BADEMCI, GUNEY; LACHGAR-RUIZ, MARÍA; DEOKAR, MANGESH; ZAFEER, MOHAMMAD FARAZ; ABAD, CLEMER; BAYLAN, MUZEYYEN YILDIRIM; INGHAM, NEIL J.; CHEN, JING; SINENI, CLAIRE J.; VADGAMA, NIRMAL; KARAKIKES, IOANNIS; GUO, SHENGRU; DUMAN, DUYGU; SINGH, NITU; HARLALKA, GAURAV; JAIN, SHIRISH P.; CHIOZA, BARRY A.; WALZ, KATHERINA; STEEL, KAREN P.; NASIR, JAMAL; TEKIN, MUSTAFA

Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; Año: 2022 vol. 119

CHEN, XIAOYA; ABAD, CLEMER; CHEN, ZHENG-YI; YOUNG, JUAN I; GURUMURTHY, CHANNABASAVAIAH B; WALZ, KATHERINA; LIU, XUE ZHONG

Generation and characterization of a P2rx2 V60L mouse model for DFNA41

HUMAN MOLECULAR GENETICS; Año: 2021 vol. 30

MYERS, HECTOR F.; FAIR, ALECIA M.; VILLALTA, FERNANDO; WALZ, KATHERINA; BEECH, BETTINA M.; SCOTT, WILLIAM K.; HAAS, DAVID W.

Transdisciplinary Perspectives on Precision Medicine

Health Equity; Año: 2021 vol. 5 p. 288 - 298

KANNAN-SUNDHARI, ABHIRAAMI; ABAD, CLEMER; MALOOF, MARIE E.; AYAD, NAGI G.; YOUNG, JUAN I.; LIU, XUE ZHONG; WALZ, KATHERINA

Bromodomain Protein BRD4 Is Essential for Hair Cell Function and Survival

Frontiers in Cell and Developmental Biology; Año: 2020 vol. 8

LI, CHONG; BADEMCI, GUNEY; SUBASIOGLU, ASLI; DIAZ-HORTA, OSCAR; ZHU, YI; LIU, JIAQI; MITCHELL, TIMOTHY GAVIN; ABAD, CLEMER; SEYHAN, SERHAT; DUMAN, DUYGU; CENGIZ, FILIZ BASAK; TOKGOZ-YILMAZ, SUNA; BLANTON, SUSAN H.; FAROOQ, AMJAD; WALZ, KATHERINA; GRACE ZHAI, R.; TEKIN, MUSTAFA

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; Año: 2019 vol. 116 p. 1347 - 1352

VARON, ALBERTO; WHITT, ZACHARY; KALIKA, PAIGE M.; POTOCKI, LORRAINE; BARBOUTH, DEBORAH S.; WALZ, KATHERINA

Arnold-Chiari type 1 malformation in Potocki–Lupski syndrome

AMERICAN JOURNAL OF MEDICAL GENETICS PART A; Año: 2019 vol. 179 p. 1366 - 1370

WALZ, KATHERINA; SRIVASTAVA, ANAND K.; ABAD, CLEMER; RAO, NALINI R.

A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation

Biology (Basel); Año: 2018

BADEMCI, GUNEY; ABAD, CLEMER; INCESULU, ARMAGAN; RAD, ABOLFAZL; ALPER, OZGUL; KOLB, SUSANNE M.; CENGIZ, FILIZ B.; DIAZ-HORTA, OSCAR; SILAN, FATMA; MIHCI, ERCAN; OCAK, EMRE; NAJAFI, MARYAM; MAROOFIAN, REZA; YILMAZ, ELANUR; NUR, BANU G.; DUMAN, DUYGU; GUO, SHENGRU; SANT, DAVID W.; WANG, GAOFENG; MONJE, PAULA V.; HAAF, THOMAS; BLANTON, SUSAN H.; VONA, BARBARA; WALZ, KATHERINA; TEKIN, MUSTAFA

