Diagnosis of Fanconi Anemia by Diepoxybutane Analysis

Current Protocols in Human Genetics ◽

10.1002/0471142905.hg0807s85 ◽

2015 ◽

pp. 8.7.1-8.7.17 ◽

Author(s):

Arleen D. Auerbach

Keyword(s):

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Abstract #838: A case of Primary Empty Sella in Fanconi Anemia: An Enigma of Findings & Dilemma in Management

Endocrine Practice ◽

10.1016/s1530-891x(20)42763-6 ◽

2015 ◽

Vol 21 ◽

pp. 166-167

Author(s):

Anirban Sinha ◽

Ravindra Shukla ◽

Biplab Mandal ◽

Asish Basu ◽

Satyam Chakraborty ◽

...

Keyword(s):

Fanconi Anemia ◽

Empty Sella ◽

Primary Empty Sella

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Immune Defects in Fanconi Anemia

Critical Reviews™ in Immunology ◽

10.1615/critrevimmunol.v26.i1.40 ◽

2006 ◽

Vol 26 (1) ◽

pp. 81-96 ◽

Author(s):

Sara R. Fagerlie ◽

Grover C. Bagby

Keyword(s):

Fanconi Anemia ◽

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Diabetes mellitus in ataxia-telangiectasia, Fanconi anemia, xeroderma pigmentosum, common variable immune deficiency, and severe combined immune deficiency families

Diabetes ◽

10.2337/diabetes.35.2.143 ◽

1986 ◽

Vol 35 (2) ◽

pp. 143-147 ◽

Author(s):

D. Morrell ◽

C. L. Chase ◽

L. L. Kupper ◽

M. Swift

Keyword(s):

Diabetes Mellitus ◽

Immune Deficiency ◽

Fanconi Anemia ◽

Ataxia Telangiectasia ◽

Xeroderma Pigmentosum ◽

Common Variable Immune Deficiency ◽

Severe Combined Immune Deficiency ◽

Combined Immune Deficiency ◽

Common Variable

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The Fanconi Anemia Pathway and Ubiquitin

Targeted Protein Database ◽

10.2970/tpdb.2007.91 ◽

2007 ◽

Author(s):

Toshiyasu Taniguchi

Keyword(s):

Fanconi Anemia ◽

Fanconi Anemia Pathway

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Lentiviral-mediated Gene Therapy for Pediatric Patients With Fanconi Anemia Subtype A

Case Medical Research ◽

10.31525/ct1-nct04069533 ◽

2019 ◽

Author(s):

Keyword(s):

Gene Therapy ◽

Fanconi Anemia ◽

Pediatric Patients ◽

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Fanconi Anemia Pathway

Reactome - a curated knowledgebase of biological pathways ◽

10.3180/r-hsa-6783310.1 ◽

2015 ◽

Vol 54 ◽

Author(s):

L Matthews ◽

M Orlic-Milacic

Keyword(s):

Fanconi Anemia ◽

Fanconi Anemia Pathway

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Faculty Opinions recommendation of A novel ubiquitin ligase is deficient in Fanconi anemia.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1015631.197563 ◽

2003 ◽

Author(s):

Vivian Cheung

Keyword(s):

Ubiquitin Ligase ◽

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Faculty Opinions recommendation of The Fanconi anemia protein FANCM can promote branch migration of Holliday junctions and replication forks.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1099285.555509 ◽

2008 ◽

Author(s):

Philippe Pasero

Keyword(s):

Fanconi Anemia ◽

Holliday Junctions ◽

Replication Forks ◽

Branch Migration

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Faculty Opinions recommendation of Fanconi anemia is a highly penetrant cancer susceptibility syndrome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1105093.561271 ◽

2008 ◽

Author(s):

Albert N Békássy

Keyword(s):

Fanconi Anemia ◽

Cancer Susceptibility

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Faculty Opinions recommendation of Diagnosis of Fanconi anemia in patients with bone marrow failure.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1158936.618927 ◽

2009 ◽

Author(s):

Albert N Békássy

Keyword(s):

Bone Marrow ◽

Fanconi Anemia ◽

Bone Marrow Failure

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