-
1
-
-
84894556457
-
Pheochromocytoma and paraganglioma pathogenesis: Learning from genetic heterogeneity
-
Dahia PL. Pheochromocytoma and paraganglioma pathogenesis: Learning from genetic heterogeneity. Nat Rev Cancer 2014;14:108-19.
-
(2014)
Nat Rev Cancer
, vol.14
, pp. 108-119
-
-
Dahia, P.L.1
-
2
-
-
84923081697
-
Paraganglioma and phaeochromocytoma: From genetics to personalized medicine
-
Favier J, Amar L, Gimenez-Roqueplo AP. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine. Nat Rev Endocrinol 2015;11:101-11.
-
(2015)
Nat Rev Endocrinol
, vol.11
, pp. 101-111
-
-
Favier, J.1
Amar, L.2
Gimenez-Roqueplo, A.P.3
-
3
-
-
84968879076
-
Multicentric giant cell tumor of bone and paraganglioma: A case report
-
Iwata S, Yonemoto T, Ishii T, Araki A, Hagiwara Y, Tatezaki S-i. Multicentric giant cell tumor of bone and paraganglioma: a case report. J Bone Joint Surg 2013;3:e23.
-
(2013)
J Bone Joint Surg
, vol.3
, pp. e23
-
-
Iwata, S.1
Yonemoto, T.2
Ishii, T.3
Araki, A.4
Hagiwara, Y.5
Tatezaki, S.6
-
4
-
-
84879468754
-
Vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas
-
Toledo RA, Qin Y, Srikantan S, Morales NP, Li Q, Deng Y, et al. In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas. Endocr Relat Cancer 2013;20:349-59.
-
(2013)
Endocr Relat Cancer
, vol.20
, pp. 349-359
-
-
Toledo, R.A.1
Qin, Y.2
Srikantan, S.3
Morales, N.P.4
Li, Q.5
Deng, Y.6
-
5
-
-
84874741731
-
MendelianIdentifyingdisease genes with the variant effect scoring tool
-
Carter H, Douville C, Stenson PD, Cooper DN, Karchin R. Identifying Mendelian disease genes with the variant effect scoring tool. BMC Genomics 2013;14 Suppl 3:S3.
-
(2013)
BMC Genomics
, vol.3
, pp. S3
-
-
Carter, H.1
Douville, C.2
Stenson, P.D.3
Cooper, D.N.4
Karchin, R.5
-
6
-
-
84874732372
-
CRAVAT: Cancer-related analysis of variants toolkit
-
Douville C, Carter H, Kim R, Niknafs N, Diekhans M, Stenson PD, et al. CRAVAT: cancer-related analysis of variants toolkit. Bioinformatics 2013;29:647-8.
-
(2013)
Bioinformatics
, vol.29
, pp. 647-648
-
-
Douville, C.1
Carter, H.2
Kim, R.3
Niknafs, N.4
Diekhans, M.5
Stenson, P.D.6
-
7
-
-
84896321422
-
Using VarScan 2 for germline variant calling and somatic mutation detection
-
Koboldt DC, Larson DE, Wilson RK. Using VarScan 2 for germline variant calling and somatic mutation detection. Curr Protoc Bioinformatics 2013;44:1541-47.
-
(2013)
Curr Protoc Bioinformatics
, vol.44
, pp. 1541-1547
-
-
Koboldt, D.C.1
Larson, D.E.2
Wilson, R.K.3
-
8
-
-
77955594623
-
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
-
Dahia PL, Ross KN, Wright ME, Hayashida CY, Santagata S, Barontini M, et al. A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. PLoS Genet 2005;1:72-80.
-
(2005)
PLoS Genet
, vol.1
, pp. 72-80
-
-
Dahia, P.L.1
Ross, K.N.2
Wright, M.E.3
Hayashida, C.Y.4
Santagata, S.5
Barontini, M.6
-
9
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
Huang da W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 2009;4:44-57.
-
(2009)
Nat Protoc
, vol.4
, pp. 44-57
-
-
Huang da, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
10
-
-
84925156346
-
The I-TASSER Suite: Protein structure and function prediction
-
Yang J, Yan R, Roy A, Xu D, Poisson J, Zhang Y. The I-TASSER Suite: protein structure and function prediction. Nat Methods 2015;12:7-8.