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

HUMAN GENETICS.; Año: 2018 vol. 137 p. 479 - 486

DIAZ-HORTA, OSCAR; ABAD, CLEMER; CENGIZ, FILIZ BASAK; BADEMCI, GUNEY; BLACKWELDER, PAT; WALZ, KATHERINA; TEKIN, MUSTAFA

Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientation

JOURNAL OF MOLECULAR MEDICINE (BERLIN, GERMANY); Año: 2018

WALZ, KATHERINA

Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain

FASEB JOURNAL; Lugar: Bethesda; Año: 2018

BADEMCI, GUNEY; ABAD, CLEMER; INCESULU, ARMAGAN; ELIAN, FAHED; REYAHI, AZADEH; DIAZ-HORTA, OSCAR; CENGIZ, FILIZ B; SINENI, CLAIRE J; SEYHAN, SERHAT; ATLI, EMINE IKBAL; BASMAK, HIKMET; DEMIR, SELMA; NIK, ALI MOUSSAVI; FOOTZ, TIM; GUO, SHENGRU; DUMAN, DUYGU; FITOZ, SUAT; GURKAN, HAKAN; BLANTON, SUSAN H; WALTER, MICHAEL A; CARLSSON, PETER; WALZ, KATHERINA; TEKIN, MUSTAFA

FOXF2 is required for cochlear development in humans and mice

HUMAN MOLECULAR GENETICS; Año: 2018

RAO, NALINI R.; ABAD, CLEMER; PEREZ, IRENE C.; SRIVASTAVA, ANAND K.; YOUNG, JUAN I.; WALZ, KATHERINA

Rai1 haploinsufficiency is associated with social abnormalities in mice

Biology; Año: 2017 vol. 6

DIAZ-HORTA, OSCAR; ABAD, CLEMER; SENNAROGLU, LEVENT; II, JOSEPH FOSTER; DESMIDT, ALEXANDRA; BADEMCI, GUNEY; TOKGOZ-YILMAZ, SUNA; DUMAN, DUYGU; CENGIZ, F. BASAK; GRATI, M'HAMED; FITOZ, SUAT; LIU, XUE Z.; FAROOQ, AMJAD; IMTIAZ, FAIQA; CURRALL, BENJAMIN B.; MORTON, CYNTHIA CASSON; NISHITA, MICHIRU; MINAMI, YASUHIRO; LU, ZHONGMIN; WALZ, KATHERINA; TEKIN, MUSTAFA

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; Año: 2016 vol. 113 p. 5993 - 5998

WALZ, KATHERINA; COHEN, DEVON; NEILSEN, PAUL M.; FOSTER, JOSEPH; BRANCATI, FRANCESCO; DEMIR, KORCAN; FISHER, RICHARD; MOFFAT, MICHELLE; VERBEEK, NIENKE E.; BJØRGO, KATHRINE; LO CASTRO, ADRIANA; CURATOLO, PAOLO; NOVELLI, GIUSEPPE; ABAD, CLEMER; LEI, CAO; ZHANG, LILY; DIAZ-HORTA, OSCAR; YOUNG, JUAN I.; CALLEN, DAVID F.; TEKIN, MUSTAFA

Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

HUMAN GENETICS.; Año: 2015 vol. 134 p. 181 - 190

GALLAGHER, DENIS; VORONOVA, ANASTASSIA; ZANDER, MARK A.; CANCINO, GONZALO I.; BRAMALL, ALEXA; KRAUSE, MATTHEW P.; ABAD, CLEMER; TEKIN, MUSTAFA; NEILSEN, PAUL M.; CALLEN, DAVID F.; SCHERER, STEPHEN W.; KELLER, GORDON M.; KAPLAN, DAVID R.; WALZ, KATHERINA; MILLER, FREDA D.

