Pituitary adenomas represent one of the key features of multiple endocrine neoplasia type 1. The gene involved in this syndrome (MEN1) is a putative tumor suppressor, that codes for a 610-amino acid nuclear protein termed 'menin'. Analyses of sporadic pituitary adenomas have so far failed to reveal MEN1 mutations or defects in MEN1 transcription in these tumors. In the present study we detected menin protein expression in a panel of normal and tumoral pituitary tissues, using a monoclonal antibody against the carboxy-terminus of menin. In the normal human pituitary gland, strong nuclear staining for menin was detectable in the majority of the endocrine cells of the anterior lobe, without a clear association with a particular hormone-produci...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple endocrine neoplasia–type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple Endocrine Neoplasia type 1 (MEN 1) is an autosomal dominant syndrome characterized by neopl...
OBJECTIVE: Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant inherited disorder c...
(Correspondence should be addressed to A B Grossman) Objective: Multiple endocrine neoplasia type 1 ...
Multiple endocrine neoplasia type 1 (MEN1) is an inherited cancer predisposition syndrome typified b...
Multiple endocrine neoplasia type 1 (MEN1), among all syndromes, causes tumors in the highest number...
Loss of menin, a tumor suppressor coded by the MEN1 gene, is a key factor in the pathogenesis of mul...
Pancreatic endocrine tumors (PETs) may be part of hereditary multiple endocrine neoplasia type-1 (ME...
non disponibilePancreatic endocrine tumors (PETs) are rare neoplasms of complex entity that can ari...
The multiple endocrine neoplasia type 1 (MEN1, OMIM 131 100) syndrome is an autosomal dominant trait...
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal-dominant inherited tumor syndrome charac...
Pituitary adenomas are a common manifestation of multiple endocrine neoplasia type 1 (MEN1) but most...
The imprinted gene, neuronatin (NNAT), is one of the most abundant transcripts in the pituitary and ...
Mutations of the multiple endocrine neoplasia type 1 (MEN1) gene lead to loss of function of its pro...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple endocrine neoplasia–type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple Endocrine Neoplasia type 1 (MEN 1) is an autosomal dominant syndrome characterized by neopl...
OBJECTIVE: Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant inherited disorder c...
(Correspondence should be addressed to A B Grossman) Objective: Multiple endocrine neoplasia type 1 ...
Multiple endocrine neoplasia type 1 (MEN1) is an inherited cancer predisposition syndrome typified b...
Multiple endocrine neoplasia type 1 (MEN1), among all syndromes, causes tumors in the highest number...
Loss of menin, a tumor suppressor coded by the MEN1 gene, is a key factor in the pathogenesis of mul...
Pancreatic endocrine tumors (PETs) may be part of hereditary multiple endocrine neoplasia type-1 (ME...
non disponibilePancreatic endocrine tumors (PETs) are rare neoplasms of complex entity that can ari...
The multiple endocrine neoplasia type 1 (MEN1, OMIM 131 100) syndrome is an autosomal dominant trait...
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal-dominant inherited tumor syndrome charac...
Pituitary adenomas are a common manifestation of multiple endocrine neoplasia type 1 (MEN1) but most...
The imprinted gene, neuronatin (NNAT), is one of the most abundant transcripts in the pituitary and ...
Mutations of the multiple endocrine neoplasia type 1 (MEN1) gene lead to loss of function of its pro...
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple endocrine neoplasia–type 1 (MEN1) is an autosomal dominant familial cancer syndrome charact...
Multiple Endocrine Neoplasia type 1 (MEN 1) is an autosomal dominant syndrome characterized by neopl...