These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 16691598)

  • 1. Evaluation of SLC35A3 as a candidate gene for human vertebral malformations.
    Ghebranious N; Burmester JK; Glurich I; McPherson E; Ivacic L; Kislow J; Rasmussen K; Kumar V; Raggio CL; Blank RD; Jacobsen FS; Faciszewski T; Womack J; Giampietro PF
    Am J Med Genet A; 2006 Jun; 140(12):1346-8. PubMed ID: 16691598
    [No Abstract]   [Full Text] [Related]  

  • 2. A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation.
    Thomsen B; Horn P; Panitz F; Bendixen E; Petersen AH; Holm LE; Nielsen VH; Agerholm JS; Arnbjerg J; Bendixen C
    Genome Res; 2006 Jan; 16(1):97-105. PubMed ID: 16344554
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine.
    Zhao S; Zhao H; Zhao L; Cheng X; Zheng Z; Wu M; Wen W; Wang S; Zhou Z; Xie H; Ruan D; Li Q; Liu X; Ou C; Li G; Zhao Z; Chen G; Niu Y; Yin X; Hu Y; Zhang X; ; Liu P; Qiu G; Liu W; Zhao C; Wu Z; Zhang J; Wu N
    Nat Commun; 2024 Feb; 15(1):1125. PubMed ID: 38321032
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gene expression profiling, chromosome assignment and mutational analysis of the porcine Golgi-resident UDP-N-acetylglucosamine transporter SLC35A3.
    Andersen PK; Veng L; Juul-Madsen HR; Vingborg RK; Bendixen C; Thomsen B
    Mol Membr Biol; 2007; 24(5-6):519-30. PubMed ID: 17710655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic counseling in a case of congenital hemivertebrae.
    Alvarez de la Rosa M; Padilla Pérez AI; de la Torre Fernández de Vega FJ; López García J; Troyano Luque JM
    Arch Gynecol Obstet; 2009 Oct; 280(4):653-8. PubMed ID: 19221776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Segmentation defects of the human axial skeleton without dysostoses or skeletal dysplasias.
    Bates AW; Nale K
    Fetal Pediatr Pathol; 2005; 24(2):121-7. PubMed ID: 16243756
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis.
    Edvardson S; Ashikov A; Jalas C; Sturiale L; Shaag A; Fedick A; Treff NR; Garozzo D; Gerardy-Schahn R; Elpeleg O
    J Med Genet; 2013 Nov; 50(11):733-9. PubMed ID: 24031089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Vertebral and multiple organ malformations in a black and white German Holstein calf].
    Buck BC; Ulrich R; Wöhlke A; Kuiper H; Baumgärtner W; Distl O
    Berl Munch Tierarztl Wochenschr; 2010; 123(5-6):251-5. PubMed ID: 20496833
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia.
    Royer-Bertrand B; Castillo-Taucher S; Moreno-Salinas R; Cho TJ; Chae JH; Choi M; Kim OH; Dikoglu E; Campos-Xavier B; Girardi E; Superti-Furga G; Bonafé L; Rivolta C; Unger S; Superti-Furga A
    Sci Rep; 2015 Nov; 5():17154. PubMed ID: 26598328
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotype characterization and natural history of spondylothoracic dysplasia syndrome: a series of 27 new cases.
    Cornier AS; Ramírez N; Arroyo S; Acevedo J; García L; Carlo S; Korf B
    Am J Med Genet A; 2004 Jul; 128A(2):120-6. PubMed ID: 15214000
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An analysis of PAX1 in the development of vertebral malformations.
    Giampietro PF; Raggio CL; Reynolds CE; Shukla SK; McPherson E; Ghebranious N; Jacobsen FS; Kumar V; Faciszewski T; Pauli RM; Rasmussen K; Burmester JK; Zaleski C; Merchant S; David D; Weber JL; Glurich I; Blank RD
    Clin Genet; 2005 Nov; 68(5):448-53. PubMed ID: 16207213
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Sagittal and frontal vertebral body fissures. On the formal regularity of congenital malformations of vertebral bodies].
    RATHKE FW
    Arch Orthop Unfallchir; 1959; 50():618-29. PubMed ID: 14436408
    [No Abstract]   [Full Text] [Related]  

  • 13. Homeotic transformations of the axial skeleton of YY1 mutant mice and genetic interaction with the Polycomb group gene Ring1/Ring1A.
    Lorente M; Pérez C; Sánchez C; Donohoe M; Shi Y; Vidal M
    Mech Dev; 2006 Apr; 123(4):312-20. PubMed ID: 16624538
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Jeune syndrome.
    O'Connor MB; Gallagher DP; Mulloy E
    Postgrad Med J; 2008 Oct; 84(996):559. PubMed ID: 19017845
    [No Abstract]   [Full Text] [Related]  

  • 15. Severe ipsilateral musculoskeletal involvement in a Cornelia de Lange patient with a novel NIPBL mutation.
    Baquero-Montoya C; Gil-Rodríguez MC; Hernández-Marcos M; Teresa-Rodrigo ME; Vicente-Gabas A; Bernal ML; Casale CH; Bueno-Lozano G; Bueno-Martínez I; Queralt E; Villa O; Hernando-Davalillo C; Armengol L; Gómez-Puertas P; Puisac B; Selicorni A; Ramos FJ; Pié J
    Eur J Med Genet; 2014 Sep; 57(9):503-9. PubMed ID: 24874887
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fibroadipose hyperplasia versus Proteus syndrome: segmental overgrowth with a mosaic mutation in the PIK3CA gene.
    Youssefian L; Vahidnezhad H; Baghdadi T; Ghaznavi A; Li Q; Tabrizi M; Uitto J
    J Invest Dermatol; 2015 May; 135(5):1450-1453. PubMed ID: 25602158
    [No Abstract]   [Full Text] [Related]  

  • 17. Congenital anomalies of the ribs and chest wall associated with congenital deformities of the spine.
    Tsirikos AI; McMaster MJ
    J Bone Joint Surg Am; 2005 Nov; 87(11):2523-36. PubMed ID: 16264130
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Anomalies associated with vertebral malformations.
    Beals RK; Robbins JR; Rolfe B
    Spine (Phila Pa 1976); 1993 Aug; 18(10):1329-32. PubMed ID: 8211365
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DLL3 as a candidate gene for vertebral malformations.
    Giampietro PF; Raggio CL; Reynolds C; Ghebranious N; Burmester JK; Glurich I; Rasmussen K; McPherson E; Pauli RM; Shukla SK; Merchant S; Jacobsen FS; Faciszewski T; Blank RD
    Am J Med Genet A; 2006 Nov; 140(22):2447-53. PubMed ID: 17041936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new trend in personalized medicine: rapid detection of SNPs in drug transporter genes by the SmartAmp method.
    Aw W; Lezhava A; Hayashizaki Y; Ishikawa T
    Clin Pharmacol Ther; 2011 Apr; 89(4):617-20. PubMed ID: 21346755
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.