, Waseem

26 C p.
artikel
45 Population genetics and gene flow of the seagrass, Syringodium isoetifolium based on Start codon targeted (SCoT) marker from Palk Bay and Chilika Lake, India Dilipan, E.

26 C p.
artikel
46 Potential association between the hopQ alleles of Helicobacter pylori and gastrointestinal diseases: A systematic review and meta-analysis Karbalaei, Mohsen

26 C p.
artikel
47 Precision medicine insight into primary prostate tumor through transcriptomic data and an integrated systems biology approach Sadeghi, Mehdi

26 C p.
artikel
48 Programmed cell death-1 rs2227981 polymorphism in patients with autoimmune skin blistering disorders: A pilot study Faina, Valentina

26 C p.
artikel
49 RAPD PCR and actA based molecular typing of L. monocytogenes isolated from human, food and domestic animals in northwest of Iran Hemmati, Azar

26 C p.
artikel
50 Relationship analysis of the miR-196a2 polymorphism (rs11614913) with colorectal cancer risk in southern Khorasan, eastern Iran Ayadilord, Malaksima

26 C p.
artikel
51 Rs4841587 in GATA4 and rs6999593 in DNMT1 gene associated with congenital heart diseases in the southeast of Iran Noori, Noor Mohammad

26 C p.
artikel
52 Screening of key modulatory genes by Degalactotigonin in Triple Negative Breast Cancer cells – An in silico approach D, Hamsa

26 C p.
artikel
53 Serum interleukin-37 (IL-37) and its gene polymorphism in Iranian Behcet's disease patients: Association with disease manifestations and activity Gholijani, Nasser

26 C p.
artikel
54 The Duffy T-33C is an insightful marker of human history and admixture Ali Albsheer, Musab M.

26 C p.
artikel
55 The polymorphism of TNFα (rs1799964) gene and schizophrenia risk: A meta-analysis Moossavi, Maryam

26 C p.
artikel
56 The Possible Role of Point Mutations and Activation of the CDC27 Gene in Progression of Multiple Myeloma Abbaspourkharyeki, Malek

26 C p.
artikel
57 The rs6265 polymorphism might not affect the secretion of BDNF protein directedly Boroujeni, Nasim Banaei

26 C p.
artikel
58 Transcripts of orphan nuclear receptor (NR4A1) & potassium channel (KCNK17) genes as new potential biomarkers for depression Dmitrzak-Weglarz, M.

26 C p.
artikel
59 Untangled the genetic structure of Kahar and Tharu, using 23 Y chromosomal paternal lineage markers Shrivastava, Pankaj

26 C p.
artikel
60 Vitamin D receptor (VDR) gene polymorphism BsmI in Syrian breast cancer patients Haddad, Shaden

26 C p.
artikel
                             60 gevonden resultaten
 
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