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development

DEVELOPMENTAL CELL; Año: 2015 vol. 32 p. 31 - 42

VORONOVA, ANASTASSIA; GALLAGHER, DENIS; ZANDER, MARK; CANCINO, GONZALO; BRAMALL, ALEXA; KRAUSE, M.P.; ABAD, C.; TEKIN, M.; NEILSEN, P.M.; CALLEN, D.F.; SCHERER, S.W.; KELLER, G.M.; KAPLAN, D.R.; WALZ, K.; MILLER, F.D.

Ankrd11 is a chromatin regulator involved in autism that is essential for neural development

SpringerPlus; Año: 2015 vol. 4 p. 1 - 32

FOSTER, J.; KAPOOR, S.; DIAZ-HORTA, O.; SINGH, A.; ABAD, C.; RASTOGI, A.; MOHARANA, R.; TEKELI, O.; WALZ, K.; TEKIN, MUSTAFA

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction

CLINICAL GENETICS; Año: 2014 vol. 86 p. 589 - 591

DIAZ-HORTA, OSCAR; SUBASIOGLU-UZAK, ASLI; GRATI, M'HAMED; DESMIDT, ALEXANDRA; FOSTER II, JOSEPH; CAO, LEI; BADEMCI, GUNEY; TOKGOZ-YILMAZ, SUNA; DUMAN, DUYGU; CENGIZ, F. BASAK; ABAD, CLEMER; MITTAL, RAHUL; BLANTON, SUSAN; LIU, XUE Z.; FAROOQ, AMJAD; WALZ, KATHERINA; LU, ZHONGMIN; TEKIN, MUSTAFA

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; Año: 2014 vol. 111 p. 9864 - 9868

CAO, LEI; MOLINA, JESSICA; ABAD, CLEMER; CARMONA-MORA, PAULINA; CÁRDENAS OYARZO, ARELI; YOUNG, JUAN I.; WALZ, KATHERINA

Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory

Human molecular genetics; Año: 2014 vol. 23 p. 1771 - 1782

WALZ, KATHERINA; YOUNG, JUAN I

The methyl binding domain containing protein MBD5 is a transcriptional regulator responsible for 2q23.1 deletion syndrome

Rare Diseases; Año: 2014 vol. 2

DROGUETT, ALEJANDRA; KRALL, PAOLA; BURGOS, M. EUGENIA; VALDERRAMA, GRACIELA; CARPIO, DANIEL; ARDILES, LEOPOLDO; RODRIGUEZ-DIEZ, RAQUEL; KERR, BREDFORD; WALZ, KATHERINA; RUIZ-ORTEGA, MARTA; EGIDO, JESUS; MEZZANO, SERGIO

Tubular overexpression of gremlin induces renal damage susceptibility in mice

PLOS ONE; Año: 2014 vol. 9

CAMARENA, VLADIMIR; CAO, LEI; ABAD, C.; ABRAMS, ALEXANDER; TOLEDO, YAIMA; ARAKI, K; ARAKI, M; WALZ, KATHERINA; YOUNG, JUAN I

Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.

EMBO MOLECULAR MEDICINE; Lugar: Londres; Año: 2014 vol. 6 p. 1003 - 1015

CANALES, CESAR P.; KRALL, PAOLA M.; KAIRATH, PAMELA; PEREZ, IRENE C.; FRAGOSO, MIRIAM; CARMONA-MORA, PAULINA; RUIZ, PHILLIP; REISER, JOCHEN; YOUNG, JUAN I.; WALZ, KATHERINA

Characterization of a Tprc6 transgenic mouse associated with early onset FSGS

British Journal of Medicine and Medical Research; Año: 2014 vol. 5

KISTLERA, ANDREAS D.; SINGH, GEETIKA; ALTINTAS, MEHMET M.; YU, HAO; FERNANDEZ, ISABEL C.; GU, CHANGKYU; WILSON, CORY; SRIVASTAVA, SANDEEP KUMAR; DIETRICH, ALEXANDER; WALZ, KATHERINA; KERJASCHKI, DONTSCHO; RUIZ, PHILLIP; DRYER, STUART; SEVER, SANJA; DINDA, AMIT K.; FAUL, CHRISTIAN; REISER, JOCHEN

