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Items: 1 to 50 of 308

1.

Memory CD4+ T cells lacking expression of CCR7 promote pro-inflammatory cytokine production in patients with diffuse cutaneous systemic sclerosis.

Almanzar G, Schmalzing M, Klein M, Hilligardt D, Morris P, Höfner K, Hajj NE, Kneitz H, Wild V, Rosenwald A, Benoit S, Hamm H, Tony HP, Haaf T, Goebeler M, Prelog M.

Eur J Dermatol. 2019 Oct 1;29(5):468-476. doi: 10.1684/ejd.2019.3645.

PMID:
31789272
2.

Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia.

Kariminejad A, Szenker-Ravi E, Lekszas C, Tajsharghi H, Moslemi AR, Naert T, Tran HT, Ahangari F, Rajaei M, Nasseri M, Haaf T, Azad A, Superti-Furga A, Maroofian R, Ghaderi-Sohi S, Najmabadi H, Abbaszadegan MR, Vleminckx K, Nikuei P, Reversade B.

Am J Hum Genet. 2019 Dec 5;105(6):1294-1301. doi: 10.1016/j.ajhg.2019.10.013. Epub 2019 Nov 21.

PMID:
31761294
3.

Genome-wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine-phosphate-guanine methylation and histological subtypes.

Fiedler D, Hirsch D, El Hajj N, Yang HH, Hu Y, Sticht C, Nanda I, Belle S, Rueschoff J, Lee MP, Ried T, Haaf T, Gaiser T.

Genes Chromosomes Cancer. 2019 Nov;58(11):783-797. doi: 10.1002/gcc.22787. Epub 2019 Aug 10.

PMID:
31334584
4.

Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss.

Hofrichter MAH, Doll J, Habibi H, Enayati S, Vahidi Mehrjardi MY, Müller T, Dittrich M, Haaf T, Vona B.

Eur J Med Genet. 2019 Oct;62(10):103724. doi: 10.1016/j.ejmg.2019.103724. Epub 2019 Jul 14.

5.

Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.

Maierhofer A, Flunkert J, Oshima J, Martin GM, Poot M, Nanda I, Dittrich M, Müller T, Haaf T.

Aging Cell. 2019 Oct;18(5):e12995. doi: 10.1111/acel.12995. Epub 2019 Jul 1.

6.

Male obesity effects on sperm and next-generation cord blood DNA methylation.

Potabattula R, Dittrich M, Schorsch M, Hahn T, Haaf T, El Hajj N.

PLoS One. 2019 Jun 27;14(6):e0218615. doi: 10.1371/journal.pone.0218615. eCollection 2019.

7.

A Note from the New Editor.

Haaf T, Nanda I.

Cytogenet Genome Res. 2019;158(2):55. doi: 10.1159/000501440. Epub 2019 Jun 26. No abstract available.

8.

Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report.

Lekszas C, Nanda I, Vona B, Böck J, Ashrafzadeh F, Donyadideh N, Ebrahimzadeh F, Ahangari N, Maroofian R, Karimiani EG, Haaf T.

BMC Med Genomics. 2019 Jun 7;12(1):83. doi: 10.1186/s12920-019-0539-y.

9.

