-
1
-
-
0036839719
-
Epidemiology of primary hyperparathyroidism in Europe
-
Adami S, Marcocci C, Gatti D. Epidemiology of primary hyperparathyroidism in Europe. J Bone Miner Res 2002 17 (Suppl 2 N18 23.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.SUPPL. 2
, pp. 18-23
-
-
Adami, S.1
Marcocci, C.2
Gatti, D.3
-
2
-
-
24344504476
-
Editorial: HRPT2 in parathyroid cancer: A piece of the puzzle
-
Rubin MR, Silverberg SJ. Editorial: HRPT2 in parathyroid cancer: a piece of the puzzle. J Clin Endocrinol Metab 2005 90 : 5505 7.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5505-7
-
-
Rubin, M.R.1
Silverberg, S.J.2
-
3
-
-
29644445010
-
Genetic disorders of calcium homeostasis caused by abnormal regulation of parathyroid hormaone secretion or responsiveness
-
In. DeGroot, L.J. Jameson, J.L. eds. Philadephia. PA. Elsevier
-
Thakker RV, Juppner H. Genetic disorders of calcium homeostasis caused by abnormal regulation of parathyroid hormaone secretion or responsiveness. In : DeGroot LJ, Jameson JL, eds. Endocrinology. Philadephia, PA : Elsevier, 2006 1511 31.
-
(2006)
Endocrinology.
, pp. 1511-31
-
-
Thakker, R.V.1
Juppner, H.2
-
4
-
-
0034700450
-
Hyperparathyroid and hypoparathyroid disorders
-
Marx SJ. Hyperparathyroid and hypoparathyroid disorders. N Engl J Med 2000 343 : 1863 75.
-
(2000)
N Engl J Med
, vol.343
, pp. 1863-75
-
-
Marx, S.J.1
-
5
-
-
0038695145
-
Hyperparathyroidism-jaw tumour syndrome
-
Chen JD, Morrison C, Zhang C, Kahnoski K, Carpten JD, Teh BT. Hyperparathyroidism-jaw tumour syndrome. J Intern Med 2003 253 : 634 42.
-
(2003)
J Intern Med
, vol.253
, pp. 634-42
-
-
Chen, J.D.1
Morrison, C.2
Zhang, C.3
Kahnoski, K.4
Carpten, J.D.5
Teh, B.T.6
-
6
-
-
0041328511
-
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
-
Howell VM, Haven CJ, Kahnoski K et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet 2003 40 : 657 63.
-
(2003)
J Med Genet
, vol.40
, pp. 657-63
-
-
Howell, V.M.1
Haven, C.J.2
Kahnoski, K.3
-
7
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
Carpten JD, Robbins CM, Villablanca A et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 2002 32 : 676 80.
-
(2002)
Nat Genet
, vol.32
, pp. 676-80
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
-
8
-
-
0025642521
-
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome
-
discussion 12-3.
-
Jackson CE, Norum RA, Boyd SB et al. Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome. Surgery 1990 108 : 1006 12 discussion 12-3.
-
(1990)
Surgery
, vol.108
, pp. 1006-12
-
-
Jackson, C.E.1
Norum, R.A.2
Boyd, S.B.3
-
9
-
-
0028958106
-
Hereditary hyperparathyroidism-jaw tumor syndrome: The endocrine tumor gene HRPT2 maps to chromosome 1q21-q31
-
Szabo J, Heath B, Hill VM et al. Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet 1995 56 : 944 50.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 944-50
-
-
Szabo, J.1
Heath, B.2
Hill, V.M.3
-
10
-
-
1842403802
-
Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas
-
Teh BT, Farnebo F, Kristoffersson U et al. Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. J Clin Endocrinol Metab 1996 81 : 4204 11.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4204-11
-
-
Teh, B.T.1
Farnebo, F.2
Kristoffersson, U.3
-
11
-
-
0142213734
-
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
-
Shattuck TM, Valimaki S, Obara T et al. Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N Engl J Med 2003 349 : 1722 9.
-
(2003)
N Engl J Med
, vol.349
, pp. 1722-9
-
-
Shattuck, T.M.1
Valimaki, S.2
Obara, T.3
-
12
-
-
19944434120
-
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism- jaw tumour syndrome
-
DOI 10.1111/j.1365-2796.2004.01421.x
-
Bradley KJ, Hobbs MR, Buley ID et al. Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. J Intern Med 2005 257 : 18 26. (Pubitemid 40129123)
-
(2005)
Journal of Internal Medicine
, vol.257
, Issue.1
, pp. 18-26
-
-
Bradley, K.J.1
Hobbs, M.R.2
Buley, I.D.3
Carpten, J.D.4
Cavaco, B.M.5
Fares, J.E.6
Laidler, P.7
Manek, S.8
Robbins, C.M.9
Salti, I.S.10
Thompson, N.W.11
Jackson, C.E.12
Thakker, R.V.13
-
13
-
-
0035060663
-
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred
-
Cavaco BM, Barros L, Pannett AA et al. The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred. QJM 2001 94 : 213 22.
