Punam Malik

researcher

Punam Malik is …
instance of (P31):
humanQ5

External links are
P269IdRef ID227012496
P213ISNI0000000499024116
P8189National Library of Israel J9U ID987007385844405171
P691NL CR AUT IDntk20211135520
P496ORCID iD0000-0002-5770-7280
P1053ResearcherIDR-5562-2018
P214VIAF ID59151963596400310450

P108employerSt. Jude Children's Research HospitalQ1164246
P101field of workhematologyQ103824
pediatricsQ123028
cancerQ12078
oncologyQ162555
gene therapyQ213901
hematopoietic system diseaseQ1963588
P735given namePunamQ122233444
PunamQ122233444
P1412languages spoken, written or signedEnglishQ1860
P106occupationscientistQ901
physicianQ39631
university teacherQ1622272
hematologistQ3144914
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q34763502A modified γ-retrovirus vector for X-linked severe combined immunodeficiency
Q92216646Abnormal submaximal cardiopulmonary exercise parameters predict impaired peak exercise performance in sickle cell anemia patients
Q52718038Angiotensin Receptor Signaling in Sickle Cell Anemia has a Reno-Protective effect on Urine Concentrating Ability but results in Sickle Glomerulopathy.
Q90282101Author Correction: Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Q93116167CRISPR-Cas9 fusion to dominant-negative 53BP1 enhances HDR and inhibits NHEJ specifically at Cas9 target sites
Q88751362Diastolic dysfunction is associated with exercise impairment in patients with sickle cell anemia
Q98240625Drug Therapies for the Management of Sickle Cell Disease
Q89532361Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Q48315547Losartan for the nephropathy of sickle cell anemia: A phase-2, multicenter trial.
Q39599891Perforin gene transfer into hematopoietic stem cells improves immune dysregulation in murine models of perforin deficiency
Q92151414Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia