87 related articles for article (PubMed ID: 9735344)
41. A spontaneous smc1b mutation causes cohesin protein dysfunction and sterility in mice.
Takabayashi S; Yamauchi Y; Tsume M; Noguchi M; Katoh H
Exp Biol Med (Maywood); 2009 Aug; 234(8):994-1001. PubMed ID: 19491376
[TBL] [Abstract][Full Text] [Related]
42. Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Puk O; Löster J; Dalke C; Soewarto D; Fuchs H; Budde B; Nürnberg P; Wolf E; de Angelis MH; Graw J
Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1525-32. PubMed ID: 18385072
[TBL] [Abstract][Full Text] [Related]
43. Characterization of a novel insertional mouse mutation, kkt: A closely linked modifier of Pax1.
Bialek P; Chan CT; Yee SP
Dev Biol; 2000 Feb; 218(2):354-66. PubMed ID: 10656775
[TBL] [Abstract][Full Text] [Related]
44. Sox18 mutations in the ragged mouse alleles ragged-like and opossum.
James K; Hosking B; Gardner J; Muscat GE; Koopman P
Genesis; 2003 May; 36(1):1-6. PubMed ID: 12748961
[TBL] [Abstract][Full Text] [Related]
45. Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7.
Chae TH; Allen KM; Davisson MT; Sweet HO; Walsh CA
Mamm Genome; 2002 May; 13(5):239-44. PubMed ID: 12016511
[TBL] [Abstract][Full Text] [Related]
46. The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation.
Mjaatvedt CH; Yamamura H; Capehart AA; Turner D; Markwald RR
Dev Biol; 1998 Oct; 202(1):56-66. PubMed ID: 9758703
[TBL] [Abstract][Full Text] [Related]
47. Synergistic interaction of two independent genetic loci causes extreme elevation of serum IgA in mice.
Schneider B; Hanke P; Jagla W; Wattler S; Nehls M; Grosse J; Schröder A; Laufs J
Genes Immun; 2004 Aug; 5(5):375-80. PubMed ID: 15175647
[TBL] [Abstract][Full Text] [Related]
48. Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse.
Hogan BL; Horsburgh G; Cohen J; Hetherington CM; Fisher G; Lyon MF
J Embryol Exp Morphol; 1986 Sep; 97():95-110. PubMed ID: 3794606
[TBL] [Abstract][Full Text] [Related]
49. Activation of the lama2 gene in muscle regeneration: abortive regeneration in laminin alpha2-deficiency.
Kuang W; Xu H; Vilquin JT; Engvall E
Lab Invest; 1999 Dec; 79(12):1601-13. PubMed ID: 10616210
[TBL] [Abstract][Full Text] [Related]
50. Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission.
Maselli RA; Arredondo J; Vázquez J; Chong JX; ; Bamshad MJ; Nickerson DA; Lara M; Ng F; Lo VL; Pytel P; McDonald CM
Am J Med Genet A; 2017 Aug; 173(8):2240-2245. PubMed ID: 28544784
[TBL] [Abstract][Full Text] [Related]
51. A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.
Maselli RA; Arredondo J; Vázquez J; Chong JX; Bamshad MJ; Nickerson DA; Lara M; Ng F; Lo VL; Pytel P; McDonald CM
Ann N Y Acad Sci; 2018 Feb; 1413(1):119-125. PubMed ID: 29377152
[TBL] [Abstract][Full Text] [Related]
52. Genetic mapping of the mouse neuromuscular mutation kyphoscoliosis.
Skynner MJ; Gangadharan U; Coulton GR; Mason RM; Nikitopoulou A; Brown SD; Blanco G
Genomics; 1995 Jan; 25(1):207-13. PubMed ID: 7774920
[TBL] [Abstract][Full Text] [Related]
53. A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defects.
Kaimori JY; Kikkawa Y; Motooka D; Namba-Hamano T; Takuwa A; Okazaki A; Kobayashi K; Tanigawa A; Kotani Y; Uno Y; Yoshimi K; Hattori K; Asahina Y; Kajimoto S; Doi Y; Oka T; Sakaguchi Y; Mashimo T; Sekiguchi K; Nakaya A; Nomizu M; Isaka Y
JCI Insight; 2022 Dec; 7(23):. PubMed ID: 36173685
[TBL] [Abstract][Full Text] [Related]
54. Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix.
Sampaolo S; Napolitano F; Tirozzi A; Reccia MG; Lombardi L; Farina O; Barra A; Cirillo F; Melone MAB; Gianfrancesco F; Iorio GD; Esposito T
J Med Genet; 2017 Oct; 54(10):710-720. PubMed ID: 28735299
[TBL] [Abstract][Full Text] [Related]
55. The neural cell cycle in the looptail (Lp) mutant mouse.
Wilson DB; Center EM
J Embryol Exp Morphol; 1974 Dec; 32(3):698-705. PubMed ID: 4477997
[No Abstract] [Full Text] [Related]
56. The site of action of the ichthyosis locus (ic) in the mouse, as determined by dermal-epidermal recombinations.
Green MC; Alpert BN; Mayer TC
J Embryol Exp Morphol; 1974 Dec; 32(3):715-21. PubMed ID: 4463225
[No Abstract] [Full Text] [Related]
57. Association of the Laminin, Alpha 5 (LAMA5) rs4925386 with height and longevity in an elderly population from Southern Italy.
De Luca M; Crocco P; De Rango F; Passarino G; Rose G
Mech Ageing Dev; 2016 Apr; 155():55-9. PubMed ID: 26968355
[TBL] [Abstract][Full Text] [Related]
58. Tumour-Derived Laminin α5 (LAMA5) Promotes Colorectal Liver Metastasis Growth, Branching Angiogenesis and Notch Pathway Inhibition.
Gordon-Weeks A; Lim SY; Yuzhalin A; Lucotti S; Vermeer JAF; Jones K; Chen J; Muschel RJ
Cancers (Basel); 2019 May; 11(5):. PubMed ID: 31064120
[TBL] [Abstract][Full Text] [Related]
59. Abnormal Wnt and PI3Kinase signaling in the malformed intestine of lama5 deficient mice.
Ritié L; Spenlé C; Lacroute J; Bolcato-Bellemin AL; Lefebvre O; Bole-Feysot C; Jost B; Klein A; Arnold C; Kedinger M; Bagnard D; Orend G; Simon-Assmann P
PLoS One; 2012; 7(5):e37710. PubMed ID: 22666383
[TBL] [Abstract][Full Text] [Related]
60. A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder.
Jones LK; Lam R; McKee KK; Aleksandrova M; Dowling J; Alexander SI; Mallawaarachchi A; Cottle DL; Short KM; Pais L; Miner JH; Mallett AJ; Simons C; McCarthy H; Yurchenco PD; Smyth IM
Development; 2020 Jun; 147(21):. PubMed ID: 32439764
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
