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| http://dx.doi.org/10.1093/nar/18.1.205 | DOI Listing |
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Polymorphism of GDF9 and BMPR1B genes and their association with litter size in Markhoz goats.
Reprod Domest Anim
August 2018
Faculty of Agricultural and Natural Resources, Department of Animal Science, University of Persian Gulf, Boushehr, I.R. Iran.
The main objective of this study was to investigate the polymorphism of GDF9 and BMPR1B genes and their relationship with litter size in Markhoz goats. The polymorphism of GDF9 and BMPR1B genes as well-documented genes regarding fecundity in sheep and goat was investigated using RFLP-PCR and a tetra-primer amplification refractory mutation system-PCR (T-ARMS-PCR) in Markhoz goats. The 164 blood samples were collected from the raised goats in Sanandaj Markhoz goat Performance Testing Station.
View Article and Find Full Text PDFGenetic dissection of five ethnic groups from Punjab, North-West India-A study based on Autosomal Markers.
Leg Med (Tokyo)
May 2017
Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab 143005, India. Electronic address:
The present study assessed the applicability of Alu insertion elements and Single Nucleotide Polymorphisms (SNPs) in forensic identification and estimated the extent of genetic variation in five major ethnic groups of Punjab, North-West India. A total of 1012 unrelated samples belonging to Banias, Brahmins, Jat Sikhs, Khatris and Scheduled Castes were genotyped for four Alu elements (ACE, APO, PLAT, D1) and six Single Nucleotide Polymorphisms [ESR (PvuII), LPL (PvuII), HTR2A (MspI), DRD2 Taq1A, Taq1B, Taq1D]. Allele frequencies observed heterozygosity and forensic efficacy parameters were determined.
View Article and Find Full Text PDFGenetic differentiation and population structure of five ethnic groups of Punjab (North-West India).
Mol Genet Genomics
December 2016
Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
The state of Punjab in the North-West part of India has acted as the main passage for all the major human invasions into the Indian subcontinent. It has resulted in the mixing of foreign gene pool into the local populations, which led to an extensive range of genetic diversity and has influenced the genetic structure of populations in Punjab, North-West India. The present study was conducted to examine the genetic structure, relationships, and extent of genetic differentiation in five Indo-European speaking ethnic groups of Punjab.
View Article and Find Full Text PDFDetection and differentiation of pigeon paramyxovirus serotype-1 (PPMV-1) isolates by RT-PCR and restriction enzyme analysis.
Trop Anim Health Prod
June 2013
Avian Diseases Section, Division of Pathology, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243 122, India.
Detection and pathotyping of Newcastle disease virus (NDV) is extremely important because the appearance of virulent virus has significant economic consequences. During 1981 to 1985, infections of racing and show pigeons with an avian paramyxovirus serotype-1 (APMV-1) hit worldwide, and a panzootic occurred due to a variant form of classical NDV. On the basis of pathogenicity and monoclonal antibody binding studies, the virus was termed 'pigeon PMV-1' (PPMV-1).
View Article and Find Full Text PDFGenetic Diversity and Balancing Selection within the Human Phenylalanine Hydroxylase (PAH) Gene Region in Iranian Population.
Iran J Public Health
November 2012
Division of Genetics, Dept. of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran ; Dept. of Molecular Genetics, Faculty of Basic Sciences, Tarbiat Modares University, Tehran, Iran.
Background: Genetic diversity of three polymorphic markers in the phenylalanine hydroxylase (PAH) gene region including PvuII (a), PAHSTR and MspI were investigated.
Methods: Unrelated individuals (n=139) from the Iranian populations were genotyped using primers specific to PAH gene markers including PvuII(a), MspI and PAHSTR. The amplified products for PvuII(a), MspI were digested using the appropriate restriction enzymes and separated on 1.
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