-
1
-
-
66949132214
-
New insights into the genetics of congenital neutropenia
-
Özbek N. New insights into the genetics of congenital neutropenia. Turk J Hematol 2009;26:1-8.
-
(2009)
Turk J Hematol
, vol.26
, pp. 1-8
-
-
Özbek, N.1
-
2
-
-
79953045205
-
Genetic defects in severe congenital neutropenia: Emerging insights into life and death of human neutrophil granulocytes
-
Klein C. Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes. Ann Rev Immunol 2011;29:399-413.
-
(2011)
Ann Rev Immunol
, vol.29
, pp. 399-413
-
-
Klein, C.1
-
3
-
-
77955122507
-
Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: Evidence for phenotype determination by modifying genes
-
Newburger PE, Pindyck TN, Zhu Z, Bolyard AA, Aprikyan AAG, Dale DC, Smith GD, Boxer LA. Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes. Pediatr Blood Cancer 2010;55:314-317.
-
(2010)
Pediatr Blood Cancer
, vol.55
, pp. 314-317
-
-
Newburger, P.E.1
Pindyck, T.N.2
Zhu, Z.3
Bolyard, A.A.4
Aprikyan, A.A.G.5
Dale, D.C.6
Smith, G.D.7
Boxer, L.A.8
-
4
-
-
79956035262
-
Congenital neutropenia: Diagnosis, molecular bases and patient management
-
Donadieu J, Fenneteau O, Beaupain B, Mahlaoui N, Chantelot CB. Congenital neutropenia: diagnosis, molecular bases and patient management. Orphanet J Rare Dis 2011;6:26.
-
(2011)
Orphanet J Rare Dis
, vol.6
, pp. 26
-
-
Donadieu, J.1
Fenneteau, O.2
Beaupain, B.3
Mahlaoui, N.4
Chantelot, C.B.5
-
5
-
-
84922393563
-
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia
-
Boztug K, Järvinen PM, Salzer E, Racek T, Mönch S, Garncarz W, Gertz EM, Schäffer AA, Antonopoulos A, Haslam SM, Schieck L, Puchałka J, Diestelhorst J, Appaswamy G, Lescoeur B, Giambruno R, Bigenzahn JW, Elling U, Pfeifer D, Conde CD, Albert MH, Welte K, Brandes G, Sherkat R, van der Werff Ten Bosch J, Rezaei N, Etzioni A, Bellanné-Chantelot C, Superti-Furga G, Penninger JM, Bennett KL, von Blume J, Dell A, Donadieu J, Klein C. JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia. Nat Genet 2014;46:1021-1027.
-
(2014)
Nat Genet
, vol.46
, pp. 1021-1027
-
-
Boztug, K.1
Järvinen, P.M.2
Salzer, E.3
Racek, T.4
Mönch, S.5
Garncarz, W.6
Gertz, E.M.7
Schäffer, A.A.8
Antonopoulos, A.9
Haslam, S.M.10
Schieck, L.11
Puchałka, J.12
Diestelhorst, J.13
Appaswamy, G.14
Lescoeur, B.15
Giambruno, R.16
Bigenzahn, J.W.17
Elling, U.18
Pfeifer, D.19
Conde, C.D.20
Albert, M.H.21
Welte, K.22
Brandes, G.23
Sherkat, R.24
van der Werff Ten Bosch, J.25
Rezaei, N.26
Etzioni, A.27
Bellanné-Chantelot, C.28
Superti-Furga, G.29
Penninger, J.M.30
Bennett, K.L.31
von Blume, J.32
Dell, A.33
Donadieu, J.34
Klein, C.35
more..
-
7
-
-
33749343053
-
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia
-
Ancliff PJ, Blundell MP, Cory GO, Calle Y, Worth A, Kempski H, Burns S, Jones GE, Sinclair J, Kinnon C, Hann IM, Gale RE, Linch DC, Thrasher AJ. Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia. Blood 2006;108:2182-2189.
-
(2006)
Blood
, vol.108
, pp. 2182-2189
-
-
Ancliff, P.J.1
Blundell, M.P.2
Cory, G.O.3
Calle, Y.4
Worth, A.5
Kempski, H.6
Burns, S.7
Jones, G.E.8
Sinclair, J.9
Kinnon, C.10
Hann, I.M.11
Gale, R.E.12
Linch, D.C.13
Thrasher, A.J.14
-
8
-
-
38949089290
-
Rapid cell senescence and apoptosis in lymphocytes and granulocytes and absence of GM-CSF receptor in congenital dysgranulopoietic neutropenia
-
Olcay L, Yetgin S, Okur H, Erdemli E. Rapid cell senescence and apoptosis in lymphocytes and granulocytes and absence of GM-CSF receptor in congenital dysgranulopoietic neutropenia. Leuk Res 2008;32:235-242.
-
(2008)
Leuk Res
, vol.32
, pp. 235-242
-
-
Olcay, L.1
Yetgin, S.2
Okur, H.3
Erdemli, E.4
-
9
-
-
0037100469
-
Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia
-
Ancliff PJ, Gale RE, Watts JM, Liesner R, Hann IM, Strobel S, Linch DC. Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia. Blood 2002;100:707-709.
-
(2002)
Blood
, vol.100
, pp. 707-709
-
-
Ancliff, P.J.1
Gale, R.E.2
Watts, J.M.3
Liesner, R.4
Hann, I.M.5
Strobel, S.6
Linch, D.C.7
-
10
-
-
36849070286
-
Congenital dysgranulopoietic neutropenia
-
Olcay L, Yetgin S, Erdemli E, Germeshausen M, Aktaş D, Büyükaşik Y, Okur H. Congenital dysgranulopoietic neutropenia. Pediatr Blood Cancer 2008;50:115-119.
-
(2008)
Pediatr Blood Cancer
, vol.50
, pp. 115-119
-
-
Olcay, L.1
Yetgin, S.2
Erdemli, E.3
Germeshausen, M.4
Aktaş, D.5
Büyükaşik, Y.6
Okur, H.7
-
11
-
-
0009763170
-
Acquired qualitative platelet disorders due to diseases, drugs and foods
-
Beutler E, Lichtman MA, Coller BS, Kipps TJ, Seligsohn U, New York, McGraw-Hill
-
Shattil SJ, Abrams CS, Bennett JS. Acquired qualitative platelet disorders due to diseases, drugs and foods. In: Beutler E, Lichtman MA, Coller BS, Kipps TJ, Seligsohn U (eds). Williams Hematology. New York, McGraw-Hill, 2001.
