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Academic Journal

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.

Authors : Rathnasiri, Asanka¹; Senarathne, Udara²; Arunath, Visvalingam¹

Source: BMC Endocrine Disorders. 10/24/2021, Vol. 21 Issue 1, p1-5. 5p.

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Academic Journal

Is hyaluronic acid production transcriptionally regulated? A transcriptional repressor gene deletion study in Streptococcus zooepidemicus.

Authors : Gao, Weixia^1,2 (AUTHOR); Zhang, Xiaoliang¹ (AUTHOR); Zhang, Guangtong¹ (AUTHOR)

Source: Applied Microbiology & Biotechnology. Nov2021, Vol. 105 Issue 21/22, p8495-8504. 10p.

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Academic Journal

New insights into the construction of wild-type Saba pig-derived Escherichia coli irp2 gene deletion strains.

Authors : Zhang, Bo¹ (AUTHOR); Wang, Hongdan² (AUTHOR); Zhao, Weiwei³ (AUTHOR)

Source: 3 Biotech. 8/13/2021, Vol. 11 Issue 9, p1-9. 9p.

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Academic Journal

Network-based gene deletion analysis identifies candidate genes and molecular mechanism involved in clear cell renal cell carcinoma.

Authors : Udayaraja, G. K.¹ (AUTHOR); Arnold Emerson, I.¹ (AUTHOR)

Source: Journal of Genetics. 2021, Vol. 100 Issue 1, p1-11. 11p.

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Academic Journal

Gene Deletion and Sleep Depletion: Exploring the Relationship Between Sleep and Affect in 22q11.2 Deletion Syndrome.

Authors : Hyde, Justyn¹ (AUTHOR); Eidels, Ami¹ (AUTHOR); van Amelsvoort, Therese² (AUTHOR)

Source: Journal of Genetic Psychology. Sep-Oct2021, Vol. 182 Issue 5, p304-316. 13p. 6 Charts.

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Academic Journal

MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report.

Authors : Cui, Shiyun¹ (AUTHOR); Zhang, Xiao² (AUTHOR); Zou, Ruihan² (AUTHOR)

Source: Oncology Research & Treatment. 2021, Vol. 44 Issue 7-8, p414-421. 8p.

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Academic Journal

Occurrence of chronic myeloid leukemia in a patient with CDC73 gene deletion: "Chance or Causality?".

Authors : De Candia, Maria Stella¹; Sgherza, Nicola² ; Bernardini, Laura³

Source: International Journal of Laboratory Hematology. Dec2021, Vol. 43 Issue 6, pe284-e286. 3p.

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Academic Journal

Combined gene deletion of dihydrofolate reductase-thymidylate synthase and pteridine reductase in Leishmania infantum.

Authors : Bhattacharya, Arijit¹ (AUTHOR); Leprohon, Philippe¹ (AUTHOR); Ouellette, Marc¹ (AUTHOR)

Source: PLoS Neglected Tropical Diseases. 4/27/2021, Vol. 15 Issue 4, p1-15. 15p.

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Delayed Diagnosis, Difficult Decisions: Novel Gene Deletion Causing X-Linked Hypophosphatemia in a Middle-Aged Man with Achondroplastic Features and Tertiary Hyperparathyroidism.

Authors : Chin, Yun Ann¹ (AUTHOR); Zhao, Yi² (AUTHOR); Tay, Gerald³ (AUTHOR)

Source: Case Reports in Endocrinology. 4/16/2021, p1-7. 7p.

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Academic Journal

Influence of the quick-to-court gene deletion on courtship behaviour of Drosophila melanogaster.

Authors : BELKINA, ELENA G.¹ (AUTHOR); LAZEBNY, OLEG E.¹ (AUTHOR); GORNOSTAEV, NIKOLAY G.¹ (AUTHOR)

Source: Journal of Genetics. 2021, Vol. 100 Issue 1, p1-12. 12p. 1 Color Photograph, 1 Diagram, 4 Charts, 3 Graphs.

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فلترة النتائج

A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.

Is hyaluronic acid production transcriptionally regulated? A transcriptional repressor gene deletion study in Streptococcus zooepidemicus.

New insights into the construction of wild-type Saba pig-derived Escherichia coli irp2 gene deletion strains.

Network-based gene deletion analysis identifies candidate genes and molecular mechanism involved in clear cell renal cell carcinoma.

Gene Deletion and Sleep Depletion: Exploring the Relationship Between Sleep and Affect in 22q11.2 Deletion Syndrome.

MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report.

Occurrence of chronic myeloid leukemia in a patient with CDC73 gene deletion: "Chance or Causality?".

Combined gene deletion of dihydrofolate reductase-thymidylate synthase and pteridine reductase in Leishmania infantum.

Delayed Diagnosis, Difficult Decisions: Novel Gene Deletion Causing X-Linked Hypophosphatemia in a Middle-Aged Man with Achondroplastic Features and Tertiary Hyperparathyroidism.

Influence of the quick-to-court gene deletion on courtship behaviour of Drosophila melanogaster.

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