H. Francová

发表

Clinical effect of stereotyped B-cell receptor immunoglobulins in chronic lymphocytic leukaemia: a retrospective multicentre study.

Lefteris Angelis, Véronique Giudicelli, Marco Montillo, 2014, The Lancet. Haematology.

Prevalence of endothelial nitric oxide synthase gene polymorphisms in patients with atopic asthma

V. Znojil, H. Francová, L. Holla, 2002, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

A NEW APPROACH TO EVALUATING THE CHEMICAL MICRO-HETEROGENEITY OF A CONTINUOUSLY CAST STEEL SLAB NOV NA^IN OCENJEVANJA KEMIJSKE MIKROHETEROGENOSTI KONTINUIRNO ULITIH SLABOV

H. Francová, K. Stránský, J. Dobrovskâ, 2013 .

New promoter mutations in the low-density lipoprotein receptor gene which induce familial hypercholesterolaemia phenotype: Molecular and functional analysis

H. Francová, M. Trbušek, V. Kuhrová, 2004, Journal of Inherited Metabolic Disease.

Identification of somatic hypermutations in the TP53 gene in B-cell chronic lymphocytic leukemia.

Š. Pospíšilová, J. Šmardová, B. Tichy, 2008, Molecular immunology.

Inactivation of p53 and deletion of ATM in B-CLL patients in relation to IgVH mutation status and previous treatment

Š. Pospíšilová, J. Šmardová, D. Dvořáková, 2006, Leukemia.

Single cell analysis revealed a coexistence of NOTCH1 and TP53 mutations within the same cancer cells in chronic lymphocytic leukaemia patients

Š. Pospíšilová, J. Šmardová, L. Radová, 2017, British journal of haematology.

Multiple productive immunoglobulin heavy chain gene rearrangements in chronic lymphocytic leukemia are mostly derived from independent clones

Š. Pospíšilová, S. Pavlova, B. Tichy, 2014, Haematologica.

Spectrum of low density lipoprotein receptor mutations in Czech hypercholesterolemic patients

L. Kozák, L. Fajkusová, H. Francová, 2001, Human mutation.

The frequency of TP53 gene defects differs between chronic lymphocytic leukaemia subgroups harbouring distinct antigen receptors

K. Stamatopoulos, R. Rosenquist, Š. Pospíšilová, 2014, British journal of haematology.

Inactivation of p53 and amplification of MYCN gene in a terminal lymphoblastic relapse in a chronic lymphocytic leukemia patient.

Š. Pospíšilová, J. Šmardová, B. Tichy, 2009, Cancer genetics and cytogenetics.

Prenatal diagnosis of Smith-Lemli-Opitz syndrome by mutation analysis.

L. Kozák, H. Francová, D. Behúlová, 2000, American journal of medical genetics.

Specific p53 mutations do not impact results of alemtuzumab therapy among patients with chronic lymphocytic leukemia

Š. Pospíšilová, J. Šmardová, B. Tichy, 2012, Leukemia & lymphoma.

Fludarabine with cytarabine followed by reduced-intensity conditioning and allogeneic hematopoietic stem cell transplantation in patients with poor-risk chronic lymphocytic leukemia

Š. Pospíšilová, J. Chovancová, M. Navrátil, 2012, Annals of Hematology.

Determination of thermophysical properties of high temperature alloy IN713LC by thermal analysis

V. Matějka, V. Vodárek, K. Konečná, 2012, Journal of Thermal Analysis and Calorimetry.

INVESTIGATION INTO SEGREGATION OF SELECTED ELEMENTS IN THE BREAKOUT AREA OF A CONTINUOUSLY CAST STEEL SLAB

H. Francová, K. Michalek, K. Stránský, 2012 .

Experimental Analysis on the Causes of the Breakout of Continuous Cast Steel Slab

H. Francová, K. Stránský, B. Smetana, 2014 .

Galactosemia: deletion in the 5′ upstream region of the GALT gene reduces promoter efficiency

L. Kozák, H. Francová, M. Trbušek, 2001, Human Genetics.

Presence of a deletion in the 5′ upstream region of the GALT gene in Duarte (D2) alleles

L. Kozák, H. Francová, J. Macků, 1999, Journal of medical genetics.

Molecular evidence for antigen drive in the natural history of mantle cell lymphoma.

E. Campo, K. Stamatopoulos, R. Rosenquist, 2015, The American journal of pathology.

Missense mutations located in structural p53 DNA-binding motifs are associated with extremely poor survival in chronic lymphocytic leukemia.

Š. Pospíšilová, J. Šmardová, P. Dobes, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

DNA damage lymphocytic leukemia: selection, impact on survival, and response to gene in chronic TP53 Monoallelic and biallelic inactivation of

Š. Pospíšilová, J. Šmardová, B. Tichy, 2010 .

Not all IGHV3-21 chronic lymphocytic leukemias are equal: prognostic considerations.

Lefteris Angelis, Véronique Giudicelli, Marco Montillo, 2015, Blood.

High expression of lymphocyte-activation gene 3 (LAG3) in chronic lymphocytic leukemia cells is associated with unmutated immunoglobulin variable heavy chain region (IGHV) gene and reduced treatment-free survival.

Š. Pospíšilová, B. Tichy, H. Francová, 2010, The Journal of molecular diagnostics : JMD.

Liquidus and solidus temperatures and latent heats of melting of steels

P. Dostál, H. Francová, B. Smetana, 2016, Journal of Thermal Analysis and Calorimetry.

Practical Wisdom in Caring for Children with a Disability in the Czech Republic

H. Francová, Aleš Novotný, 2010 .

Conditions of taking care for seniors with reduced self-sufficiency in the context of contemporary changes

H. Francová, Aleš Novotný, 2009 .

Smith–Lemli–Opitz syndrome: Molecular-genetic analysis of ten families

L. Kozák, V. Jüttnerová, H. Francová, 2000, Journal of Inherited Metabolic Disease.

Investigation Of Influence Of Cooling Rate On Back Diffusion At Solidification Of Continuously Cast Steel Billet

H. Francová, J. Dobrovskâ, V. Dobrovská, 2010 .

The Influence of Heating/Cooling Rate on Transformation Temperatures of Co-Base Alloy

H. Francová, Z. Jonšta, B. Smetana, 2014 .

Mutation analysis of the GALT gene in Czech and Slovak galactosemia populations: Identification of six novel mutations, including a stop codon mutation (X380R)

L. Kozák, L. Fajkusová, H. Francová, 2000, Human mutation.

Germline mutations in the (cid:226) -catenin gene are not associated with the FAP phenotype without an APC mutation

L. Kozák, H. Francová, A. Pijáčková, 1999 .

Multiple productive IGH rearrangements denote oligoclonality even in immunophenotypically monoclonal CLL

Š. Pospíšilová, B. Tichy, K. Plevova, 2017, Leukemia.

Identification of mutations in the glucose‐6‐phosphatase gene in Czech and Slovak patients with glycogen storage disease type Ia, including novel mutations K76N, V166A and 540del5

L. Kozák, M. Elleder, H. Francová, 2000, Human mutation.