Cargando…

Innumerable studies on single nucleotide polymorphisms: What could be its utility?

Detalles Bibliográficos
Autores principales:	Ghosh, K, Gorakshakar, Ajit
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2013
Materias:	Editorial
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897129/ https://www.ncbi.nlm.nih.gov/pubmed/24497699 http://dx.doi.org/10.4103/0971-6866.124354

Ejemplares similares

Innumerable Condyloma Acuminatum Tumors of the Bladder
por: Murray, Alexandra J., et al.
Publicado: (2017)

Are mannose-binding lectin gene 2 (MBL2) polymorphisms and MBL deficiency associated with infections?
por: Pradhan, Vandana, et al.
Publicado: (2011)

Migration of innumerable chronically retained acupuncture needles
por: Lazarow, Frances, et al.
Publicado: (2017)

Microbial proteases: ubiquitous enzymes with innumerable uses
por: Solanki, Preeti, et al.
Publicado: (2021)

Genetics of autism and mental retardation: A spoonful from the sea!
por: Ghosh, Kanjaksha, et al.
Publicado: (2009)

Integration of modern genetic knowledge and technology into public health in India
por: Ghosh, Kanjaksha, et al.
Publicado: (2010)

Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?
por: Ghosh, Kanjaksha, et al.
Publicado: (2011)

Molecular organization of ‘Rh’ gene is likely to be heterogeneous across the world
por: Gorakshakar, Ajit C., et al.
Publicado: (2013)

Dr. Bhatia's legacy in the development of immunohematology research in the country
por: Ghosh, K., et al.
Publicado: (2014)

Bombay phenotype in Orissa: What could we make out of it?
por: Ghosh, Kanjaksha, et al.
Publicado: (2007)

Prenatal diagnosis of common fetal aneuploidies: Scenario in India
por: Baburao, V., et al.
Publicado: (2013)

Is RBC discrimination index suitable for differentiating between α- and β- thalassemias?
por: Gorakshakar, Ajit C., et al.
Publicado: (2011)

National and ethnic human mutation database: A need of the day
por: Gorakshakar, A. C., et al.
Publicado: (2008)

Diffuse Leiomyomatosis: Complete Myomectomy for Innumerable Small Nodules to Achieve Fertility Sparing and Childbearing
por: Konishi, Ikuo
Publicado: (2019)

Innumerable nevi with giant congenital melanocytic nevus clinically mimicking neurofibromatosis: A diagnostic challenge
por: Boyers, Lindsay N., et al.
Publicado: (2015)

CAR-T Cell Therapy: A Door Is Open to Find Innumerable Possibilities of Treatments for Cancer Patients
por: Perez-Amill, Lorena, et al.
Publicado: (2018)

Innumerable Liver Masses in a Patient with Autoimmune Hepatitis and Primary Sclerosing Cholangitis Overlap Syndrome
por: Gharibpoor, Alireza, et al.
Publicado: (2017)

A Unique Case of Tri-Valvular Serratia marcescens Infective Endocarditis Complicated by Innumerable Emboli
por: Evangelista-Abreu, Walter, et al.
Publicado: (2022)

Time to reconsider CD33 single nucleotide polymorphism in the response to gemtuzumab ozogamicin
por: Lamba, Jatinder K., et al.
Publicado: (2021)

Could one splicing-site single nucleotide polymorphism cause the MODY2 disease?
por: Mota, Simone Brüggemann, et al.
Publicado: (2015)

Innumerable hemorrhagic brain metastases from a neuroendocrine tumor grade-1 with prolonged natural history
por: Elarjani, Turki, et al.
Publicado: (2021)

Innumerable cerebral microbleeds in hepatitis B virus-related decompensated liver cirrhosis: a case report
por: Oh, Chi Hyuk, et al.
Publicado: (2021)

Conservative Kidney Management in the United States: What It Is and What It Could Be
por: Gelfand, Samantha L.
Publicado: (2023)

Ernest Beutler (1928-2008)
por: Ghosh, Kanjaksha, et al.
Publicado: (2009)

Use of lectins in immunohematology
por: Gorakshakar, Ajit C., et al.
Publicado: (2016)

IL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis
por: Fischer, Sarah, et al.
Publicado: (2017)

Single-nucleotide Polymorphisms in Medical Nutritional Weight Loss: Challenges and Future Directions
por: Chen, Moxi, et al.
Publicado: (2022)

Evolution of technology for molecular genotyping in blood group systems
por: Gorakshakar, Ajit, et al.
Publicado: (2017)

Single nucleotide polymorphisms as the new predictors of therapy decisions in gastroesophageal junction and gastric adenocarcinoma?
por: Perkhofer, Lukas, et al.
Publicado: (2019)

Single-Nucleotide Polymorphism Masking
por: Walter, Nicole A.R., et al.
Publicado: (2008)

Intra-peritoneal rupture of large hydatid cyst of the liver containing innumerable daughter cysts after blunt abdominal trauma
por: Mohammed, Ayad Ahmad, et al.
Publicado: (2019)

Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism‐array analysis
por: Bottega, Roberta, et al.
Publicado: (2019)

A combination of strongly associated prothrombotic single nucleotide polymorphisms could efficiently predict venous thrombosis risk
por: Natae, Shewaye Fituma, et al.
Publicado: (2023)

Single nucleotide polymorphisms as the new predictors of therapy decisions in gastroesophageal junction and gastric adenocarcinoma?
por: Schulz, Christoph, et al.
Publicado: (2020)

Dr Sharad Vishwanath Apte (1930-2013)
por: Gorakshakar, Ajit C.
Publicado: (2013)

Single-Nucleotide Polymorphisms in MICA and MICB Genes Could Play a Role in the Outcome in AML Patients after HSCT
por: Machuldova, Alena, et al.
Publicado: (2021)

The Diffuse Sclerosing Variant of Papillary Thyroid Cancer Presenting as Innumerable Diffuse Microcalcifications in Underlying Adolescent Hashimoto's Thyroiditis: A Case Report
por: Jeong, Sun Hye, et al.
Publicado: (2016)

Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array
por: Zhou, Lili, et al.
Publicado: (2021)

Self-administered Fecal Microbial Transplants—What Could Possibly Go Wrong?
por: Raffals, Laura E
Publicado: (2020)

Clinical Implications of Single Nucleotide Polymorphisms in Diagnosis of Asthma and its Subtypes
por: Park, Jong-Sook, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_kls7u9rrlekucg11bgmmteuh6k