-
(2001)
Williams Hematology
-
-
Shattil, S.J.1
Abrams, C.S.2
Bennett, J.S.3
-
12
-
-
2942550593
-
Peripheral blood lymphocyte subsets in healthy Turkish children
-
İkincioğulları A, Kendirli T, Doğu F, Eğin Y, Reisli İ, Cin Ş, Babacan E. Peripheral blood lymphocyte subsets in healthy Turkish children. Turk J Pediatr 2004;46:125-130.
-
(2004)
Turk J Pediatr
, vol.46
, pp. 125-130
-
-
İkincioğulları, A.1
Kendirli, T.2
Doğu, F.3
Eğin, Y.4
Reisli, İ.5
Cin, Ş.6
Babacan, E.7
-
14
-
-
68649108160
-
Excessive naked megakaryocyte nuclei in myelodysplastic syndrome mimicking idiopathic thrombocytopenic purpura: A complicated pre-and post-transplantation course
-
Olcay L, Tuncer AM, Okur H, Erdemli E, Uysal Z, Cetin M, Duru F, Cetinkaya DU. Excessive naked megakaryocyte nuclei in myelodysplastic syndrome mimicking idiopathic thrombocytopenic purpura: a complicated pre-and post-transplantation course. Pediatr Hematol Oncol 2009;26:387-397.
-
(2009)
Pediatr Hematol Oncol
, vol.26
, pp. 387-397
-
-
Olcay, L.1
Tuncer, A.M.2
Okur, H.3
Erdemli, E.4
Uysal, Z.5
Cetin, M.6
Duru, F.7
Cetinkaya, D.U.8
-
15
-
-
0029047362
-
A biomarker that identifies senescent human cells in culture and in aging skin in vivo
-
Dimri GP, Lee X, Basile G, Acosta M, Scott G, Roskelley C, Medrano EE, Linskens M, Rubelj I, Pereira-Smith O, Peacocke M, Campisi Jl. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proc Natl Acad Sci U S A 1995;92:9363-9367.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 9363-9367
-
-
Dimri, G.P.1
Lee, X.2
Basile, G.3
Acosta, M.4
Scott, G.5
Roskelley, C.6
Medrano, E.E.7
Linskens, M.8
Rubelj, I.9
Pereira-Smith, O.10
Peacocke, M.11
-
16
-
-
0033828357
-
Dysplastic changes in idiopathic thrombocytopenic purpura and the effect of corticosteroids to increase dysplasia and cause hyperdiploid macropolycytes
-
Olcay L, Yetgin S, Okur H, Erekul S, Tuncer M. Dysplastic changes in idiopathic thrombocytopenic purpura and the effect of corticosteroids to increase dysplasia and cause hyperdiploid macropolycytes. Am J Hematol 2000;65:99-104.
-
(2000)
Am J Hematol
, vol.65
, pp. 99-104
-
-
Olcay, L.1
Yetgin, S.2
Okur, H.3
Erekul, S.4
Tuncer, M.5
-
18
-
-
0036592728
-
Rational use of the PFA-100 device for screening of platelet function disorders and von Willebrand disease
-
Buyukasik Y, Karakus S, Goker H, Haznedaroglu IC, Ozatli D, Sayinalp N, Ozcebe OI, Dundar SV, Kirazli S. Rational use of the PFA-100 device for screening of platelet function disorders and von Willebrand disease. Blood Coagul Fibrinolysis 2002;13:349-353.
-
(2002)
Blood Coagul Fibrinolysis
, vol.13
, pp. 349-353
-
-
Buyukasik, Y.1
Karakus, S.2
Goker, H.3
Haznedaroglu, I.C.4
Ozatli, D.5
Sayinalp, N.6
Ozcebe, O.I.7
Dundar, S.V.8
Kirazli, S.9
-
19
-
-
24644521152
-
High cystine in platelets from patients with nephropathic cystinosis: A chemical, ultrastructural, and functional evaluation
-
Olcay L, Erdemli E, Kesimer M, Büyükasik Y, Okur H, Kalkanoğlu HS, Coskun T, Altay C. High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation. J Clin Pathol 2005;58:939-945.
-
(2005)
J Clin Pathol
, vol.58
, pp. 939-945
-
-
Olcay, L.1
Erdemli, E.2
Kesimer, M.3
Büyükasik, Y.4
Okur, H.5
Kalkanoğlu, H.S.6
Coskun, T.7
Altay, C.8
-
20
-
-
0023696540
-
Mepacrine-labeled platelet dense-body number in patients with chronic uremia
-
Komarnichi M, Pietrzak I, Zozulinska M. Mepacrine-labeled platelet dense-body number in patients with chronic uremia. Nephron 1988;50:306-307.
-
(1988)
Nephron
, vol.50
, pp. 306-307
-
-
Komarnichi, M.1
Pietrzak, I.2
Zozulinska, M.3
-
21
-
-
18544383487
-
Reference values in infancy and childhood
-
Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux S, 8th ed. Philadelphia, Saunders
-
Brugnara C. Reference values in infancy and childhood. In: Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux S (eds). Nathan and Oski’s Hematology and Oncology of Infancy and Childhood. 8th ed. Philadelphia, Saunders, 2015.
-
(2015)
Nathan and Oski’s Hematology and Oncology of Infancy and Childhood
-
-
Brugnara, C.1
-
22
-
-
33845997120
-
Normal blood values for neonatal, pediatric and adult populations
-
Hoffman R, Benz EJ, Shattil SJ, Furie B, Cohen HJ, Silberstein LE, McGlave P, 4th ed. Philadelphia, Churchill Livingstone
-
Geaghan SM. Normal blood values for neonatal, pediatric and adult populations. In: Hoffman R, Benz EJ, Shattil SJ, Furie B, Cohen HJ, Silberstein LE, McGlave P (eds). Hematology: Basic Principles and Practice. 4th ed. Philadelphia, Churchill Livingstone, 2005.
-
(2005)
Hematology: Basic Principles and Practice
-
-
Geaghan, S.M.1
-
23
-
-
0017163667
-
Ultrastructure of platelet aggregation in refractory anemia and myelomonocytic leukemia. I. Ultrastructure of aggregation in normal controls and general defects in refractory anemia and myelomonocytic leukemia
-
Pintado T, Maldonado JE. Ultrastructure of platelet aggregation in refractory anemia and myelomonocytic leukemia. I. Ultrastructure of aggregation in normal controls and general defects in refractory anemia and myelomonocytic leukemia. Mayo Clin Proc 1976;51:379-392.
-
(1976)
Mayo Clin Proc
, vol.51
, pp. 379-392
-
-
Pintado, T.1
Maldonado, J.E.2
-
24
-
-
0017076493
-
Ultrastructure of platelet aggregation in refractory anemia and myelomonocytic leukemia. II. Individual platelet abnormalities: Thrombasthenia-like platelets, surface defects, and dissociation phenomena
-
Pintado T, Maldonado JE. Ultrastructure of platelet aggregation in refractory anemia and myelomonocytic leukemia. II. Individual platelet abnormalities: thrombasthenia-like platelets, surface defects, and dissociation phenomena. Mayo Clin Proc 1976;51:443-451.
-
(1976)
Mayo Clin Proc
, vol.51
, pp. 443-451
-
-
Pintado, T.1
Maldonado, J.E.2
-
25
-
-
0032898385
-
Increased apoptotic peripheral blood neutrophils in systemic lupus erythematosus: Relations with disease
-
Courtney PA, Crockard AD, Williamson K, Irvine AE, Kennedy RJ, Bell AL. Increased apoptotic peripheral blood neutrophils in systemic lupus erythematosus: relations with disease. Ann Rheum Dis 1999;58:309-314.
-
(1999)
Ann Rheum Dis
, vol.58
, pp. 309-314
-
-
Courtney, P.A.1
Crockard, A.D.2
Williamson, K.3
Irvine, A.E.4
Kennedy, R.J.5
Bell, A.L.6
-
26
-
-
0033972915
-
Myelokathexis, a congenital disorder of severe neutropenia characterized by accelerated apoptosis and defective expression of bcl-x in neutrophil precursors
-
Aprikyan AA, Liles WC, Park JR, Jonas M, Chi EY, Dale DC. Myelokathexis, a congenital disorder of severe neutropenia characterized by accelerated apoptosis and defective expression of bcl-x in neutrophil precursors. Blood 2000;95:320-327.
-
(2000)
Blood
, vol.95
, pp. 320-327
-
-
Aprikyan, A.A.1
Liles, W.C.2
Park, J.R.3
Jonas, M.4
Chi, E.Y.5
Dale, D.C.6
-
27
-
-
0008461995
-
Chronic neutropenia mediated by Fas ligand
-
Liu JH, Wei S, Lamy T, Epling-Burnette PK, Starkebaum G, Djeu JY, Loughran TP. Chronic neutropenia mediated by Fas ligand. Blood 2000;95:3219-3222.
-
(2000)
Blood
, vol.95
, pp. 3219-3222
-
-
Liu, J.H.1
Wei, S.2
Lamy, T.3
Epling-Burnette, P.K.4
Starkebaum, G.5
Djeu, J.Y.6
Loughran, T.P.7
-
28
-
-
0002806130
-
The immunology of human immunodeficiency virus infection
-
Mandell GL, Bennett JE, Dolin R, New York, Churchill Livingstone
-
Cohen O, Cicala C, Vaccarezza M, Fauci AS. The immunology of human immunodeficiency virus infection. In: Mandell GL, Bennett JE, Dolin R, (eds). Principles and Practice of Infectious Diseases. New York, Churchill Livingstone, 2000.
-
(2000)
Principles and Practice of Infectious Diseases
-
-
Cohen, O.1
Cicala, C.2
Vaccarezza, M.3
Fauci, A.S.4
-
29
-
-
0036867646
-
Apoptosis of cord blood neutrophils and their response to colony-stimulating factors
-
Uguz A, Coskun M, Yuzbey S, Kizilors A, Karadogan I, Gura A, Yoldas B, Oygur N, Yegin O. Apoptosis of cord blood neutrophils and their response to colony-stimulating factors. Am J Perinatol 2002;19:427-433.
-
(2002)
Am J Perinatol
, vol.19
, pp. 427-433
-
-
Uguz, A.1
Coskun, M.2
Yuzbey, S.3
Kizilors, A.4
Karadogan, I.5
Gura, A.6
Yoldas, B.7
Oygur, N.8
Yegin, O.9
-
30
-
-
0038107361
-
Impaired granulocytopoiesis in patients with chronic idiopathic neutropenia is associated with increased apoptosis of bone marrow myeloid progenitor cells
-
Papadaki HA, Eliopoulos AG, Kosteas T, Gemetzi C, Damianaki A, Koutala H, Bux J, Eliopoulos GD. Impaired granulocytopoiesis in patients with chronic idiopathic neutropenia is associated with increased apoptosis of bone marrow myeloid progenitor cells. Blood 2003;101:2591-2600.
-
(2003)
Blood
, vol.101
, pp. 2591-2600
-
-
Papadaki, H.A.1
Eliopoulos, A.G.2
Kosteas, T.3
Gemetzi, C.4
Damianaki, A.5
Koutala, H.6
Bux, J.7
Eliopoulos, G.D.8
-
31
-
-
0038383286
-
Apoptotic neutrophils in the circulation of patients with glycogen storage disease type 1b (GSD1b)
-
Kuijpers TW, Maianski NA, Tool AT, Smit GP, Rake JP, Roos D, Visser G. Apoptotic neutrophils in the circulation of patients with glycogen storage disease type 1b (GSD1b). Blood 2003;101:5021-5024.
-
(2003)
Blood
, vol.101
, pp. 5021-5024
-
-
Kuijpers, T.W.1
Maianski, N.A.2
Tool, A.T.3
Smit, G.P.4
Rake, J.P.5
Roos, D.6
Visser, G.7
-
32
-
-
0026788002
-
Key morphological features of apoptosis may occur in the absence of internucleosomal DNA fragmentation
-
Cohen GM, Sun XM, Snowden RT, Dinsdale D, Skilleter DN. Key morphological features of apoptosis may occur in the absence of internucleosomal DNA fragmentation. Biochem J 1992;286:331-334.
-
(1992)
Biochem J
, vol.286
, pp. 331-334
-
-
Cohen, G.M.1
Sun, X.M.2
Snowden, R.T.3
Dinsdale, D.4
Skilleter, D.N.5
-
34
-
-
0004235781
-
Innate immunity
-
Abbas A, Lichtman AH, Pillai S, 8th ed. Toronto, Elsevier Saunders
-
Abbas AK, Lichtman AH, Pillai S. Innate immunity. In: Abbas A, Lichtman AH, Pillai S (eds). Cellular and Molecular Immunology. 8th ed. Toronto, Elsevier Saunders, 2015.
