Wilms' tumour 1 (WT1) in development, homeostasis and disease
ND Hastie - Development, 2017 - journals.biologists.com
The study of genes mutated in human disease often leads to new insights into biology as
well as disease mechanisms. One such gene is Wilms' tumour 1 (WT1), which plays multiple …
well as disease mechanisms. One such gene is Wilms' tumour 1 (WT1), which plays multiple …
Aniridia. A review
LB Nelson, GL Spaeth, TS Nowinski, CE Margo… - Survey of …, 1984 - Elsevier
Aniridia occurs as a phenotypically heterogeneous condition which may be inherited as an
autosomal dominant disorder or as part of several systemic syndromes. It has been linked …
autosomal dominant disorder or as part of several systemic syndromes. It has been linked …
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
Familial cancer syndromes have helped to define the role of tumor suppressor genes in the
development of cancer. The dominantly inherited Li-Fraumeni syndrome (LFS) is of …
development of cancer. The dominantly inherited Li-Fraumeni syndrome (LFS) is of …
[فهرست منابع][C] DeVita, Hellman, and Rosenberg's cancer: principles & practice of oncology
VT DeVita - 2008 - books.google.com
Acclaimed by the worldwide medical community as" a staple reference text in the medical
oncologist's library"(JAMA), DeVita, Hellman, and Rosenberg's Cancer: Principles and …
oncologist's library"(JAMA), DeVita, Hellman, and Rosenberg's Cancer: Principles and …
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
We have isolated a series of genomic and cDNA clones map** within the boundaries of
constitutional and tumor deletions that define the Wilms' tumor locus on human chromsome …
constitutional and tumor deletions that define the Wilms' tumor locus on human chromsome …
[HTML][HTML] A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
JA Trofatter, MM MacCollin, JL Rutter, JR Murrell… - Cell, 1993 - cell.com
Abstract Neurofibromatosis 2 (NF2) is a dominantly inherited disorder characterized by the
occurrence of bilateral vestibular schwannomas and other central nervous system tumors …
occurrence of bilateral vestibular schwannomas and other central nervous system tumors …
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
Denys-Drash syndrome is a rare human condition inwhich severe urogenital aberrations
result in renal fail ure, pseudohermaphroditism, and Wilms' tumor (neph roblastoma). To …
result in renal fail ure, pseudohermaphroditism, and Wilms' tumor (neph roblastoma). To …
[کتاب][B] Cancer cytogenetics: chromosomal and molecular genetic aberrations of tumor cells
S Heim, F Mitelman - 2015 - books.google.com
The first three editions of this acclaimed book presented a much-needed conceptual
synthesis of this rapidly moving field. Now, Cancer Cytogenetics, Fourth Edition, offers a …
synthesis of this rapidly moving field. Now, Cancer Cytogenetics, Fourth Edition, offers a …
Positional cloning and characterization of a paired box-and homeobox-containing gene from the aniridia region
Based on the map location of the aniridia (AN) locus in human chromosomal band 11~ 13,
we have cloned a candidate AN cDNA (Dl lS812E) that Is completely or partially deleted in …
we have cloned a candidate AN cDNA (Dl lS812E) that Is completely or partially deleted in …
The candidate Wilms' tumour gene is involved in genitourinary development
WILMS'tumour is an embryonic kidney tumour thought to arise through aberrant
mesenchymal stem cell differentiation1 and to result from loss of function of a'tumour …
mesenchymal stem cell differentiation1 and to result from loss of function of a'tumour …