Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Parisa SHARAFI"'
Autor:
Leila Rezaei, Vali Alipour, Parisa Sharafi, Hamidreza Ghaffari, Amene Nematollahi, Vida Pesarakloo, Yadolah Fakhri
Publikováno v:
Environmental Health Engineering and Management, Vol 8, Iss 2, Pp 67-75 (2021)
Background: The presence of toxic heavy metals in cereal grains like rice is one of the main human and environmental health concerns. Their importance is because of their non-biodegradability nature, high half-time, and bioaccumulation ability in t
Externí odkaz:
https://doaj.org/article/f90ec16281d44f929adf5fd2119a81f2
Autor:
Parisa Sharafi, vida pesarakloo, Yadolah Fakhri, Amene Nematollahi, Vali Alipour, Leila Rezaei, Hamid Reza Ghaffari
Publikováno v:
Environmental Health Engineering and Management, Vol 8, Iss 2, Pp 67-75 (2021)
Background: The presence of toxic heavy metals in cereal grains like rice is one of the main human and environmental health concerns. Their importance is because of their non-biodegradability nature, high half-time, and bioaccumulation ability in the
Publikováno v:
Journal of Applied Oral Science v.30 2022
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 30, Article number: e20220086, Published: 09 SEP 2022
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 30, Article number: e20220086, Published: 09 SEP 2022
Bioactive molecules present the potential to be used along with biomaterials in vital pulp therapy and regenerative endodontic treatment. Objective The aim of this study was to assess the effects of the combined use of bone morphogenetic protein-7 (B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e44e70e513fc759d6de3180e08f7fb1a
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572022000100436
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572022000100436
Autor:
Sukriye Ayter, Mustafa Turan, O. F. Yılmaz, Sibel Ersoy-Evans, Ali Varan, Banu Anlar, Parisa Sharafi
Publikováno v:
Journal of Community Genetics. 9:227-232
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, and its clinical presentations are highly variable. NF1 is caused by mutations in the NF1 gene, and 50% of NF1 cases are sporadic, which occur in the absence of a fami
Autor:
Duygu Ozel Demiralp, Cemil Ozerk Demiralp, Serap Dökmeci, Aysel Yüce, Naşit İğci, Parisa Sharafi
Publikováno v:
Advances in Clinical and Experimental Medicine. 26:1053-1061
BACKGROUND Gaucher disease (GD) is defined as an autosomal recessive disorder resulting from the deficiency of glucocerebrosidase (E.C. 3.2.1.45). Glucocerebrosidase is responsible for the degradation of glucosylceramide into ceramide and glucose. Th
Autor:
Funda Çakmak Sayla, Gül Koca, Evren Özdemir, Duygu Uckan-Cetinkaya, Fatima Aerts-Kaya, Parisa Sharafi
Publikováno v:
Bone Marrow Transplantation. 53:1225-1227
Peripheral blood stem cell (PBSC) transplantation has become an established treatment option for a range of malignant and inherited diseases. PBSCs are usually cryopreserved in the presence of dimethyl sulfoxide (DMSO) and stored in liquid nitrogen.
Autor:
Sukriye Ayter, Parisa Sharafi
Publikováno v:
Journal of neurogenetics. 32(2)
This is an original manuscript / preprint of an article published by Taylor & Francis in Journal of Neurogenetics on 12 Apr 2018 available online: https://doi.org/10.1080/01677063.2018.1456538
Neurofibromatosis type 1 (NF1) is the most common ne
Neurofibromatosis type 1 (NF1) is the most common ne
Autor:
Sibel Ersoy-Evans, Parisa Sharafi, Ali Varan, Sukriye Ayter, Sibel Oguzkan-Balci, Yunus Kasim Terzi, Banu Anlar
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease that is caused by mutations of the NF1 gene. NF1 is clinically characterized by neurofibromas, pigmentation anomalies, and an increased risk of malignant tumors. The mutation rate of NF1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efcb850ad02722b17a0341b1475be7d4
http://hdl.handle.net/20.500.11851/796
http://hdl.handle.net/20.500.11851/796
Publikováno v:
Gene. 553(2)
The transcriptional events and pathways responsible for the acquisition of the myogenic phenotype during regeneration and myogenesis have been studied extensively. The modulators that shape the extracellular matrix in health and disease, however, are
Autor:
Gulsum Kayman-Kurekci, Piraye Serdaroglu-Oflazer, Parisa Sharafi, Beril Talim, Haluk Topaloglu, Petek Korkusuz, Nilufer Sayar, Turkan Sarioglu, Burcu Balci-Hayta, Nuhan Purali, Ibrahim Oncel, Hulya Gundesli, Pervin Dinçer
Publikováno v:
Neuromuscular Disorders
We performed genome-wide homozygosity mapping and mapped a novel myopathic phenotype to chromosomal region 1q25 in a consanguineous family with three affected individuals manifesting proximal and distal weakness and atrophy, rigid spine and contractu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a65cdb164231ca7ff366942fae5bf6ac
https://aperta.ulakbim.gov.tr/record/65841
https://aperta.ulakbim.gov.tr/record/65841