-
(2015)
Cellular and Molecular Immunology
-
-
Abbas, A.K.1
Lichtman, A.H.2
Pillai, S.3
-
35
-
-
0002449874
-
Differentiation and functions of CD4+ effector T cells
-
Abbas A, Lichtman AH, Pillai S, 8th ed. Toronto, Elsevier Saunders
-
Abbas AK, Lichtman AH, Pillai S. Differentiation and functions of CD4+ effector T cells. In: Abbas A, Lichtman AH, Pillai S (eds). Cellular and Molecular Immunology. 8th ed. Toronto, Elsevier Saunders, 2015.
-
(2015)
Cellular and Molecular Immunology
-
-
Abbas, A.K.1
Lichtman, A.H.2
Pillai, S.3
-
36
-
-
85056831758
-
Granulocytic and non granulocytic lineages in children with congenital neutropenia and their non neutropenic parents: Biochemical, functional, morphological and genetic evaluation
-
Olcay L, Ünal Ş, Öztürk A, Erdemli E, Billur D, Metin A, Okur H, İkincioğulları A, Yıldırmak Y, Büyükaşık Y, Yılmaz-Falay M, Özet G, Yetgin S. Granulocytic and non granulocytic lineages in children with congenital neutropenia and their non neutropenic parents: biochemical, functional, morphological and genetic evaluation. Haematologica 1012;97(Suppl 3):O65a (abstract).
-
Haematologica
, vol.97
, pp. 1012
-
-
Olcay, L.1
Ünal, Ş.2
Öztürk, A.3
Erdemli, E.4
Billur, D.5
Metin, A.6
Okur, H.7
İkincioğulları, A.8
Yıldırmak, Y.9
Büyükaşık, Y.10
Yılmaz-Falay, M.11
Özet, G.12
Yetgin, S.13
-
37
-
-
0028366535
-
Cytokine profile during high-dose rhG-CSF therapy in severe congenital neutropenia
-
Shitara T, Yugami S, Ijima H, Sotomatu M, Kuroume T. Cytokine profile during high-dose rhG-CSF therapy in severe congenital neutropenia. Am J Hematol 1994;45:58-62.
-
(1994)
Am J Hematol
, vol.45
, pp. 58-62
-
-
Shitara, T.1
Yugami, S.2
Ijima, H.3
Sotomatu, M.4
Kuroume, T.5
-
38
-
-
77954014950
-
Toll-like receptor-mediated functional activity of mononuclear cells in children with neutropenia
-
Koval’chuk LV, Khoreva MV, Nikonova AS, Finogenova NA, Mamedova EA, Polovtseva TV, Fetisova LIa, Gracheva LA, Goldyreva NG. Toll-like receptor-mediated functional activity of mononuclear cells in children with neutropenia. Zh Mikrobiol Epidemiol Immunobiol 2010;2:64-68.
-
(2010)
Zh Mikrobiol Epidemiol Immunobiol
, vol.2
, pp. 64-68
-
-
Koval’Chuk, L.V.1
Khoreva, M.V.2
Nikonova, A.S.3
Finogenova, N.A.4
Mamedova, E.A.5
Polovtseva, T.V.6
Fetisova, L.7
Gracheva, L.A.8
Goldyreva, N.G.9
-
39
-
-
48249135487
-
Lethal graft-versus-host disease in congenital neutropenia caused by p14 deficiency after allogeneic bone marrow transplantation from an HLA-identical sibling
-
Bohn G, Hardtke-Wolenski M, Zeidler C, Maecker B, Sauer M, Sykora KW, Grigull L, Welte K, Klein C. Lethal graft-versus-host disease in congenital neutropenia caused by p14 deficiency after allogeneic bone marrow transplantation from an HLA-identical sibling. Pediatr Blood Cancer 2008;51:436-438.
-
(2008)
Pediatr Blood Cancer
, vol.51
, pp. 436-438
-
-
Bohn, G.1
Hardtke-Wolenski, M.2
Zeidler, C.3
Maecker, B.4
Sauer, M.5
Sykora, K.W.6
Grigull, L.7
Welte, K.8
Klein, C.9
-
40
-
-
80052399266
-
A novel signaling pathway in TNFα-induced neutrophil apoptosis
-
Geering B, Simon HU. A novel signaling pathway in TNFα-induced neutrophil apoptosis. Cell Cycle 2011;10:2821-2822.
-
(2011)
Cell Cycle
, vol.10
, pp. 2821-2822
-
-
Geering, B.1
Simon, H.U.2
-
41
-
-
84960120477
-
Anti-tumor necrosis factor alpha (Infliximab) attenuates apoptosis, oxidative stress, and calcium ion entry through modulation of cation channels in neutrophils of patients with ankylosing spondylitis
-
Ugan Y, Nazıroğlu M, Şahin M, Aykur M. Anti-tumor necrosis factor alpha (Infliximab) attenuates apoptosis, oxidative stress, and calcium ion entry through modulation of cation channels in neutrophils of patients with ankylosing spondylitis. J Membr Biol 2016;249:437-447.
-
(2016)
J Membr Biol
, vol.249
, pp. 437-447
-
-
Ugan, Y.1
Nazıroğlu, M.2
Şahin, M.3
Aykur, M.4
-
42
-
-
2942527148
-
Akt decreases lymphocyte apoptosis and improves survival in sepsis
-
Bommhardt U, Chang KC, Swanson PE, Wagner TH, Tinsley KW, Karl IE, Hotchkiss RS. Akt decreases lymphocyte apoptosis and improves survival in sepsis. J Immunol 2004;172:7583-7591.
-
(2004)
J Immunol
, vol.172
, pp. 7583-7591
-
-
Bommhardt, U.1
Chang, K.C.2
Swanson, P.E.3
Wagner, T.H.4
Tinsley, K.W.5
Karl, I.E.6
Hotchkiss, R.S.7
-
44
-
-
83755220209
-
Tumor necrosis factor-α-induced mononuclear cell death may contribute to polymorphonuclear cell predominance in the cerebrospinal fluid of patients with bacterial meningitis
-
Kawakami Y, Tsukimoto M, Kuwabara K, Fujita T, Fujino O, Kojima S, Fukunaga Y. Tumor necrosis factor-α-induced mononuclear cell death may contribute to polymorphonuclear cell predominance in the cerebrospinal fluid of patients with bacterial meningitis. J Nippon Med Sch 2011;78:360-366.
