Expression of Mmachc and Mmadhc during mouse organogenesis

Molecular Genetics and Metabolism

Volumn 103, Issue 4, 2011, Pages 401-405

  Pupavac, Mihaela ^a   Garcia, Maira A Moreno ^a   Rosenblatt, David S ^a,b   Jerome Majewska, Loydie A ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

CblC; CblD; Cobalamin; Homocysteine; Methylmalonic acid; Vitamin B 12

Indexed keywords

COBAMAMIDE; CYANOCOBALAMIN; HOMOCYSTEINE; MECOBALAMIN; METHYLMALONIC ACID;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BLOOD VESSEL; CELL TYPE SPECIFIC GENE EXPRESSION; CENTRAL NERVOUS SYSTEM; CONCEPTION; EMBRYO; EMBRYO DEVELOPMENT; ENDODERM; ENDOTHELIUM CELL; ESOPHAGUS; FEMALE; GENE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; HEAD; HEART; HEART ATRIUM; HEART VENTRICLE SEPTUM; IN SITU HYBRIDIZATION; INTESTINE; LIVER; LUNG; MALE; MESENCHYME; MESONEPHROS; MMACHC GENE; MMADHC GENE; MOUSE; NONHUMAN; NOTOCHORD; ORGANOGENESIS; PHARYNX; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOMITE; SPINAL GANGLION; STOMACH; TISSUE SPECIFIC GENE EXPRESSION; VITAMIN METABOLISM;

ANIMALS; CARRIER PROTEINS; EMBRYO, MAMMALIAN; IN SITU HYBRIDIZATION; MICE; MICE, INBRED STRAINS; ORGAN SPECIFICITY; ORGANOGENESIS; VITAMIN B 12;

EID: 79960839041     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2011.04.004     Document Type: Article

References (10)

1. Kräutler B. Vitamin B12: chemistry and biochemistry. Biochem. Soc. Trans. 2005, 33:806-810.
2. Watkins D., Rosenblatt D.S. Inborn errors of cobalamin absorption and metabolism. Am. J. Med. Genet. 2011, 157:33-44.
3. Lerner-Ellis J.P., Tirone J.C., Pawelek P.D., Dore C., Atkinson J.L., Watkins D., Morel C.F., Fijiwara T.M., Moras E., Hosack A.R., Dunbar G.V., Antonicka H., Forgetta V., Dobson C.M., Leclerc D., Gravel R.A., Shoubridge E.A., Coulton J.W., Lepage P., Rommens J.M., Morgan K., Rosenblatt D.S. Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nat. Genet. 2006, 38:93-100.
4. Profitlich L.E., Kirmse B., Wasserstein M.P., Diaz G.A., Srivastava S. High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria. Mol. Genet. Metab. 2009, 98:344-348.
5. 12 metabolism. N. Eng. J. Med. 2008, 358:1454-1464.
6. Miousse I.R., Watkins D., Coelho D., Rupar T., Crombez E.A., Vilain E., Bernstein J.A., Cowan T., Lee-Messer C., Enns G.M., Fowler B., Rosenblatt.D.S. Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism. J. Pediatr. 2009, 154:551-556.
7. 12 metabolism. Mol. Genet. Metab. 2010, 102:139-148.
8. Neubuser A., Koseki H., Balling R. Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1. Dev. Biol. 1995, 170:701-716.
9. 1 is required for morphogenesis of the mouse embryo and placenta. Dev. Biol. 2010, 341:154-166.
10. Pagliarini D.J., Calvo S.E., Chang B., Sheth S.A., Vafai S.B., Ong S., Walford G.A., Sugiana C., Boneh A., Chen W.K., Hill D.E., Vidal M., Evans J.G., Thorburn D.R., Carr S.A., Mootha V.K. A mitochondrial protein compendium elucidates complex i disease biology. Cell 2008, 134:112-123.