-
(2001)
QJM
, vol.94
, pp. 213-22
-
-
Cavaco, B.M.1
Barros, L.2
Pannett, A.A.3
-
14
-
-
17744379773
-
A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome
-
Haven CJ, Wong FK, van Dam EW et al. A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 2000 85 : 1449 54.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 1449-54
-
-
Haven, C.J.1
Wong, F.K.2
Van Dam, E.W.3
-
15
-
-
9744232997
-
Renal neoplasia in the hyperparathyroidism-jaw tumor syndrome
-
Tan MH, Teh BT. Renal neoplasia in the hyperparathyroidism-jaw tumor syndrome. Curr Mol Med 2004 4 : 895 7.
-
(2004)
Curr Mol Med
, vol.4
, pp. 895-7
-
-
Tan, M.H.1
Teh, B.T.2
-
16
-
-
8744299920
-
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: Germline and somatic mutations in familial and sporadic parathyroid tumors
-
Cetani F, Pardi E, Borsari S et al. Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors. J Clin Endocrinol Metab 2004 89 : 5583 91.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5583-91
-
-
Cetani, F.1
Pardi, E.2
Borsari, S.3
-
17
-
-
33645033294
-
Genetic analyses in familial isolated hyperparathyroidism: Implication for clinical assessment and surgical management
-
Cetani F, Pardi E, Ambrogini E et al. Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management. Clin Endocrinol (Oxf) 2006 64 : 146 52.
-
(2006)
Clin Endocrinol (Oxf)
, vol.64
, pp. 146-52
-
-
Cetani, F.1
Pardi, E.2
Ambrogini, E.3
-
18
-
-
20044362410
-
A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome
-
Moon SD, Park JH, Kim EM et al. A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 2005 90 : 878 83.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 878-83
-
-
Moon, S.D.1
Park, J.H.2
Kim, E.M.3
-
19
-
-
33644937809
-
Utilisation of a cryptic non-canonical donor splice site of the gene encoding Parafibromin is associated with familial isolated primary hyperparathyroidism
-
Bradley KJ, Cavaco BM, Bowl MR, Harding B, Young A, Thakker RV. Utilisation of a cryptic non-canonical donor splice site of the gene encoding Parafibromin is associated with familial isolated primary hyperparathyroidism. J Med Genet 2005 42 : e51.
-
(2005)
J Med Genet
, vol.42
, pp. 51
-
-
Bradley, K.J.1
Cavaco, B.M.2
Bowl, M.R.3
Harding, B.4
Young, A.5
Thakker, R.V.6
-
20
-
-
33644943454
-
Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours
-
Bradley KJ, Cavaco BM, Bowl MR et al. Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clin Endocrinol (Oxf) 2006 64 : 299 306.
-
(2006)
Clin Endocrinol (Oxf)
, vol.64
, pp. 299-306
-
-
Bradley, K.J.1
Cavaco, B.M.2
Bowl, M.R.3
-
21
-
-
33745207986
-
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome
-
DOI 10.1111/j.1365-2265.2006.02534.x
-
Mizusawa N, Uchino S, Iwata T et al. Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome. Clin Endocrinol (Oxf) 2006 65 : 9 16. (Pubitemid 43911674)
-
(2006)
Clinical Endocrinology
, vol.65
, Issue.1
, pp. 9-16
-
-
Mizusawa, N.1
Uchino, S.2
Iwata, T.3
Tsuyuguchi, M.4
Suzuki, Y.5
Mizukoshi, T.6
Yamashita, Y.7
Sakurai, A.8
Suzuki, S.9
Beniko, M.10
Tahara, H.11
Fujisawa, M.12
Kamata, N.13
Fujisawa, K.14
Yashiro, T.15
Nagao, D.16
Golam, H.Md.17
Sano, T.18
Noguchi, S.19
Yoshimoto, K.20
more..
-
22
-
-
33847053143
-
A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone
-
Yamashita Y, Akiyama T, Mizusawa N, Yoshimoto K, Goto M. A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone. Int J Oral Maxillofac Surg 2007 36 : 365 9.
-
(2007)
Int J Oral Maxillofac Surg
, vol.36
, pp. 365-9
-
-
Yamashita, Y.1
Akiyama, T.2
Mizusawa, N.3
Yoshimoto, K.4
Goto, M.5
-
23
-
-
34447132179
-
Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma
-
Raue F, Haag C, Frank-Raue K. Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma. Dtsch Med Wochenschr 2007 132 : 1459 62.
-
(2007)
Dtsch Med Wochenschr
, vol.132
, pp. 1459-62
-
-
Raue, F.1
Haag, C.2
Frank-Raue, K.3
-
24
-
-
58249097267
-
Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism
-
Masi G, Barzon L, Iacobone M et al. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism. Endocr Relat Cancer 2008 15 : 1115 26.
-
(2008)
Endocr Relat Cancer
, vol.15
, pp. 1115-26
-
-
Masi, G.1
Barzon, L.2
Iacobone, M.3
-
25
-
-
64749095673
-
Primary hyperparathyroidism and jaw tumor syndrome: A novel mutation of the HRPT2 gene
-
Carlson AL, Smith CL. Primary hyperparathyroidism and jaw tumor syndrome: a novel mutation of the HRPT2 gene. Endocr Pract 2008 14 : 743 7.