Transient receptor potential channel 6 (trpc6) protects podocytes during complement-Mediated glomerular disease

JOURNAL OF BIOLOGICAL CHEMISTRY; Año: 2013 vol. 288 p. 36598 - 36609

BULUM, BURCU; ÖZÇAKAR, Z. BIRSIN; ÜSTÜNER, EVREN; DÜ?ÜNCELI, EBRU; KAVAZ, ASLI; DUMAN, DUYGU; WALZ, KATHERINA; FITOZ, SUAT; TEKIN, MUSTAFA; YALÇINKAYA, FATO?

High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT

PEDIATRIC NEPHROLOGY; Año: 2013 vol. 28 p. 2143 - 2147

VIEIRA, GUSTAVO H.; RODRIGUEZ, JAYSON D.; CARMONA-MORA, PAULINA; CAO, LEI; GAMBA, BRUNO F.; CARVALHO, DANIEL R.; DE REZENDE DUARTE, ANDRÉA; SANTOS, SUELY R.; DE SOUZA, DEISE H.; DUPONT, BARBARA R.; WALZ, KATHERINA; MORETTI-FERREIRA, DANILO; SRIVASTAVA, ANAND K.

Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith-Magenis syndrome

EUROPEAN JOURNAL OF HUMAN GENETICS; Año: 2012 vol. 20 p. 148 - 154

LACARIA, MELANIE; SAHA, PRADIP; POTOCKI, LORRAINE; BI, WEIMIN; YAN, JIONG; GIRIRAJAN, SANTHOSH; BURNS, BROOKE; ELSEA, SARAH; WALZ, KATHERINA; CHAN, LAWRENCE; LUPSKI, JAMES R.; GU, WENLI

A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men

PLOS GENETICS; Año: 2012 vol. 8

CARMONA-MORA, PAULINA; CANALES, CESAR P.; CAO, LEI; PEREZ, IRENE C.; SRIVASTAVA, ANAND K.; YOUNG, JUAN I.; WALZ, KATHERINA

RAI1 Transcription Factor Activity Is Impaired in Mutants Associated with Smith-Magenis Syndrome

PLOS ONE; Año: 2012 vol. 7

KERR, BREDFORD; SOTO C, JESSICA; SAEZ, MAURICIO; ABRAMS, ALEXANDER; WALZ, KATHERINA; YOUNG, JUAN I.

Transgenic complementation of MeCP2 deficiency: Phenotypic rescue of Mecp2-null mice by isoform-specific transgenes

EUROPEAN JOURNAL OF HUMAN GENETICS; Año: 2012 vol. 20 p. 69 - 76

GOH ES; PEREZ IC; CANALES, CESAR P.; RUIZ, PHILLIP; AGATEP R; YOON G; CHITAYAT D; DROR Y; SHAGO M; GOOBIE S; SGRO M; WALZ K; MENDOZA-LONDONO R

Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A; Lugar: New York; Año: 2012

CANALES, CESAR P.; WALZ, KATHERINA

Copy number variation and susceptibility to complex traits

EMBO MOLECULAR MEDICINE; Año: 2011 vol. 3 p. 1 - 4

CARMONA-MORA, PAULINA; WALZ, KATHERINA

Retinoic acid induced 1, RAI1: A dosage sensitive gene related to neurobehavioral alterations including autistic behavior

CURRENT GENOMICS; Año: 2010 vol. 11 p. 607 - 617

RICARD, GUÉNOLA; MOLINA, JESSICA; CHRAST, JACQUELINE; GU, WENLI; GHELDOF, NELE; PRADERVAND, SYLVAIN; SCHÜTZ, FRÉDÉRIC; YOUNG, JUAN I.; LUPSKI, JAMES R.; REYMOND, ALEXANDRE; WALZ, KATHERINA

Phenotypic consequences of copy number variation: Insights from smith-magenis and Potocki-Lupski syndrome mouse models

