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Items: 1 to 20 of 85

1.

Homozygosity mapping and Werner's syndrome.

Schellenberg GD, Martin GM, Wijsman EM, Nakura J, Miki T, Ogihara T.

Lancet. 1992 Apr 18;339(8799):1002. No abstract available.

PMID:
1348795
2.

Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8.

Nakura J, Miki T, Nagano K, Kihara K, Ye L, Kamino K, Fujiwara Y, Yoshida S, Murano S, Fukuchi K, et al.

Gerontology. 1993;39 Suppl 1:11-5.

PMID:
8365666
3.

Genetic linkage of Werner's syndrome to five markers on chromosome 8.

Goto M, Rubenstein M, Weber J, Woods K, Drayna D.

Nature. 1992 Feb 20;355(6362):735-8.

PMID:
1741060
4.

Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.

Ye L, Nakura J, Mitsuda N, Fujioka Y, Kamino K, Ohta T, Jinno Y, Niikawa N, Miki T, Ogihara T.

Genomics. 1995 Aug 10;28(3):566-9.

PMID:
7490095
5.

Homozygosity mapping of the Werner syndrome locus (WRN).

Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi K, Weber JL, Piussan C, Melaragno MI, et al.

Genomics. 1994 Oct;23(3):600-8.

PMID:
7851888
6.

[Werner's syndrome and familial Alzheimer's disease].

Miki T, Nakura J, Kamino K, Ogihara T.

Tanpakushitsu Kakusan Koso. 1993 Feb;38(3):366-73. Review. Japanese. No abstract available.

PMID:
8098160
7.

Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.

Kihara K, Nakura J, Ye L, Mitsuda N, Kamino K, Zhao Y, Fujioka Y, Miki T, Ogihara T.

Jpn J Hum Genet. 1994 Dec;39(4):403-9.

PMID:
7873752
8.

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T.

Genomics. 1996 Aug 15;36(1):130-41.

PMID:
8812424
9.

Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.

Salk D, Au K, Hoehn H, Martin GM.

Cytogenet Cell Genet. 1981;30(2):92-107.

PMID:
7273860
10.

Lack of effect of caffeine post-treatment on X-ray-induced chromosomal aberrations in Werner's syndrome lymphoblastoid cell lines: a preliminary report.

Franchitto A, Proietti De Santis L, Pichierri P, Mosesso P, Palitti F.

Int J Radiat Biol. 1999 Nov;75(11):1349-55.

PMID:
10597909
11.

[Werner's syndrome and intracranial meningioma].

Borroni G, Vignati G, Zaccone C, Brazzelli V, Scappaticci S, Cerimele D, Rabbiosi G.

G Ital Dermatol Venereol. 1989 May;124(5):225-9. Review. Italian.

PMID:
2695454
12.
13.

Family analysis of Werner's syndrome: a survey of 42 Japanese families with a review of the literature.

Goto M, Tanimoto K, Horiuchi Y, Sasazuki T.

Clin Genet. 1981 Jan;19(1):8-15.

PMID:
7460386
14.

Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndrome.

Scappaticci S, Forabosco A, Borroni G, Orecchia G, Fraccaro M.

Ann Genet. 1990;33(1):5-8.

PMID:
2369072
15.

Chromosome translocations in fibroblast cultures derived from patients with Werner's syndrome.

Benn PA.

Am J Hum Genet. 1985 Jan;37(1):221-3. No abstract available.

16.

A novel mutation in a patient with Werner's syndrome.

Nakayama T, Ochiai T, Takahashi Y, Ohkubo K, Hironaga T, Kokubun S.

Gerontology. 2002 Jul-Aug;48(4):215-9.

PMID:
12053110
17.

A patient with Werner's syndrome and erythroleukemia: just coincidence?

Bartal C, Yerushalmi R, Zilberman D, Yermiyahu T.

Leuk Lymphoma. 1996 May;21(5-6):509-13, color plate XXI following 5.

PMID:
9172819
18.

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, et al.

Genomics. 1994 Sep 1;23(1):100-13.

19.

[Werner's syndrome].

Haddad F, Debs R, Tohme A, Helou J, Ghayad E.

Ann Dermatol Venereol. 1998 Jan;125(1):24-6. French.

PMID:
9747202
20.

[A remarkable case of Werner's syndrome (author's transl)].

Rieger H.

Klin Monbl Augenheilkd. 1980 May;176(5):857-8. German.

PMID:
7442065

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