-
(2008)
Endocr Pract
, vol.14
, pp. 743-7
-
-
Carlson, A.L.1
Smith, C.L.2
-
27
-
-
0142213741
-
HRPT2, a marker of parathyroid cancer
-
Weinstein LS, Simonds WF. HRPT2, a marker of parathyroid cancer. N Engl J Med 2003 349 : 1691 2.
-
(2003)
N Engl J Med
, vol.349
, pp. 1691-2
-
-
Weinstein, L.S.1
Simonds, W.F.2
-
28
-
-
11144355570
-
Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene
-
Cavaco BM, Guerra L, Bradley KJ et al. Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene. J Clin Endocrinol Metab 2004 89 : 1747 52.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 1747-52
-
-
Cavaco, B.M.1
Guerra, L.2
Bradley, K.J.3
-
29
-
-
0033073851
-
Hyperparathyroidism-jaw tumor syndrome: The HRPT2 locus is within a 0.7-cM region on chromosome 1q
-
Hobbs MR, Pole AR, Pidwirny GN et al. Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. Am J Hum Genet 1999 64 : 518 25.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 518-25
-
-
Hobbs, M.R.1
Pole, A.R.2
Pidwirny, G.N.3
-
30
-
-
15144343105
-
Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families
-
Teh BT, Farnebo F, Twigg S et al. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families. J Clin Endocrinol Metab 1998 83 : 2114 20.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 2114-20
-
-
Teh, B.T.1
Farnebo, F.2
Twigg, S.3
-
31
-
-
0036238389
-
Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2
-
Hobbs MR, Rosen IB, Jackson CE. Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2. Am J Hum Genet 2002 70 : 1376 7.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1376-7
-
-
Hobbs, M.R.1
Rosen, I.B.2
Jackson, C.E.3
-
32
-
-
14644397229
-
Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression
-
Woodard GE, Lin L, Zhang JH, Agarwal SK, Marx SJ, Simonds WF. Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression. Oncogene 2005 24 : 1272 6.
-
(2005)
Oncogene
, vol.24
, pp. 1272-6
-
-
Woodard, G.E.1
Lin, L.2
Zhang, J.H.3
Agarwal, S.K.4
Marx, S.J.5
Simonds, W.F.6
-
33
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
Knudson AG Jr. Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 1971 68 : 820 3.
-
(1971)
Proc Natl Acad Sci USA
, vol.68
, pp. 820-3
-
-
Knudson, Jr.A.G.1
-
34
-
-
24344498667
-
HRPT2 mutational analysis of typical sporadic parathyroid adenomas
-
Krebs LJ, Shattuck TM, Arnold A. HRPT2 mutational analysis of typical sporadic parathyroid adenomas. J Clin Endocrinol Metab 2005 90 : 5015 7.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 5015-7
-
-
Krebs, L.J.1
Shattuck, T.M.2
Arnold, A.3
-
35
-
-
34249061535
-
Sporadic human renal tumors display frequent allelic imbalances and novel mutations of the HRPT2 gene
-
Zhao J, Yart A, Frigerio S et al. Sporadic human renal tumors display frequent allelic imbalances and novel mutations of the HRPT2 gene. Oncogene 2007 26 : 3440 9.
-
(2007)
Oncogene
, vol.26
, pp. 3440-9
-
-
Zhao, J.1
Yart, A.2
Frigerio, S.3
-
36
-
-
39149103044
-
Downregulated parafibromin expression is a promising marker for pathogenesis, invasion, metastasis and prognosis of gastric carcinomas
-
Zheng HC, Takahashi H, Li XH et al. Downregulated parafibromin expression is a promising marker for pathogenesis, invasion, metastasis and prognosis of gastric carcinomas. Virchows Arch 2008 452 : 147 55.
-
(2008)
Virchows Arch
, vol.452
, pp. 147-55
-
-
Zheng, H.C.1
Takahashi, H.2
Li, X.H.3
-
37
-
-
38449123774
-
Parafibromin expression in breast cancer: A novel marker for prognostication?
-
Selvarajan S, Sii LH, Lee A et al. Parafibromin expression in breast cancer: a novel marker for prognostication? J Clin Pathol 2008 61 : 64 7.
-
(2008)
J Clin Pathol
, vol.61
, pp. 64-7
-
-
Selvarajan, S.1
Sii, L.H.2
Lee, A.3
-
38
-
-
11844269891
-
The parafibromin tumor suppressor protein is part of a human Paf1 complex
-
Rozenblatt-Rosen O, Hughes CM, Nannepaga SJ et al. The parafibromin tumor suppressor protein is part of a human Paf1 complex. Mol Cell Biol 2005 25 : 612 20.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 612-20
-
-
Rozenblatt-Rosen, O.1
Hughes, C.M.2
Nannepaga, S.J.3
-
39
-
-
20344391925
-
The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II
-
Yart A, Gstaiger M, Wirbelauer C et al. The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II. Mol Cell Biol 2005 25 : 5052 60.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 5052-60
-
-
Yart, A.1
Gstaiger, M.2
Wirbelauer, C.3
-
40
-
-
0030045412
-
Paf1p, an RNA polymerase II-associated factor in Saccharomyces cerevisiae, may have both positive and negative roles in transcription
-
Shi X, Finkelstein A, Wolf AJ, Wade PA, Burton ZF, Jaehning JA. Paf1p, an RNA polymerase II-associated factor in Saccharomyces cerevisiae, may have both positive and negative roles in transcription. Mol Cell Biol 1996 16 : 669 76.
