Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1573-2592

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations ; day:19 ; month:1 ; year:2021 ; pages:1-13
Journal of clinical immunology ; (19.1.2021), 1-13

Creator: Giardino, Giuliana
Sharapova, Svetlana O.
Ciznar, Peter
Dhalla, Fatima
Maragliano, Luca
Radha Rama Devi, Akella
Islamoglu, Candan
Ikinciogullari, Aydan
Haskologlu, Sule
Dogu, Figen
Hanna-Wakim, Rima
Dbaibo, Ghassan
Chou, Janet
Cirillo, Emilia
Borzacchiello, Carla
Kreins, Alexandra Y.
Worth, Austen
Rota, Ioanna A.
Marques, José G.
Sayitoglu, Muge
Firtina, Sinem
Mahdi, Moaffaq
Geha, Raif
Neven, Bénédicte
Sousa, Ana E.
Benfenati, Fabio
Holländer, Georg A.
Davies, E. Graham
Pignata, Claudio

Contributor: SpringerLink (Online service)

DOI: 10.1007/s10875-021-00967-y

URN: urn:nbn:de:101:1-2021031020460469868161

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Giardino, Giuliana
Sharapova, Svetlana O.
Ciznar, Peter
Dhalla, Fatima
Maragliano, Luca
Radha Rama Devi, Akella
Islamoglu, Candan
Ikinciogullari, Aydan
Haskologlu, Sule
Dogu, Figen
Hanna-Wakim, Rima
Dbaibo, Ghassan
Chou, Janet
Cirillo, Emilia
Borzacchiello, Carla
Kreins, Alexandra Y.
Worth, Austen
Rota, Ioanna A.
Marques, José G.
Sayitoglu, Muge
Firtina, Sinem
Mahdi, Moaffaq
Geha, Raif
Neven, Bénédicte
Sousa, Ana E.
Benfenati, Fabio
Holländer, Georg A.
Davies, E. Graham
Pignata, Claudio
SpringerLink (Online service)

Other Objects (12)

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Hochschulschrift

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Hochschulschrift

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Hochschulschrift

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

G-banding and fluorescent-banding in sheep with heterozygous and homozygous translocation

Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report

CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout

Cre recombinase promotes leukemogenesis in the presence of both homozygous and heterozygous FLT3-ITD

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease

Decrypting the role of TBK1 in ageing: characterization of mice with a heterozygous or homozygous TBK1 deletion

Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

“Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”

Bone Turnover in Homozygous β2-Microglobulin Knock-Out Mice Does not Differ from That of Their Heterozygous Littermates

Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations

Related objects

Reset password