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

Parsons MT, Tudini E, Li H, Hahnen E, Wappenschmidt B, Feliubadaló L, Aalfs CM, Agata S, Aittomäki K, Alducci E, Alonso-Cerezo MC, Arnold N, Auber B, Austin R, Azzollini J, Balmaña J, Barbieri E, Bartram CR, Blanco A, Blümcke B, Bonache S, Bonanni B, Borg Å, Bortesi B, Brunet J, Bruzzone C, Bucksch K, Cagnoli G, Caldés T, Caliebe A, Caligo MA, Calvello M, Capone GL, Caputo SM, Carnevali I, Carrasco E, Caux-Moncoutier V, Cavalli P, Cini G, Clarke EM, Concolino P, Cops EJ, Cortesi L, Couch FJ, Darder E, de la Hoya M, Dean M, Debatin I, Del Valle J, Delnatte C, Derive N, Diez O, Ditsch N, Domchek SM, Dutrannoy V, Eccles DM, Ehrencrona H, Enders U, Evans DG, Farra C, Faust U, Felbor U, Feroce I, Fine M, Foulkes WD, Galvao HCR, Gambino G, Gehrig A, Gensini F, Gerdes AM, Germani A, Giesecke J, Gismondi V, Gómez C, Gómez Garcia EB, González S, Grau E, Grill S, Gross E, Guerrieri-Gonzaga A, Guillaud-Bataille M, Gutiérrez-Enríquez S, Haaf T, Hackmann K, Hansen TVO, Harris M, Hauke J, Heinrich T, Hellebrand H, Herold KN, Honisch E, Horvath J, Houdayer C, Hübbel V, Iglesias S, Izquierdo A, James PA, Janssen LAM, Jeschke U, Kaulfuß S, Keupp K, Kiechle M, Kölbl A, Krieger S, Kruse TA, Kvist A, Lalloo F, Larsen M, Lattimore VL, Lautrup C, Ledig S, Leinert E, Lewis AL, Lim J, Loeffler M, López-Fernández A, Lucci-Cordisco E, Maass N, Manoukian S, Marabelli M, Matricardi L, Meindl A, Michelli RD, Moghadasi S, Moles-Fernández A, Montagna M, Montalban G, Monteiro AN, Montes E, Mori L, Moserle L, Müller CR, Mundhenke C, Naldi N, Nathanson KL, Navarro M, Nevanlinna H, Nichols CB, Niederacher D, Nielsen HR, Ong KR, Pachter N, Palmero EI, Papi L, Pedersen IS, Peissel B, Perez-Segura P, Pfeifer K, Pineda M, Pohl-Rescigno E, Poplawski NK, Porfirio B, Quante AS, Ramser J, Reis RM, Revillion F, Rhiem K, Riboli B, Ritter J, Rivera D, Rofes P, Rump A, Salinas M, Sánchez de Abajo AM, Schmidt G, Schoenwiese U, Seggewiß J, Solanes A, Steinemann D, Stiller M, Stoppa-Lyonnet D, Sullivan KJ, Susman R, Sutter C, Tavtigian SV, Teo SH, Teulé A, Thomassen M, Tibiletti MG, Tischkowitz M, Tognazzo S, Toland AE, Tornero E, Törngren T, Torres-Esquius S, Toss A, Trainer AH, Tucker KM, van Asperen CJ, van Mackelenbergh MT, Varesco L, Vargas-Parra G, Varon R, Vega A, Velasco Á, Vesper AS, Viel A, Vreeswijk MPG, Wagner SA, Waha A, Walker LC, Walters RJ, Wang-Gohrke S, Weber BHF, Weichert W, Wieland K, Wiesmüller L, Witzel I, Wöckel A, Woodward ER, Zachariae S, Zampiga V, Zeder-Göß C; KConFab Investigators, Lázaro C, De Nicolo A, Radice P, Engel C, Schmutzler RK, Goldgar DE, Spurdle AB.

Hum Mutat. 2019 Sep;40(9):1557-1578. doi: 10.1002/humu.23818.

10.

Assessing the epigenetic risks of assisted reproductive technologies: a way forward.

Zacchini F, Sampino S, Stankiewicz AM, Haaf T, Ptak GE.

Int J Dev Biol. 2019;63(3-4-5):217-222. doi: 10.1387/ijdb.180402gp.

PMID:
31058298
11.

The DNA methylation profile of human spermatogonia at single-cell- and single-allele-resolution refutes its role in spermatogonial stem cell function and germ cell differentiation.

Fend-Guella DL, von Kopylow K, Spiess AN, Schulze W, Salzbrunn A, Diederich S, El Hajj N, Haaf T, Zechner U, Linke M.

Mol Hum Reprod. 2019 Jun 6;25(6):283-294. doi: 10.1093/molehr/gaz017.

PMID:
30892608
12.

Submaximal heart rate seems inadequate to prescribe and monitor intensified training.

Ten Haaf T, Foster C, Meeusen R, Roelands B, Piacentini MF, van Staveren S, Koenderman L, de Koning JJ.

Eur J Sport Sci. 2019 Sep;19(8):1082-1091. doi: 10.1080/17461391.2019.1571112. Epub 2019 Feb 14.

PMID:
30763148
13.