-
(1996)
Mol Cell Biol
, vol.16
, pp. 669-76
-
-
Shi, X.1
Finkelstein, A.2
Wolf, A.J.3
Wade, P.A.4
Burton, Z.F.5
Jaehning, J.A.6
-
41
-
-
0036787862
-
RNA polymerase II elongation factors of Saccharomyces cerevisiae: A targeted proteomics approach
-
Krogan NJ, Kim M, Ahn SH et al. RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approach. Mol Cell Biol 2002 22 : 6979 92.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 6979-92
-
-
Krogan, N.J.1
Kim, M.2
Ahn, S.H.3
-
42
-
-
0036123253
-
Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex
-
Mueller CL, Jaehning JA. Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex. Mol Cell Biol 2002 22 : 1971 80.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 1971-80
-
-
Mueller, C.L.1
Jaehning, J.A.2
-
43
-
-
0037007217
-
The Paf1 complex physically and functionally associates with transcription elongation factors in vivo
-
Squazzo SL, Costa PJ, Lindstrom DL et al. The Paf1 complex physically and functionally associates with transcription elongation factors in vivo. EMBO J 2002 21 : 1764 74.
-
(2002)
EMBO J
, vol.21
, pp. 1764-74
-
-
Squazzo, S.L.1
Costa, P.J.2
Lindstrom, D.L.3
-
44
-
-
0036241663
-
Exchange of RNA polymerase II initiation and elongation factors during gene expression in vivo
-
DOI 10.1016/S1097-2765(02)00502-6
-
Pokholok DK, Hannett NM, Young RA. Exchange of RNA polymerase II initiation and elongation factors during gene expression in vivo. Mol Cell 2002 9 : 799 809. (Pubitemid 34454890)
-
(2002)
Molecular Cell
, vol.9
, Issue.4
, pp. 799-809
-
-
Pokholok, D.K.1
Hannett, N.M.2
Young, R.A.3
-
45
-
-
27944450463
-
The Bur1/Bur2 complex is required for histone H2B monoubiquitination by Rad6/Bre1 and histone methylation by COMPASS
-
Wood A, Schneider J, Dover J, Johnston M, Shilatifard A. The Bur1/Bur2 complex is required for histone H2B monoubiquitination by Rad6/Bre1 and histone methylation by COMPASS. Mol Cell 2005 20 : 589 99.
-
(2005)
Mol Cell
, vol.20
, pp. 589-99
-
-
Wood, A.1
Schneider, J.2
Dover, J.3
Johnston, M.4
Shilatifard, A.5
-
46
-
-
0141483281
-
The Rtf1 component of the Paf1 transcriptional elongation complex is required for ubiquitination of histone H2B
-
Ng HH, Dole S, Struhl K. The Rtf1 component of the Paf1 transcriptional elongation complex is required for ubiquitination of histone H2B. J Biol Chem 2003 278 : 33625 8.
-
(2003)
J Biol Chem
, vol.278
, pp. 33625-8
-
-
Ng, H.H.1
Dole, S.2
Struhl, K.3
-
47
-
-
0037524702
-
The Paf1 complex is required for histone H3 methylation by COMPASS and Dot1p: Linking transcriptional elongation to histone methylation
-
Krogan NJ, Dover J, Wood A et al. The Paf1 complex is required for histone H3 methylation by COMPASS and Dot1p: linking transcriptional elongation to histone methylation. Mol Cell 2003 11 : 721 9.
-
(2003)
Mol Cell
, vol.11
, pp. 721-9
-
-
Krogan, N.J.1
Dover, J.2
Wood, A.3
-
48
-
-
0037979272
-
Methylation of histone H3 by Set2 in Saccharomyces cerevisiae is linked to transcriptional elongation by RNA polymerase II
-
Krogan NJ, Kim M, Tong A et al. Methylation of histone H3 by Set2 in Saccharomyces cerevisiae is linked to transcriptional elongation by RNA polymerase II. Mol Cell Biol 2003 23 : 4207 18.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 4207-18
-
-
Krogan, N.J.1
Kim, M.2
Tong, A.3
-
49
-
-
2442568473
-
The Paf1 complex has functions independent of actively transcribing RNA polymerase II
-
Mueller CL, Porter SE, Hoffman MG, Jaehning JA. The Paf1 complex has functions independent of actively transcribing RNA polymerase II. Mol Cell 2004 14 : 447 56.
