-
1
-
-
0002814341
-
Infantile genetic agranulocytosis: A new recessive leihal disease in man
-
Kostmann R. Infantile genetic agranulocytosis: A new recessive leihal disease in man. Acta Paediatr. 1956;105:1-78.
-
(1956)
Acta Paediatr
, vol.105
, pp. 1-78
-
-
Kostmann, R.1
-
2
-
-
0029792176
-
Dominantly inherited severe congenital neutropenia
-
Briars GL, Parry HF, Ansari BM. Dominantly inherited severe congenital neutropenia. J Infect. 1996;33:123-126.
-
(1996)
J Infect
, vol.33
, pp. 123-126
-
-
Briars, G.L.1
Parry, H.F.2
Ansari, B.M.3
-
3
-
-
0035093787
-
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia
-
Devriendt K, Kim AS, Mathijs G, et al. Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia. Nat Genet. 2001;27:313-317.
-
(2001)
Nat Genet
, vol.27
, pp. 313-317
-
-
Devriendt, K.1
Kim, A.S.2
Mathijs, G.3
-
4
-
-
0032532631
-
Cyclical neutropenia and other periodic hematological disorders: A review of mechanisms and mathematical models
-
Haurie C, Dale DC, Mackey MC. Cyclical neutropenia and other periodic hematological disorders: A review of mechanisms and mathematical models. Blood. 1998;92:2629-2640.
-
(1998)
Blood
, vol.92
, pp. 2629-2640
-
-
Haurie, C.1
Dale, D.C.2
Mackey, M.C.3
-
5
-
-
0033052104
-
Occurrence of periodic oscillations in the differential blood counts of congenital, idiopathic, and cyclical neutropenic patients before and during treatment with G-CSF
-
Haurie C, Dale DC, Mackey MC. Occurrence of periodic oscillations in the differential blood counts of congenital, idiopathic, and cyclical neutropenic patients before and during treatment with G-CSF. Exp Hematol. 1999;27:401-409.
-
(1999)
Exp Hematol
, vol.27
, pp. 401-409
-
-
Haurie, C.1
Dale, D.C.2
Mackey, M.C.3
-
6
-
-
0011982978
-
Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy
-
Freedman MH, Bonilla MA, Fier C, et al. Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy. Blood. 2000;96:429-436.
-
(2000)
Blood
, vol.96
, pp. 429-436
-
-
Freedman, M.H.1
Bonilla, M.A.2
Fier, C.3
-
7
-
-
0034651925
-
Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
-
Zeidler C, Welte K, Barak Y, et al. Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation. Blood. 2000;95:1195-1198.
-
(2000)
Blood
, vol.95
, pp. 1195-1198
-
-
Zeidler, C.1
Welte, K.2
Barak, Y.3
-
8
-
-
0029883652
-
Pathophysiology and treatment of severe chronic neutropenia
-
Welte K, Dale D. Pathophysiology and treatment of severe chronic neutropenia. Ann Hematol. 1996;72:158-165.
-
(1996)
Ann Hematol
, vol.72
, pp. 158-165
-
-
Welte, K.1
Dale, D.2
-
9
-
-
0027420671
-
Severe congenital neutropenia: Abnormal growth and differentiation of myeloid progenitors to granulocyte colony-stimulating factor (G-CSF) but normal response to G-CSF plus stem cell factor
-
Hestdal K, Welte K, Lie SO, Keller JR, Ruscetti FW, Abrahamsen TG. Severe congenital neutropenia: Abnormal growth and differentiation of myeloid progenitors to granulocyte colony-stimulating factor (G-CSF) but normal response to G-CSF plus stem cell factor. Blood. 1993;82: 2991-2997.
-
(1993)
Blood
, vol.82
, pp. 2991-2997
-
-
Hestdal, K.1
Welte, K.2
Lie, S.O.3
Keller, J.R.4
Ruscetti, F.W.5
Abrahamsen, T.G.6
-
10
-
-
0025333540
-
Abnormal responses of myeloid progenitor cells to recombinant human colony-stimulating factors in congenital neutropenia
-
Kobayashi M, Yumiba C, Kawaguchi Y, et al. Abnormal responses of myeloid progenitor cells to recombinant human colony-stimulating factors in congenital neutropenia. Blood. 1990;75:2143-2149.