Phenotypic Characterization of DFNB16-associated Hearing Loss.

Back D, Shehata-Dieler W, Vona B, Hofrichter MAH, Schroeder J, Haaf T, Rahne T, Hagen R, Schraven SP.

Otol Neurotol. 2019 Jan;40(1):e48-e55. doi: 10.1097/MAO.0000000000002059.

PMID:
30531641
14.

Expanding the clinical phenotype of IARS2-related mitochondrial disease.

Vona B, Maroofian R, Bellacchio E, Najafi M, Thompson K, Alahmad A, He L, Ahangari N, Rad A, Shahrokhzadeh S, Bahena P, Mittag F, Traub F, Movaffagh J, Amiri N, Doosti M, Boostani R, Shirzadeh E, Haaf T, Diodato D, Schmidts M, Taylor RW, Karimiani EG.

BMC Med Genet. 2018 Nov 12;19(1):196. doi: 10.1186/s12881-018-0709-3.

15.

The Arboranan Frogs: Results and Discussion.

Schmid M, Steinlein C, Haaf T, Feightinger W, Guttenbach M, Bogart JP, Gruber SL, Kasahara S, Kakampuy W, Del Pino EM, Carrillo AB, Romero-Carvajal A, Mahony M, King M, Duellman WE, Hedges SB.

Cytogenet Genome Res. 2018;155(1-4):55-221. doi: 10.1159/000489839. Epub 2018 Oct 17. No abstract available.

PMID:
30408794
16.

The Arboranan Frogs: Materials and Methods.

Schmid M, Steinlein C, Haaf T, Feightinger W, Guttenbach M, Bogart JP, Gruber SL, Kasahara S, Kakampuy W, Del Pino EM, Carrillo AB, Romero-Carvajal A, Mahony M, King M, Duellman WE, Hedges SB.

Cytogenet Genome Res. 2018;155(1-4):47-53. doi: 10.1159/000489541. Epub 2018 Oct 17. No abstract available.

PMID:
30408782
17.

The Arboranan Frogs: Introduction.

Schmid M, Steinlein C, Haaf T, Feightinger W, Guttenbach M, Bogart JP, Gruber SL, Kasahara S, Kakampuy W, Del Pino EM, Carrillo AB, Romero-Carvajal A, Mahony M, King M, Duellman WE, Hedges SB.

Cytogenet Genome Res. 2018;155(1-4):11-45. doi: 10.1159/000489540. Epub 2018 Oct 17. No abstract available.

PMID:
30408774
18.

Prenatal and postnatal experiences associated with epigenetic changes in the adult mouse brain.

Mattern F, Post A, Solger F, O'Leary A, Slattery DA, Reif A, Haaf T.

Behav Brain Res. 2019 Feb 1;359:143-148. doi: 10.1016/j.bbr.2018.10.037. Epub 2018 Oct 29.

19.

Multi-dimensional flow cytometry analysis reveals increasing changes in the systemic neutrophil compartment during seven consecutive days of endurance exercise.

van Staveren S, Ten Haaf T, Klöpping M, Hilvering B, Tinnevelt GH, de Ruiter K, Piacentini MF, Roelands B, Meeusen R, de Koning JJ, Jansen JJ, Vrisekoop N, Koenderman L.

PLoS One. 2018 Oct 30;13(10):e0206175. doi: 10.1371/journal.pone.0206175. eCollection 2018.

20.

Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors.

Potabattula R, Dittrich M, Böck J, Haertle L, Müller T, Hahn T, Schorsch M, Hajj NE, Haaf T.

Epigenomics. 2018 Oct;10(10):1315-1326. doi: 10.2217/epi-2018-0059. Epub 2018 Sep 21.

21.

DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.

Herrtwich L, Nanda I, Evangelou K, Nikolova T, Horn V, Sagar, Erny D, Stefanowski J, Rogell L, Klein C, Gharun K, Follo M, Seidl M, Kremer B, Münke N, Senges J, Fliegauf M, Aschman T, Pfeifer D, Sarrazin S, Sieweke MH, Wagner D, Dierks C, Haaf T, Ness T, Zaiss MM, Voll RE, Deshmukh SD, Prinz M, Goldmann T, Hölscher C, Hauser AE, Lopez-Contreras AJ, Grün D, Gorgoulis V, Diefenbach A, Henneke P, Triantafyllopoulou A.

