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 *

89 related articles for article (PubMed ID: 608946)

  • 1. Meander tail: a recessive mutant located in chromosome 4 of the mouse.
    Hollander WF; Waggie KS
    J Hered; 1977; 68(6):403-6. PubMed ID: 608946
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Crinkly-tail, a mild skeletal mutant in the mouse.
    Johnson DR; Wallace ME
    J Embryol Exp Morphol; 1979 Oct; 53():327-33. PubMed ID: 536693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic mapping of meander tail, a mouse mutation affecting cerebellar development.
    Fletcher C; Norman DJ; Heintz N
    Genomics; 1991 Apr; 9(4):647-55. PubMed ID: 2037292
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Morphological and morphometric features of the deformed cervical and caudal vertebrae in a new mutant knotty-tail (knt/knt) mouse.
    Matsuura T; Narama I; Nishikawa T; Nishimura M; Imagawa T; Kitagawa H; Uehara M
    Ann Anat; 1997 Jun; 179(3):277-83. PubMed ID: 9229083
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic spina bifida occulta in the mouse.
    Hollander WF
    Am J Anat; 1976 Jun; 146(2):173-9. PubMed ID: 782223
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two new mutations in linkage group XVI of the house mouse. Flaky tail and varitint-waddler-J.
    Lane PW
    J Hered; 1972; 63(3):135-40. PubMed ID: 4557539
    [No Abstract]   [Full Text] [Related]  

  • 7. Meander tail reveals a discrete developmental unit in the mouse cerebellum.
    Ross ME; Fletcher C; Mason CA; Hatten ME; Heintz N
    Proc Natl Acad Sci U S A; 1990 Jun; 87(11):4189-92. PubMed ID: 2349228
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Developmental analysis of the external granular layer in the meander tail mutant mouse: do cerebellar microneurons have independent progenitors?
    Napieralski JA; Eisenman LM
    Dev Dyn; 1993 Aug; 197(4):244-54. PubMed ID: 8292822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Kinked tail mutation results in notochord defects in heterozygotes and distal visceral endoderm defects in homozygotes.
    Farkas DR; Chapman DL
    Dev Dyn; 2009 Dec; 238(12):3237-47. PubMed ID: 19877283
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of gene action in the meander tail mutant mouse: examination of cerebellar phenotype and mitotic activity of granule cell neuroblasts.
    Hamre KM; Goldowitz D
    J Comp Neurol; 1996 Apr; 368(2):304-15. PubMed ID: 8725309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tail short variable: characterization of a new mouse mutant, and its possible analogy to certain human vascular disruption defects.
    Seller MJ; Wallace ME
    Teratology; 1993 Oct; 48(4):383-91. PubMed ID: 8278937
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage relations of dumpy, a recessive mutant on chromosome 13 of the mouse.
    Hollander WF
    J Hered; 1981; 72(5):358-9. PubMed ID: 7328306
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel murine gene, Sickle tail, linked to the Danforth's short tail locus, is required for normal development of the intervertebral disc.
    Semba K; Araki K; Li Z; Matsumoto K; Suzuki M; Nakagata N; Takagi K; Takeya M; Yoshinobu K; Araki M; Imai K; Abe K; Yamamura K
    Genetics; 2006 Jan; 172(1):445-56. PubMed ID: 16204209
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage relationships of markers on chromosome 17 of the house mouse.
    Hammerberg G; Klein J
    Genet Res; 1975 Oct; 26(2):203-11. PubMed ID: 1225760
    [No Abstract]   [Full Text] [Related]  

  • 15. Spinal dysplasia with stump tail and hind limb paralysis in a laboratory bred cat.
    Lansdown AB; Pate P
    Lab Anim; 1992 Oct; 26(4):299-300. PubMed ID: 1447909
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hairpin-tail: a case of post-reductional gene action in the mouse egg.
    JOHNSON DR
    Genetics; 1974 Apr; 76(4):795-805. PubMed ID: 4838760
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse.
    Sweet HO; Bronson RT
    J Hered; 1991; 82(2):140-4. PubMed ID: 2013688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion mapping of the t complex of chromosome 17 of the mouse.
    Erickson RP; Lewis SE; Slusser KS
    Nature; 1978 Jul; 274(5667):163-4. PubMed ID: 662013
    [No Abstract]   [Full Text] [Related]  

  • 19. Genetics analysis of mouse mutations Abnormal feet and tail and rough coat, which cause developmental abnormalities and alopecia.
    Ruvinsky I; Chertkov O; Borue XV; Agulnik SI; Gibson-Brown JJ; Lyle SR; Silver LM
    Mamm Genome; 2002 Dec; 13(12):675-9. PubMed ID: 12514744
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inheritance of alternative states of the fused gene in mice.
    Belyaev DK; Ruvinsky AO; Borodin PM
    J Hered; 1981; 72(2):107-12. PubMed ID: 7276510
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.