Willard HF - Search Results

1

X inactivation in females with X-linked disease.

Puck JM, Willard HF. Puck JM, et al. Among authors: willard hf. N Engl J Med. 1998 Jan 29;338(5):325-8. doi: 10.1056/NEJM199801293380611. N Engl J Med. 1998. PMID: 9445416 No abstract available.

2

X chromosome inactivation, XIST, and pursuit of the X-inactivation center.

Willard HF. Willard HF. Cell. 1996 Jul 12;86(1):5-7. doi: 10.1016/s0092-8674(00)80071-9. Cell. 1996. PMID: 8689687 Review. No abstract available.

3

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.

Carrel L, Willard HF. Carrel L, et al. Among authors: willard hf. Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7364-9. doi: 10.1073/pnas.96.13.7364. Proc Natl Acad Sci U S A. 1999. PMID: 10377420 Free PMC article.

4

X-inactivation profile reveals extensive variability in X-linked gene expression in females.

Carrel L, Willard HF. Carrel L, et al. Among authors: willard hf. Nature. 2005 Mar 17;434(7031):400-4. doi: 10.1038/nature03479. Nature. 2005. PMID: 15772666

5

Autosomal dominant mutations affecting X inactivation choice in the mouse.

Percec I, Plenge RM, Nadeau JH, Bartolomei MS, Willard HF. Percec I, et al. Among authors: willard hf. Science. 2002 May 10;296(5570):1136-9. doi: 10.1126/science.1070087. Science. 2002. PMID: 12004136

6

X chromosome inactivation and X-linked mental retardation.

Willard HF. Willard HF. Am J Med Genet. 1996 Jul 12;64(1):21-6. doi: 10.1002/(SICI)1096-8628(19960712)64:1<21::AID-AJMG2>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8826443 Review.

7

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.

Plenge RM, Stevenson RA, Lubs HA, Schwartz CE, Willard HF. Plenge RM, et al. Among authors: willard hf. Am J Hum Genet. 2002 Jul;71(1):168-73. doi: 10.1086/341123. Epub 2002 May 30. Am J Hum Genet. 2002. PMID: 12068376 Free PMC article.

8

Making sense (and antisense) of the X inactivation center.

Willard HF, Carrel L. Willard HF, et al. Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10025-7. doi: 10.1073/pnas.191380198. Proc Natl Acad Sci U S A. 2001. PMID: 11526224 Free PMC article. No abstract available.

9

Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.

Wolff DJ, Gustashaw KM, Zurcher V, Ko L, White W, Weiss L, Van Dyke DL, Schwartz S, Willard HF. Wolff DJ, et al. Among authors: willard hf. Hum Genet. 1997 Aug;100(2):256-61. doi: 10.1007/s004390050501. Hum Genet. 1997. PMID: 9254860

10

Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.

Plenge RM, Tranebjaerg L, Jensen PK, Schwartz C, Willard HF. Plenge RM, et al. Among authors: willard hf. Am J Hum Genet. 1999 Mar;64(3):759-67. doi: 10.1086/302286. Am J Hum Genet. 1999. PMID: 10053010 Free PMC article.

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