Cell. 2018 Aug 23;174(5):1325-1326. doi: 10.1016/j.cell.2018.08.015. No abstract available.

22.

Cell Type and Species-specific Patterns in Neuronal and Non-neuronal Methylomes of Human and Chimpanzee Cortices.

Böck J, Remmele CW, Dittrich M, Müller T, Kondova I, Persengiev S, Bontrop RE, Ade CP, Kraus TFJ, Giese A, El Hajj N, Schneider E, Haaf T.

Cereb Cortex. 2018 Oct 1;28(10):3724-3739. doi: 10.1093/cercor/bhy180.

23.

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.

Bademci G, Abad C, Incesulu A, Rad A, Alper O, Kolb SM, Cengiz FB, Diaz-Horta O, Silan F, Mihci E, Ocak E, Najafi M, Maroofian R, Yilmaz E, Nur BG, Duman D, Guo S, Sant DW, Wang G, Monje PV, Haaf T, Blanton SH, Vona B, Walz K, Tekin M.

Hum Genet. 2018 Jul;137(6-7):479-486. doi: 10.1007/s00439-018-1901-4. Epub 2018 Jul 7.

24.

Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts.

Flunkert J, Maierhofer A, Dittrich M, Müller T, Horvath S, Nanda I, Haaf T.

Exp Cell Res. 2018 Sep 15;370(2):322-332. doi: 10.1016/j.yexcr.2018.06.034. Epub 2018 Jun 28.

25.

Hereditary hearing loss SNP-microarray pilot study.

Vona B, Hofrichter MAH, Schröder J, Shehata-Dieler W, Nanda I, Haaf T.

BMC Res Notes. 2018 Jun 14;11(1):391. doi: 10.1186/s13104-018-3466-7.

26.

The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family.

Hofrichter MAH, Mojarad M, Doll J, Grimm C, Eslahi A, Hosseini NS, Rajati M, Müller T, Dittrich M, Maroofian R, Haaf T, Vona B.

BMC Med Genet. 2018 May 18;19(1):81. doi: 10.1186/s12881-018-0598-5.

27.

Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patients.

Böck J, Appenzeller S, Haertle L, Schneider T, Gehrig A, Schröder J, Rost S, Wolf B, Bartram CR, Sutter C, Haaf T.

Int J Cancer. 2018 Sep 15;143(6):1416-1425. doi: 10.1002/ijc.31526. Epub 2018 Apr 25.

28.

Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer.

Hauke J, Horvath J, Groß E, Gehrig A, Honisch E, Hackmann K, Schmidt G, Arnold N, Faust U, Sutter C, Hentschel J, Wang-Gohrke S, Smogavec M, Weber BHF, Weber-Lassalle N, Weber-Lassalle K, Borde J, Ernst C, Altmüller J, Volk AE, Thiele H, Hübbel V, Nürnberg P, Keupp K, Versmold B, Pohl E, Kubisch C, Grill S, Paul V, Herold N, Lichey N, Rhiem K, Ditsch N, Ruckert C, Wappenschmidt B, Auber B, Rump A, Niederacher D, Haaf T, Ramser J, Dworniczak B, Engel C, Meindl A, Schmutzler RK, Hahnen E.

Cancer Med. 2018 Apr;7(4):1349-1358. doi: 10.1002/cam4.1376. Epub 2018 Mar 9.

29.

Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3.

Jansch C, Günther K, Waider J, Ziegler GC, Forero A, Kollert S, Svirin E, Pühringer D, Kwok CK, Ullmann R, Maierhofer A, Flunkert J, Haaf T, Edenhofer F, Lesch KP.

Stem Cell Res. 2018 Apr;28:136-140. doi: 10.1016/j.scr.2018.02.005. Epub 2018 Feb 13.

30.

Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family.

Vona B, Maroofian R, Mendiratta G, Croken M, Peng S, Ye X, Rezazadeh J, Bahena P, Lekszas C, Haaf T, Edelmann L, Shi L.

Mol Syndromol. 2017 Dec;9(1):5-14. doi: 10.1159/000480458. Epub 2017 Sep 22.