-
(2015)
Nat Methods
, vol.12
, pp. 7-8
-
-
Yang, J.1
Yan, R.2
Roy, A.3
Xu, D.4
Poisson, J.5
Zhang, Y.6
-
11
-
-
77649175595
-
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma
-
Qin Y, Yao L, King EE, Buddavarapu K, Lenci RE, Chocron ES, et al. Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. Nat Genet 2010;42:229-33.
-
(2010)
Nat Genet
, vol.42
, pp. 229-233
-
-
Qin, Y.1
Yao, L.2
King, E.E.3
Buddavarapu, K.4
Lenci, R.E.5
Chocron, E.S.6
-
12
-
-
84937597585
-
D2HGDH regulates alpha-ketoglutarate levels and dioxygenase function by modulating IDH2
-
Lin AP, Abbas S, Kim SW, Ortega M, Bouamar H, Escobedo Y, et al. D2HGDH regulates alpha-ketoglutarate levels and dioxygenase function by modulating IDH2. Nat Commun 2015;6:7768.
-
(2015)
Nat Commun
, vol.6
, pp. 7768
-
-
Lin, A.P.1
Abbas, S.2
Kim, S.W.3
Ortega, M.4
Bouamar, H.5
Escobedo, Y.6
-
13
-
-
84927693137
-
The genomic landscape of phaeochromocytoma
-
Flynn A, Benn D, Clifton-Bligh R, Robinson B, Trainer AH, James P, et al. The genomic landscape of phaeochromocytoma. J Pathol 2015;236: 78-89.
-
(2015)
J Pathol
, vol.236
, pp. 78-89
-
-
Flynn, A.1
Benn, D.2
Clifton-Bligh, R.3
Robinson, B.4
Trainer, A.H.5
James, P.6
-
14
-
-
84923072111
-
Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas
-
Castro-Vega LJ, Letouze E, Burnichon N, Buffet A, Disderot PH, Khalifa E, et al. Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas. Nat Commun 2015;6:6044.
-
(2015)
Nat Commun
, vol.6
, pp. 6044
-
-
Castro-Vega, L.J.1
Letouze, E.2
Burnichon, N.3
Buffet, A.4
Disderot, P.H.5
Khalifa, E.6
-
15
-
-
84928566914
-
Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas
-
Fishbein L, Khare S, Wubbenhorst B, DeSloover D, D'Andrea K, Merrill S, et al. Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas. Nat Commun 2015;6:6140.
-
(2015)
Nat Commun
, vol.6
, pp. 6140
-
-
Fishbein, L.1
Khare, S.2
Wubbenhorst, B.3
DeSloover, D.4
D'Andrea, K.5
Merrill, S.6
-
16
-
-
84937509780
-
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene
-
Juhlin CC, Stenman A, Haglund F, Clark VE, Brown TC, Baranoski J, et al. Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene. Genes Chromosomes Cancer 2015;54:542-54.
-
(2015)
Genes Chromosomes Cancer
, vol.54
, pp. 542-554
-
-
Juhlin, C.C.1
Stenman, A.2
Haglund, F.3
Clark, V.E.4
Brown, T.C.5
Baranoski, J.6
-
17
-
-
84859893371
-
Histone methylation: A dynamic mark in health, disease and inheritance
-
Greer EL, Shi Y. Histone methylation: a dynamic mark in health, disease and inheritance. Nat Rev Genet 2012;13:343-57.
-
(2012)
Nat Rev Genet
, vol.13
, pp. 343-357
-
-
Greer, E.L.1
Shi, Y.2
-
18
-
-
84888353557
-
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone
-
Behjati S, Tarpey PS, Presneau N, Scheipl S, Pillay N, Van Loo P, et al. Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone. Nat Genet 2013;45:1479-82.
-
(2013)
Nat Genet
, vol.45
, pp. 1479-1482
-
-
Behjati, S.1
Tarpey, P.S.2
Presneau, N.3
Scheipl, S.4
Pillay, N.5
Van Loo, P.6
-
19
-
-
0142169926
-
The origin of the neoplastic stromal cell in giant cell tumor of bone
-
Wulling M, Delling G, Kaiser E. The origin of the neoplastic stromal cell in giant cell tumor of bone. Hum Pathol 2003;34:983-93.
-
(2003)
Hum Pathol
, vol.34
, pp. 983-993
-
-
Wulling, M.1
Delling, G.2
Kaiser, E.3
-
20
-
-
84862777348
-
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
-
Schwartzentruber J, Korshunov A, Liu XY, Jones DT, Pfaff E, Jacob K, et al. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma. Nature 2012;482:226-31.