PLOS BIOLOGY; Año: 2010 vol. 8

KRALL, PAOLA; CANALES, CESAR P.; KAIRATH, PAMELA; CARMONA-MORA, PAULINA; MOLINA, JESSICA; CARPIO, J. DANIEL; RUIZ, PHILLIP; MEZZANO, SERGIO A.; LI, JING; WEI, CHANGLI; REISER, JOCHEN; YOUNG, JUAN I.; WALZ, KATHERINA

Podocyte-specific overexpression of wild type or mutant Trpc6 in mice is sufficient to cause glomerular disease

PLOS ONE; Año: 2010 vol. 5 p. 1 - 11

CARMONA-MORA, PAULINA; ENCINA, CAROLINA A.; CANALES, CESAR P.; CAO, LEI; MOLINA, JESSICA; KAIRATH, PAMELA; YOUNG, JUAN I.; WALZ, KATHERINA

Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome

BMC MOLECULAR BIOLOGY; Año: 2010 vol. 11

KERR, BREDFORD; SILVA, PAMELA A.; WALZ, KATHERINA; YOUNG, JUAN I.

Unconventional transcriptional response to environmental enrichment in a mouse model of rett syndrome

PLOS ONE; Año: 2010 vol. 5

ALVAREZ-SAAVEDRA, MATÍAS; CARRASCO, LORETO; SURA-TRUEBA, SYLVIA; AIELLO, VERA DEMARCHI; WALZ, KATHERINA; NETO, JOSÉ XAVIER; YOUNG, JUAN I.

Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

HUMAN MOLECULAR GENETICS; Año: 2010 vol. 19 p. 2177 - 2190

SCHEIHING, RODRIGO; CARDENAS, LEYLA; NESPOLO, ROBERTO F.; KRALL, PAOLA; WALZ, KATHERINA; KOHSHIMA, SHIRO; LABARCA, PEDRO

Morphological and molecular analysis of centropagids from the high Andean plateau (Copepoda: Calanoidea)

HYDROBIOLOGIA; Año: 2010 vol. 637 p. 45 - 52

CARMONA-MORA, P.; MOLINA, J.; ENCINA, C.A.; WALZ, K.

Mouse models of genomic syndromes as tools for understanding the basis of complex traits: An example with the Smith-Magenis and the Potocki-Lupski syndromes

CURRENT GENOMICS; Año: 2009 vol. 10 p. 259 - 268

MOLINA, JESSICA; CARMONA-MORA, PAULINA; CHRAST, JACQUELINE; KRALL, PAOLA M.; CANALES, CÉSAR P.; LUPSKI, JAMES R.; REYMOND, ALEXANDRE; WALZ, KATHERINA

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome

HUMAN MOLECULAR GENETICS; Año: 2008 vol. 17 p. 2486 - 2495

WALZ, KATHERINA; PAYLOR, RICHARD; YAN, JIONG; BI, WEIMIN; LUPSKI, JAMES R.

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2)

JOURNAL OF CLINICAL INVESTIGATION; Año: 2006 vol. 116 p. 3035 - 3041

GOLDMAN, ALICIA M.; POTOCKI, LORRAINE; WALZ, KATHERINA; LYNCH, JENNIFER K.; GLAZE, DANIEL G.; LUPSKI, JAMES R.; NOEBELS, JEFFREY L.

Epilepsy and chromosomal rearrangements in Smith-Magenis syndrome [del(17)(p11.2p11.2)]

JOURNAL OF CHILD NEUROLOGY; Año: 2006 vol. 21 p. 93 - 98

YAN, JIONG; KEENER, VICTORIA W.; BI, WEIMIN; WALZ, KATHERINA; BRADLEY, ALLAN; JUSTICE, MONICA J.; LUPSKI, JAMES R.

Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome

HUMAN MOLECULAR GENETICS; Año: 2004 vol. 13 p. 2613 - 2624

BI, WEIMIN; SAIFI, G. MUSTAFA; SHAW, CHRISTINE J.; WALZ, KATHERINA; FONSECA, PATRICIA; WILSON, MEREDITH; POTOCKI, LORRAINE; LUPSKI, JAMES R.

Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

HUMAN GENETICS.; Año: 2004 vol. 115 p. 515 - 524

WALZ, KATHERINE; SPENCER, CORINNE; KAASIK, KRISTA; LEE, CHENG C.; LUPSKI, JAMES R.; PAYLOR, RICHARD

Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2)

HUMAN MOLECULAR GENETICS; Año: 2004 vol. 13 p. 367 - 378

WALZ, KATHERINA; FONSECA, PATRICIA; LUPSKI, JAMES R.

Animal models for human contiguous gene syndromes and other genomic disorders

GENETICS AND MOLECULAR BIOLOGY; Año: 2004 vol. 27 p. 305 - 320

ZELADA, ALICIA; DE SOUZA, FLÁVIO S.J.; WALZ, KATHERINA; GIASSON, LUC; PASSERON, SUSANA

cDNA cloning, biochemical and phylogenetic characterization of β- and β' -subunits of Candida albicans protein kinase CK2

YEAST; Año: 2003 vol. 20 p. 471 - 478

STANKIEWICZ P; INOUE K; BI W; WALZ K; PARK SS; KUROTAKI N; SHAW CJ; FONSECA P; YAN J; LEE JA; KHAJAVI M; LUPSKI JR

Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits.

Cold Spring Harb Symp Quant Biol; Año: 2003

WALZ K; CARATINI-RIVERA S; BI W; FONSECA P; MANSOURI DL; LYNCH J; VOGEL H; NOEBELS JL; BRADLEY A; LUPSKI JR

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

MOLECULAR AND CELLULAR BIOLOGY; Lugar: Washington; Año: 2003

YAN J; WALZ K; NAKAMURA H; CARATINI-RIVERA S; ZHAO Q; VOGEL H; WEI N; JUSTICE MJ; BRADLEY A; LUPSKI JR

COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast.

MOLECULAR AND CELLULAR BIOLOGY; Lugar: Washington; Año: 2003

BI, WEIMIN; YAN, JIONG; STANKIEWICZ, PAWE; PARK, SUNG-SUP; WALZ, KATHERINA; BOERKOEL, CORNELIUS F.; POTOCKI, LORRAINE; SHAFFER, LISA G.; DEVRIENDT, KOEN; NOWACZYK, MAGORZATA J. M.; INOUE, KEN; LUPSKI, JAMES R.

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse

GENOME RESEARCH; Año: 2002 vol. 12 p. 713 - 728

PARDO, PATRICIA S.; MURRAY, PEDRO FERNÁNDEZ; WALZ, KATHERINA; FRANCO, LORENA; PASSERON, SUSANA

In vivo and in vitro phosphorylation of the α7/PRS1 subunit of Saccharomyces cerevisiae 20 S proteasome: In vitro phosphorylation by protein kinase CK2 is absolutely dependent on polylysine

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS; Año: 1998 vol. 349 p. 397 - 401

WALZ, KATHERINA; PARDO, PATRICIA S.; PASSERON, SUSANA

Purification and characterization of protein kinase CK2 from Candida albicans: Evidence for the presence of two distinct regulatory subunits β and β'

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS; Año: 1997 vol. 340 p. 347 - 354

BIONDI, RICARDO M.; WALZ, KATHERINA; ISSINGER, OLAF-GEORG; ENGEL, MATTHIAS; PASSERON, SUSANA

Discrimination between acid and alkali-labile phosphorylated residues on Immobilon: Phosphorylation studies of nucleoside diphosphate kinase

ANALYTICAL BIOCHEMISTRY; Año: 1996 vol. 242 p. 165 - 171

BIONDI, RICARDO M.; VERON, MICHEL; WALZ, KATHERINA; PASSERON, SUSANA

Candida albicans nucleoside-diphosphate kinase: Purification and characterization

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS; Año: 1995 vol. 323 p. 187 - 194