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  • 1-9 of  9 results for ""Fanconi Anemia Complementation Group A Protein""

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Academic Journal

FANCA promotes lung adenocarcinoma progression and is a potential target for epitope vaccine immunotherapy.

  • Authors : Kang Y; Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Clinical Laboratory, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.

Subjects: Lung Neoplasms*/Lung Neoplasms*/Lung Neoplasms*/immunology ; Lung Neoplasms*/Lung Neoplasms*/Lung Neoplasms*/pathology ; Lung Neoplasms*/Lung Neoplasms*/Lung Neoplasms*/genetics

  • Source: Journal of translational medicine [J Transl Med] 2024 Oct 07; Vol. 22 (1), pp. 911. Date of Electronic Publication: 2024 Oct 07.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium:

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Academic Journal

Next-generation sequencing reveals novel variants and large deletion in FANCA gene in Polish family with Fanconi anemia.

  • Authors : Repczynska A; Department of Clinical Genetics, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland. .; Julga K

Subjects: Fanconi Anemia*/Fanconi Anemia*/Fanconi Anemia*/diagnosis ; Fanconi Anemia*/Fanconi Anemia*/Fanconi Anemia*/genetics ; Fanconi Anemia*/Fanconi Anemia*/Fanconi Anemia*/pathology

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Jul 19; Vol. 17 (1), pp. 282. Date of Electronic Publication: 2022 Jul 19.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

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Academic Journal

Whole-exome sequencing reveals the etiology of the rare primary hepatic mucoepidermoid carcinoma.

  • Authors : Hou P; Department of Hepatobiliary and Pancreatic Surgery, The Second Affiliated Hospital of Nanchang University, No.1, Minde Road, Nanchang, China.; Su X

Subjects: DNA Mutational Analysis* ; Germ-Line Mutation* ; Exome Sequencing*

  • Source: Diagnostic pathology [Diagn Pathol] 2021 Apr 08; Vol. 16 (1), pp. 29. Date of Electronic Publication: 2021 Apr 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101251558 Publication Model: Electronic Cited Medium:

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Academic Journal

High content drug screening for Fanconi anemia therapeutics.

  • Authors : Montanuy H; Department of Genetics and Microbiology, Universitat Autònoma de Barcelona, Barcelona, Spain.; Camps-Fajol C

Subjects: Fanconi Anemia*/Fanconi Anemia*/Fanconi Anemia*/drug therapy ; Fanconi Anemia*/Fanconi Anemia*/Fanconi Anemia*/genetics; DNA Damage

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2020 Jun 30; Vol. 15 (1), pp. 170. Date of Electronic Publication: 2020 Jun 30.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

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Academic Journal

Aggressive prostate cancer with somatic loss of the homologous recombination repair gene FANCA: a case report.

  • Authors : Hongo H; Department of Urology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.; Kosaka T

Subjects: Antineoplastic Agents/Antineoplastic Agents/Antineoplastic Agents/*administration & dosage ; Bone Neoplasms/Bone Neoplasms/Bone Neoplasms/*diagnostic imaging ; Fanconi Anemia Complementation Group A Protein/Fanconi Anemia Complementation Group A Protein/Fanconi Anemia Complementation Group A Protein/*genetics

  • Source: Diagnostic pathology [Diagn Pathol] 2020 Jan 13; Vol. 15 (1), pp. 5. Date of Electronic Publication: 2020 Jan 13.Publisher: BioMed Central Country of Publication: England NLM ID: 101251558 Publication Model: Electronic Cited Medium:

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Academic Journal

A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing.

  • Authors : Solomon PJ; Department of Paediatrics, Sree Balaji Medical College and Hospital, Chennai, 600 044, India. .; Margaret P

Subjects: Fanconi Anemia/Fanconi Anemia/Fanconi Anemia/*diagnosis ; Fanconi Anemia/Fanconi Anemia/Fanconi Anemia/*genetics; Child

  • Source: Italian journal of pediatrics [Ital J Pediatr] 2015 May 08; Vol. 41, pp. 38. Date of Electronic Publication: 2015 May 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium:

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Academic Journal

CpG methylation of the FHIT, FANCF, cyclin-D2, BRCA2 and RUNX3 genes in Granulosa cell tumors (GCTs) of ovarian origin

Subjects: 0301 basic medicine; Adult; DNA Repair

  • Source: Mol CancerMolecular Cancer, Vol 3, Iss 1, p 33 (2004)

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Academic Journal

A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer.

  • Authors : Thompson E; Department of Pathology, Peter MacCallum Cancer Centre, Locked Bag 1 A'Beckett St, Melbourne, Victoria 8006, Australia. ; Dragovic RL

Subjects: Gene Duplication* ; Genetic Predisposition to Disease* ; Polymorphism, Genetic*

  • Source: BMC cancer [BMC Cancer] 2005 Apr 29; Vol. 5, pp. 43. Date of Electronic Publication: 2005 Apr 29.Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium:

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Academic Journal

Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

Subjects: Science & Technology; Life Sciences & Biomedicine; Oncology

  • Source: R1016 ; R1005

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  • 1-9 of  9 results for ""Fanconi Anemia Complementation Group A Protein""