-
(2011)
J Nippon Med Sch
, vol.78
, pp. 360-366
-
-
Kawakami, Y.1
Tsukimoto, M.2
Kuwabara, K.3
Fujita, T.4
Fujino, O.5
Kojima, S.6
Fukunaga, Y.7
-
45
-
-
84890410047
-
The apoptotic actions of platelets in acute ischemic stroke
-
Cevik O, Adiguzel Z, Baykal AT, Somay G, Sener A. The apoptotic actions of platelets in acute ischemic stroke. Mol Biol Rep 2013;40:6721-6727.
-
(2013)
Mol Biol Rep
, vol.40
, pp. 6721-6727
-
-
Cevik, O.1
Adiguzel, Z.2
Baykal, A.T.3
Somay, G.4
Sener, A.5
-
46
-
-
33644654885
-
Evaluation of apoptosis in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis
-
Kawada J, Kimura H, Shibata Y, Hara S, Hoshino Y, Kojima S, Nishikawa K, Morishima T. Evaluation of apoptosis in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis. J Med Virol 2006;78:400-407.
-
(2006)
J Med Virol
, vol.78
, pp. 400-407
-
-
Kawada, J.1
Kimura, H.2
Shibata, Y.3
Hara, S.4
Hoshino, Y.5
Kojima, S.6
Nishikawa, K.7
Morishima, T.8
-
47
-
-
23044433925
-
Structure and function of the Wiskott-Aldrich syndrome protein
-
Ochs HD, Notarangelo LD. Structure and function of the Wiskott-Aldrich syndrome protein. Curr Opin Hematol 2005;12:284-291.
-
(2005)
Curr Opin Hematol
, vol.12
, pp. 284-291
-
-
Ochs, H.D.1
Notarangelo, L.D.2
-
48
-
-
33745597347
-
Identification of a homozygous deletion in the AP3B1 gene causing Hemansky-Pudlak syndrome, type 2
-
Jung J, Bohn G, Allroth A, Boztug K, Brandes G, Sandrock I, Schäffer AA, Rathinam C, Köllner I, Beger C, Schilke R, Welte K, Grimbacher B, Klein C. Identification of a homozygous deletion in the AP3B1 gene causing Hemansky-Pudlak syndrome, type 2. Blood 2006;108:362-369.
-
(2006)
Blood
, vol.108
, pp. 362-369
-
-
Jung, J.1
Bohn, G.2
Allroth, A.3
Boztug, K.4
Brandes, G.5
Sandrock, I.6
Schäffer, A.A.7
Rathinam, C.8
Köllner, I.9
Beger, C.10
Schilke, R.11
Welte, K.12
Grimbacher, B.13
Klein, C.14
-
49
-
-
33645057693
-
Hermansky-Pudlak syndrome: A disease of protein trafficking and organelle function
-
Wei ML. Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function. Pigment Cell Res 2006;19:19-42.
-
(2006)
Pigment Cell Res
, vol.19
, pp. 19-42
-
-
Wei, M.L.1
-
50
-
-
63049109925
-
Down-regulation of Gfi-1 expression by TGFB is important for differentiation of Th17 and CD103+ inducible regulatory T cells
-
Zhu J, Davidson TS, Wei G, Jankovic D, Cui K, Schones DE, Guo L, Zhao K, Shevach EM, Paul WE. Down-regulation of Gfi-1 expression by TGFB is important for differentiation of Th17 and CD103+ inducible regulatory T cells. J Exp Med 2009;206:329-341.
-
(2009)
J Exp Med
, vol.206
, pp. 329-341
-
-
Zhu, J.1
Davidson, T.S.2
Wei, G.3
Jankovic, D.4
Cui, K.5
Schones, D.E.6
Guo, L.7
Zhao, K.8
Shevach, E.M.9
Paul, W.E.10
-
51
-
-
70449464010
-
The phagocyte system and disorders of granulopoiesis and granulocyte function
-
Orkin SH, Nathan DG, Philadelphia, Saunders Elsevier
-
Dinauer MC, Newburger PP. The phagocyte system and disorders of granulopoiesis and granulocyte function. In: Orkin SH, Nathan DG, (eds). Nathan and Oski’s Hematology of Infancy and Childhood. Philadelphia, Saunders Elsevier, 2009.
-
(2009)
Nathan and Oski’s Hematology of Infancy and Childhood
-
-
Dinauer, M.C.1
Newburger, P.P.2
-
52
-
-
84860383557
-
Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis
-
Jaeger BN, Donadieu J, Cognet C, Bernat C, Ordoñez-Rueda D, Barlogis V, Mahlaoui N, Fenis A, Narni-Mancinelli E, Beaupain B, Bellanné-Chantelot C, Bajénoff M, Malissen B, Malissen M, Vivier E, Ugolini S. Neutrophil depletion impairs natural killer cell maturation, function, and homeostasis. J Exp Med 2012;209:565-580.
-
(2012)
J Exp Med
, vol.209
, pp. 565-580
-
-
Jaeger, B.N.1
Donadieu, J.2
Cognet, C.3
Bernat, C.4
Ordoñez-Rueda, D.5
Barlogis, V.6
Mahlaoui, N.7
Fenis, A.8
Narni-Mancinelli, E.9
Beaupain, B.10
Bellanné-Chantelot, C.11
Bajénoff, M.12
Malissen, B.13
Malissen, M.14
Vivier, E.15
Ugolini, S.16
-
53
-
-
0021807065
-
Impaired natural killer cell recycling in childhood chronic neutropenia with morphological abnormalities and defective chemotaxis of neutrophils
-
Komiyama A, Kawai H, Yamada S, Aoyama K, Yamazaki M, Saitoh H, Miyagawa Y, Akabane T, Uehara Y. Impaired natural killer cell recycling in childhood chronic neutropenia with morphological abnormalities and defective chemotaxis of neutrophils. Blood 1985;66:99-105.
-
(1985)
Blood
, vol.66
, pp. 99-105
-
-
Komiyama, A.1
Kawai, H.2
Yamada, S.3
Aoyama, K.4
Yamazaki, M.5
Saitoh, H.6
Miyagawa, Y.7
Akabane, T.8
Uehara, Y.9
-
54
-
-
68149179573
-
Immunosenescence: What does it mean to health outcomes in older adults?
-
McElhaney JE, Effros RB. Immunosenescence: what does it mean to health outcomes in older adults? Curr Opin Immunol 2009;21:418-424.