-
(2012)
Nature
, vol.482
, pp. 226-231
-
-
Schwartzentruber, J.1
Korshunov, A.2
Liu, X.Y.3
Jones, D.T.4
Pfaff, E.5
Jacob, K.6
-
21
-
-
84862777410
-
Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas
-
Wu G, Broniscer A, McEachron TA, Lu C, Paugh BS, Becksfort J, et al. Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas. Nat Genet 2012;44:251-3.
-
(2012)
Nat Genet
, vol.44
, pp. 251-253
-
-
Wu, G.1
Broniscer, A.2
McEachron, T.A.3
Lu, C.4
Paugh, B.S.5
Becksfort, J.6
-
22
-
-
84887617868
-
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas
-
Bender S, Tang Y, Lindroth AM, Hovestadt V, Jones DT, Kool M, et al. Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas. Cancer Cell 2013;24:660-72.
-
(2013)
Cancer Cell
, vol.24
, pp. 660-672
-
-
Bender, S.1
Tang, Y.2
Lindroth, A.M.3
Hovestadt, V.4
Jones, D.T.5
Kool, M.6
-
23
-
-
84877299145
-
The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression
-
Chan KM, Fang D, Gan H, Hashizume R, Yu C, Schroeder M, et al. The histone H3.3K27M mutation in pediatric glioma reprograms H3K27 methylation and gene expression. Genes Dev 2013;27:985-90.
-
(2013)
Genes Dev
, vol.27
, pp. 985-990
-
-
Chan, K.M.1
Fang, D.2
Gan, H.3
Hashizume, R.4
Yu, C.5
Schroeder, M.6
-
24
-
-
84877785024
-
Inhibition of PRC2 activity by a gain-of-function H3 mutation found in pediatric glioblastoma
-
Lewis PW, Muller MM, Koletsky MS, Cordero F, Lin S, Banaszynski LA, et al. Inhibition of PRC2 activity by a gain-of-function H3 mutation found in pediatric glioblastoma. Science 2013;340:857-61.
-
(2013)
Science
, vol.340
, pp. 857-861
-
-
Lewis, P.W.1
Muller, M.M.2
Koletsky, M.S.3
Cordero, F.4
Lin, S.5
Banaszynski, L.A.6
-
25
-
-
84877621282
-
Histone H3.3. Mutations drive pediatric glioblastoma through upregulation of MYCN
-
Bjerke L, Mackay A, Nandhabalan M, Burford A, Jury A, Popov S, et al. Histone H3.3. mutations drive pediatric glioblastoma through upregulation of MYCN. Cancer Discov 2013;3:512-9.
-
(2013)
Cancer Discov
, vol.3
, pp. 512-519
-
-
Bjerke, L.1
Mackay, A.2
Nandhabalan, M.3
Burford, A.4
Jury, A.5
Popov, S.6
-
26
-
-
84867606428
-
Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma
-
Sturm D, Witt H, Hovestadt V, Khuong-Quang DA, Jones DT, Konermann C, et al. Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 2012; 22:425-37.
-
(2012)
Cancer Cell
, vol.22
, pp. 425-437
-
-
Sturm, D.1
Witt, H.2
Hovestadt, V.3
Khuong-Quang, D.A.4
Jones, D.T.5
Konermann, C.6
-
27
-
-
75149188170
-
Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes
-
Dalgliesh GL, Furge K, Greenman C, Chen L, Bignell G, Butler A, et al. Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes. Nature 2010;463:360-3.
-
(2010)
Nature
, vol.463
, pp. 360-363
-
-
Dalgliesh, G.L.1
Furge, K.2
Greenman, C.3
Chen, L.4
Bignell, G.5
Butler, A.6
-
28
-
-
84907418637
-
Mutations in epigenetic regulators including SETD2 are gained during relapse in paediatric acute lymphoblastic leukaemia
-
Mar BG, Bullinger LB, McLean KM, Grauman PV, Harris MH, Stevenson K, et al. Mutations in epigenetic regulators including SETD2 are gained during relapse in paediatric acute lymphoblastic leukaemia. Nat Commun 2014;5:3469.
