Jornal de Síndromes Genéticas e Terapia Gênica

Jornal de Síndromes Genéticas e Terapia Gênica
Acesso livre

ISSN: ISSN: 2157-7412

Volume 6, Emitir 2 (2015)

Comentário

Stem Cells Transplantation in Myocardial Tissue Induces Pro- Arrhythmic Effects and Promotes 4 Reperfusion. Comparison between Intramyocardial and Intravenous Approach

Ruben Daniel Arellano-Perez Vertti, Javier Moran-Martinez, Faviel F Gonzalez-Galarza, Ana Yuritzen Garcia-Marin, J Rafael Arguello and Dealmy Delgadillo Guzman

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Artigo de revisão

Elements Involved In Promoting Eosinophilic Gastrointestinal Disorders

Anshi Shukla, Akanksha Mishra, Sathisha Upparahalli Venkateshaiah, Murli Manhoar, Chandrashekara Puthanapura Mahadevappa and Anil Mishra

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Artigo de Pesquisa

Autosomal Dominant Corneal Dystrophy with TGFBI Mutations: Lessons Learned from a Chinese Pedigree

Anli Shu, Zheng Wei, Yibin Hao, Hai Luo, Fu Tian, Fred G Biddle, Wei Wu, Min Liu and Wei Cao

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Artigo de Pesquisa

Fetal Liver-Derived Stem Cells Ameliorate Adipocyte Functions in Obese Mice

Ming Li, Kequan Guo, Yunze Cui, Yasushi Adachi and Susumu Ikehara

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Mini Revisão

Atopic Dermatitis: The Attack of Food Allergens

Arnaldo Cantani

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Artigo de Pesquisa

Molecular and Cytogenetic Evaluation of Gender in Patients Born with Ambiguous Genitalia from Different Regions of the Valley of Kashmir, North India

Arshad A Pandith, Shahnawaz Akbar, Shehjar Faheem, Tahir M Malla, Maharukh H Zargar, Zafar A Shah, Adil Lateef, Iqbal Qasim, Fayaz A Dar, Niyaz A Azad and Shahid Baba

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Artigo de Pesquisa

Identification of Unique Pattern of CFTR Gene Mutations in Cystic Fibrosis in an Ethnic Kashmiri Population (North India)

Arshad A Pandith, Shahnawaz A Sheikh, Shehjar Faheem, Mahrukh H Zargar, Tahir M Malla, Zafar A Shah, Adil Lateef, Iqbal Qasim, Niyaz A Azad, Shahid M Baba and Fayaz A Dar

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Artigo de revisão

Pros and Cons of Protein Manufacturing: Leverage Omics Data in Research, Diagnostics and Drug Discovery

Svetoslav Dimov and Anelia Atanassova

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Artigo de Pesquisa

Fetal Loss: A Genetic Insight of the De Novo Accessory Bi-Satellited Marker of Chromosome 22P

Venkata Padmalatha Oruganti, Metuku Vidyadhari, Padmavathi Buddhavarapu and Lakshmi Rao Kandukuri

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