-
(2004)
Mol Cell
, vol.14
, pp. 447-56
-
-
Mueller, C.L.1
Porter, S.E.2
Hoffman, M.G.3
Jaehning, J.A.4
-
50
-
-
36849046285
-
Histone crosstalk between H2B monoubiquitination and H3 methylation mediated by COMPASS
-
Lee JS, Shukla A, Schneider J et al. Histone crosstalk between H2B monoubiquitination and H3 methylation mediated by COMPASS. Cell 2007 131 : 1084 96.
-
(2007)
Cell
, vol.131
, pp. 1084-96
-
-
Lee, J.S.1
Shukla, A.2
Schneider, J.3
-
51
-
-
5444225805
-
Elongation by RNA polymerase II: The short and long of it
-
Sims RJ III., Belotserkovskaya R, Reinberg D. Elongation by RNA polymerase II: the short and long of it. Genes Dev 2004 18 : 2437 68.
-
(2004)
Genes Dev
, vol.18
, pp. 2437-68
-
-
Sims, III.R.J.1
Belotserkovskaya, R.2
Reinberg, D.3
-
52
-
-
47049105670
-
Direct interactions between the Paf1 complex and a cleavage and polyadenylation factor are revealed by dissociation of Paf1 from RNA polymerase II
-
Nordick K, Hoffman MG, Betz JL, Jaehning JA. Direct interactions between the Paf1 complex and a cleavage and polyadenylation factor are revealed by dissociation of Paf1 from RNA polymerase II. Eukaryot Cell 2008 7 : 1158 67.
-
(2008)
Eukaryot Cell
, vol.7
, pp. 1158-67
-
-
Nordick, K.1
Hoffman, M.G.2
Betz, J.L.3
Jaehning, J.A.4
-
53
-
-
26944435516
-
A posttranscriptional role for the yeast Paf1-RNA polymerase II complex is revealed by identification of primary targets
-
Penheiter KL, Washburn TM, Porter SE, Hoffman MG, Jaehning JA. A posttranscriptional role for the yeast Paf1-RNA polymerase II complex is revealed by identification of primary targets. Mol Cell 2005 20 : 213 23.
-
(2005)
Mol Cell
, vol.20
, pp. 213-23
-
-
Penheiter, K.L.1
Washburn, T.M.2
Porter, S.E.3
Hoffman, M.G.4
Jaehning, J.A.5
-
54
-
-
0031027465
-
Cdc73p and Paf1p are found in a novel RNA polymerase II-containing complex distinct from the Srbp-containing holoenzyme
-
Shi X, Chang M, Wolf AJ et al. Cdc73p and Paf1p are found in a novel RNA polymerase II-containing complex distinct from the Srbp-containing holoenzyme. Mol Cell Biol 1997 17 : 1160 9.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 1160-9
-
-
Shi, X.1
Chang, M.2
Wolf, A.J.3
-
55
-
-
0036460783
-
Phenotypic analysis of Paf1/RNA polymerase II complex mutations reveals connections to cell cycle regulation, protein synthesis, and lipid and nucleic acid metabolism
-
Betz JL, Chang M, Washburn TM, Porter SE, Mueller CL, Jaehning JA. Phenotypic analysis of Paf1/RNA polymerase II complex mutations reveals connections to cell cycle regulation, protein synthesis, and lipid and nucleic acid metabolism. Mol Genet Genomics 2002 268 : 272 85.
-
(2002)
Mol Genet Genomics
, vol.268
, pp. 272-85
-
-
Betz, J.L.1
Chang, M.2
Washburn, T.M.3
Porter, S.E.4
Mueller, C.L.5
Jaehning, J.A.6
-
56
-
-
0036778353
-
The yeast pafl-RNA polymerase II complex is required for full expression of a subset of cell cycle-regulated genes
-
Porter SE, Washburn TM, Chang M, Jaehning JA. The yeast pafl-RNA polymerase II complex is required for full expression of a subset of cell cycle-regulated genes. Eukaryot Cell 2002 1 : 830 42.
-
(2002)
Eukaryot Cell
, vol.1
, pp. 830-42
-
-
Porter, S.E.1
Washburn, T.M.2
Chang, M.3
Jaehning, J.A.4
-
57
-
-
23044457643
-
The human PAF complex coordinates transcription with events downstream of RNA synthesis
-
Zhu B, Mandal SS, Pham AD et al. The human PAF complex coordinates transcription with events downstream of RNA synthesis. Genes Dev 2005 19 : 1668 73.
-
(2005)
Genes Dev
, vol.19
, pp. 1668-73
-
-
Zhu, B.1
Mandal, S.S.2
Pham, A.D.3
-
58
-
-
33646691283
-
Histone H2B monoubiquitination functions cooperatively with FACT to regulate elongation by RNA polymerase II
-
Pavri R, Zhu B, Li G et al. Histone H2B monoubiquitination functions cooperatively with FACT to regulate elongation by RNA polymerase II. Cell 2006 125 : 703 17.
-
(2006)
Cell
, vol.125
, pp. 703-17
-
-
Pavri, R.1
Zhu, B.2
Li, G.3
-
59
-
-
33646555522
-
Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo
-
Mosimann C, Hausmann G, Basler K. Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo. Cell 2006 125 : 327 41.