-
(2014)
Nat Commun
, vol.5
, pp. 3469
-
-
Mar, B.G.1
Bullinger, L.B.2
McLean, K.M.3
Grauman, P.V.4
Harris, M.H.5
Stevenson, K.6
-
29
-
-
75749124332
-
Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin
-
Morin RD, Johnson NA, Severson TM, Mungall AJ, An J, Goya R, et al. Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. Nat Genet 2010;42:181-5.
-
(2010)
Nat Genet
, vol.42
, pp. 181-185
-
-
Morin, R.D.1
Johnson, N.A.2
Severson, T.M.3
Mungall, A.J.4
An, J.5
Goya, R.6
-
30
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst T, Chase AJ, Score J, Hidalgo-Curtis CE, Bryant C, Jones AV, et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet 2010;42:722-6.
-
(2010)
Nat Genet
, vol.42
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
Hidalgo-Curtis, C.E.4
Bryant, C.5
Jones, A.V.6
-
31
-
-
84929925487
-
Hijacked in cancer: The KMT2 (MLL) family of methyltransferases
-
Rao RC, Dou Y. Hijacked in cancer: the KMT2 (MLL) family of methyltransferases. Nat Rev Cancer 2015;15:334-46.
-
(2015)
Nat Rev Cancer
, vol.15
, pp. 334-346
-
-
Rao, R.C.1
Dou, Y.2
-
32
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, Bignell G, et al. Patterns of somatic mutation in human cancer genomes. Nature 2007;446: 153-8.
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.L.4
Hunter, C.5
Bignell, G.6
-
35
-
-
84875740314
-
Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal
-
Gao J, Aksoy BA, Dogrusoz U, Dresdner G, Gross B, Sumer SO, et al. Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. Sci Signal 2013;6:11.
-
(2013)
Sci Signal
, vol.6
, pp. 11
-
-
Gao, J.1
Aksoy, B.A.2
Dogrusoz, U.3
Dresdner, G.4
Gross, B.5
Sumer, S.O.6
-
36
-
-
84866002291
-
The cBio cancer genomics portal: An open platform for exploring multidimensional cancer genomics data
-
Cerami E, Gao J, Dogrusoz U, Gross BE, Sumer SO, Aksoy BA, et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer Discov 2012;2:401-4.
-
(2012)
Cancer Discov
, vol.2
, pp. 401-404
-
-
Cerami, E.1
Gao, J.2
Dogrusoz, U.3
Gross, B.E.4
Sumer, S.O.5
Aksoy, B.A.6
-
37
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET protooncogene in papillary renal carcinomas
-
Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, et al. Germline and somatic mutations in the tyrosine kinase domain of the MET protooncogene in papillary renal carcinomas. Nat Genet 1997;16:68-73.
-
(1997)
Nat Genet
, vol.16
, pp. 68-73
-
-
Schmidt, L.1
Duh, F.M.2
Chen, F.3
Kishida, T.4
Glenn, G.5
Choyke, P.6
-
38
-
-
84903785242
-
Four individually druggable MET hotspots mediate HGF-driven tumor progression
-
Basilico C, Hultberg A, Blanchetot C, de Jonge N, Festjens E, Hanssens V, et al. Four individually druggable MET hotspots mediate HGF-driven tumor progression. J Clin Invest 2014;124:3172-86.
-
(2014)
J Clin Invest
, vol.124
, pp. 3172-3186
-
-
Basilico, C.1
Hultberg, A.2
Blanchetot, C.3
De Jonge, N.4
Festjens, E.5
Hanssens, V.6
-
39
-
-
84923279397
-
Functional consequence of the MET-T1010I polymorphism in breast cancer
-
Liu S, Meric-Bernstam F, Parinyanitikul N, Wang B, Eterovic AK, Zheng X, et al. Functional consequence of the MET-T1010I polymorphism in breast cancer. Oncotarget 2015;6:2604-14.
-
(2015)
Oncotarget
, vol.6
, pp. 2604-2614
-
-
Liu, S.1
Meric-Bernstam, F.2
Parinyanitikul, N.3
Wang, B.4
Eterovic, A.K.5
Zheng, X.6
-
40
-
-
26444481568
-
Sequence survey of receptor tyrosine kinases reveals mutations in glioblastomas
-
Rand V, Huang J, Stockwell T, Ferriera S, Buzko O, Levy S, et al. Sequence survey of receptor tyrosine kinases reveals mutations in glioblastomas. Proc Natl Acad Sci U S A 2005;102:14344-9.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 14344-14349
-
-
Rand, V.1
Huang, J.2
Stockwell, T.3
Ferriera, S.4
Buzko, O.5
Levy, S.6
-
41
-
-
84880983541
-
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma
-
Jones DT, Hutter B, Jager N, Korshunov A, Kool M, Warnatz HJ, et al. Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma. Nat Genet 2013;45:927-32.