31.

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, Østergaard K, Möller C, Luxon L, Carr L, Wilson L, Rajput K, Sirimanna T, Harrop-Griffiths K, Rahman S, Vona B, Doll J, Haaf T, Bartsch O, Rosewich H, Moser T, Bitner-Glindzicz M.

Hum Genet. 2018 Mar;137(3):279-280. doi: 10.1007/s00439-018-1870-7.

PMID:
29435658
32.

The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, Østergaard K, Möller C, Luxon L, Carr L, Wilson L, Rajput K, Sirimanna T, Harrop-Griffiths K, Rahman S, Vona B, Doll J, Haaf T, Bartsch O, Rosewich H, Moser T, Bitner-Glindzicz M.

Hum Genet. 2018 Feb;137(2):111-127. doi: 10.1007/s00439-017-1862-z. Epub 2018 Jan 5. Erratum in: Hum Genet. 2018 Feb 12;:.

PMID:
29305691
33.

Changes in Choice Reaction Time During and After 8 Days Exhaustive Cycling Are Not Related to Changes in Physical Performance.

Ten Haaf T, van Staveren S, Iannetta D, Roelands B, Meeusen R, Piacentini MF, Foster C, Koenderman L, Daanen HAM, de Koning JJ.

Int J Sports Physiol Perform. 2018 Apr 1;13(4):428-433. doi: 10.1123/ijspp.2017-0218. Epub 2018 May 11.

PMID:
28872374
34.

Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals.

Haertle L, Maierhofer A, Böck J, Lehnen H, Böttcher Y, Blüher M, Schorsch M, Potabattula R, El Hajj N, Appenzeller S, Haaf T.

PLoS One. 2017 Aug 30;12(8):e0184030. doi: 10.1371/journal.pone.0184030. eCollection 2017.

35.

Epigenetic dysregulation of protocadherins in human disease.

El Hajj N, Dittrich M, Haaf T.

Semin Cell Dev Biol. 2017 Sep;69:172-182. doi: 10.1016/j.semcdb.2017.07.007. Epub 2017 Jul 8. Review.

36.

DNA methylation signatures in cord blood of ICSI children.

El Hajj N, Haertle L, Dittrich M, Denk S, Lehnen H, Hahn T, Schorsch M, Haaf T.

Hum Reprod. 2017 Aug 1;32(8):1761-1769. doi: 10.1093/humrep/dex209.

37.

Genetics of Tinnitus: Still in its Infancy.

Vona B, Nanda I, Shehata-Dieler W, Haaf T.

Front Neurosci. 2017 May 8;11:236. doi: 10.3389/fnins.2017.00236. eCollection 2017. Review.

38.

Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation.

Maierhofer A, Flunkert J, Dittrich M, Müller T, Schindler D, Nanda I, Haaf T.

PLoS One. 2017 May 10;12(5):e0177442. doi: 10.1371/journal.pone.0177442. eCollection 2017.

39.

Accelerated epigenetic aging in Werner syndrome.

Maierhofer A, Flunkert J, Oshima J, Martin GM, Haaf T, Horvath S.

Aging (Albany NY). 2017 Apr;9(4):1143-1152. doi: 10.18632/aging.101217.

40.

Epigenetic signatures of gestational diabetes mellitus on cord blood methylation.

Haertle L, El Hajj N, Dittrich M, Müller T, Nanda I, Lehnen H, Haaf T.

Clin Epigenetics. 2017 Mar 27;9:28. doi: 10.1186/s13148-017-0329-3. eCollection 2017.

41.

SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder.

Merker S, Reif A, Ziegler GC, Weber H, Mayer U, Ehlis AC, Conzelmann A, Johansson S, Müller-Reible C, Nanda I, Haaf T, Ullmann R, Romanos M, Fallgatter AJ, Pauli P, Strekalova T, Jansch C, Vasquez AA, Haavik J, Ribasés M, Ramos-Quiroga JA, Buitelaar JK, Franke B, Lesch KP.

J Child Psychol Psychiatry. 2017 Jul;58(7):798-809. doi: 10.1111/jcpp.12702. Epub 2017 Feb 22.

PMID:
28224622
42.

Gene expression and epigenetic aberrations in F1-placentas fathered by obese males.

