Yin L - Search Results

1

Frequency of RET mutations in long- and short-segment Hirschsprung disease.

Seri M, Yin L, Barone V, Bolino A, Celli I, Bocciardi R, Pasini B, Ceccherini I, Lerone M, Kristoffersson U, Larsson LT, Casasa JM, Cass DT, Abramowicz MJ, Vanderwinden JM, Kravcenkiene I, Baric I, Silengo M, Martucciello G, Romeo G. Seri M, et al. Among authors: yin l. Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8. Hum Mutat. 1997. PMID: 9090527

2

The physical map of the human RET proto-oncogene.

Pasini B, Hofstra RM, Yin L, Bocciardi R, Santamaria G, Grootscholten PM, Ceccherini I, Patrone G, Priolo M, Buys CH, et al. Pasini B, et al. Among authors: yin l. Oncogene. 1995 Nov 2;11(9):1737-43. Oncogene. 1995. PMID: 7478601

3

Heterogeneity and low detection rate of RET mutations in Hirschsprung disease.

Yin L, Barone V, Seri M, Bolino A, Bocciardi R, Ceccherini I, Pasini B, Tocco T, Lerone M, Cywes S, et al. Yin L, et al. Eur J Hum Genet. 1994;2(4):272-80. doi: 10.1159/000472371. Eur J Hum Genet. 1994. PMID: 7704557

4

Prevalence and parental origin of de novo RET mutations in Hirschsprung's disease.

Yin L, Seri M, Barone V, Tocco T, Scaranari M, Romeo G. Yin L, et al. Eur J Hum Genet. 1996;4(6):356-8. doi: 10.1159/000472232. Eur J Hum Genet. 1996. PMID: 9043870

5

Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.

Romeo G, Ceccherini I, Celli J, Priolo M, Betsos N, Bonardi G, Seri M, Yin L, Lerone M, Jasonni V, Martucciello G. Romeo G, et al. Among authors: yin l. J Intern Med. 1998 Jun;243(6):515-20. doi: 10.1046/j.1365-2796.1998.00332.x. J Intern Med. 1998. PMID: 9681852 Free article.

6

Genomic organisation of the mouse Ret proto-oncogene.

Panetta D, Yin L, Barale R, Romeo G, Ravazzolo R, Ceccherini I, Puliti A. Panetta D, et al. Among authors: yin l. DNA Seq. 2001;11(6):501-6. doi: 10.3109/10425170109041333. DNA Seq. 2001. PMID: 11696976

7

RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH.

Cinti R, Yin L, Ilc K, Berger N, Basolo F, Cuccato S, Giannini R, Torre G, Miccoli P, Amati P, Romeo G, Corvi R. Cinti R, et al. Among authors: yin l. Cytogenet Cell Genet. 2000;88(1-2):56-61. doi: 10.1159/000015485. Cytogenet Cell Genet. 2000. PMID: 10773666

8

A new candidate region for the positional cloning of the XLP gene.

Bolino A, Yin L, Seri M, Cusano R, Cinti R, Coffey A, Brooksbank R, Howell G, Bentley D, Davis JR, Lanyi A, Huang D, Stark M, Creaven M, Bjørkhaug L, Heitzmann F, Lamartine J, Gaudi S, Sylla BS, Lenoir GM, Castagnola E, Giacchino R, Porta G, Franco B, Zollo M, Sumegi J, Romeo G. Bolino A, et al. Among authors: yin l. Eur J Hum Genet. 1998 Sep-Oct;6(5):509-17. doi: 10.1038/sj.ejhg.5200249. Eur J Hum Genet. 1998. PMID: 9801876

9

Radiation hybrids for mapping and cloning DNA sequences of distal 16p.

Ceccherini I, Matera I, Sbrana M, Di Donato A, Yin L, Romeo G. Ceccherini I, et al. Among authors: yin l. Somat Cell Mol Genet. 1992 Jul;18(4):319-24. doi: 10.1007/BF01235755. Somat Cell Mol Genet. 1992. PMID: 1440054

10

Absence of SLAM mutations in EBV-associated lymphoproliferative disease patients.

Ferrand V, Li C, Romeo G, Yin L. Ferrand V, et al. Among authors: yin l. J Med Virol. 2003 May;70(1):131-6. doi: 10.1002/jmv.10373. J Med Virol. 2003. PMID: 12629654

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