Mandel JL - Search Results

1

Isolation of cDNA clone encoding human homologue of senescence marker protein-30 (SMP30) and its location on the X chromosome.

Fujita T, Mandel JL, Shirasawa T, Hino O, Shirai T, Maruyama N. Fujita T, et al. Among authors: mandel jl. Biochim Biophys Acta. 1995 Sep 19;1263(3):249-52. doi: 10.1016/0167-4781(95)00120-6. Biochim Biophys Acta. 1995. PMID: 7548213

2

Isolation and characterization of a family of sequences dispersed on the human X chromosome.

Bardoni B, Guioli S, Raimondi E, Heilig R, Mandel JL, Ottolenghi S, Camerino G. Bardoni B, et al. Among authors: mandel jl. Genomics. 1988 Jul;3(1):32-8. doi: 10.1016/0888-7543(88)90155-3. Genomics. 1988. PMID: 2851539

3

Isolation and characterization of cDNA clones for human skeletal muscle alpha actin.

Hanauer A, Levin M, Heilig R, Daegelen D, Kahn A, Mandel JL. Hanauer A, et al. Among authors: mandel jl. Nucleic Acids Res. 1983 Jun 11;11(11):3503-16. doi: 10.1093/nar/11.11.3503. Nucleic Acids Res. 1983. PMID: 6190133 Free PMC article.

4

A new human gene (DXS1357E) with ubiquitous expression, located in Xq28 adjacent to the adrenoleukodystrophy gene.

Mosser J, Sarde CO, Vicaire S, Yates JR, Mandel JL. Mosser J, et al. Among authors: mandel jl. Genomics. 1994 Jul 15;22(2):469-71. doi: 10.1006/geno.1994.1413. Genomics. 1994. PMID: 7806238

5

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

Koenig M, Camerino G, Heilig R, Mandel JL. Koenig M, et al. Among authors: mandel jl. Nucleic Acids Res. 1984 May 25;12(10):4097-109. doi: 10.1093/nar/12.10.4097. Nucleic Acids Res. 1984. PMID: 6728677 Free PMC article.

6

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.

Oberlé I, Camerino G, Kloepfer C, Moisan JP, Grzeschik KH, Hellkuhl B, Hors-Cayla MC, Van Cong N, Weil D, Mandel JL. Oberlé I, et al. Among authors: mandel jl. Hum Genet. 1986 Jan;72(1):43-9. doi: 10.1007/BF00278816. Hum Genet. 1986. PMID: 3002952

7

Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.

Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL, et al. Guioli S, et al. Among authors: mandel jl. Hum Genet. 1989 Dec;84(1):19-21. doi: 10.1007/BF00210664. Hum Genet. 1989. PMID: 2575070

8

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Oberlé I, Drayna D, Camerino G, White R, Mandel JL. Oberlé I, et al. Among authors: mandel jl. Proc Natl Acad Sci U S A. 1985 May;82(9):2824-8. doi: 10.1073/pnas.82.9.2824. Proc Natl Acad Sci U S A. 1985. PMID: 2986139 Free PMC article.

9

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Drayna D, Davies K, Hartley D, Mandel JL, Camerino G, Williamson R, White R. Drayna D, et al. Among authors: mandel jl. Proc Natl Acad Sci U S A. 1984 May;81(9):2836-9. doi: 10.1073/pnas.81.9.2836. Proc Natl Acad Sci U S A. 1984. PMID: 6326147 Free PMC article.

10

FMR1 gene and fragile X syndrome.

Bardoni B, Mandel JL, Fisch GS. Bardoni B, et al. Among authors: mandel jl. Am J Med Genet. 2000 Summer;97(2):153-63. doi: 10.1002/1096-8628(200022)97:2<153::aid-ajmg7>3.0.co;2-m. Am J Med Genet. 2000. PMID: 11180223 Review.

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