-
(1990)
Blood
, vol.75
, pp. 2143-2149
-
-
Kobayashi, M.1
Yumiba, C.2
Kawaguchi, Y.3
-
11
-
-
0032762794
-
Defective proliferation of primitive myeloid progenitor cells in patients with severe congenital neutropenia
-
Konishi N, Kobayashi M, Miyagawa S, Sato T, Katoh O, Ueda K. Defective proliferation of primitive myeloid progenitor cells in patients with severe congenital neutropenia. Blood. 1999;94: 4077-4083.
-
(1999)
Blood
, vol.94
, pp. 4077-4083
-
-
Konishi, N.1
Kobayashi, M.2
Miyagawa, S.3
Sato, T.4
Katoh, O.5
Ueda, K.6
-
12
-
-
0034672364
-
Abnormalities of primitive myeloid progenitor cells expressing granulocyte, colony-stimulating factor receptor in patients with severe congenital neutropenia
-
Nakamura K, Kobayashi M, Konishi N, et al. Abnormalities of primitive myeloid progenitor cells expressing granulocyte, colony-stimulating factor receptor in patients with severe congenital neutropenia. Blood. 2000;96:4366-4369.
-
(2000)
Blood
, vol.96
, pp. 4366-4369
-
-
Nakamura, K.1
Kobayashi, M.2
Konishi, N.3
-
13
-
-
79960970528
-
Apoptosis of bone marrow progenitor cells and neutrophil elastase mutations in the original Kostmann families
-
Aprikyan AA, Carlsson G, Stein S, et al. Apoptosis of bone marrow progenitor cells and neutrophil elastase mutations in the original Kostmann families [abstract]. Blood. 2001;98:440a.
-
(2001)
Blood
, vol.98
-
-
Aprikyan, A.A.1
Carlsson, G.2
Stein, S.3
-
14
-
-
0035161158
-
Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia
-
Aprikyan AA, Liles WC, Rodger E, Jonas M, Chi EY, Dale DC. Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia. Blood. 2001;97:147-153.
-
(2001)
Blood
, vol.97
, pp. 147-153
-
-
Aprikyan, A.A.1
Liles, W.C.2
Rodger, E.3
Jonas, M.4
Chi, E.Y.5
Dale, D.C.6
-
15
-
-
0033230361
-
Shwachman-Diamond syndrome: An inherited preleukemic bone marrow failure disorder with aberrant hematopoietic progenitors and faulty marrow microenvironment
-
Dror Y, Freedman MH, Shwachman-Diamond syndrome: An inherited preleukemic bone marrow failure disorder with aberrant hematopoietic progenitors and faulty marrow microenvironment. Blood. 1999;94:3048-3054.
-
(1999)
Blood
, vol.94
, pp. 3048-3054
-
-
Dror, Y.1
Freedman, M.H.2
-
16
-
-
0035874541
-
Shwachman-Diamond syndrome marrow cells show abnormally increased apoptosis mediated through the Fas pathway
-
Dror Y, Freedman MH. Shwachman-Diamond syndrome marrow cells show abnormally increased apoptosis mediated through the Fas pathway. Blood. 2001;97:3011-3016.
-
(2001)
Blood
, vol.97
, pp. 3011-3016
-
-
Dror, Y.1
Freedman, M.H.2
-
17
-
-
0028328265
-
Identification of a nonsense mutation in the granulocytecolony-stimulating factor receptor in severe congenital neutropenia
-
Dong F, Hoefsloot LH, Schelen AM, et al. Identification of a nonsense mutation in the granulocytecolony-stimulating factor receptor in severe congenital neutropenia. Proc Natl Acad Sci U S A. 1994;91:4480-4484.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 4480-4484
-
-
Dong, F.1
Hoefsloot, L.H.2
Schelen, A.M.3
-
18
-
-
0029129034
-
Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia
-
Dong F, Brynes RK, Tidow N, Welte K, Lowenberg B, Touw IP. Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia [see comments]. N Engl J Med. 1995;333:487-493.