-
(2013)
Nat Genet
, vol.45
, pp. 927-932
-
-
Jones, D.T.1
Hutter, B.2
Jager, N.3
Korshunov, A.4
Kool, M.5
Warnatz, H.J.6
-
42
-
-
84878969599
-
SDH mutations establish a hypermethylator phenotype in paraganglioma
-
Letouze E, Martinelli C, Loriot C, Burnichon N, Abermil N, Ottolenghi C, et al. SDH mutations establish a hypermethylator phenotype in paraganglioma. Cancer Cell 2013;23:739-52.
-
(2013)
Cancer Cell
, vol.23
, pp. 739-752
-
-
Letouze, E.1
Martinelli, C.2
Loriot, C.3
Burnichon, N.4
Abermil, N.5
Ottolenghi, C.6
-
43
-
-
67049154039
-
High frequency of cephalic neural crest cells shows coexistence of neurogenic, melanogenic, and osteogenic differentiation capacities
-
Calloni GW, Le Douarin NM, Dupin E. High frequency of cephalic neural crest cells shows coexistence of neurogenic, melanogenic, and osteogenic differentiation capacities. Proc Natl Acad Sci 2009;106:8947-52.
-
(2009)
Proc Natl Acad Sci
, vol.106
, pp. 8947-8952
-
-
Calloni, G.W.1
Le Douarin, N.M.2
Dupin, E.3
-
44
-
-
0027231568
-
Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JBJ, Healey CS, Elsdon MJ, Eng C, Gardner E, et al. Germline mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 1993;363:458-60.
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.J.2
Healey, C.S.3
Elsdon, M.J.4
Eng, C.5
Gardner, E.6
-
45
-
-
3242729164
-
A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma
-
Jimenez C, Dang GT, Schultz PN, El-Naggar A, Shapiro S, Barnes EA, et al. A novel point mutation of the RET protooncogene involving the second intracellular tyrosine kinase domain in a family with medullary thyroid carcinoma. J Clin Endocrinol Metab 2004;89:3521-6.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 3521-3526
-
-
Jimenez, C.1
Dang, G.T.2
Schultz, P.N.3
El-Naggar, A.4
Shapiro, S.5
Barnes, E.A.6
-
46
-
-
84922481128
-
The TAM family: Phosphatidylserine sensing receptor tyrosine kinases gone awry in cancer
-
Graham DK, DeRyckere D, Davies KD, Earp HS. The TAM family: phosphatidylserine sensing receptor tyrosine kinases gone awry in cancer. Nat Rev Cancer 2014;14:769-85.
-
(2014)
Nat Rev Cancer
, vol.14
, pp. 769-785
-
-
Graham, D.K.1
DeRyckere, D.2
Davies, K.D.3
Earp, H.S.4
-
47
-
-
84897504141
-
The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal function
-
Qin Y, Deng Y, Ricketts CJ, Srikantan S, Wang E, Maher ER, et al. The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal function. Hum Mol Genet 2014;23: 2428-39.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 2428-2439
-
-
Qin, Y.1
Deng, Y.2
Ricketts, C.J.3
Srikantan, S.4
Wang, E.5
Maher, E.R.6
-
48
-
-
84897570353
-
Defining early-onset kidney cancer: Implications for germline and somatic mutation testing and clinical management
-
Shuch B, Vourganti S, Ricketts CJ, Middleton L, Peterson J, Merino MJ, et al. Defining early-onset kidney cancer: implications for germline and somatic mutation testing and clinical management. J Clin Oncol 2014;32:431-7.
-
(2014)
J Clin Oncol
, vol.32
, pp. 431-437
-
-
Shuch, B.1
Vourganti, S.2
Ricketts, C.J.3
Middleton, L.4
Peterson, J.5
Merino, M.J.6
-
49
-
-
84886808679
-
Chromatin proteins and modifications as drug targets
-
Helin K, Dhanak D. Chromatin proteins and modifications as drug targets. Nature 2013;502:480-8.
-
(2013)
Nature
, vol.502
, pp. 480-488
-
-
Helin, K.1
Dhanak, D.2
|