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Academic Journal

Establishment and application of a multiplex genetic mutation-detection method of lung cancer based on MassARRAY platform.

Authors : Hong-Xia Tian¹; Xu-Chao Zhang¹; Zhen Wang¹

Source: Cancer Biology & Medicine. Mar2016, Vol. 13 Issue 1, p68-76. 9p.

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Academic Journal

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach.

Authors : Chaturvedi, Swati¹; Singh, Ashok K.¹; Keshari, Amit K.¹

Source: Scientifica. 3/9/2016, p1-14. 14p.

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Academic Journal

Pulmonary and Cerebral Infarcts Due to Secondary Thrombosis Risk of a Genetic Mutation: Life-threating Methylentetrahydrofolate Reductase (MTHFR) Deficiency with Early Onset.

Authors : Ianosi, Edith Simona¹; Simona, Szasz¹; Nemes, Roxana¹

Source: Acta Medica Marisiensis. Jun2016, Vol. 62 Issue 2, p269-271. 3p.

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Academic Journal

Emerging Helicobacter pylori levofloxacin resistance and novel genetic mutation in Nepal.

Authors : Miftahussurur, Muhammad^1,2,3; Shrestha, Pradeep Krishna⁴; Subsomwong, Phawinee¹

Source: BMC Microbiology. 11/4/2016, Vol. 16, p1-10. 10p.

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Academic Journal

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation.

Authors : Woojoong Kim¹; Eujin Park¹; Yo Han Ahn¹

Source: Korean Journal of Pediatrics. 2016, Vol. 59 Issue Suppl1, pS5-S9. 5p.

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Academic Journal

Adequacy of endobronchial ultrasound-guided transbronchial needle aspiration samples processed as histopathological samples for genetic mutation analysis in lung adenocarcinoma.

Authors : JEYABALAN, ABIRAMY¹; BHATT, NIDHI²; PLUMMERIDGE, MARTIN J.¹

Source: Molecular & Clinical Oncology. Jan2016, Vol. 4 Issue 1, p119-125. 7p.

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Academic Journal

PTEN gene mutations correlate to poor prognosis in glioma patients: a meta-analysis.

Authors : Feng Han¹; Rong Hu²; Hua Yang¹

Source: OncoTargets & Therapy. Jun2016, Vol. 9, p3485-3492. 8p.

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Academic Journal

Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report.

Authors : Cortini, Francesca^1,2 ; Marinelli, Barbara¹; Seia, Manuela²

Source: Journal of Medical Case Reports. 10/31/2016, Vol. 10, p1-5. 5p.

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Academic Journal

Case of McLeod syndrome with a novel genetic mutation.

Authors : Narumi, Shinsuke¹; Natori, Tatsunori¹; Miyazawa, Haruna¹

Source: Neurology & Clinical Neuroscience. May2016, Vol. 4 Issue 3, p115-117. 3p.

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Academic Journal

Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

Authors : Shu, Shi^1,2 (AUTHOR); Li, Xiao Ling^1,2 (AUTHOR); Liu, Qing^1,3 (AUTHOR)

Source: Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Oct/Nov2016, Vol. 17 Issue 7/8/2016, p605-607. 3p.

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فلترة النتائج

Establishment and application of a multiplex genetic mutation-detection method of lung cancer based on MassARRAY platform.

Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach.

Pulmonary and Cerebral Infarcts Due to Secondary Thrombosis Risk of a Genetic Mutation: Life-threating Methylentetrahydrofolate Reductase (MTHFR) Deficiency with Early Onset.

Emerging Helicobacter pylori levofloxacin resistance and novel genetic mutation in Nepal.

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation.

Adequacy of endobronchial ultrasound-guided transbronchial needle aspiration samples processed as histopathological samples for genetic mutation analysis in lung adenocarcinoma.

PTEN gene mutations correlate to poor prognosis in glioma patients: a meta-analysis.

Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report.

Case of McLeod syndrome with a novel genetic mutation.

Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

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