Adrian J. L. Clark

Overview

Best Publications

• Intrauterine Growth Retardation and Postnatal Growth Failure Associated with Deletion of the Insulin-Like Growth Factor I Gene

  Katie A. Woods;Cecilia Camacho-Hübner;Martin O. Savage;Adrian J.L. Clark

  1310
  Citations

• Linkage of the angiotensinogen gene to essential hypertension

  Mark Caulfield;Paul Lavender;Martin Farrall;Patricia Munroe

  849
  Citations

• Epigenetic Modification of the Renin-Angiotensin System in the Fetal Programming of Hypertension

  Irina Bogdarina;Simon Welham;Peter J. King;Shamus P. Burns

  601
  Citations

• Amplification and enhanced expression of the epidermal growth factor receptor gene in A431 human carcinoma cells

  Glenn T. Merlino;Young Hua Xu;Shunsuke Ishii;Adrian J.L. Clark

  467
  Citations

• Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2.

  Louise A Metherell;J Paul Chapple;Sadani Cooray;Alessia David

  458
  Citations

• Cloning and expression of cDNA encoding a rat adrenomedullin receptor.

  Supriya Kapas;Kevin J. Catt;Adrian J.L. Clark

  415
  Citations

• Cloning and expression of a novel angiotensin II receptor subtype.

  K. Sandberg;Hong Ji;A. J. L. Clark;H. Shapira

  378
  Citations

• DNA methylation and silencing of gene expression.

  John Newell-Price;Adrian J.L. Clark;Peter King

  378
  Citations

• Epidermal growth factor regulates the expression of its own receptor.

  Adrian J. L. Clark;Shunsuke Ishii;Nancy Richert;Glenn T. Merlino

  349
  Citations

• Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor.

  A.J.L. Clark;A. Grossman;L. McLoughlin

  345
  Citations

• Ligand-specific conformational change of the G-protein-coupled receptor ALX/FPR2 determines proresolving functional responses

  Sadani N. Cooray;Thomas Gobbetti;Trinidad Montero-Melendez;Simon McArthur

  324
  Citations

• Adrenocorticotropin Insensitivity Syndromes

  Adrian J. L. Clark;Angela Weber

  314
  Citations

• Loss of function of the melanocortin 2 receptor accessory protein 2 is associated with mammalian obesity.

  Masato Asai;Masato Asai;Shwetha Ramachandrappa;Maria Joachim;Yuan Shen

  309
  Citations

• Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene

  Katrin Handschug;Silke Sperling;Sung-Joo Kim Yoon;Steffen Hennig

  296
  Citations

• MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans

  Claire R. Hughes;Leonardo Guasti;Eirini Meimaridou;Chen-Hua Chuang

  269
  Citations

• Linkage of the angiotensinogen gene locus to human essential hypertension in African Caribbeans.

  M. Caulfield;P. Lavender;J. Newell-Price;M. Farrall

  265
  Citations

• Structure and localization of genes encoding aberrant and normal epidermal growth factor receptor RNAs from A431 human carcinoma cells

  G T Merlino;S Ishii;J Whang-Peng;T Knutsen

  263
  Citations

• A DNA Variant at the Angiotensin-Converting Enzyme Gene Locus Associates With Coronary Artery Disease in the Caerphilly Heart Study

  Raj K. Mattu;Edward W. A. Needham;David J. Galton;Evanthia Frangos

  256
  Citations

• Essential hypertension in African Caribbeans associates with a variant of the β2-adrenoceptor

  Peter Kotanko;Alexander Binder;Jacquie Tasker;Perry DeFreitas

  254
  Citations

• Osteosarcoma of the jaw.

  Vivek K. Unni;C Dahlin;Adrian J L Clark;D Devine

  0
  Citations