-
(1995)
N Engl J Med
, vol.333
, pp. 487-493
-
-
Dong, F.1
Brynes, R.K.2
Tidow, N.3
Welte, K.4
Lowenberg, B.5
Touw, I.P.6
-
19
-
-
16944361974
-
Mutations in the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia
-
Dong F, Dale DC, Bonilla MA, et al. Mutations in the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia. Leukemia. 1997;11:120-125.
-
(1997)
Leukemia
, vol.11
, pp. 120-125
-
-
Dong, F.1
Dale, D.C.2
Bonilla, M.A.3
-
20
-
-
0028961478
-
Lack of alterations in the cytoplasmic domains of the granulocyte colony-stimulating factor receptors in eight cases of severe congenital neutropenia
-
Sandoval C, Parganas E, Wang W, Ihle JN. Lack of alterations in the cytoplasmic domains of the granulocyte colony-stimulating factor receptors in eight cases of severe congenital neutropenia. Blood. 1995;85:852-860.
-
(1995)
Blood
, vol.85
, pp. 852-860
-
-
Sandoval, C.1
Parganas, E.2
Wang, W.3
Ihle, J.N.4
-
21
-
-
79960971488
-
Update on the G-CSF receptor gene mutations in patients with severe congenital neutropenia
-
Germeshausen M, Jakobs S, Zeidler C, Welte K. Update on the G-CSF receptor gene mutations in patients with severe congenital neutropenia [abstract]. Blood, 2001;98:441a.
-
(2001)
Blood
, vol.98
-
-
Germeshausen, M.1
Jakobs, S.2
Zeidler, C.3
Welte, K.4
-
22
-
-
0030945921
-
Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia
-
Tidow N, Pilz C, Teichmann B, et al. Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia. Blood. 1997;89:2369-2375.
-
(1997)
Blood
, vol.89
, pp. 2369-2375
-
-
Tidow, N.1
Pilz, C.2
Teichmann, B.3
-
23
-
-
0032126619
-
Perturbed granulopolesis in mice with a targeted mutation in the granulocyte colony-stimulating factor receptor gene associated with severe chronic neutropenia
-
Hermans MH, Ward AC, Antonissen C, Karis A, Lowenberg B, Touw IP. Perturbed granulopolesis in mice with a targeted mutation in the granulocyte colony-stimulating factor receptor gene associated with severe chronic neutropenia. Blood. 1998;92:32-39.
-
(1998)
Blood
, vol.92
, pp. 32-39
-
-
Hermans, M.H.1
Ward, A.C.2
Antonissen, C.3
Karis, A.4
Lowenberg, B.5
Touw, I.P.6
-
24
-
-
0033557171
-
Sustained receptor activation and hyperproliferation in response to granulocyte colony-stimulating factor (G-CSF) in mice with a severe congenital neutropenia/acute myeloid leukemia-derived mutation in the G-CSF receptor gene
-
Hermans MH, Antonissen C, Ward AC, Mayen AE, Ploemacher RE, Touw IP. Sustained receptor activation and hyperproliferation in response to granulocyte colony-stimulating factor (G-CSF) in mice with a severe congenital neutropenia/acute myeloid leukemia-derived mutation in the G-CSF receptor gene. J Exp Med. 1999;189:683-692.
-
(1999)
J Exp Med
, vol.189
, pp. 683-692
-
-
Hermans, M.H.1
Antonissen, C.2
Ward, A.C.3
Mayen, A.E.4
Ploemacher, R.E.5
Touw, I.P.6
-
25
-
-
0032146530
-
Increased granulocyte colony-stimulating factor responsiveness but normal resting granulopoiesis in mice carrying a targeted granulocyte colony-stimulating factor receptor mutation derived from a patient with severe congenital neutropenia
-
McLemore ML, Poursine-Laurent J, Link DC. Increased granulocyte colony-stimulating factor responsiveness but normal resting granulopoiesis in mice carrying a targeted granulocyte colony-stimulating factor receptor mutation derived from a patient with severe congenital neutropenia. J Clin Invest. 1998;102:483-492.
-
(1998)
J Clin Invest
, vol.102
, pp. 483-492
-
-
McLemore, M.L.1
Poursine-Laurent, J.2
Link, D.C.3
-
26
-
-
0032757863
-
Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis
-
Horwitz M, Benson KF, Person RE, Aprikyan AG, Dale DC. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis. Nat Genet. 1999;23:433-436.