-
(2009)
Curr Opin Immunol
, vol.21
, pp. 418-424
-
-
McElhaney, J.E.1
Effros, R.B.2
-
55
-
-
77952105389
-
Inflammatory networks during cellular senescence: Causes and consequences
-
Freund A, Orjalo AV, Desprez PY, Campisi J. Inflammatory networks during cellular senescence: causes and consequences. Trends Mol Med 2010;16:238-246.
-
(2010)
Trends Mol Med
, vol.16
, pp. 238-246
-
-
Freund, A.1
Orjalo, A.V.2
Desprez, P.Y.3
Campisi, J.4
-
56
-
-
84929715471
-
Myelodysplastic features and cellular senescence in autoimmune disorders: A pilot study on patients with collagen tissue disorders and immune thrombocytopenic purpura
-
Olcay L, Billur D, Erdemli E, Baskin SE, Balci HF, Yetgin S. Myelodysplastic features and cellular senescence in autoimmune disorders: a pilot study on patients with collagen tissue disorders and immune thrombocytopenic purpura. Turk J Med Sci 2015;45:742-744.
-
(2015)
Turk J Med Sci
, vol.45
, pp. 742-744
-
-
Olcay, L.1
Billur, D.2
Erdemli, E.3
Baskin, S.E.4
Balci, H.F.5
Yetgin, S.6
-
57
-
-
0033606852
-
Role of p53 and p21waf1/cip1 in senescence-like terminal proliferation arrest induced in human tumor cells by chemotherapeutic drugs
-
Chang BD, Xuan Y, Broude EV, Zhu H, Schott B, Fang J, Roninson IB. Role of p53 and p21waf1/cip1 in senescence-like terminal proliferation arrest induced in human tumor cells by chemotherapeutic drugs. Oncogene 1999;18:4808-4818.
-
(1999)
Oncogene
, vol.18
, pp. 4808-4818
-
-
Chang, B.D.1
Xuan, Y.2
Broude, E.V.3
Zhu, H.4
Schott, B.5
Fang, J.6
Roninson, I.B.7
-
58
-
-
38949173535
-
Assessment of DNA damage cell cycle checkpoints in G1 and G2 phases of mammalian cells
-
Studzinski GP, Robertson GP, Hufford A, Lugo TG, New York, Oxford University Press
-
O’Connor PM, Jackman J. Assessment of DNA damage cell cycle checkpoints in G1 and G2 phases of mammalian cells. In: Studzinski GP, Robertson GP, Hufford A, Lugo TG, (eds). Cell Growth, Differentiation and Senescence: A Practical Approach. New York, Oxford University Press, 1999.
-
(1999)
Cell Growth, Differentiation and Senescence: a Practical Approach
-
-
O’Connor, P.M.1
Jackman, J.2
-
59
-
-
4243305752
-
Senescence and immortalization of human cells
-
Studzinski GP, Robertson GP, Hufford A, Lugo TG, New York, Oxford University Press
-
Hubbard K, Ozer HL. Senescence and immortalization of human cells. In: Studzinski GP, Robertson GP, Hufford A, Lugo TG, (eds). Cell Growth, Differentiation and Senescence: A Practical Approach. New York, Oxford University Press, 1999.
-
(1999)
Cell Growth, Differentiation and Senescence: a Practical Approach
-
-
Hubbard, K.1
Ozer, H.L.2
-
61
-
-
0037064011
-
Expression of human telomerase (HTERT) does not prevent stress-induced senescence in normal human fibroblasts but protects the cells from stress-induced apoptosis and necrosis
-
Gorbunova V, Seluanov A, Pereira-Smith OM. Expression of human telomerase (hTERT) does not prevent stress-induced senescence in normal human fibroblasts but protects the cells from stress-induced apoptosis and necrosis. J Biol Chem 2002;277:38540-38549.
-
(2002)
J Biol Chem
, vol.277
, pp. 38540-38549
-
-
Gorbunova, V.1
Seluanov, A.2
Pereira-Smith, O.M.3
-
62
-
-
0035989631
-
Historical claims and current interpretations of replicative aging
-
Wright WE, Shay JW. Historical claims and current interpretations of replicative aging. Nat Biotechnol 2002;20:682-688.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 682-688
-
-
Wright, W.E.1
Shay, J.W.2
-
63
-
-
79951912532
-
Four faces of cellular senescence
-
Rodier F, Campisi J. Four faces of cellular senescence. J Cell Biol 2011;192:547-556.
-
(2011)
J Cell Biol
, vol.192
, pp. 547-556
-
-
Rodier, F.1
Campisi, J.2
-
64
-
-
84876407105
-
Roles and mechanisms of cellular senescence in regulation of tissue homeostasis
-
Ohtani N, Hara E. Roles and mechanisms of cellular senescence in regulation of tissue homeostasis. Cancer Sci 2013;104:525-530.
-
(2013)
Cancer Sci
, vol.104
, pp. 525-530
-
-
Ohtani, N.1
Hara, E.2
-
65
-
-
0025720598
-
Chromatin reorganization during senescence of proliferating cells
-
Macieira-Coelho A. Chromatin reorganization during senescence of proliferating cells. Mutat Res 1991;256:81-104.
-
(1991)
Mutat Res
, vol.256
, pp. 81-104
-
-
Macieira-Coelho, A.1
-
66
-
-
0019143658
-
Congenital dysgranulopoietic neutropenia: Clinical, serologic, ultrastructural, and in vitro proliferative characteristics
-
Parmley RT, Crist WM, Ragab AH, Boxer LA, Malluh A, Lui VK, Darby CP. Congenital dysgranulopoietic neutropenia: clinical, serologic, ultrastructural, and in vitro proliferative characteristics. Blood 1980;56:465-475.
-
(1980)
Blood
, vol.56
, pp. 465-475
-
-
Parmley, R.T.1
Crist, W.M.2
Ragab, A.H.3
Boxer, L.A.4
Malluh, A.5
Lui, V.K.6
Darby, C.P.7
-
67
-
-
85056861680
-
Disorders mimicking myelodysplastic syndrome and difficulties in its diagnosis
-
Fuchs O, (ed), Rijeka, InTech
-
Olcay L, Yetgin S. Disorders mimicking myelodysplastic syndrome and difficulties in its diagnosis. In: Fuchs O, (ed). Myelodysplastic Syndromes. Rijeka, InTech, 2016.
-
(2016)
Myelodysplastic Syndromes
-
-
Olcay, L.1
Yetgin, S.2
-
68
-
-
0021924451
-
Severe congenital neutropenia with unique features of dysgranulopoiesis
-
Lightsey AL, Parmley RT, Marsh WL Jr, Garg AK, Thomas WJ, Wolach B, Boxer LA. Severe congenital neutropenia with unique features of dysgranulopoiesis. Am J Hematol 1985;18:59-71.
