Search Results - "Justin Carlus, S"

The peopling of Lakshadweep Archipelago by Mustak, Mohammed S., Rai, Niraj, Naveen, Mohan Rao, Prakash, Satya, Carlus, S. Justin, Pasupuleti, Nagarjuna, Srivastava, Anshika, Singh, Prajjval Pratap, Babu, Idrees, Dubey, Pavan Kumar, Chaubey, Gyaneshwer, Thangaraj, Kumarasamy

“…The archipelago of Lakshadweep is considered as a stopover to the maritime route since ancient time. It is not very clear when the human first occupied these…”
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Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy by Abdallah, Atiyeh M, Carlus, S Justin, Al-Mazroea, Abdulhadi H, Alluqmani, Mohammad, Almohammadi, Yousef, Bhuiyan, Zahurul A, Al-Harbi, Khalid M

“…: Dilated cardiomyopathy (DCM) is a rare cardiac disease characterised by left ventricular enlargement, reduced left ventricular contractility, and impaired…”
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Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis by Carlus, S Justin, Sarkar, Saumya, Bansal, Sandeep Kumar, Singh, Vertika, Singh, Kiran, Jha, Rajesh Kumar, Sadasivam, Nirmala, Sadasivam, Sri Revathy, Gireesha, P S, Thangaraj, Kumarasamy, Rajender, Singh

“…Optimum efficiency of the folate pathway is considered essential for adequate ovarian function. 677 C>T substitution in the 5, 10-methylene…”
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Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients by Alharbi, Khalid M., Al-Mazroea, Abdelhadi H., Abdallah, Atiyeh M., Almohammadi, Yousef, Carlus, S. Justin, Basit, Sulman

“…Down syndrome (DS) is the most common autosomal chromosome anomaly. DS is frequently associated with congenital heart disease (CHD). Patients with DS have…”
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Transforming Growth Factor-β1 gene polymorphism and osteoporosis in postmenopausal egyptian women by Taha, Inass M, Abdu Allah, Azza M, Hamoudah, Maha A F, Justin Carlus, S

“…Transforming growth factor-β1 (TGF-β1) is a wide spread bone matrix protein that affect the function, formation and cell-cell interactions of osteoclasts and…”
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Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation by Mishra, Anshuman, Nizammuddin, Sheikh, Mallick, Chandana Basu, Singh, Sakshi, Prakash, Satya, Siddiqui, Niyamat Ali, Rai, Niraj, Carlus, S. Justin, Sudhakar, Digumarthi V.S., Tripathi, Vishnu P., Möls, Märt, Kim-Howard, Xana, Dewangan, Hemlata, Mishra, Abhishek, Reddy, Alla G., Roy, Biswajit, Pandey, Krishna, Chaubey, Gyaneshwer, Das, Pradeep, Nath, Swapan K., Singh, Lalji, Thangaraj, Kumarasamy

“…Our understanding of the genetics of skin pigmentation has been largely skewed towards populations of European ancestry, imparting less attention to South…”
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Mitochondrial DNA variations associated with recurrent pregnancy loss among Indian women by Vanniarajan, Ayyasamy, Govindaraj, Periyasamy, Carlus, S Justin, Aruna, Meka, Aruna, P, Kumar, Ajay, Jayakar, Richard Issac, Lionel, Anath C, Gupta, Sandeep, Rao, Lakshmi, Gupta, Nalini J, Chakravarthy, Baidyanath, Deenadayal, Mamatha, Selvaraj, Kamala, Andal, Sadaranga, Reddy, B Mohan, Singh, Lalji, Thangaraj, Kumarasamy

“…Several genetic factors have been found to be associated with recurrent pregnancy loss (RPL). However, not many attempts have been made to associate the…”
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29. No association between MTHFR C677T polymorphism and congenital heart disease in Saudi Arabian population by Carlus, S. Justin, El-Attar, Lama M., Hammoudah, Sahar A.F., Al Harbi, Ghadeer Saleh Mossad, Almuzainy, Ibrahim S., Abdallah, Atiyeh, Harbi, Khalid Al

“…Congenital heart diseases (CHD) are the most common birth defects in the world. It is a major cause of childhood mortality and morbidity worldwide with about 7…”
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Renin and CYP P450 gene variations significantly associated with essential hypertension: A prospective pharmacogenomics study by Loganathan, Lakshmanan, Carlus, S. Justin, Muthusamy, Karthikeyan

“…This study aims to investigate the association between Renin-angiotensin aldosterone system (RAAS) and Cytochrome P450 gene polymorphisms in hypertension…”
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CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia by Rani, Deepa Selvi, Carlus, S. Justin, Poongothai, J, Jyothi, Amara, Pavani, Kadupa, Gupta, Nalini J, Reddy, Alla G, Rajan, M. Mamtha, Rao, Kamini, Chakravarty, Baidyanath, Singh, Lalji, Thangaraj, Kumarasamy

“…Variations in the trinucleotide-CAG repeat number of the catalytic subunit of the mitochondrial DNA polymerase gamma (POLG) have been speculated to be…”
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Transforming Growth Factor-β1 gene polymorphism and osteoporosis in postmenopausal egyptian women by Taha, Inass M., Abdu Allah, Azza M., Hamoudah, Maha A. F., Justin Carlus, S.

“…Transforming growth factor-β1 (TGF-β1) is a wide spread bone matrix protein that affect the function, formation and cell-cell interactions of osteoclasts and…”
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Is MTHFR 677 CT Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis by Carlus, S. Justin, Sarkar, Saumya, Bansal, Sandeep Kumar, Singh, Vertika, Singh, Kiran, Jha, Rajesh Kumar, Sadasivam, Nirmala, Sadasivam, Sri Revathy, Gireesha, P. S, Thangaraj, Kumarasamy, Rajender, Singh

“…Background Optimum efficiency of the folate pathway is considered essential for adequate ovarian function. 677 C>T substitution in the 5, 10-methylene…”
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SRD5A2 Gene Polymorphisms and the Risk of Benign Prostatic Hyperplasia but not Prostate Cancer by Choubey, Vimal Kumar, Sankhwar, Satya Narayan, Carlus, S. Justin, Singh, Anand Narayan, Dalela, Divakar, Thangaraj, Kumarasamy, Rajender, Singh

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SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer by Choubey, Vimal Kumar, Sankhwar, Satya Narayan, Carlus, S Justin, Singh, Anand Narayan, Dalela, Divakar, Thangaraj, Kumarasamy, Rajender, Singh

“…Testosterone, a primary androgen in males, is converted into its most active form, dihydrotestosterone (DHT), by 5α-reductase type 2 (encoded by the SRD5A2…”
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