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  • Breast cancer is a disease in which certain cells in the breast become abnormal and multiply
  • with a high risk of developing ovarian cancer, breast cancer, and several other types of cancer in
  • blocks of proteins) is associated with several types of cancer, such as those that occur in the breast
  • are associated with an increased risk of breast cancer in both men and women, as well as several other
  • are associated with an increased risk of breast cancer in both men and women, as well as several other
  • of breast cancer in women that begins in the milk-producing glands (lobular breast cancer); prostate
  • Prostate cancer is a common disease that affects men, usually in middle age or later. In this
  • Bladder cancer is a disease in which certain cells in the bladder become abnormal and multiply
  • Lung cancer is a disease in which certain cells in the lungs become abnormal and multiply
  • particularly cancers of the breast, a gland in the lower neck called the thyroid, and the lining of the uterus
  • Found in name or synonym: serologically defined breast cancer antigen NY-BR-85
  • Lynch syndrome, often called hereditary nonpolyposis colorectal cancer (HNPCC), is an inherited
  • Fraumeni syndrome include breast cancer, a form of bone cancer called osteosarcoma, and cancers of soft
  • Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a disorder in which affected individuals
  • Inherited mutations in the PTEN gene increase the risk of developing breast cancer. In many cases
  • Found in name or synonym: cancer antigen 15-3
  • Familial adenomatous polyposis (FAP) is an inherited disorder characterized by cancer of the large
  • the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double
  • Alterations in the activity (expression) of the SEPT9 gene are associated with certain cancers. The
  • growth in breast cancer and is a valuable biomarker for breast cancer. [provided by RefSeq, Jan 2009]
  • Related term: autosomal recessive colorectal cancer
  • higher risk of breast cancer. Alternatively spliced transcript variants encoding different isoforms have
  • be involved in several types of cancer, including breast cancer and melanoma. Alternative splicing
  • apoptosis. This gene is located in a chromosomal region known to be amplified in breast cancer. The
  • alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur
  • Inherited mutations in the CDH1 gene increase a woman's risk of developing a form of breast cancer
  • BRCT (breast cancer carboxy-terminal) domains. This protein plays a critical role in maintaining genome
  • colocalizes with the breast cancer 2 early onset protein (BRCA2) in nuclear foci and likely permits the stable
  • homozygous MLH1 gene mutation have a syndrome distinct from Lynch syndrome. In addition to colorectal cancer
  • with inherited mutations in the MSH2 gene. Lynch syndrome increases the risk of many types of cancer
  • colorectal cancers, as well as other cancerous tumors. This deletion is not inherited and is found only in
  • DICER1 syndrome is an inherited disorder that increases the risk of a variety of cancerous and
  • osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers
  • an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been
  • deleted in breast and prostrate cancer. The second intron contains an apparently intronless gene, C16orf3
  • and breast cancers. Multiple transcript variants due to alternative promoters and alternative splicing
  • breast cancer, endometrial cancer, and osteoporosis. Alternative promoter usage and alternative splicing
  • lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the
  • are involved in the removal of ubiquitin from proteins. The encoded enzyme binds to the breast cancer
  • Inherited changes in the STK11 gene greatly increase the risk of developing breast cancer, as well
  • Inherited changes in the TP53 gene greatly increase the risk of developing breast cancer, as well
  • developing breast cancer and ovarian cancer. Variations in other genes, such as BARD1 and BRIP1, also
  • may be involved in breast cancer, and its protein signaling is likely a molecular switch that governs
  • lung, ovarian and breast cancers. Alternative splicing of this gene results in multiple transcript
  • disease states, including schizophrenia, bipolar disorder, depression, and breast cancer. Alternative
  • play a role in breast cancer. Alternatively spliced transcript variants encoding multiple isoforms have
  • breast cancer 1) protein and and the ATM (ataxia telangiectasia mutated) protein. ATM is thought to be a
  • associated with medulloblastomas, secretory breast carcinomas and other cancers. Several transcript variants
  • specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also
  • of heterozygosity of this gene is implicated in breast cancer.[provided by RefSeq, Sep 2009]

