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Protein-coding gene in the species Homo sapiens
in humans is encoded by the FANCB gene. The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2)
FANCB
Genetic disease causing anemia, birth defects, and cancers
[citation needed] Scientists have identified 21 FA or FA-like genes: FANCA, FANCB, FANCC, FANCD1 (BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (BRIP1)
Fanconi_anemia
Tumor or other abnormal growth of tissue
at frequencies of between 13%-100% for the DNA repair genes BRCA1, WRN, FANCB, FANCF, MGMT, MLH1, MSH2, MSH4, ERCC1, XPF, NEIL1 and ATM. These epigenetic
Neoplasm
Inherited genetic condition that predisposes a person to cancer
and hypopigmentation. To date, the genes known to cause FA are: FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, FANCN,
Hereditary_cancer_syndrome
Congenital discontinuity of the oesophagus
been discovered include the transcriptional regulators SOX2, MYCN, CHD7, FANCB, and members of FOX transcription factor family. Others plausible candidate
Esophageal_atresia
Erythropoietic protoporphyria FECH 1:75,000-200,000 Fanconi anemia (FA) FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM
List_of_genetic_disorders
Protein-coding gene in the species Homo sapiens
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, and FANCL
FANCE
Group of proteins
known as the ‘FA core complex’ which is formed by the interaction of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM and the accessory proteins (FAAP20
FANC_proteins
Region of often-methylated DNA with a cytosine followed by a guanine
non-small-cell lung cancer squamous cell carcinomas. Promoter hypermethylation of FANCB occurs in 46% of head and neck cancers. On the other hand, the promoters
CpG_site
Protein-coding gene in the species Homo sapiens
important function of FANCB and ubiquitin binding by FANCL in vivo. A nuclear complex containing FANCL (as well as FANCA, FANCB, FANCC, FANCE, FANCF,
FANCL
Protein-coding gene in the species Homo sapiens
Fanconi anaemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, and FANCL
FANCA
Aspect of cancer
occurs in 48% of squamous cell carcinomas; and promoter hypermethylation of FANCB occurs in 46% of head and neck cancers.[citation needed] On the other hand
Regulation of transcription in cancer
Regulation_of_transcription_in_cancer
HGNC:54842; P0DSO1 5449 FAN1 HGNC:29170; Q9Y2M0 5450 FANCA HGNC:3582; O15360 5451 FANCB HGNC:3583; Q8NB91 5452 FANCC HGNC:3584; Q00597 5453 FANCD2 HGNC:3585; Q9BXW9
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Protein-coding gene in the species Homo sapiens
PMID 17555773. Nomura Y, Adachi N, Koyama H (Oct 2007). "Human Mus81 and FANCB independently contribute to repair of DNA damage during replication". Genes
MUS81
Protein-coding gene in the species Homo sapiens
currently unclear. A nuclear complex containing FANCG (as well as FANCA, FANCB, FANCC, FANCE, FANCF, FANCL and FANCM) is essential for the activation of
FANCG
High frequency of mutations within the genome of a cellular lineage
frequencies of between 13–100% of epigenetic defects in genes BRCA1, WRN, FANCB, FANCF, MGMT, MLH1, MSH2, MSH4, ERCC1, XPF, NEIL1 and ATM located in cancers
Genome_instability
Process whereby cells acquire the properties of cancer
promoter hypermethylation of DNA repair genes LIG4, NEIL1, ATM, MLH1 or FANCB occurs at frequencies of between 33% and 82% in one or more of head and
Malignant_transformation
review also indicated promoter hypermethylation of LIG4, NEIL1, ATM, MLH1 or FANCB occurs at frequencies between 33% and 82% in one or more of head and neck
DNA_methylation_in_cancer
Protein-coding gene in the species Homo sapiens
involved in homology-directed DNA repair. A nuclear complex containing FANCA, FANCB, FANCC, FANCE, FANCF, FANCL, and FANCG proteins is required for activation
FANCD2
Protein-coding gene in the species Homo sapiens
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI,
FANCI
FANCB
FANCB
FANCB
FANCB
Boy/Male
Hindu
Attached, Respectful, Thoughtful
Boy/Male
Hindu
The Moon
Surname or Lastname
English and Scottish
English and Scottish : of uncertain derivation; possibly related to Bing.
Female
Finnish
Finnish form of Swedish Annika, ANNIKKI means "favor; grace."
Boy/Male
Indian
Protection, Safeguarding
Girl/Female
American, British, English, Greek, Latin
Moon; Abbreviation of Cynthia and Lucinda; Form of Cynthia; Bright
Boy/Male
Hindu, Indian, Kannada, Malayalam, Marathi, Telugu
With a Cute Personality; Someone who is Different with a Cute Personality
Boy/Male
Hindu, Indian, Marathi, Oriya, Punjabi, Sanskrit, Sikh
Clouds who Give Rain; A Star; Clouds
Girl/Female
Bengali, Gujarati, Hindu, Indian, Kannada, Sindhi, Telugu
Imagination; Creative; Imagined
Boy/Male
Hindu, Indian, Tamil
Joyful; Happy
FANCB
FANCB
FANCB
FANCB
FANCB