-
(1999)
Nat Genet
, vol.23
, pp. 433-436
-
-
Horwitz, M.1
Benson, K.F.2
Person, R.E.3
Aprikyan, A.G.4
Dale, D.C.5
-
27
-
-
0035525791
-
Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease
-
Ancliff PJ, Gale RE, Liesner R, Hann IM, Linch DC. Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease. Blood. 2001;98:2645-2650.
-
(2001)
Blood
, vol.98
, pp. 2645-2650
-
-
Ancliff, P.J.1
Gale, R.E.2
Liesner, R.3
Hann, I.M.4
Linch, D.C.5
-
28
-
-
0034307655
-
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
-
Dale DC, Person RE, Bolyard AA, et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood. 2000;96: 2317-2322.
-
(2000)
Blood
, vol.96
, pp. 2317-2322
-
-
Dale, D.C.1
Person, R.E.2
Bolyard, A.A.3
-
29
-
-
0035479832
-
Mutations in the neutrophil elastase gene in cyclic and congenital neutropenia
-
Aprikyan AA, Dale DC. Mutations in the neutrophil elastase gene in cyclic and congenital neutropenia. Curr Opin Immunol. 2001;13:535-538.
-
(2001)
Curr Opin Immunol
, vol.13
, pp. 535-538
-
-
Aprikyan, A.A.1
Dale, D.C.2
-
30
-
-
79960971229
-
Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia
-
Ancliff PJ, Gale RE, Hann IM, Strobel S, Linch DC. Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia [abstract]. Blood. 2001;98:439a.
-
(2001)
Blood
, vol.98
-
-
Ancliff, P.J.1
Gale, R.E.2
Hann, I.M.3
Strobel, S.4
Linch, D.C.5
-
31
-
-
0028568647
-
A 30-base pair element is responsible for the myeloid-specific activity of the human neutrophil elastase promoter
-
Srikanth S, Rado TA. A 30-base pair element is responsible for the myeloid-specific activity of the human neutrophil elastase promoter. J Biol Chem. 1994;269:32626-32633.
-
(1994)
J Biol Chem
, vol.269
, pp. 32626-32633
-
-
Srikanth, S.1
Rado, T.A.2
-
32
-
-
0036168150
-
Dipeptidyl peptidase I activates neutrophil-derived serine proteases and regulates the development of acute experimental arthritis
-
Adkison AM, Raptis SZ, Kelley DG, Pham CT. Dipeptidyl peptidase I activates neutrophil-derived serine proteases and regulates the development of acute experimental arthritis. J Clin Invest. 2002;109:363-371.
-
(2002)
J Clin Invest
, vol.109
, pp. 363-371
-
-
Adkison, A.M.1
Raptis, S.Z.2
Kelley, D.G.3
Pham, C.T.4
-
33
-
-
0031836105
-
Mice lacking neutrophil elastase reveal impaired host defense against gram negative bacterial sepsis
-
Belaaouaj A, McCarthy R, Baumann M, et al. Mice lacking neutrophil elastase reveal impaired host defense against gram negative bacterial sepsis. Nat Med. 1998;4:615-618.
-
(1998)
Nat Med
, vol.4
, pp. 615-618
-
-
Belaaouaj, A.1
McCarthy, R.2
Baumann, M.3
-
34
-
-
0032763069
-
Normal neutrophil function in cathepsin G-deficient mice
-
MacIvor DM, Shapiro SD, Pham CT, Belaaouaj A, Abraham SN, Ley TJ. Normal neutrophil function in cathepsin G-deficient mice. Blood. 1999;94: 4282-4293.
-
(1999)
Blood
, vol.94
, pp. 4282-4293
-
-
MacIvor, D.M.1
Shapiro, S.D.2
Pham, C.T.3
Belaaouaj, A.4
Abraham, S.N.5
Ley, T.J.6
-
35
-
-
0034144636
-
Impaired immunity and enhanced resistance to endotoxin in the absence of neutrophil elastase and cathepsin G
-
Tkalcevic J, Novelli M, Phylactides M, Iredale JP, Segal AW, Roes J. Impaired immunity and enhanced resistance to endotoxin in the absence of neutrophil elastase and cathepsin G. Immunity. 2000;12:201-210.
