4.8 Article

Germ-line mutations in WDR77 predispose to familial papillary thyroid cancer

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Multidisciplinary Sciences

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun et al.

Summary: The TOPMed program aims to study the genetic architecture and biology of heart, lung, blood, and sleep disorders to improve diagnosis, treatment, and prevention of these diseases. Resources include a variant browser, genotype imputation server, and genomic and phenotypic data available through dbGaP. The study detected a large number of rare genetic variants, providing insights into mutation processes and recent human evolutionary history.

NATURE (2021)

Article Endocrinology & Metabolism

A Germline CHEK2 Mutation in a Family with Papillary Thyroid Cancer

Yanyang Zhao et al.

THYROID (2020)

Article Multidisciplinary Sciences

The mutational constraint spectrum quantified from variation in 141,456 humans

Konrad J. Karczewski et al.

NATURE (2020)

Article Biochemistry & Molecular Biology

CADD: predicting the deleteriousness of variants throughout the human genome

Philipp Rentzsch et al.

NUCLEIC ACIDS RESEARCH (2019)

Article Biochemistry & Molecular Biology

COSMIC: the Catalogue Of Somatic Mutations In Cancer

John G. Tate et al.

NUCLEIC ACIDS RESEARCH (2019)

Article Oncology

Incidence and mortality of thyroid cancer in China, 2008-2012

Lingbin Du et al.

CHINESE JOURNAL OF CANCER RESEARCH (2019)

Article Medicine, General & Internal

Trends in Thyroid Cancer Incidence and Mortality in the United States, 1974-2013

Hyeyeun Lim et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2017)

Review Oncology

Familial non-medullary thyroid cancer: unraveling the genetic maze

Samantha Peiling Yang et al.

ENDOCRINE-RELATED CANCER (2016)

Article Medicine, General & Internal

Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer

Sudheer Kumar Gara et al.

NEW ENGLAND JOURNAL OF MEDICINE (2015)

Article Biochemistry & Molecular Biology

Loss of the Androgen Receptor Cofactor p44/WDR77 Induces Astrogliosis

Bryce Vincent et al.

MOLECULAR AND CELLULAR BIOLOGY (2012)

Article Biochemistry & Molecular Biology

SIFT web server: predicting effects of amino acid substitutions on proteins

Ngak-Leng Sim et al.

NUCLEIC ACIDS RESEARCH (2012)

Article Multidisciplinary Sciences

Crystal structure of the human PRMT5:MEP50 complex

Stephen Antonysamy et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)

Article Endocrinology & Metabolism

Familial Follicular Cell-Derived Thyroid Carcinoma

Eun Ju Son et al.

Frontiers in Endocrinology (2012)

Article Biochemistry & Molecular Biology

Predicting the functional impact of protein mutations: application to cancer genomics

Boris Reva et al.

NUCLEIC ACIDS RESEARCH (2011)

Letter Biochemical Research Methods

A method and server for predicting damaging missense mutations

Ivan A. Adzhubei et al.

NATURE METHODS (2010)

Article Endocrinology & Metabolism

Familial Nonmedullary Thyroid Cancer: A Review of the Genetics

Ayesha Khan et al.

THYROID (2010)

Article Multidisciplinary Sciences

Distinct nuclear and cytoplasmic functions of androgen receptor cofactor p44 and association with androgen-independent prostate cancer

Yi Peng et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Medicine, General & Internal

Cancer as a complex phenotype: Pattern of cancer distribution within and beyond the nuclear family

LT Amundadottir et al.

PLOS MEDICINE (2004)

Article Genetics & Heredity

Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21

JD McKay et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)