![PDF) Analysis of reninangiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects PDF) Analysis of reninangiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects](https://www.researchgate.net/profile/Johnson-Stanslas/publication/24040907/figure/fig2/AS:202630568648715@1425322300899/lane-1-represents-homozygous-CC-genotypes-lane-2-and-5-represents-heterozygous-AC_Q320.jpg)
PDF) Analysis of reninangiotensin aldosterone system gene polymorphisms in Malaysian essential hypertensive and type 2 diabetic subjects
![FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study | European Journal of Human Genetics FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fejhg.2016.186/MediaObjects/41431_2017_Article_BFejhg2016186_Fig1_HTML.jpg)
FIG4 variants in central European patients with amyotrophic lateral sclerosis: a whole-exome and targeted sequencing study | European Journal of Human Genetics
![Frontiers | Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene Frontiers | Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene](https://www.frontiersin.org/files/Articles/926070/fgene-13-926070-HTML/image_m/fgene-13-926070-g001.jpg)
Frontiers | Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene
![Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram](https://www.researchgate.net/publication/338733548/figure/fig3/AS:849987596476417@1579664243721/Indirect-proof-of-principle-on-c1213-5GT-IVS6-5GT-pathogenicity-Electropherograms.jpg)
Indirect proof of principle on c.1213+5G>T [IVS6+5G>T] pathogenicity.... | Download Scientific Diagram
![CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions: Molecular Therapy - Methods & Clinical Development CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions: Molecular Therapy - Methods & Clinical Development](https://www.cell.com/cms/attachment/783156e7-6b6a-42ed-bd5a-e490e34c96fb/fx1_lrg.jpg)
CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions: Molecular Therapy - Methods & Clinical Development
![Analysis of renin-angiotensin aldosterone system gene polymorphisms in malaysian essential hypertensive and type 2 diabetic subjects | Cardiovascular Diabetology | Full Text Analysis of renin-angiotensin aldosterone system gene polymorphisms in malaysian essential hypertensive and type 2 diabetic subjects | Cardiovascular Diabetology | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2F1475-2840-8-11/MediaObjects/12933_2008_Article_165_Fig2_HTML.jpg)
Analysis of renin-angiotensin aldosterone system gene polymorphisms in malaysian essential hypertensive and type 2 diabetic subjects | Cardiovascular Diabetology | Full Text
![Frontiers | A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia Frontiers | A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia](https://www.frontiersin.org/files/MyHome%20Article%20Library/814295/814295_Thumb_400.jpg)
Frontiers | A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia
![Genetic factors contributing to hypertension in African‐based populations: A systematic review and meta‐analysis - Yako - 2018 - The Journal of Clinical Hypertension - Wiley Online Library Genetic factors contributing to hypertension in African‐based populations: A systematic review and meta‐analysis - Yako - 2018 - The Journal of Clinical Hypertension - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/35d69bd2-6851-4beb-91d6-bf6933408dca/jch.2018.20.issue-3.cover.jpg?trick=1664038579424)
Genetic factors contributing to hypertension in African‐based populations: A systematic review and meta‐analysis - Yako - 2018 - The Journal of Clinical Hypertension - Wiley Online Library
![Two novel biallelic mutations in <em>PSMC3IP</em> in a patient affected by premature ovarian insufficiency Two novel biallelic mutations in <em>PSMC3IP</em> in a patient affected by premature ovarian insufficiency](https://www.spandidos-publications.com/article_images/mmr/25/2/mmr-25-02-12561-g02.jpg)
Two novel biallelic mutations in <em>PSMC3IP</em> in a patient affected by premature ovarian insufficiency
![Protein Encoded by the AxinFu Allele Effectively Down-regulates Wnt Signaling but Exerts a Dominant Negative Effect on c-Jun N-terminal Kinase Signaling* - Journal of Biological Chemistry Protein Encoded by the AxinFu Allele Effectively Down-regulates Wnt Signaling but Exerts a Dominant Negative Effect on c-Jun N-terminal Kinase Signaling* - Journal of Biological Chemistry](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/9efb1652-682c-40a9-b0d3-06d7fc436004/gr1_lrg.jpg)
Protein Encoded by the AxinFu Allele Effectively Down-regulates Wnt Signaling but Exerts a Dominant Negative Effect on c-Jun N-terminal Kinase Signaling* - Journal of Biological Chemistry
![Cells | Free Full-Text | Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis | HTML Cells | Free Full-Text | Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis | HTML](https://www.mdpi.com/cells/cells-10-00782/article_deploy/html/images/cells-10-00782-g001.png)
Cells | Free Full-Text | Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis | HTML
![A pair of primers facing at the double-strand break site enables to detect NHEJ-mediated indel mutations at a 1-bp resolution | Scientific Reports A pair of primers facing at the double-strand break site enables to detect NHEJ-mediated indel mutations at a 1-bp resolution | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-022-15776-5/MediaObjects/41598_2022_15776_Fig1_HTML.png)
A pair of primers facing at the double-strand break site enables to detect NHEJ-mediated indel mutations at a 1-bp resolution | Scientific Reports
![Genetic aberration in primary hepatocellular carcinoma: correlation between p53 gene mutation and loss-of-hetero- zygosity on chromosome 16q21-q23 and 9p21-p23 | Cell Research Genetic aberration in primary hepatocellular carcinoma: correlation between p53 gene mutation and loss-of-hetero- zygosity on chromosome 16q21-q23 and 9p21-p23 | Cell Research](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsj.cr.7290058/MediaObjects/41422_2000_Article_BF7290058_Fig4_HTML.gif)
Genetic aberration in primary hepatocellular carcinoma: correlation between p53 gene mutation and loss-of-hetero- zygosity on chromosome 16q21-q23 and 9p21-p23 | Cell Research
![Cureus | Genetic Markers PLEKHA7, ABCC5, and KALRN Are Not Associated With the Progression of Primary Angle Closure Glaucoma (PACG) in Malays Cureus | Genetic Markers PLEKHA7, ABCC5, and KALRN Are Not Associated With the Progression of Primary Angle Closure Glaucoma (PACG) in Malays](https://assets.cureus.com/uploads/figure/file/269336/27d5b3d0252f11ec90732bcca2d6868f-Figure3-Gen.png)
Cureus | Genetic Markers PLEKHA7, ABCC5, and KALRN Are Not Associated With the Progression of Primary Angle Closure Glaucoma (PACG) in Malays
![USB1 mutations and related aberrant transcripts identified in the PN... | Download Scientific Diagram USB1 mutations and related aberrant transcripts identified in the PN... | Download Scientific Diagram](https://www.researchgate.net/publication/325184283/figure/fig3/AS:961734282055699@1606306729497/USB1-mutations-and-related-aberrant-transcripts-identified-in-the-PN-patients.gif)
USB1 mutations and related aberrant transcripts identified in the PN... | Download Scientific Diagram
![Genotype and allele frequency distribution among hypertensives and controls | Download Scientific Diagram Genotype and allele frequency distribution among hypertensives and controls | Download Scientific Diagram](https://www.researchgate.net/profile/Lava-Kumar-3/publication/256481772/figure/tbl1/AS:203144643518470@1425444865584/Genotype-and-allele-frequency-distribution-among-hypertensives-and-controls.png)