-
(2006)
Cell
, vol.125
, pp. 327-41
-
-
Mosimann, C.1
Hausmann, G.2
Basler, K.3
-
60
-
-
35548950642
-
Paf1 complex homologues are required for Notch-regulated transcription during somite segmentation
-
Akanuma T, Koshida S, Kawamura A, Kishimoto Y, Takada S. Paf1 complex homologues are required for Notch-regulated transcription during somite segmentation. EMBO Rep 2007 8 : 858 63.
-
(2007)
EMBO Rep
, vol.8
, pp. 858-63
-
-
Akanuma, T.1
Koshida, S.2
Kawamura, A.3
Kishimoto, Y.4
Takada, S.5
-
61
-
-
33747072028
-
Drosophila Rtf1 functions in histone methylation, gene expression, and Notch signaling
-
Tenney K, Gerber M, Ilvarsonn A et al. Drosophila Rtf1 functions in histone methylation, gene expression, and Notch signaling. Proc Natl Acad Sci USA 2006 103 : 11970 4.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 11970-4
-
-
Tenney, K.1
Gerber, M.2
Ilvarsonn, A.3
-
62
-
-
33645219388
-
Drosophila Paf1 modulates chromatin structure at actively transcribed genes
-
Adelman K, Wei W, Ardehali MB et al. Drosophila Paf1 modulates chromatin structure at actively transcribed genes. Mol Cell Biol 2006 26 : 250 60.
-
(2006)
Mol Cell Biol
, vol.26
, pp. 250-60
-
-
Adelman, K.1
Wei, W.2
Ardehali, M.B.3
-
63
-
-
17244376814
-
Wnt signalling in stem cells and cancer
-
Reya T, Clevers H. Wnt signalling in stem cells and cancer. Nature 2005 434 : 843 50.
-
(2005)
Nature
, vol.434
, pp. 843-50
-
-
Reya, T.1
Clevers, H.2
-
64
-
-
4344584730
-
WNT and β-catenin signalling: Diseases and therapies
-
DOI 10.1038/nrg1427
-
Moon RT, Kohn AD, De Ferrari GV, Kaykas A. WNT and beta-catenin signalling: diseases and therapies. Nat Rev Genet 2004 5 : 691 701. (Pubitemid 39150127)
-
(2004)
Nature Reviews Genetics
, vol.5
, Issue.9
, pp. 691-701
-
-
Moon, R.T.1
Kohn, A.D.2
De Ferrari, G.V.3
Kaykas, A.4
-
65
-
-
8444251784
-
The Wnt signaling pathway in development and disease
-
DOI 10.1146/annurev.cellbio.20.010403.113126
-
Logan CY, Nusse R. The Wnt signaling pathway in development and disease. Annu Rev Cell Dev Biol 2004 20 : 781 810. (Pubitemid 39488658)
-
(2004)
Annual Review of Cell and Developmental Biology
, vol.20
, pp. 781-810
-
-
Logan, C.Y.1
Nusse, R.2
-
66
-
-
46349098659
-
Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients
-
Bjorklund P, Lindberg D, Akerstrom G, Westin G. Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients. Mol Cancer 2008 7 : 53.
-
(2008)
Mol Cancer
, vol.7
, pp. 53
-
-
Bjorklund, P.1
Lindberg, D.2
Akerstrom, G.3
Westin, G.4
-
67
-
-
36849014861
-
An LRP5 receptor with internal deletion in hyperparathyroid tumors with implications for deregulated WNT/beta-catenin signaling
-
Bjorklund P, Akerstrom G, Westin G. An LRP5 receptor with internal deletion in hyperparathyroid tumors with implications for deregulated WNT/beta-catenin signaling. PLoS Med 2007 4 : e328.
-
(2007)
PLoS Med
, vol.4
, pp. 328
-
-
Bjorklund, P.1
Akerstrom, G.2
Westin, G.3
-
68
-
-
33846077660
-
Accumulation of nonphosphorylated beta-catenin and c-myc in primary and uremic secondary hyperparathyroid tumors
-
Bjorklund P, Akerstrom G, Westin G. Accumulation of nonphosphorylated beta-catenin and c-myc in primary and uremic secondary hyperparathyroid tumors. J Clin Endocrinol Metab 2007 92 : 338 44.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 338-44
-
-
Bjorklund, P.1
Akerstrom, G.2
Westin, G.3
-
69
-
-
34347245990
-
The role of the SPT6 chromatin remodeling factor in zebrafish embryogenesis
-
Kok FO, Oster E, Mentzer L, Hsieh JC, Henry CA, Sirotkin HI. The role of the SPT6 chromatin remodeling factor in zebrafish embryogenesis. Dev Biol 2007 307 : 214 26.