Viewing: Health Conditions

  • Breast cancer is a disease in which certain cells in the breast become abnormal and multiply
  • with a high risk of developing ovarian cancer, breast cancer, and several other types of cancer in
  • of breast cancer in women that begins in the milk-producing glands (lobular breast cancer); prostate
  • Prostate cancer is a common disease that affects men, usually in middle age or later. In this
  • Bladder cancer is a disease in which certain cells in the bladder become abnormal and multiply
  • Lung cancer is a disease in which certain cells in the lungs become abnormal and multiply
  • particularly cancers of the breast, a gland in the lower neck called the thyroid, and the lining of the uterus
  • Lynch syndrome, often called hereditary nonpolyposis colorectal cancer (HNPCC), is an inherited
  • Fraumeni syndrome include breast cancer, a form of bone cancer called osteosarcoma, and cancers of soft
  • Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a disorder in which affected individuals
  • Familial adenomatous polyposis (FAP) is an inherited disorder characterized by cancer of the large
  • DICER1 syndrome is an inherited disorder that increases the risk of a variety of cancerous and

Viewing: Genes

  • blocks of proteins) is associated with several types of cancer, such as those that occur in the breast
  • are associated with an increased risk of breast cancer in both men and women, as well as several other
  • are associated with an increased risk of breast cancer in both men and women, as well as several other
  • Found in name or synonym: serologically defined breast cancer antigen NY-BR-85
  • Inherited mutations in the PTEN gene increase the risk of developing breast cancer. In many cases
  • Found in name or synonym: cancer antigen 15-3
  • the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double
  • Alterations in the activity (expression) of the SEPT9 gene are associated with certain cancers. The
  • growth in breast cancer and is a valuable biomarker for breast cancer. [provided by RefSeq, Jan 2009]
  • Related term: autosomal recessive colorectal cancer
  • higher risk of breast cancer. Alternatively spliced transcript variants encoding different isoforms have
  • be involved in several types of cancer, including breast cancer and melanoma. Alternative splicing
  • apoptosis. This gene is located in a chromosomal region known to be amplified in breast cancer. The
  • alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur
  • Inherited mutations in the CDH1 gene increase a woman's risk of developing a form of breast cancer
  • BRCT (breast cancer carboxy-terminal) domains. This protein plays a critical role in maintaining genome
  • colocalizes with the breast cancer 2 early onset protein (BRCA2) in nuclear foci and likely permits the stable
  • homozygous MLH1 gene mutation have a syndrome distinct from Lynch syndrome. In addition to colorectal cancer
  • with inherited mutations in the MSH2 gene. Lynch syndrome increases the risk of many types of cancer
  • colorectal cancers, as well as other cancerous tumors. This deletion is not inherited and is found only in
  • osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers
  • an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been
  • deleted in breast and prostrate cancer. The second intron contains an apparently intronless gene, C16orf3
  • and breast cancers. Multiple transcript variants due to alternative promoters and alternative splicing
  • breast cancer, endometrial cancer, and osteoporosis. Alternative promoter usage and alternative splicing
  • lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the
  • are involved in the removal of ubiquitin from proteins. The encoded enzyme binds to the breast cancer
  • Inherited changes in the STK11 gene greatly increase the risk of developing breast cancer, as well
  • Inherited changes in the TP53 gene greatly increase the risk of developing breast cancer, as well
  • may be involved in breast cancer, and its protein signaling is likely a molecular switch that governs
  • lung, ovarian and breast cancers. Alternative splicing of this gene results in multiple transcript
  • disease states, including schizophrenia, bipolar disorder, depression, and breast cancer. Alternative
  • play a role in breast cancer. Alternatively spliced transcript variants encoding multiple isoforms have
  • breast cancer 1) protein and and the ATM (ataxia telangiectasia mutated) protein. ATM is thought to be a
  • associated with medulloblastomas, secretory breast carcinomas and other cancers. Several transcript variants
  • specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also
  • of heterozygosity of this gene is implicated in breast cancer.[provided by RefSeq, Sep 2009]

Viewing: Help Me Understand Genetics