-
(2000)
Immunity
, vol.12
, pp. 201-210
-
-
Tkalcevic, J.1
Novelli, M.2
Phylactides, M.3
Iredale, J.P.4
Segal, A.W.5
Roes, J.6
-
36
-
-
0029954767
-
Analysis of mice containing a targeted deletion of beta-globin locus control region 5′ hypersensitive site 3
-
Hug BA, Wesselschmidt RL, Fiering S, et al. Analysis of mice containing a targeted deletion of beta-globin locus control region 5′ hypersensitive site 3. Mol Cell Biol. 1996;16:2906-2912.
-
(1996)
Mol Cell Biol
, vol.16
, pp. 2906-2912
-
-
Hug, B.A.1
Wesselschmidt, R.L.2
Fiering, S.3
-
37
-
-
0018747530
-
Mapping the extended substrate binding site of cathepsin G and human leukocyte elastase. Studies with peptide substrates related to the alpha 1-protease inhibitor reactive site
-
Nakajima K, Powers JC, Ashe BM, Zimmerman M. Mapping the extended substrate binding site of cathepsin G and human leukocyte elastase. Studies with peptide substrates related to the alpha 1-protease inhibitor reactive site. J Biol Chem. 1979;254:4027-4032.
-
(1979)
J Biol Chem
, vol.254
, pp. 4027-4032
-
-
Nakajima, K.1
Powers, J.C.2
Ashe, B.M.3
Zimmerman, M.4
-
38
-
-
0030008394
-
Deficiency of Src family kinases p59/61hck and p58c-fgr results in defective adhesion-dependent neutrophil functions
-
Lowell CA, Fumagalli L, Berton G. Deficiency of Src family kinases p59/61hck and p58c-fgr results in defective adhesion-dependent neutrophil functions. J Cell Biol. 1996;133:895-910.
-
(1996)
J Cell Biol
, vol.133
, pp. 895-910
-
-
Lowell, C.A.1
Fumagalli, L.2
Berton, G.3
-
39
-
-
0029847228
-
Long-range disruption of gene expression by a selectable marker cassette
-
Pham CT, MacIvor DM, Hug BA, Heusel JW, Ley TJ. Long-range disruption of gene expression by a selectable marker cassette. Proc Natl Acad Sci U S A. 1996;93:13090-13095.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 13090-13095
-
-
Pham, C.T.1
MacIvor, D.M.2
Hug, B.A.3
Heusel, J.W.4
Ley, T.J.5
-
40
-
-
0035957966
-
Characterization of mutant neutrophil elastase in severe congenital neutropenia
-
Li FQ, Horwitz M. Characterization of mutant neutrophil elastase in severe congenital neutropenia. J Biol Chem. 2001;276:14230-14241.
-
(2001)
J Biol Chem
, vol.276
, pp. 14230-14241
-
-
Li, F.Q.1
Horwitz, M.2
-
41
-
-
0026795415
-
Modulation of granulocyte survival and programmed cell death by cytokines and bacterial products
-
Colotta F, Re F, Polentarutti N, Sozzani S, Mantovani A. Modulation of granulocyte survival and programmed cell death by cytokines and bacterial products. Blood. 1992;80:2012-2020.
-
(1992)
Blood
, vol.80
, pp. 2012-2020
-
-
Colotta, F.1
Re, F.2
Polentarutti, N.3
Sozzani, S.4
Mantovani, A.5
-
42
-
-
0030799923
-
The granulocyte colony-stimulating factor receptor is required for the mobilization of murine hematopoietic progenitors into peripheral blood by cyclophosphamide or interleukin-8 but not flt-3 ligand
-
Liu F, Poursine-Laurent J, Link DC. The granulocyte colony-stimulating factor receptor is required for the mobilization of murine hematopoietic progenitors into peripheral blood by cyclophosphamide or interleukin-8 but not flt-3 ligand. Blood. 1997;90:2522-2528.
-
(1997)
Blood
, vol.90
, pp. 2522-2528
-
-
Liu, F.1
Poursine-Laurent, J.2
Link, D.C.3
-
43
-
-
0035801514
-
Lysosomal cysteine proteases: Facts and opportunities
-
Turk V, Turk B, Turk D. Lysosomal cysteine proteases: Facts and opportunities. EMBO J. 2001;20:4629-4633.