-
(2007)
Dev Biol
, vol.307
, pp. 214-26
-
-
Kok, F.O.1
Oster, E.2
Mentzer, L.3
Hsieh, J.C.4
Henry, C.A.5
Sirotkin, H.I.6
-
70
-
-
5144220874
-
Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma
-
Tan MH, Morrison C, Wang P et al. Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma. Clin Cancer Res 2004 10 : 6629 37.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 6629-37
-
-
Tan, M.H.1
Morrison, C.2
Wang, P.3
-
71
-
-
33847240834
-
Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal
-
Bradley KJ, Bowl MR, Williams SE et al. Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal. Oncogene 2007 26 : 1213 21.
-
(2007)
Oncogene
, vol.26
, pp. 1213-21
-
-
Bradley, K.J.1
Bowl, M.R.2
Williams, S.E.3
-
72
-
-
50549083236
-
The parafibromin tumor suppressor protein interacts with actin-binding proteins actinin-2 and actinin-3
-
Agarwal SK, Simonds WF, Marx SJ. The parafibromin tumor suppressor protein interacts with actin-binding proteins actinin-2 and actinin-3. Mol Cancer 2008 7 : 65.
-
(2008)
Mol Cancer
, vol.7
, pp. 65
-
-
Agarwal, S.K.1
Simonds, W.F.2
Marx, S.J.3
-
73
-
-
20244369068
-
New genes with roles in the C. elegans embryo revealed using RNAi of ovary-enriched ORFeome clones
-
Fernandez AG, Gunsalus KC, Huang J et al. New genes with roles in the C. elegans embryo revealed using RNAi of ovary-enriched ORFeome clones. Genome Res 2005 15 : 250 9.
-
(2005)
Genome Res
, vol.15
, pp. 250-9
-
-
Fernandez, A.G.1
Gunsalus, K.C.2
Huang, J.3
-
74
-
-
33749045892
-
Parafibromin inhibits cancer cell growth and causes G1 phase arrest
-
DOI 10.1016/j.bbrc.2006.08.169, PII S0006291X06019607
-
Zhang C, Kong D, Tan MH et al. Parafibromin inhibits cancer cell growth and causes G1 phase arrest. Biochem Biophys Res Commun 2006 350 : 17 24. (Pubitemid 44466569)
-
(2006)
Biochemical and Biophysical Research Communications
, vol.350
, Issue.1
, pp. 17-24
-
-
Zhang, C.1
Kong, D.2
Tan, M.-H.3
Pappas Jr., D.L.4
Wang, P.-F.5
Chen, J.6
Farber, L.7
Zhang, N.8
Koo, H.-M.9
Weinreich, M.10
Williams, B.O.11
Teh, B.T.12
-
75
-
-
34548685615
-
Parafibromin tumor suppressor enhances cell growth in the cells expressing SV40 large T antigen
-
Iwata T, Mizusawa N, Taketani Y, Itakura M, Yoshimoto K. Parafibromin tumor suppressor enhances cell growth in the cells expressing SV40 large T antigen. Oncogene 2007 26 : 6176 83.
-
(2007)
Oncogene
, vol.26
, pp. 6176-83
-
-
Iwata, T.1
Mizusawa, N.2
Taketani, Y.3
Itakura, M.4
Yoshimoto, K.5
-
76
-
-
33947288012
-
Nuclear localization of the parafibromin tumor suppressor protein implicated in the hyperparathyroidism-jaw tumor syndrome enhances its proapoptotic function
-
Lin L, Czapiga M, Nini L, Zhang JH, Simonds WF. Nuclear localization of the parafibromin tumor suppressor protein implicated in the hyperparathyroidism- jaw tumor syndrome enhances its proapoptotic function. Mol Cancer Res 2007 5 : 183 93.
-
(2007)
Mol Cancer Res
, vol.5
, pp. 183-93
-
-
Lin, L.1
Czapiga, M.2
Nini, L.3
Zhang, J.H.4
Simonds, W.F.5
-
77
-
-
33845234713
-
Multiple endocrine neoplasia type 1
-
In. De Groot, L.J. Jameson, J.L. eds. Philadephia. PA. Elsevier
-
Thakker RV. Multiple endocrine neoplasia type 1. In : De Groot LJ, Jameson JL, eds. Endocrinology. Philadephia, PA : Elsevier, 2006 3509 31.
-
(2006)
Endocrinology.
, pp. 3509-31
-
-
Thakker, R.V.1
-
78
-
-
26844555530
-
The menin tumor suppressor protein is an essential oncogenic cofactor for MLL-associated leukemogenesis
-
Yokoyama A, Somervaille TC, Smith KS, Rozenblatt-Rosen O, Meyerson M, Cleary ML. The menin tumor suppressor protein is an essential oncogenic cofactor for MLL-associated leukemogenesis. Cell 2005 123 : 207 18.
-
(2005)
Cell
, vol.123
, pp. 207-18
-
-
Yokoyama, A.1
Somervaille, T.C.2
Smith, K.S.3
Rozenblatt-Rosen, O.4
Meyerson, M.5
Cleary, M.L.6
-
79
-
-
42349096478
-
Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice
-
Wang P, Bowl MR, Bender S et al. Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice. Mol Cell Biol 2008 28 : 2930 40.