-
(1985)
Am J Hematol
, vol.18
, pp. 59-71
-
-
Lightsey, A.L.1
Parmley, R.T.2
Marsh, W.L.3
Garg, A.K.4
Thomas, W.J.5
Wolach, B.6
Boxer, L.A.7
-
69
-
-
0031013932
-
Apoptosis (Programmed cell death) in idiopathic (primary) osteo-/myelofibrosis: Naked nuclei in megakaryopoiesis reveal features of para-apoptosis
-
Thiele J, Lorenzen J, Manich B, Kvasnicka HM, Zirbes TK, Fischer R. Apoptosis (programmed cell death) in idiopathic (primary) osteo-/myelofibrosis: naked nuclei in megakaryopoiesis reveal features of para-apoptosis. Acta Haematol 1997;97:137-143.
-
(1997)
Acta Haematol
, vol.97
, pp. 137-143
-
-
Thiele, J.1
Lorenzen, J.2
Manich, B.3
Kvasnicka, H.M.4
Zirbes, T.K.5
Fischer, R.6
-
70
-
-
9244264090
-
Increased and pathologic emperipolesis of neutrophils within megakaryocytes associated with marrow fibrosis in GATA-1(Low) mice
-
Centurione L, Di Baldassarre A, Zingariello M, Bosco D, Gatta V, Rana RA, Langella V, Di Virgilio A, Vannucchi AM, Migliaccio AR. Increased and pathologic emperipolesis of neutrophils within megakaryocytes associated with marrow fibrosis in GATA-1(low) mice. Blood 2004;104:3573-3580.
-
(2004)
Blood
, vol.104
, pp. 3573-3580
-
-
Centurione, L.1
Di Baldassarre, A.2
Zingariello, M.3
Bosco, D.4
Gatta, V.5
Rana, R.A.6
Langella, V.7
Di Virgilio, A.8
Vannucchi, A.M.9
Migliaccio, A.R.10
-
71
-
-
0035406968
-
Megakaryocyte emperipolesis in a child with chronic neutropenia: An unusual coexistence
-
Aslan D, Yetgin S. Megakaryocyte emperipolesis in a child with chronic neutropenia: an unusual coexistence. Turk J Pediatr 2001;43:255-256.
-
(2001)
Turk J Pediatr
, vol.43
, pp. 255-256
-
-
Aslan, D.1
Yetgin, S.2
-
72
-
-
0942287736
-
Ultrastructural study shows morphologic features of apoptosis and para-apoptosis in megakaryocytes from patients with idiopathic thrombocytopenic purpura
-
Houwerzijl EJ, Blom NR, van der Want JJ, Esselink MT, Koornstra JJ, Smit JW, Louwes H, Vellenga E, de Wolf JT. Ultrastructural study shows morphologic features of apoptosis and para-apoptosis in megakaryocytes from patients with idiopathic thrombocytopenic purpura. Blood 2004;103:500-506.
-
(2004)
Blood
, vol.103
, pp. 500-506
-
-
Houwerzijl, E.J.1
Blom, N.R.2
van der Want, J.J.3
Esselink, M.T.4
Koornstra, J.J.5
Smit, J.W.6
Louwes, H.7
Vellenga, E.8
de Wolf, J.T.9
-
73
-
-
0023583912
-
Circulating micromegakaryocytes in myelodysplasia
-
Erber WN, Jacobs A, Oscier DG, O’Hea AM, Mason DY. Circulating micromegakaryocytes in myelodysplasia. J Clin Pathol 1987;40:1349-1352.
-
(1987)
J Clin Pathol
, vol.40
, pp. 1349-1352
-
-
Erber, W.N.1
Jacobs, A.2
Oscier, D.G.3
O’Hea, A.M.4
Mason, D.Y.5
-
74
-
-
0016733133
-
The platelet defect in leukemia. Platelet ultrastructure, adenine nucleotide metabolism, and the release reaction
-
Cowan DH, Graham RC, Baunach D. The platelet defect in leukemia. Platelet ultrastructure, adenine nucleotide metabolism, and the release reaction. J Clin Invest 1975;56:188-200.
-
(1975)
J Clin Invest
, vol.56
, pp. 188-200
-
-
Cowan, D.H.1
Graham, R.C.2
Baunach, D.3
-
75
-
-
84878258377
-
Inherited platelet function disorders: Overview and disorders of granules, secretion, and signal transduction
-
Rao AK. Inherited platelet function disorders: overview and disorders of granules, secretion, and signal transduction. Hematol Oncol Clin North Am 2013;27:585-611.
-
(2013)
Hematol Oncol Clin North Am
, vol.27
, pp. 585-611
-
-
Rao, A.K.1
-
77
-
-
0023608663
-
Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: Studies on one hundred and six patients
-
Nieuwenhuis HK, Akkerman JW, Sixma JJ. Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: studies on one hundred and six patients. Blood 1987;70:620-623.
-
(1987)
Blood
, vol.70
, pp. 620-623
-
-
Nieuwenhuis, H.K.1
Akkerman, J.W.2
Sixma, J.J.3
-
78
-
-
24644464010
-
Correlation of clinical severity of bleeding with electron microscopy findings in a group of pediatric patients with platelet storage pool deficiencies at a single institution
-
Jasty R, Kuerbitz S, Matthew P. Correlation of clinical severity of bleeding with electron microscopy findings in a group of pediatric patients with platelet storage pool deficiencies at a single institution. J Pediatr Hematol Oncol 2001;23:1146a (abstract).
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 1146
-
-
Jasty, R.1
Kuerbitz, S.2
Matthew, P.3
-
79
-
-
84860007854
-
The PFA-100 ® does not predict delta-granule platelet storage pool deficiencies
-
Sladky JL, Klima J, Grooms L, Kerlin BA, O’Brien SH. The PFA-100 ® does not predict delta-granule platelet storage pool deficiencies. Hemophilia 2012;18:626-629.
-
(2012)
Hemophilia
, vol.18
, pp. 626-629
-
-
Sladky, J.L.1
Klima, J.2
Grooms, L.3
Kerlin, B.A.4
O’Brien, S.H.5
-
80
-
-
0031952881
-
Use of the electron microscope for diagnosis of platelet disorders
-
White JG. Use of the electron microscope for diagnosis of platelet disorders. Semin Thromb Hemost 1998;24:163-168.
