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Tumor necrosis factor -- Therapeutic use : Tumor necrosis factor / Toma P. Rossard, editor  2009 1
Tumor Necrosis Factors   3
Tumor Necrosis Factors -- genetics : Tumor necrosis factor / Toma P. Rossard, editor  2009 1
Tumor Necrosis Factors -- immunology : TNF pathophysiology : molecular and cellular mechanisms / volume editors, G. Kollias, P.P. Sfikakis  2010 1
Tumor Necrosis Factors -- metabolism   3
Tumor Necrosis Factors -- physiology   4
Tumor Necrosis Factors -- therapeutic use : Therapeutic targets of the TNF superfamily / edited by Iqbal S. Grewal  2009 1
Tumor-Nekrose-Faktor : Death receptors and cognate ligands in cancer / Holger Kalthoff, ed  2009 1
 

Tumor, Nervous System -- See Nervous System Neoplasms


Benign and malignant neoplastic processes arising from or involving components of the central, peripheral, and autonomic nervous systems, cranial nerves, and meninges. Included in this category are primary and metastatic nervous system neoplasms
  1
 

Tumor, Neuroendocrine -- See Neuroendocrine Tumors


Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition
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Tumor of Rete Testis -- See Testicular Neoplasms


Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms
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Tumor, Osteosarcoma -- See Osteosarcoma


A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed)
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Tumor, Peripheral Nerve -- See Peripheral Nervous System Neoplasms


Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1)
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Tumor, Pineal -- See Pinealoma


Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
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Tumor, Pineal Gland -- See Pinealoma


Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
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Tumor, Pineal Parenchymal -- See Pinealoma


Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
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Tumor, Pituitary -- See Pituitary Neoplasms


Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA
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Tumor, Plasma Cell -- See Plasmacytoma


Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites
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Tumor progression -- See Cancer invasiveness


Here are entered works on the ability of cancer to infiltrate and actively destroy surrounding tissue. Works on the transfer of cancer to an organ or part of the body remote from the primary site are entered under Metastasis
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Tumor Promoters -- See Carcinogens


Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included
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Tumor promotion -- See Cocarcinogenesis


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  Tumor proteins -- 4 Related Subjects   4
Tumor proteins.   7
 

Tumor, Rectal -- See Rectal Neoplasms


Tumors or cancer of the RECTUM
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Tumor, Retinal -- See Retinal Neoplasms


Tumors or cancer of the RETINA
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Tumor, Rhabdoid -- See Rhabdoid Tumor


A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210)
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Tumor Royale -- See Neurofibroma, Plexiform


A type of neurofibroma manifesting as a diffuse overgrowth of subcutaneous tissue, usually involving the face, scalp, neck, and chest but occasionally occurring in the abdomen or pelvis. The tumors tend to progress, and may extend along nerve roots to eventually involve the spinal roots and spinal cord. This process is almost always a manifestation of NEUROFIBROMATOSIS 1. (From Adams et al., Principles of Neurology, 6th ed, p1016; J Pediatr 1997 Nov;131(5):678-82)
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Tumor, Spinal Cord -- See Spinal Cord Neoplasms


Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA
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  Tumor spread -- 2 Related Subjects   2
 

Tumor Staging -- See Neoplasm Staging


Methods which attempt to express in replicable terms the extent of the neoplasm in the patient
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Tumor Stem Cell -- See Neoplastic Stem Cells


Highly proliferative, self-renewing, and colony-forming stem cells which give rise to NEOPLASMS
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Tumor Stem Cells -- See Neoplastic Stem Cells


Highly proliferative, self-renewing, and colony-forming stem cells which give rise to NEOPLASMS
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Tumor Suppressing Gene -- See Genes, Tumor Suppressor


Genes that inhibit expression of the tumorigenic phenotype. They are normally involved in holding cellular growth in check. When tumor suppressor genes are inactivated or lost, a barrier to normal proliferation is removed and unregulated growth is possible
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  Tumor suppressing genes -- 2 Related Subjects   2
 

Tumor Suppressor Gene -- See Genes, Tumor Suppressor


Genes that inhibit expression of the tumorigenic phenotype. They are normally involved in holding cellular growth in check. When tumor suppressor genes are inactivated or lost, a barrier to normal proliferation is removed and unregulated growth is possible
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  Tumor suppressor genes -- 2 Related Subjects   2
Tumor Suppressor Protein p53   2
Tumor Suppressor Protein p53 -- analysis : P53 protocols / edited by Sumitra Deb and Swati Palit Deb  2013 1
Tumor Suppressor Protein p53 -- physiology : 25 years of p53 research / edited by Pierre Hainaut and Klas G. Wiman  2005 1
  Tumor suppressor proteins -- 3 Related Subjects   3
Tumor suppressor proteins.   8
Tumor Suppressor Proteins -- analysis   2
Tumor suppressor proteins -- Laboratory manuals : The retinoblastoma protein / edited by Pedro G. Santiago-Cardona  2018 1
Tumor Suppressor Proteins -- metabolism : SuperMEN1 : pituitary, parathyroid and pancreas / edited by Katalin Balogh, Attila Patocs  2009 1
Tumor Suppressor Proteins -- physiology : Tumor suppressor genes. Volume 223, Part 2, Regulation, function, and medicinal applications / edited by Wafik S. El-Deiry  2003 1
Tumor suppressor proteins -- Research   2
 

Tumor, Teratoid -- See Teratoma


A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642)
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Tumor, Unknown Primary -- See Neoplasms, Unknown Primary


Metastases in which the tissue of origin is unknown
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  Tumor vaccines -- 2 Related Subjects   2
 

Tumor Virus -- See Oncogenic Viruses


Viruses that produce tumors
  1
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