Mitchell M, Strick R, Strissel PL, Dittrich R, McPherson NO, Lane M, Pliushch G, Potabattula R, Haaf T, El Hajj N.

Mol Reprod Dev. 2017 Apr;84(4):316-328. doi: 10.1002/mrd.22784. Epub 2017 Mar 3.

PMID:
28186371
43.

Paternal age effects on sperm FOXK1 and KCNA7 methylation and transmission into the next generation.

Atsem S, Reichenbach J, Potabattula R, Dittrich M, Nava C, Depienne C, Böhm L, Rost S, Hahn T, Schorsch M, Haaf T, El Hajj N.

Hum Mol Genet. 2016 Nov 15;25(22):4996-5005. doi: 10.1093/hmg/ddw328.

44.

Gene-specific profiling of DNA methylation and mRNA expression in bovine oocytes derived from follicles of different size categories.

Mattern F, Heinzmann J, Herrmann D, Lucas-Hahn A, Haaf T, Niemann H.

Reprod Fertil Dev. 2017 Sep;29(10):2040-2051. doi: 10.1071/RD16327.

PMID:
28152377
45.

DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.

Herrtwich L, Nanda I, Evangelou K, Nikolova T, Horn V, Sagar, Erny D, Stefanowski J, Rogell L, Klein C, Gharun K, Follo M, Seidl M, Kremer B, Münke N, Senges J, Fliegauf M, Aschman T, Pfeifer D, Sarrazin S, Sieweke MH, Wagner D, Dierks C, Haaf T, Ness T, Zaiss MM, Voll RE, Deshmukh SD, Prinz M, Goldmann T, Hölscher C, Hauser AE, Lopez-Contreras AJ, Grün D, Gorgoulis V, Diefenbach A, Henneke P, Triantafyllopoulou A.

Cell. 2016 Nov 17;167(5):1264-1280.e18. doi: 10.1016/j.cell.2016.09.054. Epub 2016 Oct 27. Erratum in: Cell. 2018 Aug 23;174(5):1325-1326.

46.

Reduction in energy expenditure during weight loss is higher than predicted based on fat free mass and fat mass in older adults.

Ten Haaf T, Verreijen AM, Memelink RG, Tieland M, Weijs PJM.

Clin Nutr. 2018 Feb;37(1):250-253. doi: 10.1016/j.clnu.2016.12.014. Epub 2016 Dec 23.

PMID:
28062083
47.

Disease Manifestation and Inflammatory Activity as Modulators of Th17/Treg Balance and RORC/FoxP3 Methylation in Systemic Sclerosis.

Almanzar G, Klein M, Schmalzing M, Hilligardt D, El Hajj N, Kneitz H, Wild V, Rosenwald A, Benoit S, Hamm H, Tony HP, Haaf T, Goebeler M, Prelog M.

Int Arch Allergy Immunol. 2016;171(2):141-154. doi: 10.1159/000450949. Epub 2016 Dec 1.

48.

Prediction of Functional Overreaching From Subjective Fatigue and Readiness to Train After Only 3 Days of Cycling.

Ten Haaf T, van Staveren S, Oudenhoven E, Piacentini MF, Meeusen R, Roelands B, Koenderman L, Daanen HAM, Foster C, de Koning JJ.

Int J Sports Physiol Perform. 2017 Apr;12(Suppl 2):S287-S294. doi: 10.1123/ijspp.2016-0404. Epub 2016 Nov 11.

PMID:
27834554
49.

DNA methylation and mRNA expression of developmentally important genes in bovine oocytes collected from donors of different age categories.

Mattern F, Herrmann D, Heinzmann J, Hadeler KG, Bernal-Ulloa SM, Haaf T, Niemann H.

Mol Reprod Dev. 2016 Sep;83(9):802-814. doi: 10.1002/mrd.22692. Epub 2016 Sep 20.

PMID:
27567027
50.

CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development.

Schneider E, Dittrich M, Böck J, Nanda I, Müller T, Seidmann L, Tralau T, Galetzka D, El Hajj N, Haaf T.

Gene. 2016 Oct 30;592(1):110-118. doi: 10.1016/j.gene.2016.07.058. Epub 2016 Jul 25.

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