-
(1998)
Semin Thromb Hemost
, vol.24
, pp. 163-168
-
-
White, J.G.1
-
81
-
-
0037100469
-
Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia
-
Ancliff PJ, Gale RE, Watts JM, Liesner R, Hann IM, Strobel S, Linch DC. Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia. Blood 2002;100:707-709.
-
(2002)
Blood
, vol.100
, pp. 707-709
-
-
Ancliff, P.J.1
Gale, R.E.2
Watts, J.M.3
Liesner, R.4
Hann, I.M.5
Strobel, S.6
Linch, D.C.7
-
82
-
-
84937978473
-
Mosaicism of an ELANE mutation in an asymptomatic mother in a familial case of cyclic neutropenia
-
Hirata O, Okada S, Tsumura M, Karakawa S, Matsumura I, Kimura Y, Maihara T, Yasunaga S, Takihara Y, Ohara O, Kobayashi M. Mosaicism of an ELANE mutation in an asymptomatic mother in a familial case of cyclic neutropenia. J Clin Immunol 2015;35:512-516.
-
(2015)
J Clin Immunol
, vol.35
, pp. 512-516
-
-
Hirata, O.1
Okada, S.2
Tsumura, M.3
Karakawa, S.4
Matsumura, I.5
Kimura, Y.6
Maihara, T.7
Yasunaga, S.8
Takihara, Y.9
Ohara, O.10
Kobayashi, M.11
-
83
-
-
84945247193
-
Paternal somatic mosaicism of a novel frameshift mutation in ELANE causing severe congenital neutropenia
-
Kim HJ, Song MJ, Lee KO, Kim SH, Kim HJ. Paternal somatic mosaicism of a novel frameshift mutation in ELANE causing severe congenital neutropenia. Pediatr Blood Cancer 2015;62:2229-2231.
-
(2015)
Pediatr Blood Cancer
, vol.62
, pp. 2229-2231
-
-
Kim, H.J.1
Song, M.J.2
Lee, K.O.3
Kim, S.H.4
Kim, H.J.5
-
84
-
-
77349103408
-
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia
-
Malcov M, Reches A, Ben-Yosef D, Cohen T, Amit A, Dgany O, Tamary H, Yaron Y. Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia. Prenat Diagn 2010;30:207-211.
-
(2010)
Prenat Diagn
, vol.30
, pp. 207-211
-
-
Malcov, M.1
Reches, A.2
Ben-Yosef, D.3
Cohen, T.4
Amit, A.5
Dgany, O.6
Tamary, H.7
Yaron, Y.8
-
85
-
-
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
-
86
-
-
0031959590
-
Frequency of somatic and germ-line mosaicism in retinoblastoma: Implications for genetic counseling
-
Sippel KC, Fraioli RE, Smith GD, Schalkoff ME, Sutherland J, Gallie BL, Dryja TP. Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling. Am J Hum Genet 1998;62:610-619.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 610-619
-
-
Sippel, K.C.1
Fraioli, R.E.2
Smith, G.D.3
Schalkoff, M.E.4
Sutherland, J.5
Gallie, B.L.6
Dryja, T.P.7
-
87
-
-
85020661964
-
Severe congenital neutropenias
-
Skokowa J, Dale DC, Touw IP, Zeidler C, Welte K. Severe congenital neutropenias. Nat Rev Dis Primers 2017;3:17032.
-
(2017)
Nat Rev Dis Primers
, vol.3
-
-
Skokowa, J.1
Dale, D.C.2
Touw, I.P.3
Zeidler, C.4
Welte, K.5
-
88
-
-
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
-
89
-
-
85056842470
-
Genotype-phenotype interaction analyses in hemophilia
-
Batorova A, (ed)., Rijeka, InTech
-
Jaloma-Cruz AR, Beltran-Miranda CP, Gonzalez-Ramos IA, Lopez-Jimenez JJ, Luna-Zaizar H, Mantilla-Capacho JM, Mundo-Ayala JN, Galvan MJV. Genotype-phenotype interaction analyses in hemophilia. In: Batorova A, (ed). Hemophilia. Rijeka, InTech, 2012.
-
(2012)
Hemophilia
-
-
Jaloma-Cruz, A.R.1
Beltran-Miranda, C.P.2
Gonzalez-Ramos, I.A.3
Lopez-Jimenez, J.J.4
Luna-Zaizar, H.5
Mantilla-Capacho, J.M.6
Mundo-Ayala, J.N.7
Galvan, M.J.V.8
-
90
-
-
65349137591
-
Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome
-
Steinemann D, Praulich I, Otto N, Göhring G, Niemeyer CM, Schlegelberger B. Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome. Br J Haematol 2009;145:533-550.
-
(2009)
Br J Haematol
, vol.145
, pp. 533-550
-
-
Steinemann, D.1
Praulich, I.2
Otto, N.3
Göhring, G.4
Niemeyer, C.M.5
Schlegelberger, B.6
-
91
-
-
77954842713
-
Molecular analysis of two cases of severe congenital neutropenia
-
Park J, Kim M, Lim J, Kim Y, Cho B, Park JY, Han K. Molecular analysis of two cases of severe congenital neutropenia. Korean J Lab Med 2010;30:111-116.
-
(2010)
Korean J Lab Med
, vol.30
, pp. 111-116
-
-
Park, J.1
Kim, M.2
Lim, J.3
Kim, Y.4
Cho, B.5
Park, J.Y.6
Han, K.7
-
92
-
-
70349833643
-
Dysregulation of myeloid-specific transcription factors in congenital neutropenia
-
Skokowa J, Welte K. Dysregulation of myeloid-specific transcription factors in congenital neutropenia. Ann N Y Acad Sci 2009;1176:94-100.
-
(2009)
Ann N Y Acad Sci
, vol.1176
, pp. 94-100
-
-
Skokowa, J.1
Welte, K.2
-
93
-
-
70449466604
-
Neutrophil elastase is severely down-regulated in severe congenital neutropenia independent of ELA2 or HAX1 mutations but dependent on LEF-1
-
Skokowa J, Fobiwe JP, Dan L, Thakur BK, Welte K. Neutrophil elastase is severely down-regulated in severe congenital neutropenia independent of ELA2 or HAX1 mutations but dependent on LEF-1. Blood 2009;114:3044-3051.
-
(2009)
Blood
, vol.114
, pp. 3044-3051
-
-
Skokowa, J.1
Fobiwe, J.P.2
Dan, L.3
Thakur, B.K.4
Welte, K.5
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