List of works - Kati Donner

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy

scientific article

CRY2 genetic variants associate with dysthymia

scientific article

CYP2C9 genotype modifies activity of the renin-angiotensin-aldosterone system in hypertensive men.

scientific article published in October 2009

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

scientific article published on 01 December 1999

Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatment

scientific article published in May 2010

Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts

scientific article published in September 2004

Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128.

scientific article published on 24 July 2006

Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the <i>HNRNPA1</i> Gene

scientific article published on 27 October 2021

Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1.

scientific article published on 10 December 2012

Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide

scientific article published on 10 June 2013

Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

article

Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin

Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES Study

scientific article published on June 2008

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy

scientific article (publication date: February 2002)

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

scientific article

Mutations in the nebulin gene can cause severe congenital nemaline myopathy

scientific article published in October 2002

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

scientific article

Nebulin expression in patients with nemaline myopathy

scientific article published on 01 March 2001

Nebulin mutations in autosomal recessive nemaline myopathy: an update

scientific article published on 01 October 2002

Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES study

scientific article

STK39 variation predicts the ambulatory blood pressure response to losartan in hypertensive men.

scientific article

List of works by Kati Donner

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy

CRY2 genetic variants associate with dysthymia

CYP2C9 genotype modifies activity of the renin-angiotensin-aldosterone system in hypertensive men.

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatment

Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts

Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128.

Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the <i>HNRNPA1</i> Gene

Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1.

Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide

Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin

Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES Study

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Mutations in the nebulin gene can cause severe congenital nemaline myopathy

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

Nebulin expression in patients with nemaline myopathy

Nebulin mutations in autosomal recessive nemaline myopathy: an update

Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES study

STK39 variation predicts the ambulatory blood pressure response to losartan in hypertensive men.