-
(2001)
EMBO J
, vol.20
, pp. 4629-4633
-
-
Turk, V.1
Turk, B.2
Turk, D.3
-
44
-
-
0033587689
-
Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo
-
Pham CT, Ley TJ. Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo. Proc Natl Acad Sci U S A. 1999;96:8627-8632.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 8627-8632
-
-
Pham, C.T.1
Ley, T.J.2
-
45
-
-
0032709548
-
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis
-
Toomes C, James J, Wood AJ, et al. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis. Nat Genet. 1999;23:421-424.
-
(1999)
Nat Genet
, vol.23
, pp. 421-424
-
-
Toomes, C.1
James, J.2
Wood, A.J.3
-
46
-
-
0030627476
-
Characterization of the mouse neutrophil elastase gene and localization to chromosome 10
-
Belaaouaj A, Walsh BC, Jenkins NA, Copeland NG, Shapiro SD. Characterization of the mouse neutrophil elastase gene and localization to chromosome 10. Mamm Genome. 1997;8:5-8.
-
(1997)
Mamm Genome
, vol.8
, pp. 5-8
-
-
Belaaouaj, A.1
Walsh, B.C.2
Jenkins, N.A.3
Copeland, N.G.4
Shapiro, S.D.5
-
47
-
-
0036467390
-
Defensins of vertebrate animals
-
Lehrer RI, Ganz T. Defensins of vertebrate animals. Curr Opin Immunol. 2002;14:96-102.
-
(2002)
Curr Opin Immunol
, vol.14
, pp. 96-102
-
-
Lehrer, R.I.1
Ganz, T.2
-
48
-
-
13344278020
-
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia
-
Chen M, Tomkins DJ, Auerbach W, et al. Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nat Genet. 1996;12:448-451.
-
(1996)
Nat Genet
, vol.12
, pp. 448-451
-
-
Chen, M.1
Tomkins, D.J.2
Auerbach, W.3
-
49
-
-
0033852602
-
Mice with a targeted disruption of the Fanconi anemia homolog Fanca
-
Cheng NC, van de Vrugt HJ, van der Valk MA, et al. Mice with a targeted disruption of the Fanconi anemia homolog Fanca. Hum Mol Genet. 2000;9: 1805-1811.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1805-1811
-
-
Cheng, N.C.1
Van de Vrugt, H.J.2
Van der Valk, M.A.3
-
50
-
-
0035760285
-
Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9
-
Yang Y, Kuang Y, De Oca RM, et al. Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9. Blood. 2001;98:3435-3440.
-
(2001)
Blood
, vol.98
, pp. 3435-3440
-
-
Yang, Y.1
Kuang, Y.2
De Oca, R.M.3
-
51
-
-
0029587551
-
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
-
Quelle DE, Zindy F, Ashmun RA, Sherr CJ. Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell. 1995;83: 993-1000.
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
Quelle, D.E.1
Zindy, F.2
Ashmun, R.A.3
Sherr, C.J.4
-
52
-
-
0026754577
-
Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter
-
Zimmer M, Medcalf RL, Fink TM, Mattmann C, Lichter P, Jenne DE. Three human elastase-like genes coordinately expressed in the myelomonocyte lineage are organized as a single genetic locus on 19pter. Proc Natl Acad Sci U S A. 1992;89:8215-8219.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 8215-8219
-
-
Zimmer, M.1
Medcalf, R.L.2
Fink, T.M.3
Mattmann, C.4
Lichter, P.5
Jenne, D.E.6
-
53
-
-
0033485338
-
Changes in chromatin organization at the neutrophil elastase locus associated with myeloid cell differentiation
-
Wong ET, Jenne DE, Zimmer M, Porter SD, Gilks CB. Changes in chromatin organization at the neutrophil elastase locus associated with myeloid cell differentiation. Blood. 1999;94:3730-3736.
-
(1999)
Blood
, vol.94
, pp. 3730-3736
-
-
Wong, E.T.1
Jenne, D.E.2
Zimmer, M.3
Porter, S.D.4
Gilks, C.B.5
|