-
(2008)
Mol Cell Biol
, vol.28
, pp. 2930-40
-
-
Wang, P.1
Bowl, M.R.2
Bender, S.3
-
80
-
-
0342572600
-
Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19
-
Constancia M, Dean W, Lopes S, Moore T, Kelsey G, Reik W. Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. Nat Genet 2000 26 : 203 6.
-
(2000)
Nat Genet
, vol.26
, pp. 203-6
-
-
Constancia, M.1
Dean, W.2
Lopes, S.3
Moore, T.4
Kelsey, G.5
Reik, W.6
-
81
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
-
DeChiara TM, Efstratiadis A, Robertson EJ. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 1990 345 : 78 80.
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
Dechiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
82
-
-
0032160227
-
Insulin-like growth factor-I affects perinatal lethality and postnatal development in a gene dosage-dependent manner: Manipulation using the Cre/loxP system in transgenic mice
-
Liu JL, Grinberg A, Westphal H et al. Insulin-like growth factor-I affects perinatal lethality and postnatal development in a gene dosage-dependent manner: manipulation using the Cre/loxP system in transgenic mice. Mol Endocrinol 1998 12 : 1452 62.
-
(1998)
Mol Endocrinol
, vol.12
, pp. 1452-62
-
-
Liu, J.L.1
Grinberg, A.2
Westphal, H.3
-
83
-
-
0027496895
-
Mice carrying null mutations of the genes encoding insulin-like growth factor i (Igf-1) and type 1 IGF receptor (Igf1r)
-
Liu JP, Baker J, Perkins AS, Robertson EJ, Efstratiadis A. Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r). Cell 1993 75 : 59 72.
-
(1993)
Cell
, vol.75
, pp. 59-72
-
-
Liu, J.P.1
Baker, J.2
Perkins, A.S.3
Robertson, E.J.4
Efstratiadis, A.5
-
85
-
-
33745014194
-
Hormonal regulation of fetal growth
-
DOI 10.1159/000091503
-
Gicquel C, Le Bouc Y. Hormonal regulation of fetal growth. Horm Res 2006 65 (Suppl 3 28 33. (Pubitemid 44689430)
-
(2006)
Hormone Research
, vol.65
, Issue.SUPPL. 3
, pp. 28-33
-
-
Gicquel, C.1
Le Bouc, Y.2
-
86
-
-
0029094755
-
Mutation responsible for the mouse pygmy phenotype in the developmentally regulated factor HMGI-C
-
Zhou X, Benson KF, Ashar HR, Chada K. Mutation responsible for the mouse pygmy phenotype in the developmentally regulated factor HMGI-C. Nature 1995 376 : 771 4.
-
(1995)
Nature
, vol.376
, pp. 771-4
-
-
Zhou, X.1
Benson, K.F.2
Ashar, H.R.3
Chada, K.4
-
87
-
-
22544482628
-
Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice
-
Foti D, Chiefari E, Fedele M et al. Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice. Nat Med 2005 11 : 765 73.
-
(2005)
Nat Med
, vol.11
, pp. 765-73
-
-
Foti, D.1
Chiefari, E.2
Fedele, M.3
-
88
-
-
0032812704
-
Variability in the expression of trophectodermal markers beta-human chorionic gonadotrophin, human leukocyte antigen-G and pregnancy specific beta-1 glycoprotein by the human blastocyst
-
Jurisicova A, Antenos M, Kapasi K, Meriano J, Casper RF. Variability in the expression of trophectodermal markers beta-human chorionic gonadotrophin, human leukocyte antigen-G and pregnancy specific beta-1 glycoprotein by the human blastocyst. Hum Reprod 1999 14 : 1852 8.
-
(1999)
Hum Reprod
, vol.14
, pp. 1852-8
-
-
Jurisicova, A.1
Antenos, M.2
Kapasi, K.3
Meriano, J.4
Casper, R.F.5
-
89
-
-
0034152252
-
Apoptosis in rodent peri-implantation embryos: Differential susceptibility of inner cell mass and trophectoderm cell lineages - A review
-
Pampfer S. Apoptosis in rodent peri-implantation embryos: differential susceptibility of inner cell mass and trophectoderm cell lineages - a review. Placenta 2000 21 (Suppl A S3 10.
-
(2000)
Placenta
, vol.21
, Issue.SUPPL. A
, pp. 3-10
-
-
Pampfer, S.1
-
90
-
-
0035970092
-
A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors
-
Crabtree JS, Scacheri PC, Ward JM et al. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci USA 2001 98 : 1118 23.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 1118-23
-
-
Crabtree, J.S.1
Scacheri, P.C.2
Ward, J.M.3
-
91
-
-
11244318528
-
Homozygous loss of menin is well tolerated in liver, a tissue not affected in MEN1
-
Scacheri PC, Crabtree JS, Kennedy AL et al. Homozygous loss of menin is well tolerated in liver, a tissue not affected in MEN1. Mamm Genome 2004 15 : 872 7.
-
(2004)
Mamm Genome
, vol.15
, pp. 872-7
-
-
Scacheri, P.C.1
Crabtree, J.S.2
Kennedy, A.L.3
|