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Items: 1 to 20 of 111

1.

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus.

Myers JC, Jones TA, Pohjolainen ER, Kadri AS, Goddard AD, Sheer D, Solomon E, Pihlajaniemi T.

Am J Hum Genet. 1990 Jun;46(6):1024-33.

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4.

Sequence and localization of a partial cDNA encoding the human alpha 3 chain of type IV collagen.

Morrison KE, Mariyama M, Yang-Feng TL, Reeders ST.

Am J Hum Genet. 1991 Sep;49(3):545-54.

6.

Molecular genetics of Alport syndrome.

Tryggvason K, Zhou J, Hostikka SL, Shows TB.

Kidney Int. 1993 Jan;43(1):38-44. Review.

8.

Identification of mutations in the COL4A5 collagen gene in Alport syndrome.

Barker DF, Hostikka SL, Zhou J, Chow LT, Oliphant AR, Gerken SC, Gregory MC, Skolnick MH, Atkin CL, Tryggvason K.

Science. 1990 Jun 8;248(4960):1224-7.

PMID:
2349482
9.

Long-range mapping of the gene for the human alpha 5(IV) collagen chain at Xq22-q23.

Vetrie D, Flinter F, Bobrow M, Harris A.

Genomics. 1992 Jan;12(1):130-8.

PMID:
1733850
11.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
12.

Major rearrangements in the alpha 5(IV) collagen gene in three patients with Alport syndrome.

Boye E, Vetrie D, Flinter F, Buckle B, Pihlajaniemi T, Hamalainen ER, Myers JC, Bobrow M, Harris A.

Genomics. 1991 Dec;11(4):1125-32.

PMID:
1783380
13.

Human collagen genes encoding basement membrane alpha 1 (IV) and alpha 2 (IV) chains map to the distal long arm of chromosome 13.

Griffin CA, Emanuel BS, Hansen JR, Cavenee WK, Myers JC.

Proc Natl Acad Sci U S A. 1987 Jan;84(2):512-6.

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15.

Partial structure of the human alpha 2(IV) collagen chain and chromosomal localization of the gene (COL4A2).

Killen PD, Francomano CA, Yamada Y, Modi WS, O'Brien SJ.

Hum Genet. 1987 Dec;77(4):318-24.

PMID:
3692475
16.

Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.

Yoshioka K, Hino S, Takemura T, Maki S, Wieslander J, Takekoshi Y, Makino H, Kagawa M, Sado Y, Kashtan CE.

Am J Pathol. 1994 May;144(5):986-96.

17.

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Kashtan CE.

Medicine (Baltimore). 1999 Sep;78(5):338-60. Review.

18.

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome.

Mochizuki T, Lemmink HH, Mariyama M, Antignac C, Gubler MC, Pirson Y, Verellen-Dumoulin C, Chan B, Schröder CH, Smeets HJ, et al.

Nat Genet. 1994 Sep;8(1):77-81.

PMID:
7987396
19.

Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10.

Apte SS, Seldin MF, Hayashi M, Olsen BR.

Eur J Biochem. 1992 May 15;206(1):217-24.

20.

Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosis.

Zhang X, Zhou J, Reeders ST, Tryggvason K.

Genomics. 1996 May 1;33(3):473-9.

PMID:
8661006

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